Safety Related Problems
Suspected adverse reactions should be reported to the Pharmacovigilance section of the IMB. For further information on pharmacovigilance and reporting of adverse drug reactions, please refer to the guidance pages for patients/consumers and healthcare professionals.
Adverse reactions can be reported directly to the IMB be the following methods:
- Via our on-line reporting system.
- Using downloadable form from the IMB website publications section. Completed forms should be forwarded by freepost to the following address:
Human Products Monitoring Department
Irish Medicines Board
Kevin O'Malley House
- Using post-paid Report Cards (Yellow Cards)
A supply of cards can be ordered from the IMB:
Tel: (01) 6764971, email firstname.lastname@example.org
- By telephoning the Pharmacovigilance Section of the IMB, 01- 6764971