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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:

Anyone

  • 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: pharmacovigilance.mumbai@ipca.com

Phone: +91 22 6647 4630

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

 
 
 

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
Please complete captcha process first....
 

Report even if:

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

Confidentiality

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.

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