Palnox 0.25mg Injection

Palnox 0.25mg Injection

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उत्पाद विवरण

1. Technical Specifications

Attribute Details
Brand Name Palnox 0.25mg Injection
Generic Name Palonosetron Hydrochloride
Strength 0.25 mg / 5 ml vial
Dosage Form Injection (for Intravenous use only)
Packaging Size Single-use vial
Packaging Type Glass vial with rubber stopper & flip-off seal
Medicine Type Antiemetic (5-HT Receptor Antagonist)
Manufacturer Glenmark Pharmaceuticals Ltd. (commonly marketed brand in India)
Distributed By Authorized oncology distributors / specialty pharmacies

2. Product Description

Palnox 0.25mg Injection contains Palonosetron, a highly selective 5-HT receptor antagonist used to prevent nausea and vomiting caused by chemotherapy (CINV) or postoperative conditions (PONV).

It blocks serotonin activity on vagal nerve terminals in the gastrointestinal tract and in the chemoreceptor trigger zone (CTZ) of the brain, preventing vomiting reflex.

Palonosetron has a longer half-life (40 hours) compared to older 5-HT antagonists (ondansetron, granisetron), making it effective for delayed nausea and vomiting.


3. Product Highlights

Attribute Details
Therapeutic Category Antiemetic (5-HT antagonist)
Application Area Chemotherapy-induced nausea & vomiting (CINV), Postoperative nausea & vomiting (PONV)
Mechanism of Action Selective blockade of 5-HT receptors inhibition of serotonin-mediated vomiting reflex in CNS and GI tract
Administration Intravenous injection, usually as a single dose before chemotherapy or surgery
Storage Conditions Store below 30 C; protect from light; do not freeze

4. Therapeutic Uses

  • Prevention of acute nausea & vomiting associated with initial and repeat courses of moderately or highly emetogenic chemotherapy.

  • Prevention of delayed nausea & vomiting (due to long half-life).

  • Postoperative nausea & vomiting (PONV) prevention.


5. Side Effects

Common:

  • Headache

  • Constipation

  • Fatigue, dizziness

  • Insomnia

Serious / Severe (rare):

  • Hypersensitivity reactions (rash, itching, anaphylaxis)

  • QT interval prolongation, arrhythmias

  • Hypokalemia or electrolyte imbalance (with prolonged use)


6. Precautions

  • Cardiac Patients: Use with caution in patients with history of arrhythmias, prolonged QT interval, or electrolyte abnormalities.

  • Drug Interactions: Avoid combination with other QT-prolonging agents (amiodarone, sotalol, certain antibiotics/antifungals).

  • Pregnancy & Lactation: Use only if clearly needed (limited human data).

  • Hepatic/Renal Impairment: Generally safe; no major dose adjustment required.

  • Children & Elderly: Dose adjustment based on body surface area (BSA) may be required in pediatric patients.

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