Contraception

Active Ingredient: Medroxyprogesterone

Indication for Medroxyprogesterone

Population group: women, only adults (18 - 65 years old)

Medroxyprogesterone is indicated for long-term female contraception. Each injection prevents ovulation and provides contraception for at least 12 weeks (+/- 5 days). However, it should be taken into consideration that the return to fertility (ovulation) may be delayed for up to one year.

Medroxyprogesterone is suitable for use in women who have been appropriately counselled concerning the likelihood of menstrual disturbance and the potential for a delay in return to full fertility.

Medroxyprogesterone may also be used for short-term contraception in the following circumstances:

  1. For partners of men undergoing vasectomy, for protection until the vasectomy becomes effective.
  2. In women who are being immunised against rubella, to prevent pregnancy during the period of activity of the virus.
  3. In women awaiting sterilisation.

For this indication, competent medicine agencies globally authorize below treatments:

150 mg

Route of admnistration

Intramuscular

Defined daily dose

150 - 150 mg

Dosage regimen

From 150 To 150 mg once every day

Detailed description

First injection: To provide contraceptive cover in the first cycle of use, an injection of 150 mg i.m. should be given during the first five days of a normal menstrual cycle. If the injection is carried out according to these instructions, no additional contraceptive cover is required.

Post Partum: To increase assurance that the patient is not pregnant at the time of first administration, this injection should be given within 5 days post partum if not breast-feeding.

There is evidence that women prescribed medroxyprogesterone in the immediate puerperium can experience prolonged and heavy bleeding. Because of this, the drug should be used with caution in the puerperium. Women who are considering use of the product immediately following delivery or termination should be advised that the risk of heavy or prolonged bleeding may be increased. Doctors are reminded that in the non breast-feeding, post partum patient, ovulation may occur as early as week 4.

If the puerperal woman will be breast-feeding, the initial injection should be given no sooner than six weeks post partum, when the infant’s enzyme system is more fully developed. Further injections should be given at 12 week intervals.

Further doses: These should be given at 12 week intervals, however, as long as the injection is given no later than five days after this time, no additional contraceptive measures (e.g. barrier) are required. (N.B. For partners of men undergoing vasectomy, a second injection of 150 mg I.M. 12 weeks after the first may be necessary in a small proportion of patients where the partner’s sperm count has not fallen to zero.) If the interval from the preceding injection is greater than 89 days (12 weeks and five days) for any reason, then pregnancy should be excluded before the next injection is given and the patient should use additional contraceptive measures (e.g. barrier) for fourteen days after this subsequent injection.

Active ingredient

Medroxyprogesterone

Medroxyprogesterone acetate exerts anti-oestrogenic, anti-androgenic and antigonadotrophic effects.

Read more about Medroxyprogesterone

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