Product image of Levosert (Levonorgestrel) supplied by GNH India

Levosert

Active Ingredient:
Levonorgestrel
Origin:
EU

Levosert (Levonorgestrel)

Levonorgestrel, the active ingredient in Levosert, is a progestogen intrauterine system presented as a 52 mg levonorgestrel releasing device for intrauterine use. It delivers a steady low dose of hormone to prevent pregnancy in women of reproductive age, offering up to five years of continuous contraception.

GNH India supplies Levosert as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring regulatory‑approved quality and reliable logistics for global health programmes. The company adheres to WHO‑GMP standards and provides technical support for device insertion and follow‑up.

Manufacturer / TM Owner

Gedeon Richter Plc.

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Indications & Clinical Uses

Levosert, a levonorgestrel intrauterine system, is indicated for long‑acting reversible contraception in women of reproductive age.

  • Contraception: Provides up to five years of highly effective pregnancy prevention.
  • Endometrial suppression: Inhibits endometrial proliferation to maintain contraceptive efficacy.
  • Cervical mucus thickening: Increases cervical mucus viscosity, reducing sperm motility and viability.

How It Works

  • Levosert releases levonorgestrel locally within the uterine cavity at approximately 20 µg per day. The hormone binds to progesterone receptors in the endometrium, leading to reduced endometrial growth, thickened cervical mucus, and impaired sperm motility. These combined actions create an environment that prevents fertilisation and may also suppress ovulation in some users, thereby providing reliable contraception.

Side Effects

Levosert may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Irregular vaginal bleeding or spotting.
  • Amenorrhea (absence of periods) after initial months.
  • Pelvic or abdominal cramping.
  • Headache.
  • Breast tenderness.
  • Mood changes.

Serious or Rare Side Effects

  • Uterine perforation during insertion.
  • Device expulsion or displacement.
  • Pelvic inflammatory disease.
  • Ectopic pregnancy if contraception fails.
  • Severe allergic reaction (e.g., rash, swelling, anaphylaxis).

Precautions & Warnings

Before using Levosert, certain precautions should be observed.

  • Pregnancy testing: Confirm non‑pregnant status prior to insertion.
  • Infection screening: Evaluate for active pelvic infection and treat before placement.
  • Uterine anomalies: Assess for structural abnormalities that may affect device positioning.
  • Breastfeeding: Discuss benefits and potential risks with a healthcare professional.
  • Follow‑up: Schedule a post‑insertion visit to verify correct placement and address any concerns.
  • Store at ambient temperature: Keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levosert may have interactions with other medications that affect hormone levels or uterine health.

Major Interactions (Avoid)

  • Rifampicin or other strong enzyme inducers: May reduce levonorgestrel efficacy.
  • Anticonvulsants (e.g., carbamazepine, phenytoin): Can lower hormone concentrations, increasing risk of contraceptive failure.

Moderate Interactions (Monitor Closely)

  • Hormonal therapies (e.g., estrogen‑containing contraceptives): May increase risk of thromboembolic events.
  • Antifungal agents (e.g., griseofulvin): Potentially modest reduction in levonorgestrel levels.
  • Antiretroviral drugs (e.g., efavirenz): May slightly decrease contraceptive effectiveness.
  • Herbal supplements (e.g., St. John’s Wort): Possible induction of metabolism, requiring monitoring.

Frequently Asked Questions

Levosert is a levonorgestrel intrauterine system designed to provide long‑acting reversible contraception. It is inserted into the uterus and releases a low, steady dose of hormone to prevent pregnancy for up to five years in women of reproductive age.

Levonorgestrel released from Levosert binds to progesterone receptors in the endometrium, suppressing its growth, thickening cervical mucus, and impairing sperm motility. These actions together create an environment that prevents fertilisation and may also inhibit ovulation in some users.

The dose of levonorgestrel released by Levosert is fixed by the device design, delivering approximately 20 µg per day for up to five years. The prescribing clinician determines suitability and timing of insertion based on individual patient factors.

Levosert is contraindicated in pregnancy and should not be inserted in a pregnant woman. Women who are breastfeeding can use Levosert after discussing potential benefits and risks with their healthcare provider, as systemic hormone exposure is minimal.

To order Levosert, 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 daily oral contraceptives, Levosert offers continuous hormone delivery without the need for daily adherence, providing up to five years of protection. Unlike copper IUDs, it uses a hormonal mechanism, which may reduce menstrual bleeding and cramping for many users.

Levosert should be stored at ambient temperature, below 25 °C, in its original sealed packaging. Protect the device from moisture, direct sunlight and physical damage until it is inserted by a qualified healthcare professional.

Levosert is a small, flexible intrauterine system that is inserted through the cervical canal into the uterine cavity by a trained clinician. The procedure is performed in a medical setting using aseptic technique, and the device remains in place for up to five years.

Serious risks include uterine perforation during insertion, device expulsion or displacement, pelvic inflammatory disease, and the rare possibility of ectopic pregnancy if contraceptive failure occurs. Prompt medical evaluation is required if severe abdominal pain, abnormal bleeding or signs of infection develop.

Levosert is contraindicated in women who are pregnant, have known or suspected uterine anomalies, active pelvic infection, unexplained vaginal bleeding, or a history of breast cancer. Women with severe liver disease or who are allergic to levonorgestrel should also avoid its use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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