Unit Price:
৳ 45.00
(1 x 10: ৳ 450.00)
Strip Price:
৳ 450.00
Indications
Emetant is indicated for-
- Prevention of postoperative nausea and vomiting (PONV)
- Prevention of Chemotherapy induced nausea and vomiting (CINV)
Pharmacology
Aprepitant is a selective high affinity antagonist of human substance P neurokinin 1 (NK1) receptors. When substance P attaches to these receptors, it causes nausea and vomiting. Aprepitant stops substance P from binding to the NK1 receptors. By blocking the receptors, Aprepitant can prevent nausea and vomiting, which often happens after chemotherapy or as a complication of surgery.
Dosage
Post Operative Nausea and Vomiting: The recommended oral dosage of Aprepitant is 40 mg within 3 hours prior to induction of anesthesia.
Chemotherapy-Induced Nausea and Vomiting:
** The following regimen should be used for the prevention of nausea and vomiting associated with highly emetogenic cancer chemotherapy-
** The following regimen should be used for the prevention of nausea and vomiting associated with moderately emetogenic cancer chemotherapy:
Chemotherapy-Induced Nausea and Vomiting:
** The following regimen should be used for the prevention of nausea and vomiting associated with highly emetogenic cancer chemotherapy-
- Day 1: Aprepitant 125 mg orally, Dexamethasone 12 mg orally, 5-HT3 antagonist (Ondansetron): 24 mg 30 minutes before the start of chemotherapy.
- Day 2: Aprepitant 80 mg orally, Dexamethasone 8 mg orally
- Day 3: Aprepitant 80 mg orally, Dexamethasone 8 mg orally
- Day 4: Dexamethasone 8 mg orally
** The following regimen should be used for the prevention of nausea and vomiting associated with moderately emetogenic cancer chemotherapy:
- Day 1: Aprepitant 125 mg orally, Dexamethasone 12 mg orally, 5-HT3 antagonist (Ondansetron): one 8 mg tablet 30 minutes before chemotherapy followed by an 8 mg dose 8 hours later.
- Day 2: Aprepitant 80 mg orally, 5-HT3 antagonist (Ondansetron): 8 mg tablet twice a day
- Day 3: Aprepitant 80 mg orally, 5-HT3 antagonist (Ondansetron): 8 mg tablet twice a day.
Administration
Aprepitant may be taken with or without food. No dosage adjustment is necessary for the elderly patients.
Interaction
Emetant is a substrate, a weak-to-moderate (dose dependent) inhibitor, and an inducer of CYP3A4. Emetant is also an inducer of CYP2C9. Precautions should be taken while coadministering Emetant with drugs that use CYP3A4 or CYP2C9, for example- Warfarin, Tolbutamide, Phenytoin, Ketoconazole, Itraconazole, Nefazodone, Troleandomycin, Clarithromycin, Ritonavir, Nelfinavir, Diltiazem, Rifampin, Carbamazepine etc.
Upon coadministration with Emetant, the efficacy of hormonal contraceptives during and for 28 days following the last dose of Emetant may be reduced. Alternative or back-up methods of contraception should be used during treatment with Emetant and for 1 month following the last dose of Emetant.
Upon coadministration with Emetant, the efficacy of hormonal contraceptives during and for 28 days following the last dose of Emetant may be reduced. Alternative or back-up methods of contraception should be used during treatment with Emetant and for 1 month following the last dose of Emetant.
Contraindications
Aprepitant is contraindicated in patients who are hypersensitive to any component of the product. Aprepitant should not be used concurrently with Pimozide, Terfenadine, Astemizole & Cisapride.
Side Effects
Constipation, Hypotension, Pruritus, Pyrexia
Pregnancy & Lactation
Pregnancy Category B. This drug should be used during pregnancy only if clearly needed. It is not known whether this drug is excreted in human milk. A decision should be made whether to discontinue nursing or to discontinue the drug based on patient’s importance.
Use in Special Populations
Patients with Renal Impairment: No dosage adjustment is necessary for patients with renal impairment or for patients with end-stage renal disease (ESRD) undergoing hemodialysis.
Patients with Hepatic Impairment: No dosage adjustment is necessary for patients with mild to moderate hepatic impairment. There are no clinical data in patients with severe hepatic impairment.
Patients with Hepatic Impairment: No dosage adjustment is necessary for patients with mild to moderate hepatic impairment. There are no clinical data in patients with severe hepatic impairment.
Overdose Effects
No specific information is available on the treatment of overdosage with Emetant. Single doses up to 600 mg of Emetant were generally well tolerated in healthy subjects. Drowsiness and headache can be seen due to overdose. In the event of overdose, Emetant should be discontinued. General supportive treatment and monitoring should be provided. Because of the antiemetic activity of Emetant, medicine-induced emesis may not be effective. Emetant cannot be removed by hemodialysis.
Therapeutic Class
Anti-emetic drugs
Storage Conditions
Keep below 30°C temperature, away from light & moisture. Keep out of the reach of children.