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The Methodology of the Collection of Adverse Event Data
The Diagnosis of Adverse Medical Events Associated with
8 other sections not shown
abnormalities ABPI adverse drug reactions adverse event adverse experience adverse reactions algorithm assessment associated Bayes Theorem benoxaprofen Captopril causality cause Ciba-Geigy cimetidine clinical trials clinician cohort studies collected compared considered COSTART criteria detect diagnosis disease doctor dose drug surveillance Drug-induced efficacy evaluation factors further hospital hypertension identified incidence interactions investigations involved known laboratory data licence marketing medical events Medicines method Ministry of Health monitoring normal range number of patients occurring onset organised pharmaceutical company pharmaceutical industry pharmacological Pharmacovigilance Phase physician placebo PMS schemes population possible post-marketing surveillance practolol pre-marketing prescription probably problems protocol published question questionnaire rechallenge record regulatory authorities relationship relevant reporting of adverse response risk scale score serious side effects specific spontaneous reports standard statistical suspected adverse suspected drug symptoms Table therapeutic therapy treatment Type volunteers