Transforming patients’ lives today and tomorrow¹
Enbrel® is a TNFi approved for treating multiple chronic diseases in rheumatology and dermatology.2
Heritage of Enbrel®
Approved by the EMA in 2000,6 Enbrel® was the first-approved TNFi in RA.1
Enbrel® is approved across 6 therapeutic indications, including paediatric indications.²
The efficacy and safety profile of Enbrel® has been established across
What type of patients may be the best candidates for Enbrel® therapy?
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No. C-70, G Block, Bandra Kurla Complex,
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®Trademark Proprietor – Wyeth LLC, USA
Licensed User – Pfizer Limited, India
To view the summary of prescribing
information for ENBREL®, please
For the use only of Registered Medical
Practitioners or a Hospital or a Laboratory.
Full prescribing information available on
*Some studies may have evaluated (or will evaluate) etanercept biosimilars and/or evaluated (or will evaluate) indications for which Enbrel® is not approved.
EMA, European Medicines Agency; RA, rheumatoid arthritis; TNFi, tumour necrosis factor inhibitor.
Please click the Prescribing Information link to view the safety and adverse events information of Enbrel®.
For the use only of Registered Medical Practitioners or a Hospital or a Laboratory.
PP-ENB-IND-0814 August 2022
These pages are not intended for patients or for members of the general public. The web pages contain promotional content.
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For more details on, Who is a Registered medical practitioner*, please visit "https://cdsco.gov.in/opencms/export/sites/CDSCO_WEB/Pdf-documents/acts_rules/2016DrugsandCosmeticsAct1940Rules1945.pdf", Page No. 39, Rule 2 part (ee), last accessed on 26th April 2021.
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