Adverse event reporting

We at Kivonyx Healthcare are committed to providing world class medicines at affordable cost to the last man standing in society. We understand the need and importance of monitoring drug safety – right from the discovery of the medicine to the entire life cycle of the drug. The aim of pharmacovigilance is to protect health by identifying, evaluating and minimizing safety issues in all possible ways.

Drug Safety encompasses all aspects of drug reaction right from side effects/adverse events/adverse drug reactions, lack of efficacy or any undesirable response reported once a medication is administered to the patient.

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

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
Lack of efficacy
Unexpected therapeutic or clinical benefit
Use of drug in unapproved indication

Report even if:

You are not certain the product caused an adverse reaction
You don’t have all the details

Who can Report

Any Healthcare professional (Doctors, Dentists, Nurses, Pharmacists, etc)
Non Healthcare professional (Patient, relative, friend, etc)

Where to report:

407-A, Primate House, Opp. Mother Dairy, Nr. Judges Bunglows, Bodakdev, Ahmedabad-380015, INDIA Phone : +91 79400 64093

E-mail

For Global PV Reporting : drugsafety@kivonyx.com
For detailed reporting click to download Adverse Event Reporting Form

Online : To report online click here

Confidentiality :

The patient’s identity is kept confidential & protected in line with company’s policies. The information you provide will be used for the purpose of drug safety surveillance and it may be shared with health authorities. You have the right of access to your personal data which we have. Submission of a report does not constitute an admission that medical personnel or manufacturer of the product caused or contributed to the reaction.