
MM Kit200 mg+200
Ziska Pharmaceuticals Ltd.
Approved Indications Mifepristone + Misoprostol is a two-drug regimen combining a progesterone receptor antagonist (mifepristone) with a prostaglandin E1 analogue (misoprostol) and more.
Mifepristone + Misoprostol is a two-drug regimen combining a progesterone receptor antagonist (mifepristone) with a prostaglandin E1 analogue (misoprostol), used under strict medical supervision for:
Mifepristone + Misoprostol must only be used after an intrauterine pregnancy has been confirmed and an ectopic pregnancy has been excluded (see Contraindications), and requires a follow-up visit to confirm the pregnancy has been completely terminated.
| Step | Medicine & dose | Timing |
|---|---|---|
| Step 1 | Mifepristone 200 mg, one tablet, taken orally | Day 1, administered/witnessed at a medical facility |
| Step 2 | Misoprostol 800 mcg, by the buccal, vaginal, or sublingual route as specified in the approved regimen/local protocol | 24–48 hours after the mifepristone dose |
| Follow-up | Clinical review (and ultrasound/hCG testing where indicated) | Approximately 7–14 days after mifepristone, to confirm complete termination and exclude ongoing or ectopic pregnancy |
Mifepristone + Misoprostol is approved for use only up to the gestational age limit stated in the approved product labeling/local regulatory guidance; it is not intended for use beyond this limit. Treatment must be initiated and supervised by a physician who has confirmed an intrauterine pregnancy and has excluded ectopic pregnancy.
Where used for medical management of confirmed early pregnancy loss, a physician may direct a modified sequence or dose of Mifepristone + Misoprostol's components per current clinical guidelines; this must always be individualized by the treating physician.
Mifepristone + Misoprostol is used in pregnant adolescents of reproductive age under the same physician-supervised regimen as adults, with appropriate counselling; it is not used in pre-menarchal children (see Pediatric Uses).
Data on dose adjustment in significant renal or hepatic impairment are limited; Mifepristone + Misoprostol should be used with added caution and closer monitoring in these patients under specialist supervision (see Use in Special Populations).
Patients should seek urgent medical attention for soaking through more than two sanitary pads per hour for two or more consecutive hours, severe or worsening abdominal pain, fever lasting more than 24 hours, or feeling generally unwell after taking Mifepristone + Misoprostol (see Precautions and Warnings).
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