Observational prospective cohort study to evaluate the incidence of adverse events (AE), risk factors, and drug utilization patterns related to treatment with BUSCAPINA COMPOSITUM N from March to December 2016 in patients from Metropolitan Lima (PASS PERU)

31/08/2016
30/01/2025
EU PAS number:
EUPAS15008
Study
Planned
Documents
Study protocol
Initial protocol
English (224.79 KB - PDF) View document
Study results
Study report
Other information