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Takeda Biopharmaceuticals India Private Limited (formerly known as Baxalta Bioscience India Pvt. Ltd.)

6th Floor, Building 8, Tower C, DLF Cyber City

DLF Phase 2, Gurgaon 122002, Haryana, India

Tel: +91-124-4559100


Medical Information (
Intended for Health Care Professionals Only)

Tel: 0008 0005 04087

Email: [email protected]

Takeda is a patient-focused, values-based, R&D-driven global biopharmaceutical company committed to bringing Better Health and a Brighter Future to people worldwide and people in India.

Pharmacovigilance

What is Pharmacovigilance?
Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems with the ultimate goal of ensuring and improving patient safety.

What is adverse event?
An Adverse Event (AE) means “any untoward medical occurrence in a patient or clinical trial subject administered a medicinal product and which does not necessarily have a causal relationship with this treatment.”

Reporting method:

Adverse event (AE) reporting for any Takeda product can be done by following any of the methods below:

  1. Anyone, including the public, who needs to report an adverse event can fill out the AE reporting form available at https://www.gemadversereporting.com/ or by scanning the below QR code.
QR code
  1. Adverse event reporting can also be done by sending an email with the following information to [email protected]:

    A.  Details of product information
    
    B.  Adverse event:
    
    C.  Reporter information 
    
    D.  Patient information [patient initials (only), gender and age or age group].
    


  2. You can also directly call the adverse event reporting helpline at +91-9599959221 (available on all Working Days 9:00 AM to 5:30 PM).

Quality

Any product related complaint should be reported to Takeda within 01 business day at [email protected]

Media queries

For media queries, contact [email protected]