Product image of DROPERIDOL 2.5 mg/mL (Droperidol) 2.5 mg/mL INJECTION, SOLUTION supplied by GNH India

DROPERIDOL 2.5 mg/mL

Active Ingredient:
Droperidol
Form:
INJECTION, SOLUTION
Brand:
DROPERIDOL
Origin:
USA

DROPERIDOL 2.5 mg/mL (Droperidol INJECTION, SOLUTION) 2.5 mg/mL

Droperidol, the active ingredient in Droperidol 2.5 mg/mL, is a butyrophenone antipsychotic presented as a 2.5 mg/mL injection solution for intramuscular or intravenous use. It is primarily used to prevent and treat postoperative nausea and vomiting (PONV) and to manage nausea and vomiting associated with chemotherapy. GNH India supplies Droperidol 2.5 mg/mL as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals and clinics worldwide.

Droperidol 2.5 mg/mL is a sterile, non-pyrogenic, aqueous solution designed for parenteral administration. It is indicated for reducing the incidence of nausea and vomiting associated with surgical and diagnostic procedures. The drug is known for its tranquilizing and sedative effects, making it suitable for various medical settings.

Strength

2.5 mg/mL

Pack Size

25 VIAL in 1 CARTON (0143-9515-25) / 1 mL in 1 VIAL (0143-9515-01)

Manufacturer / TM Owner

Hikma Pharmaceuticals USA Inc.

1
Pack/s
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Indications & Clinical Uses

Droperidol 2.5 mg/mL is a butyrophenone derivative and dopamine antagonist used to prevent and treat postoperative nausea and vomiting (PONV).

  • Postoperative nausea and vomiting (PONV): Reduces the incidence of nausea and vomiting during and after surgical procedures.
  • Chemotherapy-induced nausea and vomiting (CINV): Manages nausea and vomiting associated with chemotherapy treatments.
  • Sedation and control of acute agitation: Provides tranquilization and sedation in various medical settings.
  • Adjunctive treatment of psychotic disorders: Used as an adjunct in the management of psychotic disorders.

How It Works

  • Droperidol works primarily by antagonizing dopamine D2 receptors in the central nervous system. This action blocks the effects of dopamine, leading to its antiemetic and antipsychotic effects. Additionally, droperidol antagonizes serotonin and histamine receptors, contributing to its sedative and tranquilizing properties. The drug also produces mild alpha-adrenergic blockade, which can result in peripheral vascular dilatation and a reduction in blood pressure.

Side Effects

Droperidol may cause various side effects, ranging from common to serious or rare.

Common Side Effects

  • Drowsiness: Mild to moderate sedation and drowsiness.
  • Hypotension: Mild to moderate decrease in blood pressure.
  • Dry mouth: Reduced saliva production.
  • Extrapyramidal symptoms: Muscle stiffness, tremors, or restlessness.
  • Dizziness: Lightheadedness or vertigo.
  • Constipation: Slowed bowel movements.
  • Blurred vision: Temporary visual disturbances.
  • Confusion: Mental disorientation or cognitive impairment.

Serious or Rare Side Effects

  • QT prolongation: Prolonged QT interval, which can lead to serious cardiac arrhythmias.
  • Neuroleptic malignant syndrome (NMS): A rare but life-threatening condition characterized by high fever, muscle rigidity, and altered mental status.
  • Torsade de pointes: A type of ventricular tachycardia that can be fatal.
  • Severe hypotension: Significant drop in blood pressure that may require medical intervention.
  • Respiratory depression: Reduced breathing rate and depth, which can be dangerous in some patients.

Precautions & Warnings

Droperidol should be used with caution in certain patient populations and conditions.

  • QT prolongation: Avoid use in patients with known or suspected QT prolongation or congenital long QT syndrome.
  • Hypersensitivity: Do not administer to patients with known hypersensitivity to droperidol or other butyrophenones.
  • Elderly patients: Use with caution in patients over 65 years old due to increased risk of side effects.
  • Alcohol abuse: Administer with extreme caution in patients who abuse alcohol.
  • Concomitant use with CNS depressants: Monitor closely when used with benzodiazepines, volatile anesthetics, and IV opiates.
  • ECG monitoring: Perform ECG monitoring prior to treatment and continue for 2 to 3 hours after completing treatment to monitor for arrhythmias.
  • Store at 20 to 25°C: Keep in the original packaging, protect from light, and do not freeze.

