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WHO GMP
Certified

15 Days Easy
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Long Expiry
(>8 Months)
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Safe Abort 200mg 200mcg Kit 5s is a combination therapeutic regimen used for the medical termination of intrauterine pregnancy through 70 days (10 weeks) of gestation. It consists of two distinct medications that work sequentially to end a pregnancy. Mifepristone acts by blocking the hormone progesterone, which is necessary to maintain a pregnancy, while Misoprostol causes the cervix to soften and the uterus to contract to expel the pregnancy tissue. This combination is also used under specialised medical guidance for the management of early pregnancy loss (miscarriage).
Safe Abort 200mg 200mcg Kit 5s is a combined treatment involving a progesterone receptor antagonist (Mifepristone) and a prostaglandin E1 analogue (Misoprostol). The two medications are used in a specific clinical sequence to achieve a medical abortion.
Mifepristone, the first medication in the regimen, binds to progesterone receptors in the uterine lining. By blocking progesterone, it causes the lining to break down and prevents the pregnancy from remaining attached to the uterine wall. It also increases the sensitivity of the uterine muscle to prostaglandins. Misoprostol, the second medication, is administered 24 to 48 hours later. It acts directly on the myometrium (uterine muscle) to induce contractions and causes cervical ripening. Together, these actions result in the evacuation of the uterus, a process that typically involves significant cramping and bleeding.
This regimen is intended for use under the supervision of a healthcare provider and requires a confirmed diagnosis of the duration of pregnancy, typically via ultrasound or clinical examination. It is not effective for ectopic pregnancies (pregnancies outside the uterus). Patients using this medication must have access to emergency medical care in the event of incomplete evacuation or excessive bleeding. A follow-up assessment is mandatory to ensure the procedure is complete and to monitor for any complications.
Safe Abort 200mg 200mcg Kit 5s may be indicated by your doctor for:
To end an intrauterine pregnancy through the 10th week (70 days) of gestation.
To assist in the completion of a miscarriage when the body does not expel the tissue naturally.
Safe Abort 200mg 200mcg Kit 5s may provide benefits such as:
Always consult your doctor if you notice any persistent or concerning symptoms while using Safe Abort 200mg 200mcg Kit 5s.
Use Safe Abort 200mg 200mcg Kit 5s exactly as directed by your doctor based on the prescribed protocol. This is usually done in a clinical setting.
Buccal: Placing two tablets in each cheek pouch for 30 minutes.
Sublingual: Placing four tablets under the tongue for 30 minutes.
Vaginal: Inserting four tablets into the vagina.
Safe Abort 200mg 200mcg Kit 5s works through a two-step biological process.
Mifepristone is a progesterone receptor antagonist. Progesterone is essential for maintaining the uterine lining and supporting pregnancy. By blocking progesterone, mifepristone causes the uterine lining to break down, detaches the pregnancy tissue, and softens the cervix, preparing the uterus for expulsion.
Misoprostol, taken 24–48 hours later, is a prostaglandin E1 analogue. It induces cervical ripening and strong uterine contractions, which lead to the expulsion of pregnancy tissue.
Together, this combination mimics a natural miscarriage process. Mifepristone initiates pregnancy termination by removing hormonal support, while misoprostol completes the process by contracting the uterus. This sequential mechanism makes the regimen highly effective for medical termination of pregnancy up to 70 days (10 weeks) of gestation.
This regimen is specifically indicated for medical termination of pregnancy up to 70 days (10 weeks). It must only be used under strict medical supervision.
Small amounts of misoprostol may pass into breast milk; guidance is required before use.
May cause dizziness, cramping, or heavy bleeding. Avoid driving or operating machinery until you feel stable.
Generally safe, but caution is advised in patients with liver impairment; monitoring may be required.
No major dose adjustments are usually necessary, but consult your doctor if you have kidney disease.
Alcohol may worsen dizziness, nausea, or increase bleeding risk. Avoid during treatment.
In the event of taking more than the prescribed amount, or if severe symptoms occur, such as extremely heavy bleeding (soaking through more than two large pads per hour for two hours), severe abdominal pain, high fever, or fainting, immediate medical attention is required.
For assistance with a suspected overdose, contact a local poison control centre or seek emergency medical services at a hospital.
If a dose is missed or if the timing between the two medications does not follow the prescribed schedule, it is necessary to contact the prescribing healthcare provider or clinic immediately. They will provide instructions on how to proceed based on the specific circumstances.
Therapeutic Class
Abortifacient / Labor Inducer
Action Class
Progesterone Receptor Antagonist / Uterotonic
Chemical Class
Antiprogestogen + Prostagandin E1 Analogue
Habit Forming
No
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