Problem
A suspected interaction can be difficult to document consistently, and AI-assisted workflows in regulated settings need evidence, accountability, and a clear human-review boundary.
A guided medication-interaction intake demo that keeps label evidence and human review in view.
Adverse Intake turns a synthetic report of a suspected medication interaction into a structured draft for human review. The guided conversation captures the products, reported experience, and timeline while showing relevant label evidence and clinical-review signals.
I built the local demo around a deterministic intake workflow, structured validation, and curated contraindication data. The separate Proveria demonstration shows how verified software, authorized actions, and portable receipts can strengthen a regulated workflow; external trust and AI paths are optional rather than required for the local intake.
A suspected interaction can be difficult to document consistently, and AI-assisted workflows in regulated settings need evidence, accountability, and a clear human-review boundary.
I designed a guided, synthetic intake that organizes the report, checks versioned label evidence, and prepares a draft record without making a treatment decision.
Collects the reporter, products, experience, and timeline one step at a time.
Checks curated contraindication assertions from a versioned snapshot.
Flags medication-safety concerns for qualified human review.
Assembles a client-owned case record that can be downloaded as JSON.
Documents the report without making an autonomous treatment decision.
Illustrates verified software, authorized actions, and receipts through Proveria.
Explore how Adverse Intake brings structured reporting, label evidence, and human review together.