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What is an Adverse Event (side effect)?
An adverse event is a response to a medicinal product which is noxious and unintended and which does not necessarily have a causal relationship (association) with a medicinal product. An adverse event can therefore be any unfavorable and unintended sign (for example, an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal product, whether or not considered related to this medicinal product. For Example: A patient suffers from vomiting and had red patches all over his body while taking medicinal product X for leg injury. In this example, vomiting and red patches all over his body are considered as adverse events.

You can report adverse event/side effect, product complaints and product related inquiries here.
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This website page is for reporting adverse event(s)/side effect(s) experienced by patient, raising product quality complaints, medical/other product related enquiry by patient or his/her representative for products of Alembic Pharmaceuticals Limited.

Any person who misuses or posts inappropriate content unrelated to the adverse event/side effect, product complaints, inquiry on this website shall be accountable or liable for consequences related thereto. We further reserve our right to take appropriate action against such person. Further, all your personal information submitted while reporting any adverse event/side effects on this website are sent to the pharmacovigilance team and may be shared with the relevant authorities to report adverse drug effects/side effects.

If you are contacting for any other information than adverse event please visit https://www.alembicpharmaceuticals.com/

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