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The data behind the verdict
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14 sources, all live
Every Scan Dose verdict is cross-referenced against these 14 authoritative public-health datasets. Tap any database to read the source.
U.S. FDA
FDA adverse event reports, drug labels, recalls, and approval data. Primary source for safety signals.
Real adverse events for any drug or supplement; recall alerts.
U.S. Department of Agriculture
Authoritative nutrient profiles for foods and ingredients.
Nutrient-level lookups for whole-food alternatives to supplements.
U.S. National Library of Medicine
Registry of every clinical trial conducted globally. We index trials relevant to supplement ingredients.
Verify whether a supplement claim has clinical trial backing.
U.S. National Library of Medicine
Standardized nomenclature for clinical drugs across systems.
Match user-entered medication names to canonical drug records.
Stanford University
Pharmacogenomics knowledge base linking genetic variants to drug response.
23andMe / AncestryDNA upload → personalized drug-response insights.
Regenstrief Institute
Universal codes for clinical lab tests and observations.
Map blood-panel rows from any lab to a standard biomarker schema.
U.S. National Library of Medicine
Official structured product labels (SPL) for every FDA-approved drug.
Pull authoritative warnings, contraindications, and interaction data.
NCBI / National Library of Medicine
Index of 36+ million biomedical citations and abstracts.
Source of citation backing for every ingredient grade.
NCBI
Clinical interpretations of human genetic variants.
Interpret rare variants surfaced by genome upload.
Clinical Pharmacogenetics Implementation Consortium
Peer-reviewed dosing guidelines for drug-gene pairs.
Translate raw genotype data into actionable dose adjustments for medications.
European Bioinformatics Institute (EBI)
Comprehensive protein sequence and functional annotation database.
Resolve enzyme names referenced in pharmacokinetic mechanisms.
SNOMED International
Multilingual clinical health terminology used by 80+ national health systems.
Standardize the user's self-reported conditions for cross-database matching.
Jackson Laboratory
Standardized vocabulary of phenotypic abnormalities in human disease.
Tie symptom descriptions to disease and gene associations.
Johns Hopkins University
Online Mendelian Inheritance in Man — catalog of human genes and disorders.
Map genome-derived variants back to known Mendelian disease entries.