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BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH                Reconstitute              To Give:               Vial               Product             Product Stability     Special
  (Storage Prior to Use,             With:                                       Stability                                                      Precautions/Notes
Manufacturer, Preservative
         Status)
      Aldesleukin
      22 million IU          1.2 mL SWI1,2             18 million IU/mL          48 h F1           50 mL D5W1                 48 h F1           - cytotoxic3
        (1.3 mg)                                        (1.1 mg/mL)1,2                                                                          - do not use in-line
       (Novartis)            direct diluent against                                              30 – 70 mcg/mL1                                filter1,2
        (F)(PFL)             side of vial during                                                                                                - avoid
    no preservative1         reconstitution1                                                   < 30 mcg/mL: dilute in                           bacteriostatic water
                                                                                                  D5W containing                                for injection or NS
                             do not shake1                                                     human albumin 0.1%2                              due to increased
                                                                                                                                                aggregation1

    Alemtuzumab                                                                                                                                 - cytotoxic7
                                                                          5                                     6
      30 mg/mL                        N/A             filter NOT required     discard unused        SC syringe          discard at the end of   - do not shake8
 (Genzyme previously                                                              portion5                                 the day F or RT
        Bayer)4                                           30 mg/mL5
       (F)(PFL)
     do not shake
   no preservative5

                                                                                               100 mL NS or D5W5            8 h F or RT5

                                                                                                                              **(PFL)8

     Alemtuzumab
      30 mg/3 mL                      N/A             use 5 micron filter     discard unused        SC syringe6         discard at the end of   - cytotoxic7
     (Schering/Ilex)                                  to withdraw drug            portion9                                the day F or RT8      - do not shake8
        (F)(PFL)                                       from ampoule8
      do not shake
    no preservative9                                      10 mg/mL9



        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                        1/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH               Reconstitute            To Give:                Vial               Product           Product Stability      Special
  (Storage Prior to Use,            With:                                      Stability                                                     Precautions/Notes
Manufacturer, Preservative
         Status)

                                                                                              100 mL NS or D5W9         8 h F or RT8

                                                                                                                          **(PFL)8

     Amifostine
       500 mg                 9.7 mL NS only10         50 mg/mL10          24 h F, 5 h RT10   25–50 mL*NS only10       5–40 mg/mL:           - noncytotoxic10
    (MedImmune)                                                                                                       24 h F,10 5 h RT       - discard cloudy
         (RT)                                                                                                                                solution11
   no preservative10

     Amsacrine
    75 mg/1.5 mL               glass syringes           5 mg/mL12             24 h RT12         500 mL D5W12        7 d F, 48 h RT12,13,14   - cytotoxic15
    (Erfa Canada)             preferred during
         (RT)                  reconstitution;                                  PFL12           (plastic or glass
   no preservative12         max. time in plastic                                                 container)12
                             syringe12: 15 min

                              13.5 mL supplied
                               diluent (L-lactic
                                    acid)1

                             transfer 1.5mL from
                               ampoule into the
                                 diluent vial12




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                    2/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
    DRUG & STRENGTH               Reconstitute           To Give:                Vial             Product             Product Stability       Special
   (Storage Prior to Use,            With:                                     Stability                                                      Precautions/Notes
Manufacturer, Preservative
          Status)
     Asparaginase16
 (asparaginase E. coli)      do not shake; roll to    2500 units/mL16        48 h F, RT16        syringe16               14 d F20, 16         - cytotoxic3
       10,000 units              reconstitute18,11
         (Orphan                   4 mL SWI19
     Pharmaceutical          Intradermal test11:
      International)          Reconstitute with
            (F)                 5 mL SWI to give
    no preservative17           2000 units/mL
                              Transfer 0.1 mL to
                                10 mL vial (or 12
                                mL syringe)
                              Add 9.9 mL SWI
                                roll to dissolve to
                                give 20 units/mL
                              2 unit test dose =
                                0.1 mL
                             (Note: the rest of the
                               reconstituted vial
                              has a concentration
                              of 2000 units/mL)11




                                                                                            50 mL*NS or D5W20,13   14 d F,20,13 2 d RT20,21




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                    3/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH               Reconstitute            To Give:                Vial              Product      Product Stability   Special
  (Storage Prior to Use,            With:                                      Stability                                            Precautions/Notes
Manufacturer, Preservative
         Status)
Erwinia asparaginase
(asparaginase Erwinia        do not shake; roll to     10000-5000         15 min in original       glass or     8 h in a glass or   - cytotoxic3
     chrysanthemi)              reconstitute22          units/mL          container; 8 h in a   polypropylene    polypropylene
      10,000 units                                                             glass or           syringe22         syringe22
        (Orphan                  1-2 mL NS22                                polypropylene
   Pharmaceuticals                                                            syringe22
     International)
           (F)
   no preservative22




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                             4/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial              Product        Product Stability   Special
  (Storage Prior to Use,           With:                                       Stability                                              Precautions/Notes
Manufacturer, Preservative
         Status)
 PEG-asparaginase
   (pegasparagase)                 N/A               750 units/mL23        discard unused   IM: maximum volume    syringe: 4 h23,24   - cytotoxic3
       (pegylated                                                             portion23      2 mL; if >2 mL use                       - discard cloudy
 asparaginase E. coli)                                                                         multiple sites23                       solution23
      750 units/mL                                                                                                                    - do not shake23
        (Enzon)                                                                                                                       - do not use if
           (F)                                                                                                                        stored out of
   no preservative23                                                                                                                  refrigerator for > 48
                                                                                                                                      h23
                                                                                                                                      - do not use if
                                                                                                                                      previously frozen23



                                                                                            IV: 100 mL NS or       bag: 4 h23,24
                                                                                            D5W23




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                               5/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH               Reconstitute            To Give:                Vial        Product        Product Stability   Special
  (Storage Prior to Use,            With:                                      Stability                                        Precautions/Notes
Manufacturer, Preservative
         Status)
      Azacitidine
        100 mg               4 mL SWI25                25 mg/mL25               8 h F,     SC syringe25      45 min RT25        - cytotoxic3
       (Celgene)                                                             45 min RT25
          (RT)               shake vigorously25                                                           prepare immediately   - discard if contains
   no preservative25                                                                                      before use and use    large particles25
                                                                                                            within 45 min, or
                                                                                                                discard.        - re-suspend
                                                                                                                                syringe contents
                                                                                                                                before injection by
                                                                                                                                vigorously rolling
                                                                                                                                syringe between
                                                                                                                                palms25
          BCG
         81 mg               do not shake; roll to   10.5 ± 8.7×108          2 h F, RT26   50 mL NS26      2 h F or RT after    - cytotoxic7
    (Sanofi Pasteur)            reconstitute26          CFU/vial                                            reconstitution26
        (F)(PFL)                                      (Connaught
     preservative26             3 mL supplied           strain)26                                              **(PFL)26
                                   diluent26

                                record time of
                                reconstitution




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                         6/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH               Reconstitute            To Give:                Vial              Product           Product Stability   Special
  (Storage Prior to Use,            With:                                      Stability                                                 Precautions/Notes
Manufacturer, Preservative
         Status)
          BCG
   (Tice substrain)          1 mL preservative          1 to 8×108          2 h F (PFL)27    transfer from vial to       2 h F27         - cytotoxic3
 50 mg = 1 to 8 x 108           free NS for             CFU/vial27                           60 mL syringe, rinse                        - overfill unknown
          CFU                    injection27                                                vial with another 1 mL                       - protect from
  (Hospira/Organon)                                                                            NS. Add rinse to                          light27
        (F)(PFL)             use reconstitution                                             same 60 mL syringe.                          - do not filter27
   no preservative27          device provided                                               qs to 50 mL with NS27

                             allow to stand for a
                             few minutes, then
                                gently swirl to
                                  suspend27




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                  7/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH                Reconstitute           To Give:                Vial           Product            Product Stability   Special
  (Storage Prior to Use,             With:                                     Stability                                               Precautions/Notes
Manufacturer, Preservative
         Status)
    Bendamustine
 25 mg single-use vial        25 mg vial: add 5         5 mg/mL28           30 minutes28      500 mL NS28      24 h F, 3 h RT28        - cytotoxic3
100 mg single-use vial            mL SWI
      (Cephalon)             100 mg vial: add 20                                            0.2-0.6 mg/mL28
       (RT)(PFL)                  mL SWI28
   no preservative28
                             Shake well to yield a
                             clear, colourless to a
                             pale yellow solution.
                                  Expected to
                              completely dissolve
                               within 5 minutes28

    Bevacizumab
     100 mg/4 mL                      N/A              25 mg/mL29          discard unused   1.4-16.5 mg/mL30      48 h F, RT21,29,30   - cytotoxic7
    400 mg/16 mL                                                              portion29                                                - do not shake29
       (Roche)                                                                              100-250 mL NS
       (F)(PFL)                                                                                only29,30
     do not shake
   no preservative29
      Bleomycin
         15 IU                    6 mL*NS31             2.5 IU/mL              48 h F31       50 mL*NS31             24 h RT31         - cytotoxic7
(NB: dose in units only)                                                                                                               - no overfill32
        (Bristol)
          (F)
   no preservative31




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                8/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial             Product        Product Stability   Special
  (Storage Prior to Use,           With:                                       Stability                                             Precautions/Notes
Manufacturer, Preservative
          Status)
      Bleomycin
           15 IU             6 mL*NS or SWI33          2.5 IU/mL33        48 h F, 24 h RT33   50 mL *NS, SWI33     24 h RT34         - cytotoxic7
(NB: dose in units only)                                                                                                             - no overfill35
        (Hospira)
         (F)(PFL)
   no preservative33
      Bortezomib
          3.5 mg               3.5 mL NS36              1 mg/mL36             2d RT13,37          syringe36         8 h RT38         - cytotoxic7
(Ortho Biotech formally
      Millennium)
       (RT)(PFL)
   no preservative36




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                              9/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial              Product           Product Stability     Special
  (Storage Prior to Use,           With:                                       Stability                                                   Precautions/Notes
Manufacturer, Preservative
         Status)
       Busulfan
     60 mg/10 mL                   N/A             use 5-micron nylon      discard unused   NS or D5W (dilute in        complete           - cytotoxic7
   (Orphan Medical)                                filter provided with       portion39     volume 10 times the    administration within
           (F)                                          ampoule to                          busulfan volume to ~       12 h F: NS39
   no preservative39                                 withdraw drug39                            0.5 mg/mL)39        8 h RT: NS, D5W

                                                        6 mg/mL39

     Carboplatin
     50 mg/5 mL                     N/A                10 mg/mL40          discard unused      0.3-10 mg/mL41      24 h RT,42 48 h F40     - cytotoxic7
    150 mg/15 mL                                                              portion40                                                    - do NOT use
    450 mg/45 mL                                                                                NS, D5W11,40                               aluminum-
       (Hospira)                                                                                                                           containing needle,
      (RT)(PFL)                                                                                 do NOT use                                 syringe or tubing41
   no preservative40                                                                        aluminum-containing
                                                                                             needle or syringe41

