Indications |
Extra-amniotic Pregnancy termination in the 2nd trimester Adult: As 100 mcg/mL soln: Instill 1 mL through a suitable foley catheter followed by 1-2 mL at 2-hr intervals according to patient's response. Vaginal Cervical priming, induction and augmentation of labour Adult: As cervical gel: Apply 500 mcg in 2.5 mL preparation. May be repeated after 6 hr if necessary. Max: 1.5 mg/24 hr. Vaginal Labour induction Adult: As vaginal gel: 1 mg (or 2 mg for primigravid patients with unfavourable induction features) followed by another 1 or 2 mg after 6 hr if necessary. Max: 3 mg (or 4 mg in unfavourable primigravid patients). As pessary: Initially, 3 mg followed by a further 3 mg after 6-8 hr if necessary. Max: 6 mg. |
Contraindications |
Hypersensitivity to prostaglandins. Patients in whom oxytocics are generally contraindicated. History of pelvic inflammatory disease; active cardiac, pulmonary, renal or hepatic disease. |
Warnings / Precautions |
Raised intraocular pressure. Previous caesarean section; history of asthma, epilepsy, hepatic or renal dysfunction, cardiovascular disease; pregnancy. |
Adverse Reactions |
Hypersensitivity reactions, nausea, vomiting, diarrhoea, abdominal pain; flushing, shivering, headache, dizziness; hypertension; convulsions, ECG changes,local tissue irritation, erythema; pyrexia, increased WBC. Uterine contractile abnormalities with or without foetal distress. Dosage >0.5 mg intracervically can cause hypertonic uterine contractions. Intra/extra-amniotic inj: Local infection, vomiting, diarrhoea, pyrexia, transient hypotension. Potentially Fatal: Sudden CV collapse due to accidental IV absorption and intra-amniotic inj. Uterine rupture, amniotic fluid embolism during labour. Foetal distress and death in rare cases. |
Overdose Reactions |
Rigors, vomiting, severe abdominal pain, uterine hypercontractility and uterine hypertonus. Management: conservative management may be sufficient in most cases. β-adrenergic drugs may be used as a treatment of hyperstimulation following admin for cervical ripening. |
Drug Interactions |
Potentially Fatal: Concomitant use of oxytocin may lead to uterine rupture. See Below for More dinoprostone Drug Interactions |
Mechanism of Actions |
Dinoprostone causes induction of uterine muscle contraction during pregnancy. It is both a vasoconstrictor and bronchodilator. The pattern of uterine contraction is similar to that in normal labour at term. It can also stimulate the smooth muscle of the GI tract. Onset: 10 min. Duration: 2-3 hr (vaginal supp). Absorption: Small amounts absorbed by the uterus. Distribution: Diffuses into the maternal blood. Metabolism: Hepatic, renal, spleen and other tissues: Rapid. Excretion: Urine; faeces (small amounts). |
Storage Conditions |
Extra-amniotic: Cervical gel: Refrigerate at 2-8°C. Vag supp: Store in a freezer below -20°C. Vag insert: Store in a freezer between -20°C & -10°C. Vaginal: Cervical gel: Refrigerate at 2-8°C. Vag supp: Store in a freezer below -20°C. Vag insert: Store in a freezer between -20°C & -10°C. |
ATC Classification |
G02AD02 - dinoprostone ; Belongs to the class of prostaglandins. Used to induce abortion or augment labour and to minimize blood loss from the placental site. |
Storage |
Extra-amniotic: Cervical gel: Refrigerate at 2-8°C. Vag supp: Store in a freezer below -20°C. Vag insert: Store in a freezer between -20°C & -10°C. Vaginal: Cervical gel: Refrigerate at 2-8°C. Vag supp: Store in a freezer below -20°C. Vag insert: Store in a freezer between -20°C & -10°C. |
Available As |
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Dinoprostone
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Dinoprostone Containing Brands
Dinoprostone is used in following diseases
Drug - Drug Interactions of Dinoprostone
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