MM Kit 200 mg+200 mcg (Tablet)

(1+4) tablet kit: ৳ 300.00

Medicine Details

Indications

  • Early Menstrual Regulation (MR)
  • Termination of pregnancy up to 9 weeks of gestation

Composition

  • Each box contains 2 blister strips
  • One strip contains 1 tablet of Mifepristone INN 200 mg
  • Another strip contains 4 tablets of Misoprostol USP 200 microgram each

Pharmacology

  • Mifepristone is a synthetic steroid with anti-progestational activity
  • Mifepristone inhibits the activity of endogenous or exogenous progesterone
  • Mifepristone sensitizes the myometrium to the contraction-inducing activity of prostaglandins
  • Misoprostol is a synthetic analogue of prostaglandin E1
  • Misoprostol causes myometrial contraction by interacting with specific receptors
  • Misoprostol causes the cervix to soften and the uterus to contract

Dosage & Administration

  • Mifepristone administration: One tablet of Mifepristone (200 mg) is taken in a single oral dose
  • Misoprostol administration: 800 micrograms of Misoprostol is taken buccally or sublingually 24-48 hours after Mifepristone
  • Post-treatment examination is required within 10 to 14 days after Mifepristone administration

Interaction

  • Mifepristone metabolism may be inhibited by Ketoconazole, Itraconazole, Erythromycin, and grapefruit juice
  • Misoprostol does not interfere with the beneficial effects of aspirin

Contraindications

  • Known allergy or hypersensitivity to Mifepristone, Misoprostol, or other prostaglandins
  • Confirmed or suspected ectopic pregnancy
  • Chronic adrenal failure
  • Haemorrhagic disorders or concurrent anticoagulant therapy
  • Inherited porphyria

Side Effects

  • Nausea
  • Vomiting
  • Diarrhoea
  • Pelvic pain
  • Fainting
  • Headache
  • Dizziness
  • Asthenia
  • Abdominal pain
  • Flatulence
  • Dyspepsia
  • Shivering
  • Hyperthermia
  • Severe vaginal bleeding
  • Shock
  • Uterine rupture

Pregnancy & Lactation

  • Mifepristone is indicated for Menstrual Regulation (MR) and has no other approved indication for use during pregnancy
  • Mifepristone effects on infants through breast milk is unknown
  • Misoprostol should not be administered to nursing mothers

Precautions & Warnings

  • Combination of Mifepristone & Misoprostol should not be given to anyone else
  • Intra Uterine Device (IUD) should be removed before treatment with Mifepristone
  • Surgical termination is recommended in cases of treatment failure
  • Patients with hepatic disease should receive a decreased dose of Misoprostol

Use in Special Populations

  • Patients with hepatic impairment should receive a decreased dose of Misoprostol
  • No routine dosage adjustment is recommended in older patients or patients with renal impairment for Misoprostol

Overdose Effects

  • No serious adverse reactions reported in tolerance studies for Mifepristone
  • Clinical signs of Misoprostol overdose are sedation, tremor, convulsions, dyspnea, abdominal pain, diarrhoea, fever, palpitations, hypotension, or bradycardia

Therapeutic Class

  • Drugs acting on the Uterus
  • Prostaglandin analogues

Storage Conditions

  • Store in a cool and dry place
  • Protected from light

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