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Alzheimer’s Disease Medications
FA C T S H E E T

S

everal prescription drugs are
currently approved by the U.S.
Food and Drug Administration
(FDA) to treat people who have been
diagnosed with Alzheimer’s disease.
Treating the symptoms of Alzheimer’s
can provide patients with comfort,
dignity, and independence for a longer
period of time and can encourage and
assist their caregivers as well.

It is important to understand that none
of these medications stops the disease
itself.

Treatment for Mild to
Moderate Alzheimer’s
Medications called cholinesterase inhibitors are prescribed for mild to moderate
Alzheimer’s disease. These drugs may
help delay or prevent symptoms from
becoming worse for a limited time and
may help control some behavioral symptoms. The medications include Razadyne®
(galantamine), Exelon® (rivastigmine),
and Aricept® (donepezil). Another drug,
Cognex® (tacrine), was the first approved
cholinesterase inhibitor but is rarely
prescribed today due to safety concerns.
Scientists do not yet fully understand
how cholinesterase inhibitors work to
treat Alzheimer’s disease, but research
indicates that they prevent the breakdown of acetylcholine, a brain chemical
believed to be important for memory and

thinking. As Alzheimer’s progresses, the
brain produces less and less acetylcholine;
therefore, cholinesterase inhibitors may
eventually lose their effect.
No published study directly compares
these drugs. Because they work in a
similar way, switching from one of these
drugs to another probably will not produce significantly different results.
However, an Alzheimer’s patient may
respond better to one drug than another.

Treatment for Moderate
to Severe Alzheimer’s
A medication known as Namenda®
(memantine), an N-methyl D-aspartate
(NMDA) antagonist, is prescribed to treat
moderate to severe Alzheimer’s disease.
This drug’s main effect is to delay progression of some of the symptoms of
moderate to severe Alzheimer’s. It may
allow patients to maintain certain daily
functions a little longer than they would
without the medication. For example,
Namenda® may help a patient in the
later stages of the disease maintain his
or her ability to use the bathroom independently for several more months, a
benefit for both patients and caregivers.
Namenda® is believed to work by regulating glutamate, an important brain
chemical. When produced in excessive
amounts, glutamate may lead to brain
cell death. Because NMDA antagonists
(continued on back)

Alzheimer’s Disease Education & Referral (ADEAR) Center
A Service of the National Institute on Aging
National Institutes of Health
U.S. Department of Health and Human Services
Medications to Treat

This brief summary does not include all information import
for professional medical advice. Consult the prescribing d
any other medications or supplements. Drugs are listed

DRUG NAME

DRUG TYPE
AND USE

HOW IT WORKS

COMMON SIDE
EFFECTS

Namenda®
(memantine)

N-methyl D-aspartate
(NMDA) antagonist
prescribed to treat
symptoms of moderate
to severe Alzheimer’s

Blocks the toxic effects
associated with excess
glutamate and regulates
glutamate activation

Dizziness, headache,
constipation, confusion

Razadyne®
(galantamine)

Cholinesterase inhibitor
prescribed to treat
symptoms of mild to
moderate Alzheimer’s

Prevents the breakdown
of acetylcholine and stimulates nicotinic receptors to
release more acetylcholine
in the brain

Nausea, vomiting,
diarrhea, weight loss,
loss of appetite

Exelon®
(rivastigmine)

Cholinesterase inhibitor
prescribed to treat
symptoms of mild to
moderate Alzheimer’s

Prevents the breakdown
of acetylcholine and butyrylcholine (a brain chemical
similar to acetylcholine) in
the brain

Nausea, vomiting,
diarrhea, weight
loss, loss of appetite,
muscle weakness

Aricept®
(donepezil)

Cholinesterase inhibitor
prescribed to treat
symptoms of mild to
moderate, and moderate
to severe Alzheimer’s

Prevents the breakdown
of acetylcholine in the brain

Nausea, vomiting,
diarrhea

*Available as a generic drug.
Alzheimer’s Disease

tant for patient use and should not be used as a substitute
doctor and read the package insert before using these or
in order of FDA approval, starting with the most recent.

