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Drug Safety|March 17, 2017
Pharmacovigilance of Regenerative Medicine Under the Amended Pharmaceutical Affairs Act in JapanYasuko InokumaDrug Safety|February 4, 2017
Validation of New Signal Detection Methods for Web Query Log Data Compared to Signal Detection Algorithms Used With FAERSSusan Colilla, Elad Yom Tov, Ling Zhang, et al.Drug Safety|March 2, 2017
A Survey on Pharmacovigilance Activities in ASEAN and Selected Non-ASEAN Countries, and the Use of Quantitative Signal Detection AlgorithmsCheng Leng Chan, Pei San Ang, Shu Chuen LiDrug Safety|March 2, 2017
Causality Assessment in Pharmacovigilance: Still a ChallengeI Ralph EdwardsDrug Safety|February 4, 2021
Adverse Drug Reactions from Real-World Data in Inflammatory Bowel Disease Patients in the IBDREAM RegistryEline L Giraud, Pepijn W A Thomas, Jette A van Lint, et al.Drug Safety|October 5, 2019
Reported Severe Hypersensitivity Reactions after Intravenous Iron Administration in the European Economic Area (EEA) Before and After Implementation of Risk Minimization MeasuresLennart Nathell, Annegret Gohlke, Stefan WohlfeilDrug Safety|May 20, 1998
A risk-benefit assessment of natural and synthetic exogenous surfactants in the management of neonatal respiratory distress syndromeH Walti, M Monset-CouchardDrug Safety|May 20, 1998
Safety issues in the treatment of paediatric supraventricular tachycardiasJ P Pfammatter, U BauersfeldDrug Safety|May 20, 1998
Safety considerations in treating concomitant diseases in patients with asthmaL W HuntDrug Safety|November 24, 2004
Overview of the tolerability of gefitinib (IRESSA) monotherapy : clinical experience in non-small-cell lung cancerBeverley Forsythe, Karen FaulknerPageof 308