Reporting of Adverse Events
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