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Adverse Event Reporting

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TARO Pharma 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.

Report even in situations where:
You are not certain that the product caused the adverse reaction
You do not have all the details

Who can report:
Any health care professional (Doctors, Dentists, Nurses, Pharmacists, 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.

Note: Submission of a report does not constitute an admission that medical personnel or manufacturer or the product caused or contributed to the reaction.

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

 
 

Taro Pharmaceutical Industries Ltd.
14 Hakitor Street, P.O. Box 10347
Haifa Bay 26110, Israel
Tel: 972-4-847-5700

E-Mail: drugsafety@taropharma.com

Adverse Experience Reporting Form

Reporter Details
Consent to contact Healthcare Professional (HCP) / Prescribing Physician
Patient Details ?
or
Taro Product Details ?
* Suspect Drug details   Strength   Lot/Batch Number
1.
 
 
2.
 
 
3.
 
 
* Start Date   Stop Date Of Drug   Dose   Frequency
1.
 
 
 
2.
 
 
 
3.
 
 
 
Event Description ?