MANUFACTURER’S
RECOMMENDED DOSAGE

FOR MORE
INFORMATION

• Tablet: Initial dose of 5 mg once a day
• May increase dose to 10 mg/day (5 mg twice a
day), 15 mg/day (5 mg and 10 mg as separate
doses), and 20 mg/day (10 mg twice a day) at
minimum 1-week intervals if well tolerated
• Oral solution: same dosage as above
• Extended-release tablet: Initial dose of 7 mg once

a day; may increase dose to 14 mg/day, 21mg/day,
and 28 mg/day at minimum 1-week intervals if well
tolerated

For current information about this drug’s
safety and use, visit www.namenda.com.
Click on “Prescribing Information” to see the
drug label.

• Tablet*: Initial dose of 8 mg/day (4 mg twice a day)
• May increase dose to 16 mg/day (8 mg twice a
day) and 24 mg/day (12 mg twice a day) at
minimum 4-week intervals if well tolerated
• Oral solution*: same dosage as above
• Extended-release capsule*: same dosage as above
but taken once a day

For current information about this drug’s
safety and use, visit www.razadyneer.com.
Click on “Important Safety Information” to
see links to prescribing information.

• Capsule*: Initial dose of 3 mg/day (1.5 mg twice
a day)
• May increase dose to 6 mg/day (3 mg twice a
day), 9 mg (4.5 mg twice a day), and 12 mg/day
(6 mg twice a day) at minimum 2-week intervals
if well tolerated
• Patch: Initial dose of 4.6 mg once a day; may increase to 9.5 mg once a day and 13.3 mg once a day
at minimum 4-week intervals if well tolerated
• Oral solution: same dosage as capsule

For current information about this drug’s
safety and use, visit www.fda.gov/cder.
Click on “Drugs@FDA,” search for Exelon,
and click on drug-name links to see “Label
Information.”

• Tablet*: Initial dose of 5 mg once a day
• May increase dose to 10 mg/day after 4-6 weeks
if well tolerated, then to 23 mg/day after at least
3 months
• Orally disintegrating tablet*: same dosage as above
• 23-mg dose available as brand-name tablet only

For current information about this drug’s
safety and use, visit www.fda.gov/cder.
Click on “Drugs@FDA,” search for Aricept,
and click on drug-name links to see “Label
Information.”
(continued from front)

work very differently from cholinesterase inhibitors, the two types of drugs
can be prescribed in combination.
The FDA has also approved Aricept®
for the treatment of moderate to severe
Alzheimer’s disease.

Dosage and Side Effects
Doctors usually start patients at low
drug doses and gradually increase the
dosage based on how well a patient
tolerates the drug. There is some evidence that certain patients may benefit
from higher doses of the cholinesterase
inhibitors. However, the higher the
dose, the more likely are side effects.
The recommended effective dosages of
drugs prescribed to treat the symptoms
of Alzheimer’s and the drugs’ possible
side effects are summarized in the table
(see inside).

Patients should be monitored when a
drug is started. Report any unusual
symptoms to the prescribing doctor
right away. It is important to follow
the doctor’s instructions when taking
any medication, including vitamins
and herbal supplements. Also, let the
doctor know before adding or changing
any medications.
Testing New Alzheimer’s Drugs
Clinical trials are the best way to find
out if promising new treatments are
safe and effective in humans. Volunteer
participants are needed for many
Alzheimer’s trials conducted around the
United States. To learn more, talk with
your doctor or visit the ADEAR Center’s
listing of clinical trials at www.nia.nih.
gov/Alzheimers/ResearchInformation/
Clinical Trials. More information is
available at www.ClinicalTrials.gov.

For More Information
To learn about support groups, research
centers, research studies, and publications about Alzheimer’s disease, contact
the following resources:

ADEAR website provides free, online
publications in English and Spanish;
email alerts; an Alzheimer’s clinical
trials database; and more.

Alzheimer’s Disease Education and
Referral (ADEAR) Center
P Box 8250
.O.
Silver Spring, MD 20907-8250
1-800-438-4380 (toll-free)
www.nia.nih.gov/alzheimers

Alzheimer’s Association
225 North Michigan Avenue, Floor 17
Chicago, IL 60601-7633
1-800-272-3900 (toll-free)
1-866-403-3073 (TDD/toll-free)
www.alz.org

The National Institute on Aging’s
ADEAR Center offers information and
publications for families, caregivers, and
professionals on diagnosis, treatment,
patient care, caregiver needs, long-term
care, education, training, and research
related to Alzheimer’s disease. Staff
members answer telephone, email, and
written requests and make referrals to
local and national resources. The

The Alzheimer’s Association is a
national nonprofit association with a
network of local chapters that provide
education and support for people diagnosed with Alzheimer’s, their families,
and caregivers. The Association also
supports research on Alzheimer’s.

