SiteCheck Health & Travel

Ingested from the official MCP Registry

FastDrop pulled this entry from the official MCP Registry as io.github.bck-stack/sitecheck-health-travel and probed the endpoint. The maker did not submit it, so the outbound link is not endorsed and the description is not theirs.

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Tools this endpoint exposes

Read directly from the endpoint on 23 Oct 2026. Not supplied by the maker.

• health_pubmed_abstracts

  PubMed search (NCBI E-utilities): matching articles with PMID, title, authors, journal, publication date and DOI. Citation metadata only, no abstract text. Up to 20 results. Price: $0.002 in USDC per

• health_clinical_trials_gov

  ClinicalTrials.gov study search (API v2): NCT ID, title, status, phase, start and completion dates, sponsor, conditions, interventions, enrollment and primary outcome. Up to 10 studies per call. Price

• health_fda_orange_book

  FDA Drugs@FDA approved applications (openFDA) by active ingredient: application number, sponsor, brand names, dosage form, marketing status and Orange Book therapeutic equivalence (TE) code. Up to 10

• health_fda_purple_book

  FDA Purple Book licensed biological products matching a name (brand or proper name, e.g. adalimumab): applicant, BLA number, license type (351(a) originator, 351(k) biosimilar or interchangeable), str

• health_fda_drug_shortages

  FDA drug shortage listings (openFDA): generic name, availability status (e.g. Available, Currently in Shortage), manufacturer, package NDC, posting dates and FDA contact number. Up to 10 listings per

• health_fda_medical_device_510k

  FDA 510(k) premarket notifications (openFDA): K-number, device name, applicant, decision (e.g. Substantially Equivalent), decision and received dates, product code and advisory committee. Up to 10 per

• health_fda_recalls_enforcement

  FDA drug recall enforcement reports (openFDA) matching a product word: recall number, class I/II/III, status, recalling firm, reason, product description and dates. Drug recalls only, not food or cosm

• health_fda_adverse_events_faers

  FDA FAERS drug adverse event reports (openFDA) for a generic drug name: report ID, receive date, seriousness, patient age and sex, drugs and reported reactions. Spontaneous reports only; a report does