1 PATIENT’S DETAILS Full Name or Initials: Patient Record No: Age/Date of Birth: Sex: * M: F: Weight(kg): Hospital/Treatment Centre: 2 ADVERSE DRUG REACTION (ADR) DESCRIPTION DATE Reaction Started DATE Reaction Stopped OUTCOME OF REACTION TICK AS APPROPRIATE Congenital Abnormally Life-threatening Recovered fully Recovered with disability Death Others (specify) Was the patient Admitted Due to ADR Yes No If already Hospitalized, was it prolonged due to ADR Yes No Duration of Admission (days): Treatment of Reaction: 3 SUSPECTED SWIPHA DRUG (Including Biologicals Medicines & Nutraceuticals) DRUG DETAILS (State name and other details if available / Attach product label / Sample (if available) Brand Name: Generic Name: Batch No: NAFDAC No: Expiry Date: Name & Address of Manufacturer: Indications for Use Dosage Route of Administration Date Started Date Stopped 4 CONCOMITANT MEDICINES (All medicines taken within the last 3 months including Nutraceutical and self-medication) Brand/Generic Dosage Route Date Started Date Stopped Reason for Use 5 SOURCE OF REPORT: Name of Reporter: Address: Profession: Telephone: Email Address: