Safety Related Problems

Suspected adverse reactions should be reported to the Pharmacovigilance section of the IMB.

Information on reporting of adverse drug reactions may be found in the guidance document 'Advice for healthcare professionals on reporting of adverse drug reactions'.

Adverse reactions can be reported via our on-line reporting system.

Alternatively, adverse reaction report forms can be downloaded from the 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

The Irish Medicines Board - www.imb.ie

Safety Related Problems