Product image of Gynipral (Hexoprenaline Sulfate) supplied by GNH India

Gynipral

Active Ingredient:
Hexoprenaline Sulfate
Origin:
EU

Gynipral (Hexoprenaline Sulfate)

Gynipral is a prescription medication that contains the active ingredient hexoprenaline sulfate, supplied as an intravenous solution. It belongs to the beta‑2 adrenergic agonist class and is used primarily as a tocolytic agent to manage uterine activity. The product is marketed in the European Union and is administered under medical supervision. The formulation does not contain additional excipients that alter its pharmacologic profile, and dosing is individualized based on clinical assessment.

Manufacturer / TM Owner

Takeda Austria Gmbh

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Indications & Clinical Uses

Gynipral is indicated for situations where suppression of uterine contractions is clinically required.

  • Management of preterm labor to delay delivery.
  • Treatment of uterine tachysystole during labor induction.
  • Adjunct therapy in obstetric procedures requiring uterine relaxation.
  • Short‑term use when rapid inhibition of uterine activity is needed.
  • Off‑label use may include experimental protocols under research settings.

Side Effects

The safety profile of Gynipral includes both frequently observed and less common adverse reactions.

Common

  • Tremor or shaking.
  • Palpitations or increased heart rate.
  • Nausea.

Serious

  • Significant arrhythmias.
  • Severe hypotension.
  • Allergic reactions including rash or anaphylaxis.

Precautions & Warnings

When prescribing Gynipral, clinicians should evaluate patient history and monitor specific parameters to minimize risk.

  • Use only under continuous cardiac and fetal monitoring.
  • Contraindicated in patients with known hypersensitivity to hexoprenaline or related beta‑2 agonists.
  • Caution in individuals with cardiovascular disease, especially arrhythmias or hypertension.
  • Avoid in uncontrolled hyperthyroidism.
  • Assess blood glucose in diabetic patients, as beta‑2 stimulation may affect glycemic control.
  • Limit duration of therapy to the shortest effective period.

Avoid Interactions

Gynipral may interact with other medications that influence cardiovascular or smooth‑muscle function.

Avoid

  • Concurrent use with non‑selective beta‑blockers, which can diminish tocolytic effect.
  • Combination with other potent vasodilators, increasing risk of hypotension.

Use with caution

  • Concurrent administration of other beta‑2 agonists (e.g., terbutaline) may enhance side‑effects.
  • Drugs that affect electrolyte balance, such as diuretics, may increase risk of cardiac arrhythmias.
  • Anticoagulants, because uterine relaxation may alter bleeding risk.

Frequently Asked Questions

Hexoprenaline sulfate selectively stimulates beta‑2 adrenergic receptors, leading to relaxation of uterine smooth muscle and bronchial smooth muscle, which helps suppress uterine contractions.

Gynipral is used for the management of preterm labor and uterine tachysystole, and may be employed when rapid uterine relaxation is required during obstetric procedures.

Gynipral is supplied as an intravenous solution and is given under continuous medical supervision, usually via infusion.

Continuous fetal heart rate monitoring and maternal cardiac monitoring, including blood pressure and heart rhythm, are recommended while the drug is infused.

Common adverse reactions include tremor, palpitations, and mild nausea.

Serious events may include significant arrhythmias, severe hypotension, and allergic reactions such as rash or anaphylaxis.

Patients with known hypersensitivity to hexoprenaline or other beta‑2 agonists, those with uncontrolled cardiovascular disease, and individuals with uncontrolled hyperthyroidism are generally contraindicated.

Concurrent use with non‑selective beta‑blockers is generally avoided because they can reduce the drug’s tocolytic effectiveness.

Beta‑2 stimulation can raise blood glucose, so diabetic patients should have glucose levels monitored during treatment.

Gynipral is a prescription‑only medication and must be prescribed by a qualified healthcare professional.

The infusion should be stopped, and appropriate supportive measures such as fluid resuscitation and vasopressors should be initiated under medical supervision.

The product should be stored according to the manufacturer’s instructions, typically at controlled room temperature and protected from light.

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GNH India Pharmaceuticals Limited

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