Safety Signals
Adverse events extracted, classified by severity, and rated by evidence weight — pooled from regulators and the peer-reviewed literature.
Drug safety signals, interactions, dosing, and Africa formulary status — any drug, any patient, in under sixty seconds. Built on eleven million papers and live regulatory feeds, written for the bedside.
Every signal that matters — safety, dosing, interactions, formulary — surfaced in parallel and cross-referenced against the literature, the trials registry, and the regulators that ship in your market.
Adverse events extracted, classified by severity, and rated by evidence weight — pooled from regulators and the peer-reviewed literature.
Publication velocity tracked at 30 days versus the trailing six-month baseline. New safety concerns flagged before they reach the label.
Active ClinicalTrials.gov studies pulled in and flagged against open signals — including trials marked for immediate safety review.
Therapeutic alternatives ranked head-to-head on a single, source-cited score from zero to one hundred — class-aware, indication-aware.
Severity-ranked pairings with proposed mechanism, expected timing, and clinical management — not a wall of yellow warnings.
Patient-specific dosing with renal, hepatic, body-surface-area, and weight adjustments — and the citation behind each rule.
Pregnancy, lactation, geriatric, and paediatric considerations surfaced as first-class flags — with the FDA category and the trial evidence behind it.
Gene–drug interactions read against CPIC and PharmGKB — flagged for the metabolisers and HLA variants most likely to matter at the bedside.
Registration, prequalification, and market availability checked against NAFDAC, SAHPRA, and the WHO list — the data your hospital pharmacy actually uses.
Type a drug, an INN, or paste a list. Add co-medications, renal function, weight, and any flags that matter.
Eleven million papers, 225K FDA documents, and live WHO, NAFDAC, and SAHPRA feeds — read in parallel.
Signals classified, weighted by evidence, and ranked against therapeutic alternatives in the same class.
One source-cited clinical brief, exportable as PDF, written for the bedside — not the literature.
One query, one document. Severity on the left, the finding in the middle, the source on the right. No tabs. No PDFs to chase.
A clinician in Lagos, Nairobi, or Accra monitoring drug safety manually checks FDA, WHO, NAFDAC, and SAHPRA across separate browser tabs — and still misses the rising signal. Vigil does it in one scan, cites every source, and writes the brief in the time it takes to read the chart.
A drug safety signal nobody reads is a drug safety signal nobody acts on.Editorial principle · Vigil, vol. i