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Revom

Revom Tablet is a medication manufactured by Deurali Janta Pharmaceuticals Pvt. Ltd. in Nepal. Its generic name is Domperidone. It is primarily used as an antiemetic and prokinetic agent.

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Description

Revom Tablet (Domperidone)

Manufacturer: Deurali Janta Pharmaceuticals Pvt. Ltd. Generic Name: Domperidone Availability: Nepal

Overview: Revom Tablet, containing Domperidone, is a peripheral dopamine-receptor blocker primarily used to improve gastrointestinal motility and manage various related symptoms.

Indications for Use: Revom Tablet is indicated for the treatment of:

  • Gastritis
  • Nausea and Vomiting
  • Gastroparesis (delayed gastric emptying)
  • Non-ulcer Dyspepsia (indigestion not caused by ulcers)
  • Migraine (for associated nausea and vomiting)
  • Lactation (to promote milk production, off-label use in some regions)

Dosage Information:

Adults (Oral):

  • Nausea and Vomiting: 10-20 mg every 4-8 hours. Maximum daily dose: 80 mg.
  • Non-ulcer Dyspepsia: 10 mg three to four times daily. May be increased to 20 mg three to four times daily. The last dose should be taken at bedtime.
  • Migraine: 20 mg every 4 hours. Maximum: 4 doses per 24 hours.

Adults (Rectal):

  • Nausea and Vomiting: 60 mg twice daily.

Elderly:

  • No dosage adjustment is typically needed.

Hepatic Impairment:

  • No dosage adjustment is typically needed.

Children (Oral):

  • 0.2 – 0.4 mg/kg every 4 – 8 hours daily.

Children (Rectal):

  • Under 12 years and over 15 kg: 30 mg twice daily.
  • Over 12 years and over 35 kg: 60 mg twice daily.

Renal Impairment:

  • Mild to Moderate: No dosage adjustment needed.
  • Severe: Dosing should be reduced to 1-2 times daily with prolonged treatment.

Administration:

  • Revom Tablet should be taken on an empty stomach.
  • Administer 15-30 minutes before meals.

Contraindications: Revom Tablet is contraindicated in patients with:

  • Known hypersensitivity to Domperidone or any of its components.
  • Gastrointestinal hemorrhage, obstruction, or perforation.
  • Prolactin-releasing pituitary tumors.
  • It is not recommended for chronic administration or routine prophylaxis of postoperative nausea and vomiting.

Precautions: Exercise caution when administering Revom Tablet to:

  • Patients with pheochromocytoma.
  • Children under 2 years of age.
  • Elderly patients.
  • Patients with renal or hepatic impairment.
  • There is a risk of cardiac arrhythmias and hypokalemia, especially if administered intravenously.
  • Use with caution during pregnancy and lactation.

Interactions:

  • May reduce the effectiveness of bromocriptine (hypoprolactinemic effect).
  • The prokinetic effect may be antagonized by opioid analgesics and antimuscarinics.
  • Potentially Fatal Interaction: Concomitant use with potent CYP3A4 inhibitors (e.g., ketoconazole, erythromycin, ritonavir) can significantly increase serum domperidone levels, leading to an elevated risk of QT prolongation and serious cardiac arrhythmias.

Adverse Effects: Common side effects of Domperidone include:

  • Drowsiness
  • Extrapyramidal reactions (involuntary movements)
  • Galactorrhea (abnormal milk production)
  • Gynecomastia (breast enlargement in males)
  • Constipation or diarrhea
  • Lassitude (lack of energy)
  • Decreased libido
  • Skin rash, itch

Potentially Fatal Adverse Effects:

  • Convulsions
  • Arrhythmias and cardiac arrest
  • Dysrhythmias in patients with pre-existing cardiovascular disease or hypokalemia
  • Seizures
  • Hypertensive crisis in patients with pheochromocytoma

Mechanism of Action: Domperidone acts as a peripheral dopamine-receptor blocker. Its primary actions include:

  • Increasing esophageal peristalsis.
  • Enhancing gastroduodenal coordination.
  • Lowering esophageal sphincter pressure.
  • Improving gastric motility and peristalsis, thereby facilitating gastric emptying and decreasing small bowel transit time.

Important Note: This information on Revom Tablet from Farmaco Nepal drug index is provided for general knowledge and is not intended for diagnosis, medical advice, or treatment. It should not be considered a substitute for professional medical judgment or consultation with a healthcare provider

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