Advisory, Warning & Recall Notices
From time to time notices relating to the safety and/or quality of medicinal products are published by the Irish Medicines Board.
These notices are classified under several priority related categories and may relate to human and veterinary medicines, or medical devices.
The issues covered by these notices will range from quality defect information and medicinal product safety information through to updated information on the appropriate usage of medicines or devices.
Notices are categorised in accordance with their importance at time of publication.
The four notice categories are outlined as follows:-
- Advisory (routine safety information)
- Warning (urgent safety information)
- Recall (urgent safety information relating to a product recall)
- Publications (general safety information provided by the IMB for publication via 3rd parties e.g. MIMS)
The Irish Medicines Board Drug Safety Newsletter is also published on a regular basis.