Product image of Mirena (Levonorgestrel) supplied by GNH India

Mirena

Active Ingredient:
Levonorgestrel
Origin:
EU

Mirena (Levonorgestrel)

Levonorgestrel, the active ingredient in Mirena, is a progestin presented as a 20 µg/day (total 52 mg) intrauterine system for intrauterine use. It provides up to five years of reversible contraception, reduces heavy menstrual bleeding, and offers endometrial protection for women receiving estrogen therapy.

GNH India supplies Mirena as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring regulatory‑approved quality for the EU market and other regions, with comprehensive documentation and support for import compliance and timely delivery.

Manufacturer / TM Owner

Bayer Healthcare

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Indications & Clinical Uses

  • Mirena (levonorgestrel intrauterine system) is used in the reproductive health field to provide hormonal contraception and manage menstrual disorders.
  • Contraception: provides up to five years of highly effective, reversible birth control by preventing ovulation and creating a cervical mucus barrier.
  • Heavy menstrual bleeding: reduces menstrual blood loss by thinning the endometrial lining, leading to lighter periods and improvement of anemia associated with excessive bleeding.
  • Endometrial protection during estrogen therapy: maintains a stable endometrial environment, preventing estrogen‑induced hyperplasia in women using combined hormone replacement therapy.

How It Works

  • Levonorgestrel released from the intrauterine system acts locally on the uterine tissue. It suppresses the hypothalamic‑pituitary‑ovarian axis, inhibiting the mid‑cycle LH surge and thereby preventing ovulation. In addition, it thickens cervical mucus, reducing sperm penetration, and induces endometrial atrophy, creating an environment unsuitable for implantation. These combined actions result in effective contraception and also modulate the endometrial response, which accounts for the reduction in menstrual blood loss.

Side Effects

Levonorgestrel delivered via the Mirena intrauterine system may be associated with a range of adverse reactions.

Common Side Effects

  • Irregular bleeding or spotting: occasional light bleeding between periods, usually resolves over time.
  • Amenorrhea (absence of periods): menstrual cycles may stop during use, often returning after removal.
  • Headache: mild to moderate tension‑type headaches, may improve with analgesics.
  • Breast tenderness: temporary soreness or swelling of the breasts, typically diminishes after initial months.
  • Acne: emergence or worsening of facial pimples, generally mild.
  • Mood changes: irritability or mild depressive symptoms, should be monitored.

Serious or Rare Side Effects

  • Pelvic inflammatory disease: infection of the reproductive organs requiring medical attention.
  • Uterine perforation: rare injury to the uterine wall during insertion.
  • Ectopic pregnancy: pregnancy occurring outside the uterus, most commonly in the fallopian tube.

Precautions & Warnings

Before using Mirena, healthcare providers should consider several precautionary measures to ensure safety and effectiveness.

  • Patient selection: confirm no active pelvic infection or uterine anomalies.
  • Pregnancy status: contraindicated in known or suspected pregnancy; ensure negative test before insertion.
  • Breastfeeding: evaluate risks and benefits, as levonorgestrel is excreted in milk.
  • Smoking: advise against use in women over 35 who smoke heavily due to cardiovascular risk.
  • Follow‑up: schedule pelvic exam 4‑6 weeks after insertion to verify placement.
  • Store at room temperature: keep the device in original packaging, protect from moisture and extreme heat.

Avoid Interactions

Levonorgestrel released from Mirena can interact with other medications, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Antiepileptic enzyme inducers (e.g., carbamazepine, phenytoin, rifampicin): may reduce levonorgestrel levels and compromise contraceptive effectiveness.
  • Antitubercular agents (rifampin): similar enzyme induction leading to decreased hormone concentrations.

Moderate Interactions (Monitor Closely)

  • Antifungal azoles (ketoconazole, itraconazole): can increase levonorgestrel exposure, potentially heightening side effects.
  • Antiretroviral drugs (efavirenz, nevirapine): may modestly lower hormone levels, requiring additional contraceptive measures.
  • St. John’s wort: herbal inducer that may lower efficacy; advise patient to avoid or use backup contraception.

Frequently Asked Questions

Mirena is a levonorgestrel-releasing intrauterine system indicated for up to five years of reversible contraception, for the treatment of heavy menstrual bleeding, and for endometrial protection in women receiving estrogen therapy.

Levonorgestrel released from the intrauterine system suppresses ovulation, thickens cervical mucus to block sperm, and induces endometrial atrophy, creating an environment that prevents implantation and reduces menstrual blood loss.

The device is designed to release approximately 20 µg of levonorgestrel per day (total 52 mg) for up to five years. The exact dosing schedule is set by the prescribing clinician based on individual patient needs.

Mirena is contraindicated in pregnancy (Category X) and should not be inserted in women who are pregnant or suspect they might be. Levonorgestrel is excreted in breast milk, so clinicians weigh benefits and risks before recommending use while breastfeeding.

Enquiries are submitted via the product page on gnhindia.com, where you specify the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Compared with oral contraceptives, Mirena offers continuous low‑dose hormone delivery, eliminates daily adherence, and can reduce menstrual bleeding. Unlike copper IUDs, it provides hormonal benefits but is not suitable for women who prefer a non‑hormonal method.

Mirena should be stored at room temperature, below 25 °C, in its original sealed packaging. Protect the device from moisture, direct sunlight and extreme heat to maintain its integrity until insertion.

A trained healthcare professional inserts Mirena through the cervical canal into the uterine cavity using a specialized inserter. The procedure is performed in a clinical setting under aseptic conditions, and placement is confirmed by pelvic examination or ultrasound.

Serious risks include pelvic inflammatory disease, uterine perforation during insertion, and ectopic pregnancy if conception occurs. Prompt medical evaluation is required if severe abdominal pain, abnormal bleeding, or signs of infection develop.

Mirena is contraindicated in women with current pregnancy, suspected pregnancy, active pelvic infection, unexplained vaginal bleeding, uterine anomalies that could impede placement, or a history of breast cancer. Smoking women over 35 should also avoid its use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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