https://docs.google.com/forms/d/e/1FAIpQLSe8QIasHs2itDSdhjYVznIfy6fcqawZ2HSI3XcmQHSDMvHC8A/viewform
Suspected Adverse Drug Reaction Reporting Form
(For Drugs used in Prophylaxis & Treatment of COVID-19)
Suspected Adverse Drug Reaction Reporting Form
(For Voluntary Reporting of Adverse Drug Reactions by Health care Professionals)
Medicine Side Effect Reporting Form for Consumers/ Patients in TAMIL
Information provided in this form is handled in strict confidence.
The causality assessment is carried out at AMCs by using WHO-UMC scale.
The analyzed forms are forwarded to the NCC through ADR database.
Finally the data is analyzed and forwarded to the Global Pharmacovigilance Database managed by WHO Uppsala Monitoring Centre in Sweden.
The reports are periodically reviewed by the National Coordination Centre-Pharmacovigilance Programme of India.
The information generated on the basis of these reports helps in continuous assessment of the benefit-risk ratio of medicines.
The information is submitted to the Steering committee of PvPI constituted by the Ministry of Health & Family Welfare.
The Committee is entrusted with the responsibility to review the data and suggest any interventions that may be required