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Journal Abstract Search

257 related items for PubMed ID: 9192053

  • 1. Two UK Government proposals bearing on drug safety.
    Griffin JP.
    Adverse Drug React Toxicol Rev; 1997 Mar; 16(1):1-7. PubMed ID: 9192053
    [No Abstract] [Full Text] [Related]

  • 2. Sequential surveillance for drug safety in a regulatory environment.
    Martin D, Gagne JJ, Gruber S, Izem R, Nelson JC, Nguyen MD, Ouellet-Hellstrom R, Schneeweiss S, Toh S, Walker AM.
    Pharmacoepidemiol Drug Saf; 2018 Jul; 27(7):707-712. PubMed ID: 29504168
    [No Abstract] [Full Text] [Related]

  • 3. The new EU legislation on pharmacovigilance and changing models for drug development.
    Callréus T.
    Drug Saf; 2011 Jun 01; 34(6):529-30; author reply 530-1. PubMed ID: 21585224
    [No Abstract] [Full Text] [Related]

  • 4. European legislators tighten rules on drug safety.
    Watson R.
    BMJ; 2012 Sep 18; 345():e6260. PubMed ID: 22991010
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  • 8. European commission consultation on pharmacovigilance.
    Waller P, Beard K, Egberts T, Evans S, Hallas J, Hasford J, Laporte JR, Moore N, Shakir S, Sturkenboom M.
    Pharmacoepidemiol Drug Saf; 2008 Feb 18; 17(2):108-9. PubMed ID: 18058839
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  • 11. [Farmacovigilance: the way towards a safer drug use].
    Dobrić S.
    Vojnosanit Pregl; 2007 Apr 18; 64(4):229-30. PubMed ID: 17580530
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  • 12. How should we react to adverse drug reactions?
    Ferner RE, Beard K.
    Postgrad Med J; 2011 Feb 18; 87(1024):81-2. PubMed ID: 21303818
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  • 15. Adverse drug reaction reporting systems: the United Kingdom and the United States.
    Scott HD, Thacher A, Rosenbaum SE, Waters WJ, Green M.
    R I Med J (1976); 1988 May 18; 71(5):179-84. PubMed ID: 3387803
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