Avoid Interactions

Droperidol may interact with other medications, leading to potential adverse effects or altered drug efficacy.

Major Interactions (Avoid)

  • QT-prolonging drugs: Avoid concomitant use with other drugs that prolong the QT interval, as this can increase the risk of serious cardiac arrhythmias.
  • CNS depressants: Avoid use with other CNS depressants, such as benzodiazepines and opioids, due to the risk of excessive sedation and respiratory depression.
  • Antiarrhythmic drugs: Avoid use with drugs that can cause cardiac arrhythmias, as droperidol may exacerbate this risk.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: Monitor blood pressure closely when used with antihypertensive drugs, as droperidol can cause hypotension.
  • Antipsychotics: Monitor for increased side effects when used with other antipsychotic drugs, as this can enhance the risk of extrapyramidal symptoms and sedation.
  • Anticholinergics: Monitor for increased anticholinergic effects, such as dry mouth and constipation, when used with other anticholinergic drugs.

Frequently Asked Questions

Droperidol 2.5 mg/mL is primarily used to prevent and treat postoperative nausea and vomiting (PONV). It is also used to manage nausea and vomiting associated with chemotherapy, provide sedation and control acute agitation, and as an adjunctive treatment for psychotic disorders. The drug is administered intramuscularly or intravenously and is known for its tranquilizing and antiemetic effects.

Droperidol works by antagonizing dopamine D2 receptors in the central nervous system. This action blocks the effects of dopamine, leading to its antiemetic and antipsychotic effects. Additionally, droperidol antagonizes serotonin and histamine receptors, contributing to its sedative and tranquilizing properties. The drug also produces mild alpha-adrenergic blockade, which can result in peripheral vascular dilatation and a reduction in blood pressure.

The dosage of Droperidol 2.5 mg/mL is determined by the prescribing healthcare professional based on the patient's age, weight, and medical condition. The maximum recommended initial dose for adults is 2.5 mg intramuscularly or intravenously. Additional doses may be administered with caution, and only if the potential benefit outweighs the potential risk. The dosage for children is based on body weight and should be individualized.

Droperidol is classified as a pregnancy category C drug, meaning that animal reproduction studies have shown an adverse effect on the fetus, and there are no adequate and well-controlled studies in humans. The drug should be used during pregnancy only if the potential benefits justify the potential risks to the fetus. It is not known whether droperidol is excreted in human milk, so caution should be exercised when administering the drug to nursing mothers.

To order Droperidol 2.5 mg/mL from GNH India, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams across international markets. The team will ask you to confirm your trade or institutional credentials and will reply with pricing, availability, shipping (including cold-chain where relevant), and the import paperwork.

Droperidol is a potent antiemetic drug that is particularly effective in preventing and treating postoperative nausea and vomiting (PONV). Compared to other antiemetic drugs, such as ondansetron or metoclopramide, droperidol has a broader range of actions, including sedative and antipsychotic effects. However, it is associated with a higher risk of side effects, such as QT prolongation and extrapyramidal symptoms, which should be carefully monitored.

Droperidol 2.5 mg/mL should be stored at 20 to 25°C (68 to 77°F), with excursions permitted to 15 to 30°C (59 to 86°F). The drug should be kept in the original packaging, protected from light, and should not be frozen. It is important to inspect the solution visually for particulate matter and discoloration prior to administration. If any abnormalities are observed, the drug should not be administered.

Droperidol 2.5 mg/mL is administered either intramuscularly or intravenously. The intravenous administration should be done slowly to minimize the risk of adverse effects. The dosage and administration route should be determined by the prescribing healthcare professional based on the patient's individual needs and medical condition. Vital signs and ECG should be monitored routinely during and after administration.

The most serious risks associated with Droperidol use include QT prolongation, which can lead to serious cardiac arrhythmias such as torsade de pointes. Other serious risks include neuroleptic malignant syndrome (NMS), severe hypotension, and respiratory depression. Patients should be monitored closely for these adverse effects, and ECG monitoring should be performed prior to treatment and continued for 2 to 3 hours after completing treatment.

Droperidol 2.5 mg/mL should not be used in patients with known or suspected QT prolongation, congenital long QT syndrome, or known hypersensitivity to the drug. It is also contraindicated in patients for whom other treatments for perioperative nausea and vomiting are effective or appropriate. The drug should be used with caution in elderly patients, those who abuse alcohol, and patients taking other CNS depressants or QT-prolonging drugs.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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