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 provides long‑acting reversible contraception by preventing ovulation and implantation in women of reproductive age.

GNH India supplies Levosert as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent quality and regulatory compliance across markets. The company leverages a robust supply chain and quality assurance processes to meet the needs of global healthcare providers.

Manufacturer / TM Owner

Ceres Pharma Nv

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Indications & Clinical Uses

  • Levosert (levonorgestrel) is a hormonal contraceptive that acts within the reproductive system to prevent pregnancy.
  • Contraception (long‑acting reversible contraceptive): Provides continuous birth control for up to five years after insertion of the intrauterine system.

How It Works

  • Levonorgestrel released from the intrauterine system binds to progesterone receptors in the hypothalamus and pituitary, suppressing the luteinizing hormone surge and thereby inhibiting ovulation. The hormone also thickens cervical mucus, creating a barrier to sperm, and induces endometrial changes that reduce the likelihood of implantation. This localized release maintains effective contraceptive concentrations within the uterine cavity while keeping plasma levels low.

Side Effects

Levosert may be associated with a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Irregular bleeding or spotting: Unpredictable menstrual bleeding patterns, especially during the first six months.
  • Cramps or pelvic pain: Mild to moderate discomfort in the lower abdomen.
  • Headache: Transient headache episodes.
  • Breast tenderness: Mild soreness or swelling of the breasts.
  • Acne or skin changes: Occasional worsening of acne.

Serious or Rare Side Effects

  • Uterine perforation: Rare injury to the uterine wall during insertion.
  • Expulsion of the device: The IUS may be partially or completely expelled.
  • Pelvic inflammatory disease: Infection that can affect reproductive organs.
  • Allergic reaction: Severe hypersensitivity to levonorgestrel or device components.

Precautions & Warnings

Before using Levosert, certain precautions and warnings should be considered to ensure safe and effective use.

  • Pregnancy status: Do not insert in women who are already pregnant; confirm negative pregnancy test prior to placement.
  • Breastfeeding: Use with caution; discuss benefits and risks with healthcare provider.
  • Uterine abnormalities: Evaluate for fibroids, septum, or scarring that may increase insertion complications.
  • Infection risk: Treat any active pelvic infection before insertion.
  • Copper IUD use: Not applicable; avoid concurrent use of other intrauterine devices.
  • Store at room temperature: Keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levosert can interact with other medicines or substances that affect hormone metabolism or uterine environment.

Major Interactions (Avoid)

  • Enzyme inducers (e.g., rifampin, carbamazepine, phenytoin): May reduce levonorgestrel levels, decreasing contraceptive efficacy.
  • Antifungal agents (e.g., griseofulvin): Can lower hormone concentrations, risking failure.

Moderate Interactions (Monitor Closely)

  • Antibiotics (e.g., tetracycline, metronidazole): May have a modest effect on hormone levels; monitor for breakthrough bleeding.
  • Antiretroviral drugs (e.g., efavirenz): May slightly reduce efficacy; consider additional contraception.
  • Herbal supplements (e.g., St. John’s wort): Potential enzyme induction; advise caution.

Frequently Asked Questions

Levosert is a levonorgestrel‑releasing intrauterine system indicated for long‑acting reversible contraception in women of reproductive age. It provides up to five years of birth control after insertion and is intended for use as a primary contraceptive method.

Levonorgestrel binds to progesterone receptors, suppressing the luteinizing hormone surge and preventing ovulation. It also thickens cervical mucus, creating a barrier to sperm, and induces endometrial changes that reduce the chance of implantation. The intrauterine system releases a low, steady dose directly to the uterus, limiting systemic exposure.

The dosage of Levosert is determined by the prescribing healthcare professional. The device contains 52 mg of levonorgestrel and is inserted once by a qualified provider, providing contraceptive effect for up to five years. No self‑adjustment of dose is required.

Levosert is contraindicated in pregnancy; it must not be inserted in a woman who is already pregnant. For breastfeeding women, the device can be used, but clinicians should discuss potential benefits and risks, as levonorgestrel exposure through breast milk is minimal.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying 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 copper IUDs, Levosert releases levonorgestrel, which can reduce menstrual bleeding and provide hormonal contraception, whereas copper devices are non‑hormonal and may increase bleeding. Both offer long‑term protection, but the hormonal IUS may be preferred for women seeking lighter periods or additional acne improvement.

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

Levosert is inserted into the uterine cavity by a trained healthcare professional using a specialized inserter. The procedure is performed in a clinical setting, typically after confirming a negative pregnancy test and ensuring the absence of active pelvic infection. Once placed, the device remains in situ for up to five years.

Serious risks, though rare, include uterine perforation during insertion, expulsion of the device, and pelvic inflammatory disease. Women should be monitored for signs of severe abdominal pain, abnormal bleeding, or infection, and seek immediate medical attention if such symptoms occur.

Levosert is not suitable for women who are currently pregnant, have known or suspected uterine abnormalities (such as large fibroids, uterine septum, or extensive scarring), have active pelvic infections, or have a history of hypersensitivity to levonorgestrel or device components. Consultation with a healthcare provider is essential before use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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