Table 2.
Objectives | Main variables |
---|---|
To document the long-term safety and tolerability profile of everolimus in the treatment of patients with TSC residing in the European Union who are prescribed everolimus for approved indications | Incidence of AEs, SAEs, and everolimus-related AEs in the observation period |
Incidence of events of special interest (e.g., noninfectious pneumonitis, severe infections, hypersensitivity, stomatitis, secondary amenorrhea in post-adolescent females, etc.) | |
To collect everolimus therapeutic drug monitoring data within routine clinical practice as per the Summary of Product Characteristics | Everolimus blood concentration, if available |
Abbreviations: AE adverse event, PASS post-authorization safety study, SAE serious adverse event, TOSCA TuberOus SClerosis registry to increase disease Awareness, TSC tuberous sclerosis complex.