ADR Reporting - Best WHO-GMP&ISO Certified PCD Pharma franchise and third party manufacturing Company in India

ADVERSE DRUG REACTION REPORTING FORM

For VOLUNTARY reporting of ADRs

Voizmed Pharmacovigilance Helpline : +91-8814892777‬ (10:00 AM to 6:00 PM, Monday-Saturday)

Adverse Event Reporting
Adverse Event/Side EffectPregnancy/lactationOverdoseLack of efficacyMisuseAbuseProduct Complaint
Select

Patient Information

Event Description

Complete RecoveryOngoingRecoveringUnknownDied
Select

Drug Use Detail

Treatment Dates

Reporter Information

If you would like to send us information by post, please download the form and mail to the following address:

Voizmed Pharmacovigilance Department
Voizmed Pharma Pvt Ltd.
Plot No – 363, 2nd Floor,
Industrial Area, Phase – 2
Panchkula, Haryana , 134113, India

Toll Free Number : +91-8814892777‬
safety@voizmed.com

 

To report adverse events, we recommend you to use the email address safety@voizmed.com. If more information specific to your Country is required, you may also navigate to the Worldwide tab available on the website.

Voizmed Pharma Pvt Ltd has a strong commitment to manufacturing quality products. A comprehensive adverse event reporting database is maintained in order to ensure compliance regulations are met globally. Please help us by filling the form below in the event of adverse reactions. The information generated on the basis of these reports helps in continuous assessment of the benefit-risk ratio of medicines.

 

Who can report:

Any health care professional (Doctors, Dentists, Nurses, Pharmacists,Patients etc)
Non healthcare professional (Patient, relative, friend, etc)

 

Confidentiality: 

The patient’s identity is held in strict confidence and protected to the fullest extent. The company shall not disclose the reporter’s identity in response to a request from the public.

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