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Book
Pharmacovigilance Essentials : Advances, Challenges and Global Perspectives.
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ISBN: 9819989493 Year: 2024 Publisher: Springer Nature

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Book
European medicines research : perspectives in clinical trial.
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ISBN: 0952664305 Year: 1996 Publisher: Cambridge European conference publications

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Book
Bericht über die Tagung Unerwünschte Arzneimittelwirkungen Erfassungsmethoden und Bewertung, Kiel, 26.-29. November 1990
ISBN: 3537835019 Year: 1991 Publisher: Sankt Augustin Asgard-Verlag

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Dissertation
Medication errors and adverse drug events in hospitalised patients; methodological issues and computerised intervention.
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ISBN: 9789077113981 Year: 2009 Publisher: S.l. s.n.

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Dissertation
From research on rare diseases to new orphan drug development.
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ISBN: 9789039352595 Year: 2010 Publisher: Rotterdam Optima grafische communicatie

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Current challenges in pharmacovigilance : pragmatic approaches.
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ISBN: 9290360747 Year: 2001 Publisher: Geneva CIOMS

European medicines research : perspectives in pharmacotoxicology and pharmacovigilance
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ISBN: 9051991541 Year: 1994 Publisher: Amsterdam ; Oxford ; Washington, DC ; Tokyo IOS Press

Adverse drug reactions : a practical guide to diagnosis and management
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ISBN: 0471942111 Year: 1994 Publisher: Chichester Wiley

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This text will be of enormous value to anyone involved in the monitoring and investigation of adverse medical events occurring during the clinical trials, or during the post marketing period of a drug. The book reviews the biochemical and physiological abnormalities in each of the bodys organ systems and helps the investigator decide if the problem is of drug-induced origin. Most of the information is presented as a series of observations with accompanying questions which should be addressed in order to make an accurate diagnosis. Easy-to-read with useful flow charts for the management of adverse drug events and examples of specific report forms, this text will be of interest to all those involved in drug monitoring in clinical medicine, pharmaceutical companies, contract research organisations or regulatory authorities.

MedWatch : the FDA safety information and adverse event reporting program
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Year: 1997 Publisher: Rockville, Md. : U.S. Food and Drug Administration

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