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:

1. Via our on-line reporting system.

2. Using downloadable form from the IMB website publications section. Completed forms should be forwarded by freepost to the following address:                     
   
   'FREEPOST'                
   Pharmacovigilance Section
   Human Products Monitoring Department              
   Irish Medicines Board      
   Kevin O'Malley House
   Earlsfort Centre  
   Earlsfort Terrace                
   Dublin 2  

3. Using post-paid Report Cards (Yellow Cards)

A supply of cards can be ordered from the IMB:

Tel: (01) 6764971, email imbpharmacovigilance@imb.ie

4. By telephoning the Pharmacovigilance Section of the IMB, 01- 6764971