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Abstract
Mesh: See more » Adverse Drug Reaction Reporting SystemsAdvisory CommitteesDrug ApprovalDrug-Related Side Effects and Adverse ReactionsHumansSafetyUnited StatesUnited States Food and Drug Administration/organization & administration
Year: 2005 PMID: 15733696 DOI: 10.1016/S0140-6736(05)17994-X
Source DB: PubMed Journal: Lancet ISSN: 0140-6736 Impact factor: 79.321