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Hemabate

Active Ingredient:
Carboprost
Origin:
EU

Hemabate (Carboprost)

Hemabate is a prescription injectable medication that contains the prostaglandin F2α analog carboprost tromethamine. It is supplied as an intramuscular or intraamniotic injection, with the specific strength varying by market. Hemabate is marketed in the European Union and is classified as a uterotonic agent used to promote uterine contraction. The drug works by activating prostaglandin F2α receptors, leading to increased uterine tone and reduced bleeding after delivery.

Manufacturer / TM Owner

Pfizer Limited

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Indications & Clinical Uses

Hemabate is indicated for the management of obstetric conditions that involve insufficient uterine contraction.

  • Treatment of postpartum hemorrhage due to uterine atony.
  • Control of bleeding after cesarean section when uterine tone is inadequate.
  • Management of retained placenta when uterine contraction is required.
  • Adjunct therapy for severe primary postpartum hemorrhage unresponsive to oxytocin.
  • Prevention of excessive bleeding during manual removal of the placenta.
  • Use in cases of uterine inversion where rapid contraction is needed.

Side Effects

Side effects of Hemabate are related to its stimulation of uterine smooth muscle and systemic prostaglandin activity, and they can range from mild gastrointestinal symptoms to serious hypersensitivity reactions.

Common

  • Abdominal cramping or uterine pain, often transient.
  • Diarrhea or loose stools, sometimes accompanied by abdominal discomfort.
  • Nausea, vomiting, or loss of appetite.
  • Fever, chills, or mild headache.
  • Injection site pain or erythema.

Serious

  • Severe allergic reaction (anaphylaxis) with rash, swelling, or hypotension.
  • Bronchospasm or respiratory distress, particularly in patients with asthma.
  • Cardiovascular effects such as hypertension, tachycardia, or arrhythmia.
  • Uterine rupture in cases of excessive dosing.

Precautions & Warnings

When prescribing Hemabate, clinicians should evaluate patient history and monitor for conditions that may increase the risk of adverse reactions.

  • Contraindicated in patients with known hypersensitivity to carboprost or other prostaglandin analogs.
  • Use with caution in individuals with asthma or a history of bronchospasm.
  • Avoid in patients with active gastrointestinal bleeding or ulcer disease.
  • Caution in patients with cardiovascular disease, hypertension, or arrhythmias.
  • Monitor uterine tone and bleeding closely after administration.
  • Consider dose adjustment in patients with severe liver impairment.

Avoid Interactions

Hemabate may interact with other medications that affect uterine contractility, prostaglandin pathways, or respiratory function.

Avoid

  • Concurrent use with other uterotonic agents (e.g., oxytocin, misoprostol) may cause excessive uterine contraction.
  • Co‑administration with non‑steroidal anti‑inflammatory drugs (NSAIDs) can increase gastrointestinal irritation.
  • Use with beta‑agonist bronchodilators may reduce the risk of bronchospasm but requires monitoring.

Use with caution

  • Caution when combined with antihypertensive agents, as Hemabate may cause transient blood pressure changes.
  • Use with caution in patients receiving anesthetic agents that depress respiration, due to potential bronchospasm.
  • Caution with drugs that prolong the QT interval, as prostaglandin effects may affect cardiac rhythm.

Frequently Asked Questions

Hemabate (carboprost tromethamine) activates prostaglandin F2α receptors in uterine smooth muscle, causing strong contractions and increased uterine tone, which helps control postpartum bleeding.

Hemabate is primarily used to treat postpartum hemorrhage caused by uterine atony, a condition where the uterus fails to contract adequately after delivery.

Yes, Hemabate can be given intramuscularly after a cesarean section to improve uterine tone and reduce bleeding when standard uterotonics are insufficient.

Hemabate should be used with caution in patients with asthma because prostaglandin F2α analogs can provoke bronchospasm; monitoring of respiratory status is recommended.

Common gastrointestinal side effects include abdominal cramping, diarrhea, nausea, and vomiting, which are usually mild and transient.

Hemabate is supplied as a sterile injectable solution intended for intramuscular or intraamniotic administration.

Combining Hemabate with other uterotonics may increase the risk of excessive uterine contraction and should generally be avoided unless specifically directed by a physician.

After administration, clinicians should monitor uterine tone, bleeding volume, vital signs, and for any signs of respiratory distress or allergic reaction.

Yes, Hemabate is classified as a prescription‑only (Rx) medication in the European Union.

Patients with cardiovascular disease should be monitored closely because Hemabate can cause transient increases in blood pressure and heart rate.

If an allergic reaction such as rash, swelling, or difficulty breathing occurs, the injection should be stopped immediately and emergency medical treatment initiated.

Severe liver impairment may affect the metabolism of Hemabate; dose adjustment or careful monitoring may be required in such patients.

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GNH India Pharmaceuticals Limited

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Last updated:

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