The FDA (U.S. Food and Drug Administration) has over 12 thousands adverse effects (AE) registered under FAERS. These AEs are monitored by life science professionals for different use cases: Pharmacovigilance/Drug Safety, Post-marketing Surveillance and Competitive Landscape.
We extracted 700 most common adverse effects from FDA, and benchmarked them towards PubMed and then towards PapersHive.
- Results do not contain duplicates.
- Results only take in consideration PubMed sources (PubMed, MEDLINE, PubMed Central).
On average PapersHive finds 66% more references. 🔥
⏬ Check the report! ⏬
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