Determination of Adverse Drug Reactions in Individual Cases
Protocols
Determination of Adverse Drug Reactions in Individual Cases
·Reviewed·Published ·Updated ·8 min read
Summary
The procedure for the detection and determination of ADRs should consist of three main processes: first, the physician should make a diagnosis of the adverse condition (event AE) present in the patient and determine the type of disease or syndrome the patient is suffering from; second, he or she should perform an identification of the AE and determine that it is likely to be due to the drug and draw a conclusion about the ADE; and finally, he or she should perform a validation test, thus determining that the ADE is likely to be due to the drug and drawing a conclusion about the ADR. Conclusion.
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Da — when not otherwise indicated, molecular weight units are daltons. Mw — weight-average molecular weight. Mn — number-average molecular weight.
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Cite this article
Aladdin Scientific. "Determination of Adverse Drug Reactions in Individual Cases" Aladdin Knowledge Base, updated Dec 24, 2024. https://www.aladdinsci.com/us_en/faqs/determination-of-adverse-drug-reactions-en.html
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