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Page 1 of 47
Date Title
19/02/2008 IMB Guide to Electronic Transmission of ICSRs and SUSARs Associated with Use of Human Medicines. Latest Information
01/01/2007 A Simple Guide to Reporting Adverse Reactions to Veterinary Medicinal Products
23/04/2008 Abacavir & Didanosine-Important Safety Information from GlaxoSmithKline and Bristol-Myers Squibb as approved by the IMB
16/07/2009 Abelcet (amphotericin B-lipid complex) - Important Safety Information from Cephalon as approved by the Irish Medicines Board
21/01/2014 Abraxane (paclitaxel) - Important Safety Information from Celgene Europe Ltd. as approved by the Irish Medicines Board
01/11/2006 Academic Clinical Research - support from ICRIN and IDA Ireland
21/10/2009 ACERYCAL (perindopril, amlodipine) - Important Safety Information from Les Laboratoires Servier
15/03/2010 Aclasta (zoledronic acid) - Important Safety Information from Novartis as approved by the Irish Medicines Board
27/07/2007 Acomplia (rimonabant) 20mg film-coated tablet - Important Safety Information from Sanofi Aventis as approved by the Irish Medicines Board
14/07/2008 Acomplia (rimonabant)-Important Safety Information from Sanofi Aventis as approved by the IMB
24/10/2008 Acomplia (rimonabant)-Important Safety Information from Sanofi Aventis concerning the suspension of Acomplia
08/12/2008 Acomplia (08 Dec)
03/08/2011 Actos (pioglitazone hydrochloride) and Competact (pioglitazone hydrochloride and metformin hydrochloride) - Important Safety Information from Takeda as approved by the Irish Medicines Board
27/03/2007 Actos (Pioglitazone) - Important Safety Information from Takeda as approved by the Irish Medicines Board
01/10/2013 Additional monitoring: Black triangle introduced as prompt to report suspected adverse reactions
21/05/2012 Adenuric (febuxostat) - Important Safety Information from Menarini as approved by the Irish Medicines Board
20/02/2009 Advanced Therapy Medicinal Products Regulation - Frequently Asked Questions
23/04/2013 Adverse Reaction Form - Human Medicines
18/05/2011 Adverse Reaction Form - Veterinary Medicines
07/09/2009 Adverse reaction reporting to the IMB for 2008 - update
Page 1 of 47



Date Printed: 19 April 2014

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