Miltefos 50 50 mg Capsule

    Miltefos 50 50 mg

    Miltefosine

    Category: Capsule

    Manufacturer: Popular Pharmaceuticals Ltd.

    Price: 165.0

    30 in Blister Pack

    Uses of Miltefos 50: - Kala-azar Visceral leishmaniasis, Mycosis fungoides, Skin metastases of breast cancer Pregnancy, lactation, concurrent radiation therapy.
    How to use Miltefosine: Take this medicine in the dose and duration as advised by your doctor. Do not chew, crush or break it. Miltefosine is to be taken with food. Adult Dose: Adult : PO Visceral Leishmaniasis 100-150 mg/day for 28 days. Child Dose: Child: PO 2.5 mg/kg/day bid >12 y: 30–44 kg: 100 mg/day bid >45 kg: 150 mg/day tid
    Miltefosine did not inhibit human cytochrome P450 enzymes in vitro. Miltefosine did not induce cytochrome 3A activity in rats.
    Pregnancy, lactation, concurrent radiation therapy.
    Common - Headache - Nausea - Itching - Sleepiness - Decreased appetite - Abdominal pain - Diarrhea - Vomiting - Dizziness - Increased creatinine level in blood - Increased liver enzymes >10% Visceral leishmaniasis Increased transaminases, <3 x ULN (94%),Decreased platelets <150,000 (62%),Vomiting (37.8%),Decreased appetite (23.1%),Diarrhea (20.4%) 1-10% Visceral leishmaniasis Increased serum creatinine, >1.5 x baseline (10%),Asthenia (6.3%),Increased transaminases, 3-5 x ULN (6%),Decreased platelets <50,000 (2.4%)
    Precaution: Metastases grown over breast implants. Increased serum creatinine, ALT, AST, bilirubin reported; monitor. Thrombocytopenia reported; monitor platelets Stevens-Johnson syndrome reported; discontinue if an exfoliative or bullous rash occurs Lactation: Unknown if distributed in human breast milk; avoid breastfeeding during therapy and for 5 months following therapy
    Keep below 30°C temperature, away from light & moisture. Keep out of the reach of children.
    Leishmaniacides
    Miltefosine is a phospholipid derivative thought to work by disrupting cell-membrane function.
    Pregnancy: Miltefosine should not be used during pregnancy. Obtain a urine or serum pregnancy test in females of reproductive potential prior to prescribing.Nursing Mothers: Discontinue drug or nursing depending on the importance of drug to the mother. Avoid breastfeeding for 5 months after Miltefosine therapy.Females and Males of Reproductive Potential: Advise females to use effective contraception during therapy and for 5 months after therapy. Advise patients of reproductive toxicities in animals, and that the potential for impaired fertility in humans has not been adequately evaluated
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