     Carboplatin
      50 mg/5 mL                   N/A                 10 mg/mL43          discard unused   0.5-10 mg/mL44               8 h RT43          - cytotoxic7
    150 mg/15 mL                                                             portion RT43                                                  - do NOT use
    450 mg/45 mL                                                                               NS, D5W11,43,45                             aluminum-
     (Novopharm)                                                                                                                           containing needle,
       (RT)(PFL)                                                                                do NOT use                                 syringe or tubing43
   no preservative43                                                                        aluminum-containing
                                                                                             needle or syringe43




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                   10/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH               Reconstitute            To Give:                Vial                 Product             Product Stability     Special
  (Storage Prior to Use,            With:                                      Stability                                                        Precautions/Notes
Manufacturer, Preservative
         Status)
      Carmustine
        100 mg                  3 mL diluent        3.3 mg/mL in 10%       24 h F, 8 h RT46    glass46 or polyolefin   24 h F: in glass,46 or   - cytotoxic7
     (Bristol Labs)             (supplied)46            ethanol46                                  container11         polyolefin container11   - do not use if
           (F)                                                                                                                                  product has oily
   no preservative46         diluent to reach RT,                                              500 mL NS or D5W46        use within 4 h of      droplets46
                              then dissolve drug                                                                        reconstitution RT46
                               with 3 mL diluent;
                               add 27 mL SWI46

                               record time of
                               reconstitution

      Cetuximab
     100 mg/50 mL                    N/A                2 mg/mL47          discard unused            syringe47           12 h F, 8 h RT47       - cytotoxic3
    200 mg/100 mL                                                         portion after 12 h                                                    - administer with a
    (ImClone/BMS)                                                            F, 8 h RT47                                                        0.2 or 0.22 micron
          (F)                                                                                                                                   low protein binding
      do not dilute                                                                              sterile evacuated       12 h F, 8 h RT47       in-line filter47
      do not shake                                                                             container or bag e.g.                            - normal saline
   no preservative47                                                                                 polyolefin,                                may be used to
                                                                                                   polyethylene,                                flush the line47
                                                                                                   ethylene vinyl                               - solution may
                                                                                                  acetate, DEHP                                 contain white
                                                                                               plasticized PVC, PVC                             particulates which
                                                                                                  bag, or glass47                               do not affect
                                                                                                                                                product quality47




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                       11/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial              Product           Product Stability   Special
  (Storage Prior to Use,           With:                                       Stability                                                 Precautions/Notes
Manufacturer, Preservative
         Status)
       Cisplatin
     10 mg/10 mL                    N/A                 1 mg/mL48             48 h RT49     < 60 mg: 100 mL NS*        48 h RT49         - cytotoxic7
     50 mg/50 mL                                                                            > 60 mg: 250 mL NS*                          - do NOT use
    100 mg/100mL                                                                                                                         aluminum-
        (Hospira)                                                                           500 or 1000 mL *NS,                          containing needle,
       (RT)(PFL)                                                                            D5-NS, D5-1/2S; D5-                          syringe or tubing48
   no preservative48                                                                        NS with mannitol; D5-
                                                                                                  1/2S with
                                                                                             mannitol48,50; D5W-
                                                                                             1/3S with mannitol48

                                                                                                do NOT use
                                                                                            aluminum-containing
                                                                                             needle or syringe48

      Cladribine
     10 mg/10 mL                   N/A                  1 mg/mL51          discard unused       SC syringe52        48h F, end of day    - cytotoxic7
   (Janssen-Ortho)                                                            portion51                                RT13,51,53,54     - shake vigorously
       (F)(PFL)                                                                                  cassette51                              to dissolve any
   no preservative51                                                                                                                     precipitates from
                                                                                                                                         refrigeration11
                                                                                                                                         - bacteriostatic NS
                                                                                                                                         contains benzyl
                                                                                                                                         alcohol51

                                                                                             500 mL NS only51          24 h RT51

                                                                                            Do NOT use D5W51


        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                  12/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial              Product            Product Stability   Special
  (Storage Prior to Use,           With:                                       Stability                                                  Precautions/Notes
Manufacturer, Preservative
         Status)

                                                                                             qs to 100 mL with        at least 7 days51
                                                                                             bacteriostatic NS
                                                                                               only via SIMS
                                                                                               DELTEC INC.
                                                                                               MEDICATION
                                                                                            CASSETTES®51; filter
                                                                                                drug and diluent
                                                                                            through 0.22u filter as
                                                                                            each solution is being
                                                                                              introduced into the
                                                                                                   medication

     Clodronate
    300 mg/10 mL                    N/A                 30 mg/mL           discard unused   500 mL NS or D5W55           12 h RT55        - noncytotoxic
        (Oryx)                                                                portion55
         (RT)
   no preservative55




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                    13/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial                 Product                Product Stability      Special
  (Storage Prior to Use,           With:                                       Stability                                                            Precautions/Notes
Manufacturer, Preservative
          Status)
 Cyclophosphamide
         200 mg                    NS56                20 mg/mL56          72 h F,56,57 24 h    < 1 g: 100 mL NS*         72 h F,56,57 24 h RT56    - cytotoxic7
         500 mg                                                                 RT56            > 1 g: 250 mL NS*
        1000 mg                200 mg: 10 mL                                                    high dose in BMT:
        2000 mg                500 mg: 25 mL                                                    may need 500 NS*
         (Baxter)             1000 mg: 50 mL
       (RT)(PFL)             2000 mg: 100 mL56                                                  NS, D5W, D5NS56
   no preservative56


    Cyclosporine                   N/A                 50 mg/mL58          discard unused           NS, D5W58            dilute immediately prior   - cytotoxic3
     50 mg/1 mL                                                               portion58                                           to use58
     250 mg/5 mL                                                                               dilute to concentration
      (Novartis)                                                                                  between 1:20 and                                  - polyoxyethylated
      (RT)(PFL)                                                                                         1:10058                                     castor oil/ethanol
   no preservative58                                                                                                                                vehicle58

                                                                                                                                                    - do NOT
                                                                                                                                                    refrigerate or
                                                                                                                                                    freeze58

                                                                                                                                                    - use non-PVC bag
                                                                                                                                                    and tubing59




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                          14/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial             Product               Product Stability       Special
  (Storage Prior to Use,           With:                                       Stability                                                        Precautions/Notes
Manufacturer, Preservative
         Status)
      Cytarabine
     100 mg/1 mL                    N/A               100 mg/mL60             24 h RT60    100 mL*NS, Water for     72 h F, 24 h RT from        - cytotoxic7
    1000 mg/10mL                                                                              Injection, D5W,       initial vial puncture60     - do not use for IT
    2000 mg/20mL              record time of                                                Lactated Ringer’s60                                 injection
        (Hospira)               puncture
       (RT)(PFL)
   no preservative60


      Cytarabine
     IT injection60                N/A                100 mg/mL60             24 h RT60     diluents containing     use within 4 h of initial   - cytotoxic7
     100 mg/1 mL                                                                           preservatives should       vial puncture11,13        - auxiliary label62:
    1000 mg/10mL              record time of                                                 NOT be used for                                    “IT”
    2000 mg/20mL                puncture                                                        intrathecal                                     - label to include
        (Hospira)                                                                             administration60                                  route in full (i.e.,
       (RT)(PFL)                                                                                                                                INTRATHECAL
   no preservative60                                                                          qs to 6 mL with                                   injection) attached
                                                                                           preservative free NS61                               to both syringe and
                                                                                                                                                outer ziplock bag62




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                     15/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH               Reconstitute            To Give:                Vial               Product          Product Stability   Special
  (Storage Prior to Use,            With:                                      Stability                                                 Precautions/Notes
Manufacturer, Preservative
         Status)
      Cytarabine
     SC injection:           100 mg: 5 mL BWI63         100 mg:              48 h RT63,64           syringe         14 d F, 48 h RT64    - cytotoxic7
        100 mg                                         20 mg/mL63                                                                        - for high dose
        (Pfizer)                                                                                                                         use, do not use
       (RT)(PFL)                                                                                                                         diluent containing
   no preservative63                                                                                                                     benzyl alcohol65
                                                                                                                                         - do not use for IT
                                                                                                                                         injection

    Dacarbazine
        100 mg                 100 mg: 9.9 mL          10 mg/mL66          72 h F, 8 h RT66   250-500 mL*NS or       24 h F, 8 h RT66    - cytotoxic7
        200 mg                     SWI66                                                            D5W                                  - protect container
       (Abraxis)              200 mg: 19.7 mL                                                                          **(PFL)11,66      from light during
       (F)(PFL)                    SWI66                                                                               see Special       storage and
   no preservative66                                                                                                Precautions/Notes    administration67
                                                                                                                         Column          - overfill unknown

    Dacarbazine
         200 mg               200 mg: 19.7 mL          10 mg/mL68          48 h F, 8 h RT68   0.19–3.0 mg/mL13,68       24 h F68         - cytotoxic7
         600 mg                    SWI68                                                                                                 - protect container
       (Hospira)              600 mg: 59.1 mL                                  (PFL)69        250-500 mL*NS or          **(PFL)67        from light during
        (F)(PFL)                   SWI68                                                            D5W                see Special       storage and
   no preservative68                                                                                                Precautions/Notes    administration67
                                                                                                                         Column          - no overfill69,35




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                  16/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial                Product                Product Stability   Special
  (Storage Prior to Use,           With:                                       Stability                                                        Precautions/Notes
Manufacturer, Preservative
         Status)
    Dactinomycin
         0.5 mg                  1.1 mL                0.5 mg/mL71           24 h F, RT72          syringe71,73         24 h F, RT
                                                                                                                                    74
                                                                                                                                                - cytotoxic3
       (Ovation)70           SWI(preservative         (500 mcg/mL)                                                                              - do not filter71,73
       (RT)(PFL)                 free)71                                                                                                        .
   no preservative71
                             Do NOT use SWI
                             with preservative
                                (may form
                               precipitate)71




                                      BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial                Product                Product Stability   Special
  (Storage Prior to Use,           With:                                       Stability                                                        Precautions/Notes
Manufacturer, Preservative
         Status)
     Daunorubicin
         20 mg                 4 mL SWI75             5 mg/mL75,78        48 h F, 24 h RT77       100-250 mL in           24 h RT, 48 h F75     - cytotoxic3
 (Erfa Canada Inc.)75                                                                         isotonic solution e.g.,
      (RT)(PFL)76                                                                                      NS75
   no preservative77
                                                                                               no data for D5W77




