PharmaPulse
The life-sciences vertical — spanning clinical & competitive intelligence and deep research bioinformatics. 180+ tools across 40+ data sources: clinical trials, FDA safety, drug/target pharmacology, genomics, proteomics & structures, pathways & interactions, and biomedical literature.
Included Packs
Search 400K+ clinical trials. Filter by phase, status, sponsor, condition. Track pipeline progress.
Drug adverse events (FAERS), FDA approvals, drug labels, recalls, safety signal detection.
Drug name normalization (brand ↔ generic), drug interactions, NDC codes.
Pharma company financials, 10-K/10-Q filings, R&D spend, revenue, patent cliff disclosures.
Search 40M+ biomedical citations and research publications.
Search patent filings for drug compounds, methods, formulations.
BioThings (MyGene / MyVariant / MyDisease / MyChem), GWAS Catalog, Ensembl, gnomAD — gene, variant, and disease annotation.
NCI GDC and cBioPortal — cancer studies, cases, mutations, and genomic files across TCGA/TARGET/CPTAC.
UniProt, AlphaFold, RCSB PDB, Human Protein Atlas, InterPro — sequences, 3D structures, expression, and domains.
KEGG, Reactome, WikiPathways, Rhea, QuickGO — metabolic/signaling pathways, biochemical reactions, and Gene Ontology.
IntAct, STRING, Guide to PHARMACOLOGY — protein interactions and quantitative drug-target pharmacology.
PubChem, ChEMBL, NCI CACTUS — compound properties, bioactivity, and chemical identifier resolution.
Expression Atlas (transcriptomics), PRIDE (proteomics), MetaboLights (metabolomics) — the EBI omics trio.
SGD (yeast), PomBase (fission yeast), Europe PMC, DailyMed, MedlinePlus — curated genetics and biomedical references.
Common questions
What data sources are included in PharmaPulse?
ClinicalTrials.gov (active and completed trials by phase, sponsor, condition), OpenFDA (adverse events, drug approvals, label data), RxNorm (drug normalization, ingredient mapping), DailyMed (structured labels), SEC EDGAR (pharma company filings), and USPTO (patents and trademarks). Covers competitive intelligence, safety analysis, and clinical pipeline tracking.
Can I get a complete safety profile for a drug from one call?
Yes — the drug_safety_profile prompt and the pharma_drug_profile _intel tool fan out across RxNorm, OpenFDA adverse events, ClinicalTrials, and DailyMed in parallel. A query like "What are the side effects of Ozempic?" returns adverse event counts (54k+ reports for semaglutide), interaction warnings, and label sections in one round trip.
How do I track Phase 3 trials or competitive pipelines for a condition?
ClinicalTrials.gov tools let an agent filter trials by phase, status (recruiting, active, completed), condition, sponsor, and intervention type. Combine with EDGAR filings on the sponsor companies and USPTO patent search on the molecule for a full competitive-intelligence brief.
Is the drug data live or cached?
ClinicalTrials.gov updates are typically reflected within hours. OpenFDA adverse events are refreshed quarterly by FDA, with the most recent quarter usually 2–3 months behind. RxNorm releases monthly. Every response includes _meta.cache.fresh_until so agents can decide whether to refetch.