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 synthetic progestogen presented as a 52 mg intrauterine system for intrauterine use. The device releases approximately 20 µg of levonorgestrel per day, creating a local hormonal environment that prevents pregnancy and reduces menstrual blood loss. It provides long‑acting reversible contraception and is also indicated for the management of heavy menstrual bleeding in women of reproductive age.

GNH India supplies Mirena as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and offers reliable global logistics for this IUS product.

Manufacturer / TM Owner

Bayer Hellas Sa

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Indications & Clinical Uses

Levonorgestrel, a synthetic progestogen, is employed within hormonal contraceptive and menstrual‑management pathways.

  • Contraception (long‑acting reversible contraceptive): Provides highly effective pregnancy prevention for up to five years.
  • Heavy menstrual bleeding: Reduces menstrual blood loss and can improve anemia associated with excessive bleeding.

How It Works

  • Levonorgestrel released from the intrauterine system acts locally on the endometrium and cervical mucus. It thickens cervical mucus, impairing sperm motility and function, induces endometrial atrophy, and may suppress ovulation. The combined actions create an environment unfavorable for fertilisation and implantation, thereby preventing pregnancy while also decreasing endometrial growth that contributes to heavy menstrual bleeding. The low systemic exposure minimizes hormonal side effects compared with oral progestogens.

Side Effects

Levonorgestrel IUS may be associated with a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Irregular vaginal bleeding or spotting.
  • Amenorrhea (absence of periods) after several months.
  • Pelvic or abdominal cramping.
  • Hormonal changes such as breast tenderness or mood swings.

Serious or Rare Side Effects

  • Uterine perforation during insertion.
  • Device expulsion or displacement.
  • Pelvic inflammatory disease or severe infection.

Precautions & Warnings

Prior to insertion and during use, several precautions should be observed to ensure safety and effectiveness.

  • Pregnancy testing: Confirm the patient is not pregnant before insertion.
  • Uterine evaluation: Screen for fibroids, polyps, or congenital anomalies that may impede placement.
  • Active infection: Defer insertion in the presence of pelvic inflammatory disease or genital infection.
  • Expulsion risk: Counsel patients on signs of device displacement and schedule follow‑up checks.
  • Hormonal contraindications: Avoid use in women with known thrombophilia or hormone‑sensitive cancers.
  • Store at room temperature: Keep the device in its original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levonorgestrel released from an intrauterine system can interact with other medicines that affect hormone metabolism or increase infection risk.

Major Interactions (Avoid)

  • Enzyme‑inducing antiepileptics (e.g., carbamazepine, phenytoin): May lower levonorgestrel levels and reduce efficacy.
  • Rifampicin or rifabutin: Strong hepatic inducers that can diminish contraceptive protection.
  • Antiretroviral efavirenz: Can decrease hormonal concentrations, increasing pregnancy risk.

Moderate Interactions (Monitor Closely)

  • St John’s wort: Herbal inducer that may modestly reduce levonorgestrel exposure.
  • Antifungal azoles (e.g., ketoconazole): May increase levonorgestrel levels, potentially heightening side‑effect risk.
  • Estrogen‑containing hormonal therapies: Combined use can raise the risk of thromboembolic events.

Frequently Asked Questions

Mirena is an intrauterine system that delivers levonorgestrel locally. It is approved for long‑acting reversible contraception and for the management of heavy menstrual bleeding, helping to reduce menstrual blood loss and improve related anemia.

Levonorgestrel released from the device thickens cervical mucus, impairs sperm motility, induces endometrial atrophy, and may suppress ovulation. These combined actions create an environment that prevents fertilisation and implantation while also decreasing the growth of the uterine lining that contributes to heavy bleeding.

Mirena is a pre‑loaded intrauterine system that releases approximately 20 µg of levonorgestrel per day. The exact duration of use, typically up to five years, and any replacement schedule are determined by the prescribing healthcare professional.

Mirena must not be used in women who are pregnant or who suspect pregnancy; it is contraindicated for that purpose. After insertion, it is generally considered compatible with breastfeeding, but patients should discuss individual risks and benefits with their clinician.

To order Mirena, submit an enquiry on the product page at gnhindia.com, specifying 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 necessary import documentation.

Compared with oral progestins or combined pills, Mirena offers higher contraceptive efficacy, a lower systemic hormone exposure, and a duration of up to five years without daily dosing. It also provides the added benefit of reducing menstrual blood loss, which many oral formulations do not address.

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

Mirena is inserted by a trained healthcare provider using a sterile applicator. The device is placed through the cervical canal into the uterine cavity under aseptic conditions, after which the applicator is removed, leaving the IUS in place for up to five years.

Serious but rare risks include uterine perforation during insertion, expulsion or displacement of the device, and pelvic inflammatory disease. In very uncommon cases, an ectopic pregnancy can occur if contraception fails.

Mirena is contraindicated in women with a confirmed or suspected pregnancy, active pelvic infection, unexplained vaginal bleeding, uterine anomalies that impede placement, known or suspected hormone‑sensitive cancers, and in those with a history of thrombophilia or severe liver disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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