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 presented as a 52 mg intrauterine system for intrauterine use. It prevents pregnancy by providing continuous hormonal contraception for up to five years.

GNH India supplies Levosert as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Gedeon Richter Plc.

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Indications & Clinical Uses

Levosert, a levonorgestrel‑based intrauterine system, is indicated for hormonal contraception.

  • Contraception: provides up to five years of highly effective pregnancy prevention.
  • Heavy menstrual bleeding: reduces menstrual blood loss and improves bleeding patterns.
  • Endometrial protection in estrogen therapy: induces endometrial atrophy to lower bleeding risk.

How It Works

  • Levonorgestrel is released locally from the intrauterine system at approximately 20 µg per day. The hormone binds to progesterone receptors in the endometrium, suppressing ovulation, thickening cervical mucus, and causing endometrial atrophy, collectively creating an environment that prevents fertilisation and implantation.

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).
  • Pelvic or uterine cramping.
  • Breast tenderness or enlargement.
  • Acne or skin changes.
  • Mood swings or headache.

Serious or Rare Side Effects

  • Uterine perforation during insertion.
  • Pelvic inflammatory infection.
  • Expulsion of the device.
  • Ectopic pregnancy if contraception fails.
  • Ovarian cyst formation or rupture.
  • Severe allergic reaction to device components.

Precautions & Warnings

Before prescribing Levosert, clinicians should assess patient suitability and counsel on potential risks.

  • Confirm uterine cavity size: ensure appropriate fit of the intrauterine system.
  • Exclude current pregnancy: verify negative pregnancy test before insertion.
  • Avoid in active pelvic infection: postpone insertion until infection resolves.
  • Counsel on bleeding pattern changes: inform patients that irregular bleeding is common initially.
  • Review thromboembolic risk: consider medical history of clotting disorders.
  • Store at room temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levosert may interact with other medicines that affect hormone metabolism or efficacy.

Major Interactions (Avoid)

  • Rifampicin and other enzyme inducers: may reduce levonorgestrel levels, decreasing contraceptive effectiveness.
  • Anticonvulsants such as phenytoin, carbamazepine, or phenobarbital: can lower hormone concentrations.
  • Efavirenz (HIV antiretroviral): may diminish contraceptive protection.

Moderate Interactions (Monitor Closely)

  • Ketoconazole and other strong antifungals: may increase levonorgestrel exposure, requiring monitoring for side effects.
  • St. John's wort: may modestly reduce hormone levels, warranting additional contraceptive measures.

Frequently Asked Questions

Levosert is an intrauterine system that delivers levonorgestrel directly to the uterus. It is used as a long‑acting hormonal contraceptive to prevent pregnancy for up to five years in women of reproductive age.

Levonorgestrel released from Levosert binds to progesterone receptors in the endometrium, suppresses ovulation, thickens cervical mucus, and causes endometrial atrophy. These actions together create conditions that block fertilisation and implantation.

Levosert contains a total of 52 mg of levonorgestrel, releasing about 20 µg per day. The specific dosing schedule, including insertion and removal timing, is determined by the prescribing clinician based on individual patient needs.

Levosert is intended for use in women who are not pregnant. If pregnancy occurs, the device should be removed promptly. Limited data are available on breastfeeding; clinicians should weigh benefits and risks before recommending use in lactating women.

To request Levosert, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India works with 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 progestin pills, Levosert offers continuous low‑dose hormone delivery without daily adherence, providing up to five years of protection. Unlike copper IUDs, it uses a hormonal mechanism, which often results in reduced menstrual bleeding and cramping.

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

Levosert is inserted by a trained healthcare professional into the uterine cavity using a specialized inserter. The procedure is performed in a clinical setting under aseptic conditions, and the device remains in place for up to five years before removal.

Serious risks include uterine perforation during insertion, pelvic inflammatory infection, expulsion of the device, and the rare possibility of ectopic pregnancy if contraceptive failure occurs. Patients should seek immediate medical attention if they experience severe abdominal pain, fever, or abnormal bleeding.

Levosert is contraindicated in women with active pelvic infection, known or suspected uterine anomalies, current pregnancy, unexplained vaginal bleeding, or a history of breast cancer. It should also be used with caution in individuals with clotting disorders or severe liver disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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