Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Search in posts
Search in pages

Drug Safety

Advice About Adverse Event (Side Effects) Reporting

At Ipca, our commitment to ensuring safety of drugs goes beyond mere compliance. We understand the need and importance of monitoring drug safety – right from the discovery of the medicine throughout the life of the drug. We strive to ensure safe and rational use of medicines.

If you wish to report an adverse event occurring with our drug, please read below:

Who can report:


  • Any health care professional (Doctors, Dentists, Nurses, Pharmacists, etc.)
  • Non healthcare professional (Patient, relative, friend, etc.)

What to report

  • All types of adverse events (Side effects occurring after administration of drug)
  • Other scenario/situations (even if not associated with adverse event)
    • Overdose
    • Accidental use
    • Abuse and misuse
    • Medication errors
    • Use of drug during pregnancy
    • Use of drug during breast feeding
    • Paternal exposure
    • Drug interactions
    • Occupational exposure
    • Lack of efficacy
    • Unexpected therapeutic or clinical benefit
    • Use of drug in unapproved indication

Where to report

Ipca Laboratories Ltd., Corporate Pharmacovigilance Cell, 142-AB, Kandivli Industrial Estate, Kandivli (West), Mumbai 400 067, India. E-Mail:

Phone: +91 22 6647 4105

US Toll free number: 1-888-472-2651

UK number: 00800 890 13370

Malta Toll Free Number: 00 800 2660 4571

Online submission

Note: Fields marked by * are compulsory

Patient's Initial *
Adverse event *
Suspect drugs *
Name of the reporter *
Email ID of the reporter *
Please enter valid e-mail ID
Telephone/Cell number of the reporter *
Number should be in international format like +919999988888.
Please fill all compulsory marked fields

Report even if:

  • You’re not certain the product caused adverse reaction
  • You don’t have all the details


All the information and personal data you share with us will be protected and kept confidential in line with Company SOP. The information you provide will be used for the purpose of drug safety surveillance [and to enable us to deal with your enquiry appropriately] and it may be shared with health authorities. You have a right of access to your personal data which we hold about you.

Submission of a report does not constitute an admission that medical personnel or manufacturer or the product caused or contributed to the reaction.


Leave us your details so we can get in touch with you.

Fields marked by * are compulsory.

Please enter valid Telephone number like +919999988888.
Please enter valid e-mail ID
Please fill all compulsory marked fields
We use cookies to give you the best possible experience on our site. By continuing to use the site you agree to our use of cookies. More information
OK, got it!