The Role of the Clinical Pharmacologist in the Management of Adverse Drug Reactions
- 1 January 2001
- journal article
- review article
- Published by Springer Nature in Drug Safety
- Vol. 24 (1) , 1-7
- https://doi.org/10.2165/00002018-200124010-00001
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Quantitative estimation of rare adverse events which follow a biological progression: a new model applied to chronic NSAID usePAIN®, 2000
- Incidence and Costs of Adverse Drug Reactions During HospitalisationDrug Safety, 2000
- Adverse drug reaction monitoring in Jena — experiences of a regionalized pharmacovigilance centreExperimental and Toxicologic Pathology, 1998
- Frequency and cost of serious adverse drug reactions in a department of general medicineBritish Journal of Clinical Pharmacology, 1998
- Preliminary Report: Effect of Encainide and Flecainide on Mortality in a Randomized Trial of Arrhythmia Suppression after Myocardial InfarctionNew England Journal of Medicine, 1989
- Spontaneous reporting of adverse drug reactions. II: Uses.British Journal of Clinical Pharmacology, 1988
- Spontaneous reporting of adverse drug reactions. I: the data.British Journal of Clinical Pharmacology, 1988
- ADVERSE DRUG REACTION MONITORING: DOING IT THE FRENCH WAYThe Lancet, 1985
- Clinical pharmacology. Adverse reactions to drugs.BMJ, 1981
- The Definition and Scope of Clinical PharmacologyPublished by American Medical Association (AMA) ,1980