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New search Medicine profile Dinoprostone (Prostaglandin E2)

Clinical medicine profile

Dinoprostone (Prostaglandin E2)

Therapeutic agent (verify pharmacological class)

POM
Evidence state Source not available Reviewed 14 Aug 2026
Route
See product SmPC
Schedule
POM
ATC
Not assigned
PPB status
registered
Patient advice Check interactions
Verification required

This profile needs source confirmation

A traceable source link is not attached to this profile. Confirm prescribing decisions against the current SmPC and Kenya STG/EML.

01 Risk first

Safety essentials

The information most likely to change a prescribing or dispensing decision.

Contraindications

  • Allergic reaction to dinoprostone or related drugs
  • history of asthma
  • active pulmonary disease
  • significant cephalopelvic disproportion
  • malpresentation of fetus
  • active pelvic inflammatory disease
  • ruptured mem- branes.

Precautions

  • Pregnancy termination can fail
  • history of anaemia
  • hypertension or hypotension
  • cardiovascular disease
  • diabetes mellitus
  • renal disease
  • pre-eclampsia
  • uterine fibroids
  • cervical stenosis
  • uterine surgery
  • epilepsy
  • glaucoma
02 Point of care

Dosing matrix

Population and organ-function guidance, shown together for faster comparison.

Adult

Vaginally. Insert high into posterior fornix 3mg followed by another 3mg 6-8hrs later incase the labour is not established [max. 6mg]

Paediatric

See label paediatric section if present; otherwise use paediatric formulary — do not extrapolate adult doses.

Renal

Review renal impairment dosing; many agents need CrCl/eGFR adjustment.

  • CrCl 0–120: Confirm renal dosing in product SmPC / primary label.
Hepatic

Review hepatic impairment dosing; monitor LFTs if agent is hepatically cleared or hepatotoxic.

03 Clinical use

Use, effects & interactions

Indications

  • Induction of labour
  • elective abor- tion [between 12-18 wks of gestation]
  • treatment of incomplete abortion
  • therapeutic abortion [e.g. in cases of intra-uterine fetal death and congenital abnormalities incompatible with life]
  • cervical ripening
  • treatment of postpartum haemorrhage
  • treatment of benign hydatidiform mole

Adverse effects

  • Anaphylaxis
  • bronchoconstriction
  • burning eyes
  • endometritis
  • second-degree heart block
  • urinary retention
  • bradycardia
  • adynamic ileus
  • peripheral vasoconstriction
  • tachycardia
  • and increased uterine bleeding or pain
  • severe and continuing abdominal or stomach pain
  • double vision
  • hematuria
  • Professional use: confirm indication, dose, duration, monitoring and patient counselling points against current Kenya STG / EML and the product SmPC.
  • Document allergy status and key interactions.
04 Pharmacology

Mechanism & disposition

It stimulates myometrial con- tractions in the gravid uterus.

It stimulates myometrial con- tractions in…It also facilitates cervical dilatation an…In addition, it stimulates the smooth musc…
Read complete mechanism

It stimulates myometrial con- tractions in the gravid uterus. It also facilitates cervical dilatation and softening. In addition, it stimulates the smooth muscle of the gastrointesti- nal tract, arterioles, and bronchioles. For cervical ripening, it softens the cervix and facilitates cervical dilation and effacement. It also stimu- lates collagenase secretion hence reducing the collagen network within the cervix.

Onset

Product-specific

Duration

Product-specific

Route

See product SmPC

Elimination

are product-specific. Consider food effects, protein binding, hepatic CYP/UGT

Half-life

when adjusting for organ impairment, age and drug interactions. Verify parameters in the current SmPC.

05 Special populations

Pregnancy, lactation & diet

Pregnancy

Use only if potential benefit justifies potential risk; prefer agents with better reproductive data when alternatives exist.

Lactation

Assess infant risk vs benefit of maternal therapy; prefer agents with lactation data.

06 Kenya market

Brands & loaded prices

From
Median
Listings2
BrandManufacturerPackObserved price
Glandin E2 Gel 2mg NABIQASIM INDUSTRIES (PVT.) LTD. Gel 2mg Unavailable
Glandin E 2 Tablet 3mg Nabiqasim Industries (Pvt). Ltd. Vaginal Tablet 3mg Unavailable
07 Provenance

Sources & review state

Primary sourceLocal active-ingredient clinical extract; Professional class pharmacology (Therapeutic agent (verify pharmacological class))
Last reviewed14 Aug 2026
EvidenceSource not available

Decision support only. Confirm patient-specific decisions against the current product SmPC, Kenya STG/EML, and professional judgement.