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                         17/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH                Reconstitute           To Give:                Vial               Product           Product Stability     Special
  (Storage Prior to Use,             With:                                     Stability                                                    Precautions/Notes
Manufacturer, Preservative
         Status)
     Daunorubicin
         20 mg                   4 mL SWI79             5 mg/mL79         24 h RT, 48 h F79      100-250 mL          48 h F, 24 h RT79      - cytotoxic7
     (Novopharm)                                                                                 NS or D5W11
       (RT)(PFL)                                                               (PFL)79                                   **(PFL)79
   no preservative79
     Dexrazoxane
        250 mg                supplied diluent80:      10 mg/mL80               6 h F80       empty viaflex bag80         6 h RT81          - cytotoxic82
        500 mg                 250 mg: 25 mL
        (Pfizer)               500 mg: 50 mL
          (RT)
   no preservative80
       Docetaxel
     20 mg/0.5 mL              supplied diluent :      10 mg/mL83           48 h F, RT13,85    0.3–0.74 mg/mL            complete           - cytotoxic7
      80 mg/2 mL                  - if vials were                                                                   administration within   - non-PVC bag and
    (Sanofi-Aventis)         refrigerated, allow to                                           (e.g., 250 mL NS or   4 h F,83 48 h RT86,87   tubing only83
     (F, RT) (PFL)             warm for 5 min at                                                     D5W)83
   no preservative83         RT. Withdraw entire
                                 contents of the
                             diluent and inject the
                               entire contents of
                              the syringe into the
                                 corresponding
                             concentrate vial. Mix
                                   by repeated
                             inversions for 45 sec
                                DO NOT SHAKE
                                   Let sit for 5
                                   minutes83,84




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                    18/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial          Product          Product Stability    Special
  (Storage Prior to Use,           With:                                       Stability                                             Precautions/Notes
Manufacturer, Preservative
         Status)

     Doxorubicin
        10 mg                 NS, SWI, D5W88            2 mg/mL88            48 h F, 24 h     syringe88     48 h F, 24 h RT13,89     - cytotoxic7
        50 mg                (NS reconstitution                                RT13,88
        150 mg                 takes longer)
       (Hospira)               10 mg: 5 mL
      (RT)(PFL)                50 mg: 25 mL
   no preservative88          150 mg: 75 mL

                                                                                            0.2–2 mg/mL90     48 h F, 24 h RT13,90

                                                                                            100 mL*NS88




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                             19/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial              Product         Product Stability   Special
  (Storage Prior to Use,           With:                                       Stability                                               Precautions/Notes
Manufacturer, Preservative
         Status)
     Doxorubicin
      10 mg/5 mL                   N/A                  2 mg/mL                 8 h91             syringe91       48 h F, 24 h RT91    - cytotoxic7
     20 mg/10 mL                                                                                                   from initial vial
     50 mg/25 mL              record time of                                                                          puncture
    200 mg/100 mL               puncture
     (Novopharm)
        (F)(PFL)
   no preservative91


     Doxorubicin
     10 mg/5 mL                    N/A                  2 mg/mL92          discard unused         syringe92       48 h F, 24 h RT92    - cytotoxic3
     50 mg/25 mL                                                              portion92,74
    200 mg/100 mL
        (Pfizer)
          (F)
   no preservative92

    Doxorubicin
Pegylated Liposomal                N/A                  2 mg/mL93          discard unused      < 90 mg: 250 mL        24 h F93         - cytotoxic7
    20 mg/10 mL                                                               portion93          D5W only93                            - do not filter93
    50 mg/25 mL
     (Schering)                                                                              ≥ 90 mg: 500mL D5W
         (F)                                                                                         only
  no preservative93




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                20/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial            Product           Product Stability      Special
  (Storage Prior to Use,           With:                                       Stability                                                  Precautions/Notes
Manufacturer, Preservative
          Status)
       Epirubicin
      10 mg/5 mL                   N/A                  2 mg/mL94               8 h94           syringe94       48 h F, 24 h RT from      - cytotoxic7
     50 mg/25 mL                                                                                                initial vial puncture94
    200 mg/100 mL             record time of
         (Pfizer)               puncture
        (F)(PFL)
   no preservative94

                                                                                           100 mL*NS or D5W11     2 d F, RT: NS or
                                                                                                                       D5W49




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                21/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                 Vial                  Product            Product Stability    Special
  (Storage Prior to Use,           With:                                        Stability                                                       Precautions/Notes
Manufacturer, Preservative
         Status)
       Etoposide
      100 mg/5 mL                   N/A                20 mg/mL95         14 d RT11,13,96,97,98    0.2– 0.4 mg/mL95    0.2 mg/mL:               - cytotoxic7
     500 mg/25 mL                                                                                                      48 h RT13,95             - use non-PVC bag
    1000 mg/50 mL                                                                                 500 mL*NS or D5W95   0.4 mg/mL:               and tubing only
         (BMS)                                                                                                         24 h RT95
          (RT)
     preservative95

      Etoposide                                                                                                        0.2-0.3 mg/mL:
     100 mg/5 mL                   N/A                 20 mg/mL99          discard unused                NS            7 d F,100 2 d RT87,100   - cytotoxic7
    200 mg/10 mL                                                              portion99                                0.4-0.5 mg/mL:           - use non-PVC bag
    500 mg/25 mL                                                                                       Stabilty is     1 d F,100 1 d RT100      and tubing only
    1000 mg/50 mL                                                                                    concentration     0.6-9.0mg/mL:
     (Novopharm)                                                                                      dependent        generally unstable100
      (RT)(PFL)                                                                                                        9.5 mg/mL:
   no preservative99                                                                                                   2 d F,100 1d RT100
                                                                                                                       10-12 mg/mL:
                                                                                                                       7 d F,100 2 d RT87,100


                                                                                                        D5W99                4 h RT99,101




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                        22/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial               Product           Product Stability   Special
  (Storage Prior to Use,           With:                                       Stability                                                  Precautions/Notes
Manufacturer, Preservative
         Status)
      Fludarabine
         50 mg                 2 mL SWI102            25 mg/mL102         48 h F or RT13,49   dilute to maximum of    48 h F, RT13,49     - cytotoxic7
        (Berlex)                                                                                  1 mg/mL102,103
           (F)
   no preservative102                                                                         100 mL*NS or D5W102


     Fludarabine
         50 mg                      N/A               25 mg/mL104          discard unused     dilute to maximum of   48 h F, 24 h RT104   - cytotoxic7
     (Novopharm)                                                              portion104            1 mg/mL104
          (F)
   no preservative104                                                                          100 mL*NS or D5W




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                   23/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial            Product        Product Stability   Special
  (Storage Prior to Use,           With:                                       Stability                                            Precautions/Notes
Manufacturer, Preservative
         Status)
     Fluorouracil
   5000 mg/100 mL                  N/A                50 mg/mL105            8 h RT105,106      syringe13       48 h RT13,21,106    - cytotoxic7
        (Hospira)
       (RT)(PFL)
   no preservative105




                                                                                              2-10 mg/mL in      24 h RT105,106
                                                                                                D5W105,106

                                                                                             50-1000 mL*D5W




                                                                                             CIVI: ambulatory   complete within
                                                                                                 pump106          8 d11,13,107




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                             24/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial           Product      Product Stability     Special
  (Storage Prior to Use,           With:                                       Stability                                           Precautions/Notes
Manufacturer, Preservative
         Status)




     Gemcitabine
        200 mg               200 mg: 5 mL NS          38 mg/mL108           48 h RT108,109    syringe108     48 h RT,13,108,109    - cytotoxic7
       1000 m g              1000 mg: 25 mL
       (Eli-Lilly)                NS108
         (RT)
   no preservative108




                                                                                             0.1–10 mg/mL   48 h F, RT13,108,109
                                                                                                NS108,109




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                           25/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH               Reconstitute            To Give:                Vial               Product        Product Stability    Special
  (Storage Prior to Use,            With:                                      Stability                                                Precautions/Notes
Manufacturer, Preservative
         Status)
     Gemcitabine
         200 mg               200 mg vial: 5 mL       38 mg/mL110           48 RT110,112,74       syringe110        24 h RT110,112      - cytotoxic7
        1000 mg                     NS
        2000 mg              1000 mg vial: 25 mL
        (Hospira)                   NS
          RT110              2000 mg vial: 50 mL
   no preservative111              NS110


                                                                                              26 mg/mL-0.1 mg/mL     48 h RT112,74
                                                                                                   NS110,112

     Gemcitabine
        200 mg                200 mg vial: 5mL        38 mg/mL114             24 h RT114        38 mg/mL – 0.1         24 RT114         - cytotoxic7
       1000 mg                      NS                                                           mg/mL NS114
     (Novopharm)             1000 mg vial: 25 mL
          RT                       NS114
   no preservative113

     Gemcitabine
        200 mg                200 mg vial: 5 mL       38 mg/mL115           48 h RT115,116        syringe115       48 h RT115,117,116   - cytotoxic7
       1000 mg                      NS
  (Sandoz Standard)          1000 mg vial: 25 mL
          RT                       NS115
   no preservative115




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                 26/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial            Product            Product Stability   Special
  (Storage Prior to Use,           With:                                       Stability                                                Precautions/Notes
Manufacturer, Preservative
         Status)

                                                                                           38 mg/mL-0.1 mg/mL   48 h RT13,119
                                                                                             NS or D5W115,118




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                 27/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial               Product             Product Stability      Special
  (Storage Prior to Use,           With:                                       Stability                                                       Precautions/Notes
Manufacturer, Preservative
          Status)
       Idarubicin
           5 mg              vial under negative       1 mg/mL120         48 h F,120 24 h RT        syringe         48 h F,13, 120 24 h RT13   - cytotoxic7
          10 mg                   pressure120                                  (PFL)120                                     (PFL)120
         (Pfizer)
       (RT)(PFL)              5 mg: 5 mL SWI
   no preservative120          10 mg: 10 mL
                                  SWI120
      Idarubicin
      5 mg/5 mL                     N/A                1 mg/mL120             same as               syringe         Discard 48 h F,13,120 24   - cytotoxic7
     10 mg/10 mL                                                            reconstituted                           h RT13
     20 mg/20 mL                                                             solution121                                   (PFL)120
         (Pfizer)
        (F)(PFL)
   no preservative120
      Ifosfamide
       1000 m g               1000 mg: 20 mL          50 mg/mL122            48 h F13,122       0.6–20 mg/mL122            72 h F122           - cytotoxic7
        3000 mg                   SWI122                                                                            24 h F, RT when mixed
        (Baxter)              3000 mg: 60 mL                                                   500–1000 mL*NS,           with mesna11
         (RT) 11                   SWI                                                           D5W, D5-NS,
   no preservative122                                                                          D5-1/2NS, Lactated      D5W or Lactated
                                 shake well                                                       Ringer’s11,122     Ringer’s when mixed

  Interferon Alfa -2b
   18 million IU/3 mL               N/A             6 million IU/mL123       48 h F13,123          syringe123              2 d F13,124         - cytotoxic7
       (Schering)
 (F)(or up to 7 days at
    RT before use)
   no preservative123


        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                     28/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH               Reconstitute             To Give:               Vial              Product           Product Stability   Special
  (Storage Prior to Use,            With:                                      Stability                                                 Precautions/Notes
Manufacturer, Preservative
         Status)

