Consolidate drug information, intelligent safety analysis, and clinical evidence into a single workspace. Stop navigating dozens of fragmented databases. 100% free. Zero subscriptions.
AI Grounded in Peer-Reviewed Literature From
Whether you're a clinical pharmacist running complex consults, a specialist seeking trial data beyond the EMR, or a medical director managing formularies, you face a fragmented information landscape. Statim—latin for "immediately"—cuts your research time in half by synthesizing global medical literature and FDA data into cited, actionable intelligence.
Prescribing info, adverse event data, clinical trials, and adherence research live across separate websites with no integration.
Basic drug directories list side effects but ignore demographic-specific risks, interaction severity, or real-world adherence barriers.
Learning about new drugs relies on fragmented news, missing critical regulatory tags like Breakthrough Therapy or Priority Review.
Real-time tracking of novel drugs, regulatory tags, and concise clinical summaries of new treatments.
Search the way you think—using natural clinical language and patient intent, not just exact drug names.
Advanced analysis of FDA adverse event data with confidence indicators and direct evidence citations.
Ask complex medication questions and get precise answers grounded directly in official prescribing info and literature.
We don’t just list side effects. We generate five distinct types of structured insights by analyzing FDA Adverse Event (FAERS) data, surfacing demographic risk, severity distribution, interactions, adherence tolerability, and off-label effects.
Evaluate age and gender-specific safety profiles so you can personalize risk assessments for individual patient populations.
Identify unexpected adverse reactions that fall outside standard labeling, prioritized by clinical severity and confidence level.
Analyze concurrent medication reports to flag combination risks, and review real-world tolerability factors that impact patient compliance.
CSI safety signals are enriched with clinical trial evidence sourced from ClinicalTrials.gov. Statim compares active safety events against rates observed in registered trials, making discrepancies visible.
Evaluate how post-market adverse event frequency compares to historic results recorded during regulatory trials.
Identify potential safety gaps when standard trial populations do not match the real-world age and gender patient demographics using the drug.
Every insight includes report counts, confidence intervals, and citations.
statim:csi:slug) designed for academic publications and AI pipelines.
Statim is not just a reference tool—it's a personalized clinical intelligence platform that helps you cut research time in half and protects against missed safety signals.
Bookmark complex drug profiles, attach private clinical notes, and spot visual indicators for medications with co-pay assistance for formulary reviews.
Automated monitoring with concise clinical summaries, regulatory significance tags, and validated source tracking for P&T committees.
Ask natural language questions. Statim instantly synthesizes data from official prescribing info, clinical trials, and PubMed to give you clear, cited answers.
Cut your drug consult research time in half with an AI workspace built for pharmaceutical intelligence. Synthesize global medical literature and real-time FDA data into a single, natural-language workspace.
Protect your margins and accelerate utilization management reviews with real-time, zero-PHI drug intelligence. Bypass red tape to access instant, aggregate data on drug efficacy, demographic risks, and adverse events.
Survive clinical rounds. Get instant, peer-reviewed drug data and citations in five seconds flat. Act as an instant, cited cognitive cheat-code for rapid medical literature synthesis right before rounds.
When your EMR database runs out of answers, get instant visibility into the latest clinical trials and FDA data. Bridge the gap where the EMR ends by providing instant access to the absolute fringes of medical literature.
Get the depth of analysis and speed of access modern clinical practice demands. Unify comprehensive drug data, real-time FDA monitoring, and AI-powered safety intelligence in a single secure platform.
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