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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

DINOPROSTONE for Cervical dilatation: Side Effects & Safety Data

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There are 5 adverse event reports in the FDA FAERS database where DINOPROSTONE was used for Cervical dilatation.

Most Reported Side Effects for DINOPROSTONE

Side Effect Reports % Deaths Hosp.
Foetal exposure during pregnancy 67 9.3% 3 23
Uterine hyperstimulation 65 9.0% 1 13
Off label use 52 7.2% 1 25
Premature separation of placenta 48 6.6% 0 7
Maternal exposure during pregnancy 46 6.4% 0 25
Postpartum haemorrhage 40 5.5% 7 16
Premature baby 40 5.5% 1 16
Drug ineffective 36 5.0% 0 5
Foetal heart rate deceleration abnormality 36 5.0% 1 8
Premature delivery 33 4.6% 1 14
Exposure during pregnancy 32 4.4% 1 9
Uterine rupture 32 4.4% 1 11
Haemoglobin decreased 31 4.3% 0 14
Uterine hypertonus 31 4.3% 0 10
Foetal exposure during delivery 30 4.2% 3 3

Other Indications for DINOPROSTONE

Labour induction (286) Induction of cervix ripening (182) Product used for unknown indication (154) Induced labour (23) Foetal exposure during pregnancy (8) Delivery (5)

Other Drugs Used for Cervical dilatation

MISOPROSTOL (17)

Related Pages

DINOPROSTONE Full Profile All Cervical dilatation Drugs DINOPROSTONE Demographics DINOPROSTONE Timeline