                                                                                            ≥ 0.3 million IU/mL123   24 h F, RT124

                                                                                                50 mL NS123

  Interferon Alfa -2b
  25 million IU/2.5 mL               N/A             10 million IU/mL123     48 h F13,123        syringe123            2 d F13,124       - cytotoxic7
       (Schering)
 (F)(or up to 7 days at
    RT before use)
   no preservative123


                                                                                            ≥ 0.3 million IU/mL123   24 h F, RT124

                                                                                                50 mL NS123

  Interferon Alfa -2b
      10 million IU            1 mL supplied         10 million IU/mL123      24 h F123          syringe123          24 h F, RT124       - cytotoxic7
       (Schering)             diluent (SWI) 123
          (F)
   no preservative123        do not shake; roll to
                               reconstitute123

                                                                                            > 0.1 million IU/mL124    48 h RT11,13

                                                                                               100 mL NS125




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                  29/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH               Reconstitute             To Give:               Vial                Product               Product Stability   Special
  (Storage Prior to Use,            With:                                      Stability                                                       Precautions/Notes
Manufacturer, Preservative
         Status)

                                 1 mL BWI123                               48 h F, RT13,123        syringe125          14 d F, 48 h RT13,125

                             do not shake; roll to
                                reconstitute123

                                                                                                 100 mL NS125                48 h RT11,13

  Interferon Alfa -2b
      18 million IU             1 mL supplied        18 million IU/mL123      24 h F123            syringe123               24 h F, RT124      - cytotoxic7
       (Schering)                 diluent123
          (F)
   no preservative123        do not shake; roll to
                               reconstitute123

                                                                                              > 0.1 million IU/mL126         48 h RT11,13

                                                                                                 100 mL NS125


                                 1 mL BWI123                                 48 h F, RT13          syringe123                14 d F13,125

                             do not shake; roll to
                               reconstitute123

                                                                                                 100 mL NS125                48 h RT11,13




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                        30/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial                 Product           Product Stability   Special
  (Storage Prior to Use,           With:                                       Stability                                                    Precautions/Notes
Manufacturer, Preservative
          Status)
       Irinotecan
      40 mg/2 mL                    N/A               20 mg/mL127         2 days RT13,128,129   0.12– 2.8 mg/mL127    24 h RT: D5W, NS127   - cytotoxic7
      100 mg/5 mL                                                                                                                           - do NOT
     500 mg/25 mL                                                                                 500 mL11 D5W           48 h F: D5W        refrigerate if in
        (Hospira)                                                                                (preferred), NS127        (PFL)127         NS130
       (RT)(PFL)
   no preservative127

      Irinotecan
      40 mg/2 mL                   N/A                20 mg/mL130          discard unused       0.12– 2.8 mg/mL130    24 h RT: D5W, NS130   - cytotoxic7
     100 mg/5 mL                                                              portion130                                                    - do NOT
        (Pfizer)                                                                                  500 mL11 D5W           48 h F: D5W        refrigerate if in
       (RT)(PFL)                                                                                 (preferred), NS130        (PFL)130         NS130
   no preservative130

      Irinotecan
      40 mg/2 mL                   N/A                20 mg/mL131          discard unused        0.12-2.8 mg/mL131    24 h RT: D5W NS131    - cytotoxic3
     100 mg/5 mL                                                             portion131,74                              48 h F: D5W131
        (Sandoz)                                                                                D5W (recommended)
       (RT)(PFL)                                                                                       NS131                (PFL)131
   no preservative131




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                      31/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial               Product             Product Stability   Special
  (Storage Prior to Use,           With:                                       Stability                                                    Precautions/Notes
Manufacturer, Preservative
         Status)
      Ixabepilone
         15 mg                8 mL supplied             2 mg/mL               1 h RT132        0.2 – 0.6 mg/mL in          6 h RT132        - cytotoxic3
   (contains 16 mg)              diluent                                                        Lactated Ringer’s                           - use 0.2-1.2
         45 mg                                                                                 Injection USP (use                           micron in-line
   (contains 47 mg)          23.5 mL supplied           2 mg/mL                                 non-PVC infusion                            filter132
         (BMS)                    diluent                                                          container)132                            - use non-PVC
        (F)(PFL)                                                                                                                            (i.e., DEHP-free)
   no preservative132                                                                                                                       administration
                                                                                                                                            set132

      Leucovorin
      50 mg/5 mL                    N/A               10 mg/mL133         5 mL vial: discard       syringe134              7 d F134         - noncytotoxic
    500 mg/50 mL                                                          unused portion133                              48 h RT87,134
       (Hospira)
        (F)(PFL)                                                           50 mL vial: 8 h
   no preservative133

                                                                                               0.05-10 mg/mL133      24 h RT133: NS, D5W,
                                                                                                                      Lactated Ringer’s,
                                                                                                                           Ringer’s


                                                                                                50-250 mL* NS,       8 h RT133: D10W, D5-
                                                                                                D5W, Lactated                 NS
                                                                                               Ringer’s, Ringer’s,
                                                                                                 D10W, D5-NS




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                     32/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial               Product             Product Stability     Special
  (Storage Prior to Use,           With:                                       Stability                                                      Precautions/Notes
Manufacturer, Preservative
         Status)
       Leucovorin
       50 mg/5 mL                 N/A135              10 mg/mL135         5 mL vial: discard        syringe                 8 h135,13         - noncytotoxic
     500 mg/50 mL                                                         unused portion135
      (Novopharm)
       (F)(PFL)135                                                           50 mL vial:
                                                                           discard unused
                                                                              portion135


                                                                                               0.060-1.0 mg/mL135    24 h RT NS, Lactated
                                                                                                                      Ringer’s, Ringer’s135


                                                                                                50-250 mL* NS,          12 h RT D5W,
                                                                                                D5W, Lactated             D10W135
                                                                                               Ringer’s, Ringer’s,
                                                                                               D10W, D10NS135          6 h RT D5NS135




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                     33/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH               Reconstitute            To Give:                Vial              Product         Product Stability     Special
  (Storage Prior to Use,            With:                                      Stability                                                 Precautions/Notes
Manufacturer, Preservative
         Status)
  Mechlorethamine
         10 mg                  do NOT use if          1 mg/mL136          use within 4 h of     syringe136           complete           - cytotoxic7
        (Ovation             discoloured or water                           reconstitution                          administration
Pharmaceuticals/Merck)       droplets form in vial                             RT11,13                           4 h of reconstitution
   no preservative136               before                                                                            RT11,13,136
                               reconstitution136

                             10 mL SWI or NS136

                                record time of
                                reconstitution




                                                                                               100 mL NS49,136         complete
                                                                                                                 administration within
                                                                                                                 4 h of reconstitution
                                                                                                                       RT13,49,136




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                 34/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                Vial                Product              Product Stability       Special
  (Storage Prior to Use,           With:                                       Stability                                                          Precautions/Notes
Manufacturer, Preservative
         Status)
Medroxyprogesterone
     250 mg/5 mL                    N/A                50 mg/mL18          use within 4 h of    syringe: IM only18    use within 4 h of initial   - cytotoxic7
        (Pfizer)                                                                initial                                 vial puncture11,137       - auxiliary label:
          (RT)                 record time of                               puncture11,137                                                        shake before use18
     preservative18              puncture


Medroxyprogesterone
        Depo                        N/A               150 mg/mL18          use within 4 h of    syringe: IM only18    use within 4 h of initial   - cytotoxic7
     150 mg/1mL                                                                 initial                                   puncture11,137          - auxiliary label:
       (Pfizer)                record time of                               puncture11,137                                                        shake before use18
         (RT)                    puncture
    preservative18
      Melphalan
        50 mg                  10mL supplied           5 mg/mL138             2 h RT138        0.1– 0.45 mg/mL in              complete           - cytotoxic7
        (GSK)                    diluent138                                                        NS only138          administration within
      (RT)(PFL)                                                               do NOT                                    60 min from time of
  no preservative138          immediately after                              refrigerate       (e.g., > 45 mg and <   initial reconstitution at
                               adding diluent,                                                  110 mg in 250 mL                 RT11
                             shake vigorously138                                                        NS)*

                               record time of
                               reconstitution




        BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                       35/77
        Activation Date: 2 March 2006
        Revised Date: 1 July 2010
Mesna
 1000 mg/10mL                   N/A                100 mg/mL139         14 d F, RT13,139       > 1mg/mL139          48 h F, 24 h RT139    - noncytotoxic
     (PPC)
      (RT)                                                                                     NS or D5W
 preservative139

  Methotrexate
   50 mg/2mL                     N/A               25 mg/mL140          50mg: discard             syringe           2 d F, RT11,141,142   - cytotoxic7
  500 mg/20mL                                                          unused portion140                                                  - for high-dose
    1 g/40mL                                                                                                                              regimens (e.g., 1-8
   5 g/200mL                                                            500mg, 1 g, 5 g:                                                  g/m2 as a single
     (Hospira)                                                            8 h F, RT140                                                    dose)143 use
    (RT)(PFL)                                                                                                                             preservative-free
no preservative140                                                                                                                        methotrexate11
                                                                                                                                          - do not use for IT
                                                                                                                                           injection


                                                                                             0.4–2 mg/mL140            24 h RT140

                                                                                                100 mL*
                                                                                                NS, D5W

                                                                                           high dose (e.g., 1-8
                                                                                             g/m2 as a single
                                                                                           dose)143,144-146: 500–
                                                                                                1000 mL*




     BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                     36/77
     Activation Date: 2 March 2006
     Revised Date: 1 July 2010
Methotrexate
   IT Injection140:               N/A                25 mg/mL140          discard unused        qs to 6 mL with       use within 4 h of initial   - cytotoxic7
Only preservative free                                                       portion140      preservative free NS61       puncture11,13           - auxiliary label62:
methotrexate may be                                                                                                                               “IT”
 administered by the                                                                                                                              - label to include
 intrathecal route140                                                                                                                             route in full (i.e.,
    50 mg/2mL147                                                                                                                                  INTRATHECAL
       (Hospira)                                                                                                                                  injection) attached
      (RT)(PFL)                                                                                                                                   to both syringe and
  no preservative140                                                                                                                              outer ziplock bag62

   Methotrexate
     50 mg/2mL                    N/A                25 mg/mL140             24 h F141              syringe                 14 d F87,141          - cytotoxic7
   500 mg/20mL                                                                                                                                    - high-dose
      (Hospira)                                                                                                                                   regimen(e.g., 1-8
     (RT)(PFL)                                                                                                                                    g/m2 as a single
   preservative140                                                                                                                                dose)144-146: use
                                                                                                                                                  preservative-free
                                                                                                                                                  methotrexate11
                                                                                                                                                  - do not use for IT
                                                                                                                                                  injection


                                                                                                0.4–2 mg/mL140               4 h RT140

                                                                                               e.g., 100 mL*NS,
                                                                                                     D5W140

