Reporting Adverse Event and Quality Defect

A service that allows you to report adverse events, medication errors, and product quality defects of the companies products.


 

What is Pharmacovigilance ?

A service that allows you to report adverse events, medication errors, and product quality defects of Advanced Pharmaceutical Industries Products.

What is Adverse Event ?

Defined as a response to a medicinal product, which is noxious and unintended.

What is Quality Defect ?

Defined as any difference in the appearance, physical-chemical, microbiological and pharmaceutical-technological properties of the actual situation of medicinal product and information from marketing authorization.

Why do we report Adverse Event ?

Advanced Pharmaceutical Industries maintains active surveillance to ensure the safety of our patients and that our products have a complete safe profile.
Your information will allow us to take the necessary action to increase the safety of the Advanced Pharmaceutical Industries product.

If you experienced adverse event or found a quality defect while using any of our products, please fill the below report form.

 

Adverse Drug Reaction (ADR) Reporting Form

Oral
Injection
* Indicates required fields
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