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Pharmacovigilance activities in Iran
Experience in managing medication
errors
reported by:
Iranian Pharmacovigilance Center
Edited :
Behrouz Mansouri
Mahmoud Nasseri
Muhammad Tanvir
Amirmasoud Nikahd
• 16.8% (n = 62) of the 370 patients had at least one ADR.
(102 ADRs).
• 58.8% of the ADRs (60 reactions) :preventable
reactions
• Preventable ADRs were more severe than those that
were nonpreventable.
• the incidence of preventable ADRs increased with the
patients' age and caused longer hospitalization than did
nonpreventable ones.
Number of ADRs and reports from hospitals
before and after interventions
• Every manufacturer is responsible for safety of its products
and must implement pharmacovigilance system.
• Every manufacturer must introduce a trained person in the
field of pharmacovigilance to Iranian ADR Monitoring
Center. This person should be able to evaluate ADEs and
conduct risk- benefit assessment for related pharmaceutical
products.
• Manufacturers must submit PSUR for their product
according to published guidelines of Iranian Food and Drug
Organization.
• Immediate reporting
• The following ADEs must report immediately:
• Fatal ADEs
• Life threatening ADEs
• ADEs with permanent disability
• ADEs leading to hospitalization
• ADEs resulted in prolonged hospital stay
• Birth defects suspected to an ADE
Pharmacovigilance in Iran
Pharmacovigilance in Iran
Pharmacovigilance in Iran
Pharmacovigilance in Iran
Pharmacovigilance in Iran
Pharmacovigilance in Iran
Pharmacovigilance in Iran

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Pharmacovigilance in Iran

  • 1. Pharmacovigilance activities in Iran Experience in managing medication errors reported by: Iranian Pharmacovigilance Center Edited : Behrouz Mansouri Mahmoud Nasseri Muhammad Tanvir Amirmasoud Nikahd
  • 2. • 16.8% (n = 62) of the 370 patients had at least one ADR. (102 ADRs). • 58.8% of the ADRs (60 reactions) :preventable reactions • Preventable ADRs were more severe than those that were nonpreventable. • the incidence of preventable ADRs increased with the patients' age and caused longer hospitalization than did nonpreventable ones.
  • 3.
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9. Number of ADRs and reports from hospitals before and after interventions
  • 10.
  • 11. • Every manufacturer is responsible for safety of its products and must implement pharmacovigilance system. • Every manufacturer must introduce a trained person in the field of pharmacovigilance to Iranian ADR Monitoring Center. This person should be able to evaluate ADEs and conduct risk- benefit assessment for related pharmaceutical products. • Manufacturers must submit PSUR for their product according to published guidelines of Iranian Food and Drug Organization.
  • 12. • Immediate reporting • The following ADEs must report immediately: • Fatal ADEs • Life threatening ADEs • ADEs with permanent disability • ADEs leading to hospitalization • ADEs resulted in prolonged hospital stay • Birth defects suspected to an ADE