Summary of safety profile: The most commonly reported adverse drug reactions in placebo-controlled and active comparator efficacy clinical trials (N=1116) were "foetal heart rate disorder" (6.9%), "uterine contractions abnormal" (6.2%) and "abnormal labour affecting foetus" (2.6 %).
The table as follows displays the main ADRs distributed by system organ classes (SOC) and frequency. Further, the ADRs seen during post-marketing experience are mentioned with unknown frequency.
Adverse reactions observed in clinical studies are presented according to their incidence, post authorisation reported adverse reactions are presented in the column frequency unknown. (See table.)
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