Adverse Event Reporting Form
PATIENT INFORMATION
Pateint Name/Initial
*
* required
Contact Number
Gender
Male
Female
Age
DETAILS OF THE SIDE EFFECTS
Reaction onset Date:
* Please enter a valid date
Describe the event (e.g Diarrhoea, Vomiting, Headache, Bleeding etc)
* required
PRODUCT INFORMATION
Pharmevo Product Name
*
* required
Daily Dose
Start Date
* Please enter a valid date
Stop Date
* Please enter a valid date
Frequency
Batch#
REPORTER'S PARTICULARS
Reporter Name
*
* required
City
Contact No.
*
* required
Email
Profession
Select
Doctor
Nurse
Pharmacist
Patient
Other
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