Safety Notices

The purpose of these notices relating to the safety and/or quality of medicinal products is to update users and health care professionals of important changes to medicines, and to explain the reasons for those changes. The notices are classified under a number of 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 HPRA for publication via 3rd parties e.g. EMA

Date Title Type
18/12/2010 Suspected Adverse Reactions to Veterinary Medicinal Products 2010 3rd Party Publications
11/02/2010 Ivermectin products with amended withdrawal periods 3rd Party Publications
31/12/2009 Suspected Adverse Reactions to Veterinary Medicinal Products 2009 3rd Party Publications
31/12/2008 Suspected Adverse Reactions to Veterinary Medicinal Products 2008 3rd Party Publications
31/01/2008 Suspected Adverse Reactions to Veterinary Medicinal Products 2006 - 2007 3rd Party Publications
31/01/2006 Suspected Adverse Reactions to Veterinary Medicinal Products 2005 3rd Party Publications
31/01/2005 Suspected Adverse Reactions to Veterinary Medicinal Products 2004 3rd Party Publications
31/01/2004 Suspected Adverse Reactions to Veterinary Medicinal Products 2003 3rd Party Publications
31/01/2003 Suspected Adverse Reactions to Veterinary Medicinal Products 2001 - 2002 3rd Party Publications
31/05/2001 Suspected Adverse Reactions to Veterinary Medicinal Products 2000 3rd Party Publications