NIH Publication No. 08-3431

November 2008 (updated November 2012)

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Global Medical Cures™ | Alzheimers disease medications

  • 1. Alzheimer’s Disease Medications FA C T S H E E T S everal prescription drugs are currently approved by the U.S. Food and Drug Administration (FDA) to treat people who have been diagnosed with Alzheimer’s disease. Treating the symptoms of Alzheimer’s can provide patients with comfort, dignity, and independence for a longer period of time and can encourage and assist their caregivers as well. It is important to understand that none of these medications stops the disease itself. Treatment for Mild to Moderate Alzheimer’s Medications called cholinesterase inhibitors are prescribed for mild to moderate Alzheimer’s disease. These drugs may help delay or prevent symptoms from becoming worse for a limited time and may help control some behavioral symptoms. The medications include Razadyne® (galantamine), Exelon® (rivastigmine), and Aricept® (donepezil). Another drug, Cognex® (tacrine), was the first approved cholinesterase inhibitor but is rarely prescribed today due to safety concerns. Scientists do not yet fully understand how cholinesterase inhibitors work to treat Alzheimer’s disease, but research indicates that they prevent the breakdown of acetylcholine, a brain chemical believed to be important for memory and thinking. As Alzheimer’s progresses, the brain produces less and less acetylcholine; therefore, cholinesterase inhibitors may eventually lose their effect. No published study directly compares these drugs. Because they work in a similar way, switching from one of these drugs to another probably will not produce significantly different results. However, an Alzheimer’s patient may respond better to one drug than another. Treatment for Moderate to Severe Alzheimer’s A medication known as Namenda® (memantine), an N-methyl D-aspartate (NMDA) antagonist, is prescribed to treat moderate to severe Alzheimer’s disease. This drug’s main effect is to delay progression of some of the symptoms of moderate to severe Alzheimer’s. It may allow patients to maintain certain daily functions a little longer than they would without the medication. For example, Namenda® may help a patient in the later stages of the disease maintain his or her ability to use the bathroom independently for several more months, a benefit for both patients and caregivers. Namenda® is believed to work by regulating glutamate, an important brain chemical. When produced in excessive amounts, glutamate may lead to brain cell death. Because NMDA antagonists (continued on back) Alzheimer’s Disease Education & Referral (ADEAR) Center A Service of the National Institute on Aging National Institutes of Health U.S. Department of Health and Human Services
  • 2. Medications to Treat This brief summary does not include all information import for professional medical advice. Consult the prescribing d any other medications or supplements. Drugs are listed DRUG NAME DRUG TYPE AND USE HOW IT WORKS COMMON SIDE EFFECTS Namenda® (memantine) N-methyl D-aspartate (NMDA) antagonist prescribed to treat symptoms of moderate to severe Alzheimer’s Blocks the toxic effects associated with excess glutamate and regulates glutamate activation Dizziness, headache, constipation, confusion Razadyne® (galantamine) Cholinesterase inhibitor prescribed to treat symptoms of mild to moderate Alzheimer’s Prevents the breakdown of acetylcholine and stimulates nicotinic receptors to release more acetylcholine in the brain Nausea, vomiting, diarrhea, weight loss, loss of appetite Exelon® (rivastigmine) Cholinesterase inhibitor prescribed to treat symptoms of mild to moderate Alzheimer’s Prevents the breakdown of acetylcholine and butyrylcholine (a brain chemical similar to acetylcholine) in the brain Nausea, vomiting, diarrhea, weight loss, loss of appetite, muscle weakness Aricept® (donepezil) Cholinesterase inhibitor prescribed to treat symptoms of mild to moderate, and moderate to severe Alzheimer’s Prevents the breakdown of acetylcholine in the brain Nausea, vomiting, diarrhea *Available as a generic drug.
