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What data and content sources are available in PharmaPendium?
Last updated on November 01, 2019PharmaPendium is the go-to database to support informed decision-making during pharmaceutical development. It provides access to hard-to-find full text searchable regulatory documents and high-quality extracted data on Drug safety, DMPK and Efficacy. Further, the PharmaPendium drug-drug interaction risk calculator helps DMPK specialist to predicts harmful drug-drug interactions.
You can find the most current content statistics here
PharmaPendium provides access to the following full text searchable documents:
- FDA approval packages
- EMA approval documents
- FDA Advisory Committee Documents
- DESI documents
- Meyler's Side Effects of Drugs: The International Encyclopedia of Adverse Drug Reactions and Interactions
- Mosby's Drug Consult™
PharmaPendium contains high quality preclinical, clinical and post-market drug safety data that is extracted from various sources:
- FDA approval packages
- EMA approval documents
- FDA Adverse event reporting system (FAERS)
- Meyler's Side Effects of Drugs: The International Encyclopedia of Adverse Drug Reactions and Interactions
- Mosby's Drug Consult™
- PharmaPendium Published Toxicity (literature sources)
The high quality PK data in PharmaPendium Pharmacokinetic module is extracted from:
- FDA approval packages
- EMA approval documents
- PharmaPendium Published PK (literature sources)
The unique MET data in the Metabolizing enzymes and transporter module is extracted from:
- FDA approval packages
- EMA approval documents
- FDA Advisory Committee Documents
- PharmaPendium Published MET (literature sources)
The Efficacy data in the Efficacy module is extracted from:
- FDA approval packages
- EMA approval documents
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