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PvPI

Adverse drug reaction reporting to India’s Pharmacovigilance Programme.

Offered in: India only.

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What it is

For any hospital or clinic that reports to an ADR Monitoring Centre. A suspected adverse drug reaction is logged against the patient by whoever saw it — a doctor, a nurse or the pharmacist: the reaction in their words, when it began and when the hospital learnt of it, the medicines on the form (at least one suspected, with batch, dose, route and dates as given), whether it is serious on the ICH E2A criteria the PvPI form uses, what was done, and whether it abated when the medicine stopped or returned when it was given again. A prescriber then assigns the causality on the WHO-UMC categories, once, against their name and with their reasons — the screen never suggests one. The pharmacovigilance desk records the submission: the date, the AMC it went to and the reference it gave. A submitted report is kept as submitted. A due date shows only when your practice sets its own reporting window, with the source it read; none ships. The suspected ADR form prints from the record. The PvPI portal and VigiFlow are not connected: the desk submits there and records it here.

Who uses it: Built for: Every specialty
Reads: The patient record
Writes: ADR reports, causality assessments, submissions to the AMC
Never: It does not decide causality, judge seriousness or send anything to PvPI on its own — a clinician grades the reaction and a person submits it, and this keeps the record of both.
Access: Only people whose role includes it — the clinic owner decides who
Your data: Full PHI. Hosted in Boston, United States. On uninstall: The register stops; every report, assessment and submission is kept on the record.

In the product

Who uses it: Quality officer — the demo profile it is best tried as
Where it opens: Compliance › ADR reporting /pvpi
Permission: pvpi.read

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How it works

Report the reactionThe patient, what happened, the medicines suspected.
Assess causalityA prescriber’s WHO-UMC category, with reasons, once.
Submit to the AMCRecord the date and the reference it gave.
Print the formThe suspected ADR form, from the record.

Rules it keeps

What it does not do, by design. A listing with only benefits is an advertisement.

It does not decide causality, judge seriousness or send anything to PvPI on its own — a clinician grades the reaction and a person submits it, and this keeps the record of both.

AI in PvPI

AskQuestions about what is on screen — “What needs attention in PvPI today?” — answered with the records it read.

DraftSummaries and notes for the team, marked as drafts until a person signs.

Every answer shows its sources. Nothing AI writes is saved until a person accepts it.

See it on screen

PvPI — ADR reporting — Report a suspected drug reaction, record its causality and its submission to the AMC — 01ADR reporting — Report a suspected drug reaction, record its causality and its submission to the AMCCaptured from the running demo clinic

01ADR reporting — Report a suspected drug reaction, record its causality and its submission to the AMCCaptured from the running demo clinic

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Connected to

Read out of the code, not the brochure: each app below is here because one service queries the other’s tables. Install either side and the hand-over is already wired.

Reads from · 1

Patient Registry

See the whole clinic →

Questions clinics ask

What does PvPI do?

Adverse drug reaction reporting to India’s Pharmacovigilance Programme. For any hospital or clinic that reports to an ADR Monitoring Centre. A suspected adverse drug reaction is logged against the patient by whoever saw it — a doctor, a nurse or the pharmacist: the reaction in their words, when it began and when the hospital learnt of it, the medicines on the form (at least one suspected, with batch, dose, route and dates as given), whether it is serious on the ICH E2A criteria the PvPI form uses, what was done, and whether it abated when the medicine stopped or returned when it was given again. A prescriber then assigns the causality on the WHO-UMC categories, once, against their name and with their reasons — the screen never suggests one. The pharmacovigilance desk records the submission: the date, the AMC it went to and the reference it gave. A submitted report is kept as submitted. A due date shows only when your practice sets its own reporting window, with the source it read; none ships. The suspected ADR form prints from the record. The PvPI portal and VigiFlow are not connected: the desk submits there and records it here.

What data does PvPI read and write?

PvPI reads the patient record and writes ADR reports, causality assessments, submissions to the AMC. Its data class is Full PHI. Every app works on the same patient record — nothing is copied into a silo.

What does PvPI deliberately not do?

It does not decide causality, judge seriousness or send anything to PvPI on its own — a clinician grades the reaction and a person submits it, and this keeps the record of both.

What happens to our data if we uninstall PvPI?

The register stops; every report, assessment and submission is kept on the record.

Is PvPI available today?

Yes — PvPI is live in clinics today. Set up your practice on MedAppz and install it from your dashboard.

Where is PvPI offered?

PvPI is offered in India only: it is built on that market's own systems and rules.

Want to see PvPI running on your own patients?

Tell us what you run and we will show you this app inside a practice shaped like yours — or answer the question the page above did not.

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