Indications
Vorifend is an azole antifungal medicine. It is indicated for
use in patients 12 years of age and older in the treatment of following fungal
infections-
Invasive aspergillosis
Candidemia (nonneutropenic) and disseminated candidiasis in
skin, abdomen, kidney, bladder wall and wounds
Esophageal candidiasis
Serious infections caused by Scedosporium apiospermum and
Fusarium Species including Fusarium solani
Patients intolerant of, or refractory to other therapy.
* রেজিস্টার্ড
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Pharmacology
Voriconazole is a triazole antifungal medication used to
treat serious fungal infections. Voriconazole binds and inhibits ergosterol
synthesis by inhibiting CYP450-dependent 14-alpha sterol demethylase. The
inhibition of 14-alpha sterol demethylase results in a depletion of ergosterol
in fungal cell membrane.
Dosage & Administration
Oral-
Voriconazole tablet and powder for suspension are to be
taken at least one hour before or one hour following a meal
At or over 40 kg body weight: Loading dose regimen is 400 mg
or 10 ml every 12 hours (for the first 24 hours) and maintenance dose (after
first 24 hours) is 200 mg or 5 ml twice daily.
Below 40 Kg body weight: Loading dose regimen is 200 mg or 5 ml every 12 hours (for the first 24 hours) and maintenance dose (after first 24 hours) is 100 mg or 2.5 ml twice daily. Or, as directed by the registered physician.
Injection-
Invasive Aspergillosisd :
Loading dose: 6 mg/kg 12 hourly for the first 24 hours.
Maintenance Dose: 4 mg/kg 12 hourly.
Candidemia in nonneutropenic patients and other deep tissue Candida
infections:
Loading dose: 6 mg/kg 12 hourly for the first 24 hours.
Maintenance Dose: 3-4 mg/kg 12 hourly.
Scedosporiosis and Fusariosis:
Loading dose: 6 mg/kg 12 hourly for the first 24 hours.
Maintenance Dose: 4 mg/kg 12 hourly.
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Interaction
CYP3A4, CYP2C9 and CYP2C19 inhibitors and inducers: Adjust
Vorifend dosage and monitor for adverse reactions or lack of efficacy
Vorifend may increase the concentrations and activity of
drugs that are CYP3A4, CYP2C9 and CYP2C19 substrates. Reduce doses of these
other drugs and monitor for adverse reactions
Increase maintenance oral and intravenous dosage of Vorifend
with co-administration of Phenytoin or Efavirenz
Contraindications
Known hypersensitivity to Voriconazole or any other
components of this drug-
Co-administration with terfenadine, astemizole, cisapride,
pimozide or quinidine, sirolimus due to risk of serious adverse reactions
Co-administration with rifampin, carbamazepine, long-acting
barbiturates, efavirenz, ritonavir, rifabutin, ergot alkaloids and St. John's
Wort due to risk of loss of efficacy
Side Effects
The most common side effects are abdominal pain, anemia,
blurred vision, headache, chest pain, nausea and diarrhea.
Pregnancy & Lactation
There are no adequate and well-controlled studies in
pregnant woman. It should be used during pregnancy only if the potential
benefit justifies the potential risk to the fetus.
Precautions & Warnings
Long term exposure (treatment or prophylaxis) greater than
180 days requires careful assessment of the benefit-risk balance. Squamous cell
carcinoma of the skin (SCC) has been reported in relation with long-term
Vorifend treatment.
Use in Special Populations
The efficacy to the children under 12 years of age is not
established.
Overdose Effects
There is no data found about overdose of Vorifend.
Therapeutic Class
Other Antifungal preparations
Reconstitution
Reconstitution Instructions of suspension: Shake the bottle
well before adding water to loosen the powder. Add 25 ml of boiled and cooled
water to the bottle (5 spoons of a provided spoon). Shake the closed bottle
vigorously until powder mixed completely with the water. Store reconstituted
suspension between 15°-30° C. Discard suspension 14 days after reconstitution.
Storage Conditions
Keep out of reach of children. Store in a dry place, below 25°C temperature and protected from light. Store Vorifend powder for suspension between 2° to 8°C temperature
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