  • 3. Alzheimer’s Disease tant for patient use and should not be used as a substitute doctor and read the package insert before using these or in order of FDA approval, starting with the most recent. MANUFACTURER’S RECOMMENDED DOSAGE FOR MORE INFORMATION • Tablet: Initial dose of 5 mg once a day • May increase dose to 10 mg/day (5 mg twice a day), 15 mg/day (5 mg and 10 mg as separate doses), and 20 mg/day (10 mg twice a day) at minimum 1-week intervals if well tolerated • Oral solution: same dosage as above • Extended-release tablet: Initial dose of 7 mg once a day; may increase dose to 14 mg/day, 21mg/day, and 28 mg/day at minimum 1-week intervals if well tolerated For current information about this drug’s safety and use, visit www.namenda.com. Click on “Prescribing Information” to see the drug label. • Tablet*: Initial dose of 8 mg/day (4 mg twice a day) • May increase dose to 16 mg/day (8 mg twice a day) and 24 mg/day (12 mg twice a day) at minimum 4-week intervals if well tolerated • Oral solution*: same dosage as above • Extended-release capsule*: same dosage as above but taken once a day For current information about this drug’s safety and use, visit www.razadyneer.com. Click on “Important Safety Information” to see links to prescribing information. • Capsule*: Initial dose of 3 mg/day (1.5 mg twice a day) • May increase dose to 6 mg/day (3 mg twice a day), 9 mg (4.5 mg twice a day), and 12 mg/day (6 mg twice a day) at minimum 2-week intervals if well tolerated • Patch: Initial dose of 4.6 mg once a day; may increase to 9.5 mg once a day and 13.3 mg once a day at minimum 4-week intervals if well tolerated • Oral solution: same dosage as capsule For current information about this drug’s safety and use, visit www.fda.gov/cder. Click on “Drugs@FDA,” search for Exelon, and click on drug-name links to see “Label Information.” • Tablet*: Initial dose of 5 mg once a day • May increase dose to 10 mg/day after 4-6 weeks if well tolerated, then to 23 mg/day after at least 3 months • Orally disintegrating tablet*: same dosage as above • 23-mg dose available as brand-name tablet only For current information about this drug’s safety and use, visit www.fda.gov/cder. Click on “Drugs@FDA,” search for Aricept, and click on drug-name links to see “Label Information.”
  • 4. (continued from front) work very differently from cholinesterase inhibitors, the two types of drugs can be prescribed in combination. The FDA has also approved Aricept® for the treatment of moderate to severe Alzheimer’s disease. Dosage and Side Effects Doctors usually start patients at low drug doses and gradually increase the dosage based on how well a patient tolerates the drug. There is some evidence that certain patients may benefit from higher doses of the cholinesterase inhibitors. However, the higher the dose, the more likely are side effects. The recommended effective dosages of drugs prescribed to treat the symptoms of Alzheimer’s and the drugs’ possible side effects are summarized in the table (see inside). Patients should be monitored when a drug is started. Report any unusual symptoms to the prescribing doctor right away. It is important to follow the doctor’s instructions when taking any medication, including vitamins and herbal supplements. Also, let the doctor know before adding or changing any medications. Testing New Alzheimer’s Drugs Clinical trials are the best way to find out if promising new treatments are safe and effective in humans. Volunteer participants are needed for many Alzheimer’s trials conducted around the United States. To learn more, talk with your doctor or visit the ADEAR Center’s listing of clinical trials at www.nia.nih. gov/Alzheimers/ResearchInformation/ Clinical Trials. More information is available at www.ClinicalTrials.gov. For More Information To learn about support groups, research centers, research studies, and publications about Alzheimer’s disease, contact the following resources: ADEAR website provides free, online publications in English and Spanish; email alerts; an Alzheimer’s clinical trials database; and more. Alzheimer’s Disease Education and Referral (ADEAR) Center P Box 8250 .O. Silver Spring, MD 20907-8250 1-800-438-4380 (toll-free) www.nia.nih.gov/alzheimers Alzheimer’s Association 225 North Michigan Avenue, Floor 17 Chicago, IL 60601-7633 1-800-272-3900 (toll-free) 1-866-403-3073 (TDD/toll-free) www.alz.org The National Institute on Aging’s ADEAR Center offers information and publications for families, caregivers, and professionals on diagnosis, treatment, patient care, caregiver needs, long-term care, education, training, and research related to Alzheimer’s disease. Staff members answer telephone, email, and written requests and make referrals to local and national resources. The The Alzheimer’s Association is a national nonprofit association with a network of local chapters that provide education and support for people diagnosed with Alzheimer’s, their families, and caregivers. The Association also supports research on Alzheimer’s. NIH Publication No. 08-3431 November 2008 (updated November 2012)