Adverse event reporting


Drug Safety Monitoring: Objective and Importance

Systematic drug safety monitoring or pharmacovigilance involves continual monitoring of unwanted effects and other safety-related aspects of drugs which are already available in the market. This strives to promote rational use of drugs with minimum risk to the consumers.

INTAS is firmly committed to fulfilling its pharmacovigilance responsibilities and INTAS encourages reporting by the concerned parties of complaints associated with intake or administration of any INTAS drug product. This activity helps in continuous assessment of the benefit-risk ratio of INTAS drug products.

WHAT CAN BE REPORTED (I.E., EVENT) WHO CAN REPORT (I.E., REPORTER)
Any Adverse Experience / Side Effect that occurred after taking an INTAS drug product A healthcare professional / person who experienced it or his/her relative, friend, lawyer, acquaintance / anyone who has sufficient knowledge of the event
Lack of expected clinical response after taking an INTAS drug product A healthcare professional / person who experienced it or his/her relative, friend, lawyer, acquaintance / anyone who has sufficient knowledge of the event
Overdosing, abuse, misuse of a drug, off-label use with or without adverse experience / side effects, medication errors with or without adverse experience / side effects, interactions, occupational exposure with an INTAS drug product A healthcare professional / person who experienced it or his/her relative, friend, lawyer, acquaintance / anyone who has sufficient knowledge of the event
INTAS drug product in original package found damaged, discoloured, misshaped, or tampered with, or any product quality-related complaint A healthcare professional / person who experienced it or his/her relative, friend, lawyer, acquaintance / anyone who has sufficient knowledge of the event
Having taken an INTAS drug product while being pregnant, breast feeding or lactating with or without adverse events A healthcare professional / person who experienced it or his/her relative, friend, lawyer, acquaintance / anyone who has sufficient knowledge of the event

To report an adverse event in India, please follow the below mentioned steps. To report an adverse event in Europe, UK, US or MENA region, please click here.

Healthcare Professionals (Doctor / Nurse / Dentist / Physiotherapist / Pharmacist) to report here:

To report an adverse event (side effect) / lack of efficacy / overdose / misuse / unintended use while being pregnant or lactating or breastfeeding / other event:

Click here to fill out the Intas Suspected ADR Report Form for Healthcare Professionals online. Alternatively, download the Printable Version of Intas’ Suspected ADR Report Form for Healthcare Professionals, fill-up its print copy and post it to the following address:

PV Cell, Medical Services Dept.,
INTAS Pharmaceuticals Limited,
Corporate House, Opposite Sola Bridge,
Off S. G. Highway, Thaltej,
Ahmedabad – 380054. Gujarat. India.

To report product quality-related complaints:

Click here to fill out the Intas Product Complaint Form online. Alternatively, download the Printable Version of Intas Product Complaint Form, fill-up its print copy and send by post to the following address:

PV Cell, Medical Services Dept.,
INTAS Pharmaceuticals Limited,
Corporate House, Opposite Sola Bridge,
Off S. G. Highway, Thaltej,
Ahmedabad – 380054. Gujarat. India.

Non-healthcare Professionals (Patient / Relative / Friend / Acquaintance) to report here:

To report an adverse event (side effect) / lack of efficacy / overdose / misuse / unintended use while being pregnant or lactating or breastfeeding / other event:

Click here to fill out the Intas Suspected ADR Report Form for Non-healthcare Professionals online. Alternatively, download the Printable Version of Intas Suspected ADR Report Form for Non-healthcare Professionals, fill-up its print copy and send by post to the following address:

PV Cell, Medical Services Dept.,
INTAS Pharmaceuticals Limited,
Corporate House, Opposite Sola Bridge,
Off S. G. Highway, Thaltej,
Ahmedabad – 380054. Gujarat. India.

To report product quality-related issues:

Click here to fill out the Intas Product Complaint Form online. Alternatively, download the Printable Version of Intas Product Complaint Form, fill-up its print copy and send by post to the following address:

PV Cell, Medical Services Dept.,
INTAS Pharmaceuticals Limited,
Corporate House, Opposite Sola Bridge,
Off S. G. Highway, Thaltej,
Ahmedabad – 380054. Gujarat. India.