MSF SAE Report Form

This form allows you to capture relevant information on Serious Adverse Events occurring in study participants. We also used the same form for Adverse Events of Special Interest and Overdoses in the study (see PV-TB-D01 for details on how to capture). This form is filled by the site doctor and can be used for reporting to the Pharmacovigilance unit but also reporting to Ethics Committees and National Regulatory Agencies if accepted. 

Target user: TB doctors