Reporting of Adverse Events

"An adverse event is any untoward medical occurrence in a patient administered a medicinal product and which does not necessarily have to have a causal relationship with this treatment."

If you wish to report an adverse event (side effect) or product complaint with a Themis product, please download the ADR reporting form, fill in the details and email it to us at drugsafety@themismedicare.com

You may also call us on this telephone no.

+91. 22 6760 7080, Ext- 359