Reporting of Adverse Events

 

"An adverse event is any untoward medical occurrence in a patient administered a medicinal product and which does not necessarily have to have a causal relationship with this treatment."
- ICH E2D

"If you wish to report an adverse event (side effect)/product complaint with a Dr. Reddy's product in India please call Dr. Reddy's Laboratories Ltd. India on Toll free No. 1800 425 0014 (Monday to Friday 8am to 6pm and on out of office hours and on weekends, the callers can record their messages for us to call back) or write to the email ID: customerservices@drreddys.com.

Please ensure that the below mentioned, minimum information is provided:

Guidelines to fill the CIOMS form

Pharmacovigilance Form

Reporter Information
Patient Details
M
F
I- REACTION INFORMATION
M
F
Patient Died
Involved or Prolonged Inpatient Hospitalisatoin
Involved Persistence or Significant Disability or Incapacity
Life Threarening
II- SUSPECT DRUG(S) INFORMATION
Yes
No
NA
Yes
No
NA
III- CONCOMITANT DRUG(S) AND HISTORY
IV - MANUFACTURE INFORMATION
Study

Literature

Health Professional
Initial

Follow Up

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