     Mitomycin
         5 mg                    SWI                 0.5 mg/mL148         48 h F, RT13,148         syringe13           14 d F, 48 h RT13,148      - cytotoxic7
        20 mg                5 mg: 10 mL                                     (PFL)148
    (Novopharm)              20 mg: 40 mL
      (RT)(PFL)
  no preservative148          shake well148



       BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                        37/77
       Activation Date: 2 March 2006
       Revised Date: 1 July 2010
0.02-0.04 mg/mL148       3 h RT: D5W
                                                                                                                    12 h RT: NS
                                                                                          NS, D5W, sodium         24 h RT: sodium
                                                                                              lactate148             lactate148

   Mitomycin
       5 mg                    SWI                 0.5 mg/mL149        48 h F, RT13,149       syringe11        14 d F, 48 h RT11,21      - cytotoxic7
      20 mg                5 mg: 10 mL
      (BMS)                20 mg: 40 mL                                     (PFL)149
    (RT)(PFL)
no preservative149          shake well149

                                                                                          0.02–0.04 mg/mL           12 h RT: NS
                                                                                                                      3h: D5W
                                                                                          NS, D5W, sodium      24 h: sodium lactate149
                                                                                              lactate149




     BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                   38/77
     Activation Date: 2 March 2006
     Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH             Reconstitute              To Give:                 Vial           Product         Product Stability   Special
  (Storage Prior to Use,          With:                                         Stability                                            Precautions/Notes
Manufacturer, Preservative
         Status)
     Mitoxantrone
     20 mg/10 mL                   N/A                 2 mg/mL150           discard unused   0.2-0.6 mg/mL150   NS: 24 h F, RT150    - cytotoxic7
    25 mg/12.5 mL                                                              portion150
        (Hospira)                                                                              NS, D5W150          **(PFL)150
       (RT)(PFL)
   no preservative150                                                                          > 50 mL*150

    Mitoxantrone
     20 mg/10 mL                   N/A                 2 mg/mL151           discard unused     NS, D5W151          24 h RT151        - cytotoxic7
     (Novopharm)                                                               portion151
      (RT)(PFL)                                                                                > 50 mL*151         **(PFL)152
  no preservative151
    Mitoxantrone
     20 mg/10 mL                   N/A                 2 mg/mL153           discard unused      NS, D5W2           24 h RT153        - cytotoxic7
   (Pharmaceutical                                                             portion153      > 50 mL*153
 Partners of Canada)
         (RT)
  no preservative153




         BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                             39/77
         Activation Date: 2 March 2006
         Revised Date: 1 July 2010
Octreotide
  50 mcg/mL; 100                 N/A                 50 mcg/mL            discard unused       sc syringe154       single use vials: use   - noncytotoxic
mcg/mL; 500 mcg/mL                                  100 mcg/mL               portion154                                  within 4 h
    (Novopharm)                                    500 mcg/mL154                                                   multidose vials: use
       (F)(PFL)                                                                                                     within 14 d F74,154
  no preservative
multidose vials (5mL):
      200 µg/mL
       (F)(PFL)
                 154
   preservative


                                                   200 mcg/mL154            14 d F74,154      infusion: NS154       single use vials or
                                                                                                                   multidose vials: 24 h
                                                                                                                           RT154

     Octreotide
    (Sandostatin)                N/A               200 mcg/mL18           discard unused   50–200 mL NS18,11,156        24 h RT18          - noncytotoxic10
   1000 mcg/5 mL                                                             portion155
      (Novartis)
      (F)(PFL)                                                                              SC infusion: adjust
    preservative18                                                                           volume to ensure
                                                                                            infusion rate of 25
                                                                                                  mcg/h18




       BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                    40/77
       Activation Date: 2 March 2006
       Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                 Vial             Product               Product Stability       Special
  (Storage Prior to Use,           With:                                        Stability                                                        Precautions/Notes
Manufacturer, Preservative
         Status)
       Octreotide
     (Sandostatin)                 N/A                 50 mcg/mL            discard unused     50-100 mL11,156              24 h RT18            - noncytotoxic10
      50 mcg/1 mL                                     100 mcg/mL               portion18
     100 mcg/1 mL                                    500 mcg/mL18                                    NS18
     500 mcg/1 mL
       (Novartis)                                                                            SC infusion: adjust
        (F)(PFL)                                                                              volume to ensure
   no preservative18                                                                         infusion rate of 25
                                                                                                   mcg/h18

      Octreotide
  (Sandostatin LAR)           2 mL supplied         10 mg: 5 mg/mL          discard unused    deep intragluteal      use within 4 h of initial   - noncytotoxic10
        10 mg                    diluent            20 mg: 10 mg/mL            portion18     administration only18     reconstitution18,13       - do NOT shake
        20 mg                                      30 mg: 15 mg/mL18
        30 mg                 gently run 2 mL
      (Novartis)             down sides of the
       (F)(PFL)                vial; do NOT
    preservative155           disturb for 2–5
                              min, then swirl
                               moderately18

                              record time of
                              reconstitution




         BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                     41/77
         Activation Date: 2 March 2006
         Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH             Reconstitute              To Give:                 Vial              Product               Product Stability       Special
  (Storage Prior to Use,          With:                                         Stability                                                         Precautions/Notes
Manufacturer, Preservative
         Status)
       Oxaliplatin
      50 mg/10 mL                  N/A                 5 mg/mL157           discard unused     0.2-1.3 mg/mL158           0.2-1.3 mg/mL:          - cytotoxic7
     100 mg/20 mL                                                              portion157                             14 d F, 48 h RT159,87,158   - do NOT use
     200 mg/40 mL                                                                             1.3–2 mg/mL157,158                                  aluminum-
    (Sanofi-Aventis)                                                                                                      1.3-2 mg/mL:            containing needle,
       (RT)(PFL)                                                                             250–500 mL D5W157          48 h F, 24 h RT157        syringe or
   no preservative157                                                                                                                             tubing157
                                                                                              do NOT use NS or
                                                                                                other chloride-
                                                                                             containing solution157

                                                                                                 do NOT use
                                                                                             aluminum-containing
                                                                                             needle and syringe157




         BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                      42/77
         Activation Date: 2 March 2006
         Revised Date: 1 July 2010
BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART
   DRUG & STRENGTH              Reconstitute             To Give:                 Vial             Product              Product Stability   Special
  (Storage Prior to Use,           With:                                        Stability                                                   Precautions/Notes
Manufacturer, Preservative
         Status)
      Oxaliplatin
         50 mg                  SWI, D5W:              5 mg/mL160              24 h F160        500 mL D5W             24 h F, 6 h RT160    - cytotoxic7
        100 mg                 50 mg: 10 mL                                                                                                 - do NOT use
      (Sigmacon)              100 mg: 20 mL                                                   do NOT use NS or                              aluminum-
          (RT)                                                                                  other chloride-                             containing needle,
   no preservative160        do NOT use NS or                                                containing solutions                           syringe or tubing160
                               other chloride-                                                  (degrades)160
                                 containing
                                 solution160                                                    do NOT use
                                                                                            aluminum-containing
                                do NOT use                                                  needle and syringe160
                                 aluminum-
                             containing needle
                               and syringe160

       Paclitaxel
      30 mg/5 mL                   N/A                 6 mg/mL162              8 h RT162    0.3–1.2 mg/mL in NS,    0.3-1.2 mg/mL:          - cytotoxic7
    100 mg/16.7 mL                                                                          D5W162                  24 h RT162              - use non-PVC bag
     300 mg/50 mL                                                                           (e.g., 100–1000 mL)*                            and tubing with in-
        (Biolyse)                                                                                                   0.1 mg/mL:              line filter162
         (RT)161                                                                                                    44 h F, RT163
    no preservative                                                                         0.1 mg/mL in NS163
                                                                                                                    0.012-0.09 mg/mL:
                                                                                            0.012-0.1 mg/mL164      16 h RT164




         BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00                                    43/77
         Activation Date: 2 March 2006
         Revised Date: 1 July 2010
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART
CHEMOTHERAPY PREPARATION AND STABILITY CHART

