15 Services from med.halowerk.com

Searches the FDA medical device recall database by product name, manufacturer, or model and returns matching recalls with classification, reason, recalling firm, dates, status, and verbatim product descriptions including lot numbers and serial ranges.

Checks whether a drug carries an FDA boxed warning by scanning multiple manufacturer labels and returns the warning text and label version if found.

Summarizes FDA adverse event reports for a drug, including top reactions, serious outcome distribution, reporter type split, and temporal trend — with explicit causation limitations.

Aggregates FDA medical device adverse event reports by product code, device name, or manufacturer into annual trend statistics including outcome splits, top problem codes, and manufacturer evaluation rates.

Returns the GHS hazard profile of a chemical including pictograms, signal word, hazard and precautionary statements, and physical handling properties like flash point, boiling point, and vapour pressure.

Resolves a gene symbol or identifier and returns cross-referenced identifiers (Entrez, Ensembl), genomic location, biotype, description, and associated transcripts with protein products.

Resolves two drug products to their RxNorm concepts and returns a detailed, field-by-field comparison of active ingredients, strengths, dose form, and route of administration — listing every difference individually.

Resolves any common chemical identifier to a canonical PubChem compound record with full structural, physicochemical, and computed properties

Searches the clinical trial registry and returns matching studies with recruitment status, phase, type, enrolment target, conditions, interventions, sponsor, dates, and site countries.

Monitors registered clinical trials for changes over time by storing a baseline snapshot on first call and reporting diffs in status, enrollment, dates, sites, and results on subsequent calls using a session token.

Returns the complete, unabridged sections of an official FDA drug label reordered by clinical significance rather than document order, preserving all text verbatim.

Searches the FDA enforcement database for drug recalls by product name, company, or date range and returns each recall with its classification spelled out in plain language (e.g. Class I = risk of serious harm or death).

Parses a clinical trial's eligibility section into structured inclusion and exclusion criteria items, each with classification and verbatim source sentence

Resolves any drug name or alias to its canonical RxNorm concept, returning identifiers, term types, active ingredients, strengths, dose forms, and brand names.

Returns per-site details for a registered clinical trial, including facility name, location, coordinates, site-specific recruitment status, and public contact information.