Paloxi-ODT
Generic Name
Palonosetron 0.5 mg Orally Disintegrating Tablet
Manufacturer
Example Pharma Ltd.
Country
Bangladesh
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Price Details
Current market pricing information
| Variant | Unit Price | Strip Price |
|---|---|---|
| paloxi odt 05 mg tablet | ৳ 22.00 | ৳ 220.00 |
Description
Overview of the medicine
Palonosetron ODT is an orally disintegrating tablet containing 0.5 mg of palonosetron, a selective serotonin 5-HT3 receptor antagonist. It is used for the prevention of acute and delayed nausea and vomiting associated with moderately emetogenic chemotherapy, and for acute nausea and vomiting associated with highly emetogenic chemotherapy. It is also indicated for the prevention of postoperative nausea and vomiting.
Uses & Indications
Dosage
Adults
For CINV: 0.5 mg orally, taken approximately 1 hour prior to chemotherapy. For PONV: 0.5 mg orally, taken approximately 1 hour prior to induction of anesthesia.
Elderly
No dosage adjustment required based on age.
Renal_impairment
No dosage adjustment recommended for patients with renal impairment.
How to Take
The ODT tablet should be placed on the tongue where it will disintegrate rapidly and can be swallowed with or without water. Do not chew or crush the tablet. Take approximately 1 hour before chemotherapy or anesthesia.
Mechanism of Action
Palonosetron is a highly selective 5-HT3 receptor antagonist. Serotonin 5-HT3 receptors are located both peripherally on vagal nerve terminals in the gastrointestinal tract and centrally in the chemoreceptor trigger zone. Chemotherapeutic agents and radiation therapy are thought to cause the release of serotonin from enterochromaffin cells of the small intestine, which then activates vagal afferents via 5-HT3 receptors, initiating the vomiting reflex. Palonosetron blocks this action, thereby preventing nausea and vomiting.
Pharmacokinetics
Onset
Within 30 minutes to 1 hour (for anti-emetic effect).
Excretion
Primarily excreted renally (approximately 50% unchanged in urine).
Half life
Approximately 40 hours (for CINV), 9-10 hours (for PONV).
Absorption
Well absorbed orally. Bioavailability is approximately 60%.
Metabolism
Metabolized to a minor extent by multiple CYP enzymes (CYP2D6, CYP3A4, CYP1A2) to form two inactive metabolites.
Side Effects
Contraindications
- •Hypersensitivity to palonosetron or any component of the formulation.
- •Known hypersensitivity to other 5-HT3 receptor antagonists.
Drug Interactions
Serotonergic drugs
Concurrent use with other serotonergic drugs (e.g., SSRIs, SNRIs, MAOIs, tricyclic antidepressants) may increase the risk of serotonin syndrome, although this risk is generally low with 5-HT3 antagonists.
QT prolonging agents
Caution when co-administering with drugs that prolong the QT interval (e.g., antiarrhythmics, antipsychotics, some antibiotics).
Storage
Store below 30°C in a dry place, away from light and moisture. Keep out of reach of children.
Overdose
There is no specific antidote for palonosetron overdose. Treatment should be symptomatic and supportive. Patients should be monitored for signs of serotonin syndrome and QT prolongation.
Pregnancy & Lactation
Pregnancy Category B. Use only if clearly needed. It is not known whether palonosetron is excreted in human milk; caution should be exercised when administered to a nursing woman.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
Typically 24-36 months from manufacturing date.
Availability
Pharmacies, hospitals
Approval Status
Approved by major regulatory bodies (e.g., FDA, EMA, DGDA for specific regions)
Patent Status
Generic versions available, original patent expired
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Global Brand Names
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