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CHEMOTHERAPY PREPARATION AND STABILITY CHART

  • 1. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Aldesleukin 22 million IU 1.2 mL SWI1,2 18 million IU/mL 48 h F1 50 mL D5W1 48 h F1 - cytotoxic3 (1.3 mg) (1.1 mg/mL)1,2 - do not use in-line (Novartis) direct diluent against 30 – 70 mcg/mL1 filter1,2 (F)(PFL) side of vial during - avoid no preservative1 reconstitution1 < 30 mcg/mL: dilute in bacteriostatic water D5W containing for injection or NS do not shake1 human albumin 0.1%2 due to increased aggregation1 Alemtuzumab - cytotoxic7 5 6 30 mg/mL N/A filter NOT required discard unused SC syringe discard at the end of - do not shake8 (Genzyme previously portion5 the day F or RT Bayer)4 30 mg/mL5 (F)(PFL) do not shake no preservative5 100 mL NS or D5W5 8 h F or RT5 **(PFL)8 Alemtuzumab 30 mg/3 mL N/A use 5 micron filter discard unused SC syringe6 discard at the end of - cytotoxic7 (Schering/Ilex) to withdraw drug portion9 the day F or RT8 - do not shake8 (F)(PFL) from ampoule8 do not shake no preservative9 10 mg/mL9 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 1/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 2. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) 100 mL NS or D5W9 8 h F or RT8 **(PFL)8 Amifostine 500 mg 9.7 mL NS only10 50 mg/mL10 24 h F, 5 h RT10 25–50 mL*NS only10 5–40 mg/mL: - noncytotoxic10 (MedImmune) 24 h F,10 5 h RT - discard cloudy (RT) solution11 no preservative10 Amsacrine 75 mg/1.5 mL glass syringes 5 mg/mL12 24 h RT12 500 mL D5W12 7 d F, 48 h RT12,13,14 - cytotoxic15 (Erfa Canada) preferred during (RT) reconstitution; PFL12 (plastic or glass no preservative12 max. time in plastic container)12 syringe12: 15 min 13.5 mL supplied diluent (L-lactic acid)1 transfer 1.5mL from ampoule into the diluent vial12 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 2/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 3. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Asparaginase16 (asparaginase E. coli) do not shake; roll to 2500 units/mL16 48 h F, RT16 syringe16 14 d F20, 16 - cytotoxic3 10,000 units reconstitute18,11 (Orphan 4 mL SWI19 Pharmaceutical Intradermal test11: International)  Reconstitute with (F) 5 mL SWI to give no preservative17 2000 units/mL  Transfer 0.1 mL to 10 mL vial (or 12 mL syringe)  Add 9.9 mL SWI roll to dissolve to give 20 units/mL  2 unit test dose = 0.1 mL (Note: the rest of the reconstituted vial has a concentration of 2000 units/mL)11 50 mL*NS or D5W20,13 14 d F,20,13 2 d RT20,21 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 3/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 4. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Erwinia asparaginase (asparaginase Erwinia do not shake; roll to 10000-5000 15 min in original glass or 8 h in a glass or - cytotoxic3 chrysanthemi) reconstitute22 units/mL container; 8 h in a polypropylene polypropylene 10,000 units glass or syringe22 syringe22 (Orphan 1-2 mL NS22 polypropylene Pharmaceuticals syringe22 International) (F) no preservative22 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 4/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 5. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) PEG-asparaginase (pegasparagase) N/A 750 units/mL23 discard unused IM: maximum volume syringe: 4 h23,24 - cytotoxic3 (pegylated portion23 2 mL; if >2 mL use - discard cloudy asparaginase E. coli) multiple sites23 solution23 750 units/mL - do not shake23 (Enzon) - do not use if (F) stored out of no preservative23 refrigerator for > 48 h23 - do not use if previously frozen23 IV: 100 mL NS or bag: 4 h23,24 D5W23 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 5/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 6. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Azacitidine 100 mg 4 mL SWI25 25 mg/mL25 8 h F, SC syringe25 45 min RT25 - cytotoxic3 (Celgene) 45 min RT25 (RT) shake vigorously25 prepare immediately - discard if contains no preservative25 before use and use large particles25 within 45 min, or discard. - re-suspend syringe contents before injection by vigorously rolling syringe between palms25 BCG 81 mg do not shake; roll to 10.5 ± 8.7×108 2 h F, RT26 50 mL NS26 2 h F or RT after - cytotoxic7 (Sanofi Pasteur) reconstitute26 CFU/vial reconstitution26 (F)(PFL) (Connaught preservative26 3 mL supplied strain)26 **(PFL)26 diluent26 record time of reconstitution BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 6/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 7. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) BCG (Tice substrain) 1 mL preservative 1 to 8×108 2 h F (PFL)27 transfer from vial to 2 h F27 - cytotoxic3 50 mg = 1 to 8 x 108 free NS for CFU/vial27 60 mL syringe, rinse - overfill unknown CFU injection27 vial with another 1 mL - protect from (Hospira/Organon) NS. Add rinse to light27 (F)(PFL) use reconstitution same 60 mL syringe. - do not filter27 no preservative27 device provided qs to 50 mL with NS27 allow to stand for a few minutes, then gently swirl to suspend27 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 7/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 8. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Bendamustine 25 mg single-use vial 25 mg vial: add 5 5 mg/mL28 30 minutes28 500 mL NS28 24 h F, 3 h RT28 - cytotoxic3 100 mg single-use vial mL SWI (Cephalon) 100 mg vial: add 20 0.2-0.6 mg/mL28 (RT)(PFL) mL SWI28 no preservative28 Shake well to yield a clear, colourless to a pale yellow solution. Expected to completely dissolve within 5 minutes28 Bevacizumab 100 mg/4 mL N/A 25 mg/mL29 discard unused 1.4-16.5 mg/mL30 48 h F, RT21,29,30 - cytotoxic7 400 mg/16 mL portion29 - do not shake29 (Roche) 100-250 mL NS (F)(PFL) only29,30 do not shake no preservative29 Bleomycin 15 IU 6 mL*NS31 2.5 IU/mL 48 h F31 50 mL*NS31 24 h RT31 - cytotoxic7 (NB: dose in units only) - no overfill32 (Bristol) (F) no preservative31 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 8/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 9. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Bleomycin 15 IU 6 mL*NS or SWI33 2.5 IU/mL33 48 h F, 24 h RT33 50 mL *NS, SWI33 24 h RT34 - cytotoxic7 (NB: dose in units only) - no overfill35 (Hospira) (F)(PFL) no preservative33 Bortezomib 3.5 mg 3.5 mL NS36 1 mg/mL36 2d RT13,37 syringe36 8 h RT38 - cytotoxic7 (Ortho Biotech formally Millennium) (RT)(PFL) no preservative36 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 9/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 10. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Busulfan 60 mg/10 mL N/A use 5-micron nylon discard unused NS or D5W (dilute in complete - cytotoxic7 (Orphan Medical) filter provided with portion39 volume 10 times the administration within (F) ampoule to busulfan volume to ~ 12 h F: NS39 no preservative39 withdraw drug39 0.5 mg/mL)39 8 h RT: NS, D5W 6 mg/mL39 Carboplatin 50 mg/5 mL N/A 10 mg/mL40 discard unused 0.3-10 mg/mL41 24 h RT,42 48 h F40 - cytotoxic7 150 mg/15 mL portion40 - do NOT use 450 mg/45 mL NS, D5W11,40 aluminum- (Hospira) containing needle, (RT)(PFL) do NOT use syringe or tubing41 no preservative40 aluminum-containing needle or syringe41 Carboplatin 50 mg/5 mL N/A 10 mg/mL43 discard unused 0.5-10 mg/mL44 8 h RT43 - cytotoxic7 150 mg/15 mL portion RT43 - do NOT use 450 mg/45 mL NS, D5W11,43,45 aluminum- (Novopharm) containing needle, (RT)(PFL) do NOT use syringe or tubing43 no preservative43 aluminum-containing needle or syringe43 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 10/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 11. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Carmustine 100 mg 3 mL diluent 3.3 mg/mL in 10% 24 h F, 8 h RT46 glass46 or polyolefin 24 h F: in glass,46 or - cytotoxic7 (Bristol Labs) (supplied)46 ethanol46 container11 polyolefin container11 - do not use if (F) product has oily no preservative46 diluent to reach RT, 500 mL NS or D5W46 use within 4 h of droplets46 then dissolve drug reconstitution RT46 with 3 mL diluent; add 27 mL SWI46 record time of reconstitution Cetuximab 100 mg/50 mL N/A 2 mg/mL47 discard unused syringe47 12 h F, 8 h RT47 - cytotoxic3 200 mg/100 mL portion after 12 h - administer with a (ImClone/BMS) F, 8 h RT47 0.2 or 0.22 micron (F) low protein binding do not dilute sterile evacuated 12 h F, 8 h RT47 in-line filter47 do not shake container or bag e.g. - normal saline no preservative47 polyolefin, may be used to polyethylene, flush the line47 ethylene vinyl - solution may acetate, DEHP contain white plasticized PVC, PVC particulates which bag, or glass47 do not affect product quality47 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 11/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 12. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Cisplatin 10 mg/10 mL N/A 1 mg/mL48 48 h RT49 < 60 mg: 100 mL NS* 48 h RT49 - cytotoxic7 50 mg/50 mL > 60 mg: 250 mL NS* - do NOT use 100 mg/100mL aluminum- (Hospira) 500 or 1000 mL *NS, containing needle, (RT)(PFL) D5-NS, D5-1/2S; D5- syringe or tubing48 no preservative48 NS with mannitol; D5- 1/2S with mannitol48,50; D5W- 1/3S with mannitol48 do NOT use aluminum-containing needle or syringe48 Cladribine 10 mg/10 mL N/A 1 mg/mL51 discard unused SC syringe52 48h F, end of day - cytotoxic7 (Janssen-Ortho) portion51 RT13,51,53,54 - shake vigorously (F)(PFL) cassette51 to dissolve any no preservative51 precipitates from refrigeration11 - bacteriostatic NS contains benzyl alcohol51 500 mL NS only51 24 h RT51 Do NOT use D5W51 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 12/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 13. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) qs to 100 mL with at least 7 days51 bacteriostatic NS only via SIMS DELTEC INC. MEDICATION CASSETTES®51; filter drug and diluent through 0.22u filter as each solution is being introduced into the medication Clodronate 300 mg/10 mL N/A 30 mg/mL discard unused 500 mL NS or D5W55 12 h RT55 - noncytotoxic (Oryx) portion55 (RT) no preservative55 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 13/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 14. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Cyclophosphamide 200 mg NS56 20 mg/mL56 72 h F,56,57 24 h < 1 g: 100 mL NS* 72 h F,56,57 24 h RT56 - cytotoxic7 500 mg RT56 > 1 g: 250 mL NS* 1000 mg 200 mg: 10 mL high dose in BMT: 2000 mg 500 mg: 25 mL may need 500 NS* (Baxter) 1000 mg: 50 mL (RT)(PFL) 2000 mg: 100 mL56 NS, D5W, D5NS56 no preservative56 Cyclosporine N/A 50 mg/mL58 discard unused NS, D5W58 dilute immediately prior - cytotoxic3 50 mg/1 mL portion58 to use58 250 mg/5 mL dilute to concentration (Novartis) between 1:20 and - polyoxyethylated (RT)(PFL) 1:10058 castor oil/ethanol no preservative58 vehicle58 - do NOT refrigerate or freeze58 - use non-PVC bag and tubing59 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 14/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 15. