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
Healthcare professionals face a fragmented information landscape. Statim—latin for "immediately", solves the core friction points that hinder modern clinical practice by providing intelligence, not just information.
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 companion that keeps you informed of the data that matters most to you.
Bookmark drugs, attach private clinical notes, and instantly spot visual indicators for medications offering co-pay assistance.
Automated monitoring with concise clinical summaries, regulatory significance tags, and validated source tracking.
Ask natural language questions. Statim instantly synthesizes data from official prescribing info, clinical trials, and PubMed to give you clear, cited answers.
Access demographic-specific risk data at the point of prescribing and stay effortlessly updated on novel treatment options and approvals.
Support medication therapy management with advanced interaction analysis, adherence tolerability insights, and formulary support.
Quickly verify safety profiles, identify options with co-pay assistance, and track updates to commonly administered medications.
Inform formularies with data-driven safety intelligence, or use our stable canonical identifiers for academic citations and AI pipelines.
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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