Reporting of Adverse Events

“An adverse event is any uptoward 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 NEON product, please click on the below link to download

ADR Presentation

ADR Reporting Form

Monograph - Cisatracurium Inj.

Patient Information Leaflet - Cisastracurium Inj.

Ropin Heavy Leaflet PIL

Fill in the details and email it to us at drugsafety@neonegroup.com
You may also call or Whatsapp us on this no. +91 87675 59938