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By Nucleati Team

FAERS: FDA Adverse Event Reporting System

The FDA Adverse Event Reporting System (FAERS) is a public database containing information on adverse events and medication errors. An adverse event is any symptom ...

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By Nucleati Team

Importance of Compiling Case Reports of Adverse Drug Reactions & Their Role in Precision Medicine

It is nearly impossible to design a drug molecule that only has targetted effect in all living individuals. Even commonly used over-the-counter drugs, deemed and recognized by authorities as safe, can cause undesirable effects in some "hypersensitive" individuals.

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By Nucleati Team

Adverse drug reactions (ADRs) caused by genomic variations through modulation of Pharmacokinetics and Pharmacodynamics of a Drug

How does genetic make-up determine the possibility of developing ADRs to medications?

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