Medical, clinical trial and drug databases your AI assistant can search
Clinical and pharmaceutical research draws on many authoritative but separate databases. Kahubi connects to PubMed and clinical-evidence search, ClinicalTrials.gov, EU medicine authorisations from the EMA, US drug labels in DailyMed, the RxNorm drug vocabulary, openFDA adverse-event reports, NCATS Inxight Drugs and DrugCentral, ClinGen curations and WHO, CDC and nutrition data.
Ask a clinical question and the assistant searches the right registries, then cites PMIDs, NCT numbers, EPAR product numbers or the exact label section it used. Spontaneous adverse-event reports are labelled as such, so a count is never presented as proof of causation.
14 sources you can connect
- PubMed & Europe PMCBiomedical literature: search, MeSH terms, related articles, citations and lawful full text.Community server
- ClinicalTrials.govSearch registered clinical trials, read full study records, posted results and eligibility criteria.Community server
- Clinical evidence (trials, FDA labels, adverse events)ClinicalTrials.gov, openFDA drug labels, adverse-event reports and approvals alongside PubMed.Community server
- CDC data and WONDERUS public-health datasets (data.cdc.gov) and CDC WONDER mortality and natality queries.Community server
- NCATS Inxight DrugsEvery FDA-registered substance with its UNII, plus NCATS-curated approval status, indications, targets and pharmacokinetics.Hosted by Kahubi
- openFDAFDA drug and device adverse events, recalls, labels and shortages.Community server
- EMA medicines (EU authorisations)Centrally authorised EU medicines, orphan designations, safety communications and shortages from the European Medicines Agency.Hosted by Kahubi
- WHO Global Health ObservatoryWHO health indicators for every member state: life expectancy, mortality, disease burden, health systems.Hosted by Kahubi
- DailyMed (US drug labels)Current FDA-submitted prescribing information for every US drug, section by section.Hosted by Kahubi
- USDA FoodData CentralNutrient composition of foods from the USDA reference database.Community server
- RxNorm (NLM drug vocabulary)Normalised US drug names: ingredients, brands, clinical drugs with strength and form, and NDC codes.Hosted by Kahubi
- Open Food FactsCrowd-sourced database of 3M+ packaged food products: ingredients, nutrition, labels, Nutri-Score.Community server
- DrugCentralApproved drugs worldwide: approvals by agency, indications and contraindications, mechanism targets and FAERS safety signals.Hosted by Kahubi
- ClinGen (clinical gene and variant curation)Expert-panel gene-disease validity, dosage sensitivity and ACMG variant classifications.Hosted by Kahubi
Questions researchers ask these sources
“Find randomised controlled trials since 2020 on exercise interventions for depression in older adults.”
Articles with PMIDs, publication types, MeSH headings and abstracts.
PubMed & Europe PMC“List completed phase 3 trials of GLP-1 receptor agonists in heart failure that have posted results.”
Studies with NCT numbers, enrolment, primary outcomes and the posted results.
ClinicalTrials.gov“What does the FDA label say about liver-related adverse reactions for this drug, and what has been reported since approval?”
Label sections and adverse-event report summaries from openFDA, for evidence review.
Clinical evidence“How many US deaths were attributed to drug overdoses each year from 2015 to 2022?”
Counts and rates by year from CDC WONDER mortality data, with the query parameters stated.
CDC data and WONDER“What are the half-life and main CYP interactions of apixaban?”
Curated human pharmacokinetics with dose and population, plus CYP and transporter interactions with sources.
NCATS Inxight Drugs“What are the most frequently reported adverse events for semaglutide in FAERS?”
Reaction terms with report counts, noted as spontaneous reports that do not prove causation.
openFDA
Frequently asked questions
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