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Cytarabine 100 mg/1 mL N/A 100 mg/mL60 24 h RT60 100 mL*NS, Water for 72 h F, 24 h RT from - cytotoxic7 1000 mg/10mL Injection, D5W, initial vial puncture60 - do not use for IT 2000 mg/20mL record time of Lactated Ringer’s60 injection (Hospira) puncture (RT)(PFL) no preservative60 Cytarabine IT injection60 N/A 100 mg/mL60 24 h RT60 diluents containing use within 4 h of initial - cytotoxic7 100 mg/1 mL preservatives should vial puncture11,13 - auxiliary label62: 1000 mg/10mL record time of NOT be used for “IT” 2000 mg/20mL puncture intrathecal - label to include (Hospira) administration60 route in full (i.e., (RT)(PFL) INTRATHECAL no preservative60 qs to 6 mL with injection) attached preservative free NS61 to both syringe and outer ziplock bag62 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 15/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 16. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Cytarabine SC injection: 100 mg: 5 mL BWI63 100 mg: 48 h RT63,64 syringe 14 d F, 48 h RT64 - cytotoxic7 100 mg 20 mg/mL63 - for high dose (Pfizer) use, do not use (RT)(PFL) diluent containing no preservative63 benzyl alcohol65 - do not use for IT injection Dacarbazine 100 mg 100 mg: 9.9 mL 10 mg/mL66 72 h F, 8 h RT66 250-500 mL*NS or 24 h F, 8 h RT66 - cytotoxic7 200 mg SWI66 D5W - protect container (Abraxis) 200 mg: 19.7 mL **(PFL)11,66 from light during (F)(PFL) SWI66 see Special storage and no preservative66 Precautions/Notes administration67 Column - overfill unknown Dacarbazine 200 mg 200 mg: 19.7 mL 10 mg/mL68 48 h F, 8 h RT68 0.19–3.0 mg/mL13,68 24 h F68 - cytotoxic7 600 mg SWI68 - protect container (Hospira) 600 mg: 59.1 mL (PFL)69 250-500 mL*NS or **(PFL)67 from light during (F)(PFL) SWI68 D5W see Special storage and no preservative68 Precautions/Notes administration67 Column - no overfill69,35 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 16/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 17. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Dactinomycin 0.5 mg 1.1 mL 0.5 mg/mL71 24 h F, RT72 syringe71,73 24 h F, RT 74 - cytotoxic3 (Ovation)70 SWI(preservative (500 mcg/mL) - do not filter71,73 (RT)(PFL) free)71 . no preservative71 Do NOT use SWI with preservative (may form precipitate)71 BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Daunorubicin 20 mg 4 mL SWI75 5 mg/mL75,78 48 h F, 24 h RT77 100-250 mL in 24 h RT, 48 h F75 - cytotoxic3 (Erfa Canada Inc.)75 isotonic solution e.g., (RT)(PFL)76 NS75 no preservative77 no data for D5W77 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 17/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 18. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Daunorubicin 20 mg 4 mL SWI79 5 mg/mL79 24 h RT, 48 h F79 100-250 mL 48 h F, 24 h RT79 - cytotoxic7 (Novopharm) NS or D5W11 (RT)(PFL) (PFL)79 **(PFL)79 no preservative79 Dexrazoxane 250 mg supplied diluent80: 10 mg/mL80 6 h F80 empty viaflex bag80 6 h RT81 - cytotoxic82 500 mg 250 mg: 25 mL (Pfizer) 500 mg: 50 mL (RT) no preservative80 Docetaxel 20 mg/0.5 mL supplied diluent : 10 mg/mL83 48 h F, RT13,85 0.3–0.74 mg/mL complete - cytotoxic7 80 mg/2 mL - if vials were administration within - non-PVC bag and (Sanofi-Aventis) refrigerated, allow to (e.g., 250 mL NS or 4 h F,83 48 h RT86,87 tubing only83 (F, RT) (PFL) warm for 5 min at D5W)83 no preservative83 RT. Withdraw entire contents of the diluent and inject the entire contents of the syringe into the corresponding concentrate vial. Mix by repeated inversions for 45 sec DO NOT SHAKE Let sit for 5 minutes83,84 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 18/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 19. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Doxorubicin 10 mg NS, SWI, D5W88 2 mg/mL88 48 h F, 24 h syringe88 48 h F, 24 h RT13,89 - cytotoxic7 50 mg (NS reconstitution RT13,88 150 mg takes longer) (Hospira) 10 mg: 5 mL (RT)(PFL) 50 mg: 25 mL no preservative88 150 mg: 75 mL 0.2–2 mg/mL90 48 h F, 24 h RT13,90 100 mL*NS88 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 19/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 20. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Doxorubicin 10 mg/5 mL N/A 2 mg/mL 8 h91 syringe91 48 h F, 24 h RT91 - cytotoxic7 20 mg/10 mL from initial vial 50 mg/25 mL record time of puncture 200 mg/100 mL puncture (Novopharm) (F)(PFL) no preservative91 Doxorubicin 10 mg/5 mL N/A 2 mg/mL92 discard unused syringe92 48 h F, 24 h RT92 - cytotoxic3 50 mg/25 mL portion92,74 200 mg/100 mL (Pfizer) (F) no preservative92 Doxorubicin Pegylated Liposomal N/A 2 mg/mL93 discard unused < 90 mg: 250 mL 24 h F93 - cytotoxic7 20 mg/10 mL portion93 D5W only93 - do not filter93 50 mg/25 mL (Schering) ≥ 90 mg: 500mL D5W (F) only no preservative93 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 20/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 21. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Epirubicin 10 mg/5 mL N/A 2 mg/mL94 8 h94 syringe94 48 h F, 24 h RT from - cytotoxic7 50 mg/25 mL initial vial puncture94 200 mg/100 mL record time of (Pfizer) puncture (F)(PFL) no preservative94 100 mL*NS or D5W11 2 d F, RT: NS or D5W49 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 21/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 22. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Etoposide 100 mg/5 mL N/A 20 mg/mL95 14 d RT11,13,96,97,98 0.2– 0.4 mg/mL95 0.2 mg/mL: - cytotoxic7 500 mg/25 mL 48 h RT13,95 - use non-PVC bag 1000 mg/50 mL 500 mL*NS or D5W95 0.4 mg/mL: and tubing only (BMS) 24 h RT95 (RT) preservative95 Etoposide 0.2-0.3 mg/mL: 100 mg/5 mL N/A 20 mg/mL99 discard unused NS 7 d F,100 2 d RT87,100 - cytotoxic7 200 mg/10 mL portion99 0.4-0.5 mg/mL: - use non-PVC bag 500 mg/25 mL Stabilty is 1 d F,100 1 d RT100 and tubing only 1000 mg/50 mL concentration 0.6-9.0mg/mL: (Novopharm) dependent generally unstable100 (RT)(PFL) 9.5 mg/mL: no preservative99 2 d F,100 1d RT100 10-12 mg/mL: 7 d F,100 2 d RT87,100 D5W99 4 h RT99,101 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 22/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 23. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Fludarabine 50 mg 2 mL SWI102 25 mg/mL102 48 h F or RT13,49 dilute to maximum of 48 h F, RT13,49 - cytotoxic7 (Berlex) 1 mg/mL102,103 (F) no preservative102 100 mL*NS or D5W102 Fludarabine 50 mg N/A 25 mg/mL104 discard unused dilute to maximum of 48 h F, 24 h RT104 - cytotoxic7 (Novopharm) portion104 1 mg/mL104 (F) no preservative104 100 mL*NS or D5W BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 23/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 24. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Fluorouracil 5000 mg/100 mL N/A 50 mg/mL105 8 h RT105,106 syringe13 48 h RT13,21,106 - cytotoxic7 (Hospira) (RT)(PFL) no preservative105 2-10 mg/mL in 24 h RT105,106 D5W105,106 50-1000 mL*D5W CIVI: ambulatory complete within pump106 8 d11,13,107 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 24/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 25. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Gemcitabine 200 mg 200 mg: 5 mL NS 38 mg/mL108 48 h RT108,109 syringe108 48 h RT,13,108,109 - cytotoxic7 1000 m g 1000 mg: 25 mL (Eli-Lilly) NS108 (RT) no preservative108 0.1–10 mg/mL 48 h F, RT13,108,109 NS108,109 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 25/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 26. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Gemcitabine 200 mg 200 mg vial: 5 mL 38 mg/mL110 48 RT110,112,74 syringe110 24 h RT110,112 - cytotoxic7 1000 mg NS 2000 mg 1000 mg vial: 25 mL (Hospira) NS RT110 2000 mg vial: 50 mL no preservative111 NS110 26 mg/mL-0.1 mg/mL 48 h RT112,74 NS110,112 Gemcitabine 200 mg 200 mg vial: 5mL 38 mg/mL114 24 h RT114 38 mg/mL – 0.1 24 RT114 - cytotoxic7 1000 mg NS mg/mL NS114 (Novopharm) 1000 mg vial: 25 mL RT NS114 no preservative113 Gemcitabine 200 mg 200 mg vial: 5 mL 38 mg/mL115 48 h RT115,116 syringe115 48 h RT115,117,116 - cytotoxic7 1000 mg NS (Sandoz Standard) 1000 mg vial: 25 mL RT NS115 no preservative115 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 26/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 27. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) 38 mg/mL-0.1 mg/mL 48 h RT13,119 NS or D5W115,118 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 27/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 28. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Idarubicin 5 mg vial under negative 1 mg/mL120 48 h F,120 24 h RT syringe 48 h F,13, 120 24 h RT13 - cytotoxic7 10 mg pressure120 (PFL)120 (PFL)120 (Pfizer) (RT)(PFL) 5 mg: 5 mL SWI no preservative120 10 mg: 10 mL SWI120 Idarubicin 5 mg/5 mL N/A 1 mg/mL120 same as syringe Discard 48 h F,13,120 24 - cytotoxic7 10 mg/10 mL reconstituted h RT13 20 mg/20 mL solution121 (PFL)120 (Pfizer) (F)(PFL) no preservative120 Ifosfamide 1000 m g 1000 mg: 20 mL 50 mg/mL122 48 h F13,122 0.6–20 mg/mL122 72 h F122 - cytotoxic7 3000 mg SWI122 24 h F, RT when mixed (Baxter) 3000 mg: 60 mL 500–1000 mL*NS, with mesna11 (RT) 11 SWI D5W, D5-NS, no preservative122 D5-1/2NS, Lactated D5W or Lactated shake well Ringer’s11,122 Ringer’s when mixed Interferon Alfa -2b 18 million IU/3 mL N/A 6 million IU/mL123 48 h F13,123 syringe123 2 d F13,124 - cytotoxic7 (Schering) (F)(or up to 7 days at RT before use) no preservative123 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 28/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 29. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) ≥ 0.3 million IU/mL123 24 h F, RT124 50 mL NS123 Interferon Alfa -2b 25 million IU/2.5 mL N/A 10 million IU/mL123 48 h F13,123 syringe123 2 d F13,124 - cytotoxic7 (Schering) (F)(or up to 7 days at RT before use) no preservative123 ≥ 0.3 million IU/mL123 24 h F, RT124 50 mL NS123 Interferon Alfa -2b 10 million IU 1 mL supplied 10 million IU/mL123 24 h F123 syringe123 24 h F, RT124 - cytotoxic7 (Schering) diluent (SWI) 123 (F) no preservative123 do not shake; roll to reconstitute123 > 0.1 million IU/mL124 48 h RT11,13 100 mL NS125 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 29/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 30. