CERVIDIL® Vaginal Delivery System contains 10 mg dinoprostone (Prostaglandin E2) and is indicated for the initiation of cervical ripening in patients, at or near term, who have favourable induction features and in whom there is a medical or obstetrical indication for induction of labour1.
CERVIDIL® should only be administered by qualified healthcare personnel in hospitals and clinics with obstetric units with facilities for continuous fetal and uterine monitoring1.
This video will provide a step-by-step administration guide and important safety information for healthcare personnel.
Reference: 1. Cervidil® Approved Product Information; 07 December 2021
“For Healthcare Professionals Only”
SG-CV-2200003