Cadila Pharmaceuticals

Every report matters. By sharing what you experience, you help us detect issues early and protect others from harm. Together, we can make every medicine safer and healthcare more trustworthy.

Your Safety, Our Priority!

Pharmacovigilance is like a health detective, watching out for any issues with medications and vaccines.
If you experience any side effect, let us know – together, we can keep healthcare safe and effective!

Help Us, Help You

We are committed to keeping medicines and vaccines safe for everyone. Our mission is to catch any unexpected side effects or issues before they become serious problems.

So, share your experiences.

Your Experience Matters

Report a strange reaction to a medication or vaccine.

You help us protect millions and ensure healthcare remains safe and effective.

patients

Patients

patients

Doctors

patients

Nurses

patients

Relatives

patients

Pharmacists

patients

Lawyers

patients

Other Healthcare professionals

You can report all suspected adverse drug reactions (ADR - side effects), including:

Severe reactions, such as those that are:

  • starFatal (causing death)
  • starLife-threatening
  • starDisabling or incapacitating
  • starResult in or prolong hospitalisation
  • starCause congenital abnormalities or are otherwise medically significant

Other side effects:

  • starProduct quality-related complaints
  • starIssues related to identity, purity, quality, strength, efficacy, safety, physical changes, labelling defects, packaging, storage, handling, or any other product defects. 

*It is important that you complete and submit the Initial Information on Adverse Drug Reactions (ADR) report form within 24 hours of receipt.

Download Adverse Drug Reactions (ADR) Reporting Form:

If you notice any ADR, please report the essential information:

Patient Information

Age, gender, existing conditions, and any other medications being taken.ation

Reporter Information

Name, contact number, and address.

Drug Information

Drug name (brand and generic), batch number, manufacturing and expiry dates.

Event Description

Name of the event, date of occurrence, outcome, and actions taken.

Make medicines safer for everyone

Make medicines safer for everyone

Prevent harm before it happens

Prevent harm before it happens

Ensure safe prescribing and use of medicines

Ensure safe prescribing and use of medicines

Protect patients and public health

Protect patients and public health

Strengthen medicine information and education

Strengthen medicine information and education

 

Patient can report suspected side effects:

For Global PV Reporting (Except US & UK)

For PV Reporting in 
the USA

For PV Reporting in 
the UK

Download Adverse Drug Reactions (ADR) Reporting Form:

Vaccines Marketed in India

Topiramate Safety Information - United Kingdom

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Corporate Identification No : U24231GJ1991PLC015132

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