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) 1 mL BWI123 48 h F, RT13,123 syringe125 14 d F, 48 h RT13,125 do not shake; roll to reconstitute123 100 mL NS125 48 h RT11,13 Interferon Alfa -2b 18 million IU 1 mL supplied 18 million IU/mL123 24 h F123 syringe123 24 h F, RT124 - cytotoxic7 (Schering) diluent123 (F) no preservative123 do not shake; roll to reconstitute123 > 0.1 million IU/mL126 48 h RT11,13 100 mL NS125 1 mL BWI123 48 h F, RT13 syringe123 14 d F13,125 do not shake; roll to reconstitute123 100 mL NS125 48 h RT11,13 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 30/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 31. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Irinotecan 40 mg/2 mL N/A 20 mg/mL127 2 days RT13,128,129 0.12– 2.8 mg/mL127 24 h RT: D5W, NS127 - cytotoxic7 100 mg/5 mL - do NOT 500 mg/25 mL 500 mL11 D5W 48 h F: D5W refrigerate if in (Hospira) (preferred), NS127 (PFL)127 NS130 (RT)(PFL) no preservative127 Irinotecan 40 mg/2 mL N/A 20 mg/mL130 discard unused 0.12– 2.8 mg/mL130 24 h RT: D5W, NS130 - cytotoxic7 100 mg/5 mL portion130 - do NOT (Pfizer) 500 mL11 D5W 48 h F: D5W refrigerate if in (RT)(PFL) (preferred), NS130 (PFL)130 NS130 no preservative130 Irinotecan 40 mg/2 mL N/A 20 mg/mL131 discard unused 0.12-2.8 mg/mL131 24 h RT: D5W NS131 - cytotoxic3 100 mg/5 mL portion131,74 48 h F: D5W131 (Sandoz) D5W (recommended) (RT)(PFL) NS131 (PFL)131 no preservative131 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 31/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 32. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Ixabepilone 15 mg 8 mL supplied 2 mg/mL 1 h RT132 0.2 – 0.6 mg/mL in 6 h RT132 - cytotoxic3 (contains 16 mg) diluent Lactated Ringer’s - use 0.2-1.2 45 mg Injection USP (use micron in-line (contains 47 mg) 23.5 mL supplied 2 mg/mL non-PVC infusion filter132 (BMS) diluent container)132 - use non-PVC (F)(PFL) (i.e., DEHP-free) no preservative132 administration set132 Leucovorin 50 mg/5 mL N/A 10 mg/mL133 5 mL vial: discard syringe134 7 d F134 - noncytotoxic 500 mg/50 mL unused portion133 48 h RT87,134 (Hospira) (F)(PFL) 50 mL vial: 8 h no preservative133 0.05-10 mg/mL133 24 h RT133: NS, D5W, Lactated Ringer’s, Ringer’s 50-250 mL* NS, 8 h RT133: D10W, D5- D5W, Lactated NS Ringer’s, Ringer’s, D10W, D5-NS BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 32/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 33. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Leucovorin 50 mg/5 mL N/A135 10 mg/mL135 5 mL vial: discard syringe 8 h135,13 - noncytotoxic 500 mg/50 mL unused portion135 (Novopharm) (F)(PFL)135 50 mL vial: discard unused portion135 0.060-1.0 mg/mL135 24 h RT NS, Lactated Ringer’s, Ringer’s135 50-250 mL* NS, 12 h RT D5W, D5W, Lactated D10W135 Ringer’s, Ringer’s, D10W, D10NS135 6 h RT D5NS135 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 33/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 34. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Mechlorethamine 10 mg do NOT use if 1 mg/mL136 use within 4 h of syringe136 complete - cytotoxic7 (Ovation discoloured or water reconstitution administration Pharmaceuticals/Merck) droplets form in vial RT11,13 4 h of reconstitution no preservative136 before RT11,13,136 reconstitution136 10 mL SWI or NS136 record time of reconstitution 100 mL NS49,136 complete administration within 4 h of reconstitution RT13,49,136 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 34/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 35. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Medroxyprogesterone 250 mg/5 mL N/A 50 mg/mL18 use within 4 h of syringe: IM only18 use within 4 h of initial - cytotoxic7 (Pfizer) initial vial puncture11,137 - auxiliary label: (RT) record time of puncture11,137 shake before use18 preservative18 puncture Medroxyprogesterone Depo N/A 150 mg/mL18 use within 4 h of syringe: IM only18 use within 4 h of initial - cytotoxic7 150 mg/1mL initial puncture11,137 - auxiliary label: (Pfizer) record time of puncture11,137 shake before use18 (RT) puncture preservative18 Melphalan 50 mg 10mL supplied 5 mg/mL138 2 h RT138 0.1– 0.45 mg/mL in complete - cytotoxic7 (GSK) diluent138 NS only138 administration within (RT)(PFL) do NOT 60 min from time of no preservative138 immediately after refrigerate (e.g., > 45 mg and < initial reconstitution at adding diluent, 110 mg in 250 mL RT11 shake vigorously138 NS)* record time of reconstitution BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 35/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 36. Mesna 1000 mg/10mL N/A 100 mg/mL139 14 d F, RT13,139 > 1mg/mL139 48 h F, 24 h RT139 - noncytotoxic (PPC) (RT) NS or D5W preservative139 Methotrexate 50 mg/2mL N/A 25 mg/mL140 50mg: discard syringe 2 d F, RT11,141,142 - cytotoxic7 500 mg/20mL unused portion140 - for high-dose 1 g/40mL regimens (e.g., 1-8 5 g/200mL 500mg, 1 g, 5 g: g/m2 as a single (Hospira) 8 h F, RT140 dose)143 use (RT)(PFL) preservative-free no preservative140 methotrexate11 - do not use for IT injection 0.4–2 mg/mL140 24 h RT140 100 mL* NS, D5W high dose (e.g., 1-8 g/m2 as a single dose)143,144-146: 500– 1000 mL* BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 36/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 37. Methotrexate IT Injection140: N/A 25 mg/mL140 discard unused qs to 6 mL with use within 4 h of initial - cytotoxic7 Only preservative free portion140 preservative free NS61 puncture11,13 - auxiliary label62: methotrexate may be “IT” administered by the - label to include intrathecal route140 route in full (i.e., 50 mg/2mL147 INTRATHECAL (Hospira) injection) attached (RT)(PFL) to both syringe and no preservative140 outer ziplock bag62 Methotrexate 50 mg/2mL N/A 25 mg/mL140 24 h F141 syringe 14 d F87,141 - cytotoxic7 500 mg/20mL - high-dose (Hospira) regimen(e.g., 1-8 (RT)(PFL) g/m2 as a single preservative140 dose)144-146: use preservative-free methotrexate11 - do not use for IT injection 0.4–2 mg/mL140 4 h RT140 e.g., 100 mL*NS, D5W140 Mitomycin 5 mg SWI 0.5 mg/mL148 48 h F, RT13,148 syringe13 14 d F, 48 h RT13,148 - cytotoxic7 20 mg 5 mg: 10 mL (PFL)148 (Novopharm) 20 mg: 40 mL (RT)(PFL) no preservative148 shake well148 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 37/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 38. 0.02-0.04 mg/mL148 3 h RT: D5W 12 h RT: NS NS, D5W, sodium 24 h RT: sodium lactate148 lactate148 Mitomycin 5 mg SWI 0.5 mg/mL149 48 h F, RT13,149 syringe11 14 d F, 48 h RT11,21 - cytotoxic7 20 mg 5 mg: 10 mL (BMS) 20 mg: 40 mL (PFL)149 (RT)(PFL) no preservative149 shake well149 0.02–0.04 mg/mL 12 h RT: NS 3h: D5W NS, D5W, sodium 24 h: sodium lactate149 lactate149 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 38/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 39. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Mitoxantrone 20 mg/10 mL N/A 2 mg/mL150 discard unused 0.2-0.6 mg/mL150 NS: 24 h F, RT150 - cytotoxic7 25 mg/12.5 mL portion150 (Hospira) NS, D5W150 **(PFL)150 (RT)(PFL) no preservative150 > 50 mL*150 Mitoxantrone 20 mg/10 mL N/A 2 mg/mL151 discard unused NS, D5W151 24 h RT151 - cytotoxic7 (Novopharm) portion151 (RT)(PFL) > 50 mL*151 **(PFL)152 no preservative151 Mitoxantrone 20 mg/10 mL N/A 2 mg/mL153 discard unused NS, D5W2 24 h RT153 - cytotoxic7 (Pharmaceutical portion153 > 50 mL*153 Partners of Canada) (RT) no preservative153 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 39/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 40. Octreotide 50 mcg/mL; 100 N/A 50 mcg/mL discard unused sc syringe154 single use vials: use - noncytotoxic mcg/mL; 500 mcg/mL 100 mcg/mL portion154 within 4 h (Novopharm) 500 mcg/mL154 multidose vials: use (F)(PFL) within 14 d F74,154 no preservative multidose vials (5mL): 200 µg/mL (F)(PFL) 154 preservative 200 mcg/mL154 14 d F74,154 infusion: NS154 single use vials or multidose vials: 24 h RT154 Octreotide (Sandostatin) N/A 200 mcg/mL18 discard unused 50–200 mL NS18,11,156 24 h RT18 - noncytotoxic10 1000 mcg/5 mL portion155 (Novartis) (F)(PFL) SC infusion: adjust preservative18 volume to ensure infusion rate of 25 mcg/h18 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 40/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 41. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Octreotide (Sandostatin) N/A 50 mcg/mL discard unused 50-100 mL11,156 24 h RT18 - noncytotoxic10 50 mcg/1 mL 100 mcg/mL portion18 100 mcg/1 mL 500 mcg/mL18 NS18 500 mcg/1 mL (Novartis) SC infusion: adjust (F)(PFL) volume to ensure no preservative18 infusion rate of 25 mcg/h18 Octreotide (Sandostatin LAR) 2 mL supplied 10 mg: 5 mg/mL discard unused deep intragluteal use within 4 h of initial - noncytotoxic10 10 mg diluent 20 mg: 10 mg/mL portion18 administration only18 reconstitution18,13 - do NOT shake 20 mg 30 mg: 15 mg/mL18 30 mg gently run 2 mL (Novartis) down sides of the (F)(PFL) vial; do NOT preservative155 disturb for 2–5 min, then swirl moderately18 record time of reconstitution BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 41/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 42. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Oxaliplatin 50 mg/10 mL N/A 5 mg/mL157 discard unused 0.2-1.3 mg/mL158 0.2-1.3 mg/mL: - cytotoxic7 100 mg/20 mL portion157 14 d F, 48 h RT159,87,158 - do NOT use 200 mg/40 mL 1.3–2 mg/mL157,158 aluminum- (Sanofi-Aventis) 1.3-2 mg/mL: containing needle, (RT)(PFL) 250–500 mL D5W157 48 h F, 24 h RT157 syringe or no preservative157 tubing157 do NOT use NS or other chloride- containing solution157 do NOT use aluminum-containing needle and syringe157 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 42/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010
  • 43. BC CANCER AGENCY CHEMOTHERAPY PREPARATION AND STABILITY CHART DRUG & STRENGTH Reconstitute To Give: Vial Product Product Stability Special (Storage Prior to Use, With: Stability Precautions/Notes Manufacturer, Preservative Status) Oxaliplatin 50 mg SWI, D5W: 5 mg/mL160 24 h F160 500 mL D5W 24 h F, 6 h RT160 - cytotoxic7 100 mg 50 mg: 10 mL - do NOT use (Sigmacon) 100 mg: 20 mL do NOT use NS or aluminum- (RT) other chloride- containing needle, no preservative160 do NOT use NS or containing solutions syringe or tubing160 other chloride- (degrades)160 containing solution160 do NOT use aluminum-containing do NOT use needle and syringe160 aluminum- containing needle and syringe160 Paclitaxel 30 mg/5 mL N/A 6 mg/mL162 8 h RT162 0.3–1.2 mg/mL in NS, 0.3-1.2 mg/mL: - cytotoxic7 100 mg/16.7 mL D5W162 24 h RT162 - use non-PVC bag 300 mg/50 mL (e.g., 100–1000 mL)* and tubing with in- (Biolyse) 0.1 mg/mL: line filter162 (RT)161 44 h F, RT163 no preservative 0.1 mg/mL in NS163 0.012-0.09 mg/mL: 0.012-0.1 mg/mL164 16 h RT164 BC Cancer Agency Chemotherapy Preparation and Stability Chart© version 2.00 43/77 Activation Date: 2 March 2006 Revised Date: 1 July 2010