How to report a suspected side effect (adverse event) with the use of Jetrea?
If you wish to report to ThromboGenics a safety related event (adverse event, use during pregnancy or lactation, suspected interaction with other products, treatment errors such as overdose, usage outside the conditions in the label) in a patient treated with JETREA, please complete the form provided below.
ThromboGenics will only use the data you provide in the form to contact you and to comply with the applicable laws on this type of information. By completing your details you agree that ThromboGenics may use the information that you have submitted for the purposes of:
- contacting you for more information on the suspected adverse event you have reported
- disclosing information to Government healthcare agencies as required by law
You also agree that ThromboGenics may transfer, store and process the information outside your country (including outside of the USA) as required by other countries laws.