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 progestin presented as a 20 µg/day release intrauterine system for intrauterine use. It prevents pregnancy in women of reproductive age by providing continuous hormonal contraception.

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‑releasing intrauterine system, provides long‑acting reversible contraception.

  • Prevention of pregnancy: delivers a steady hormone dose to inhibit ovulation and prevent fertilisation for up to five years.
  • Long‑acting reversible contraception: offers a convenient, hormone‑based method without daily dosing.
  • Management of menstrual symptoms: can reduce heavy bleeding and dysmenorrhoea in users seeking hormonal regulation.

How It Works

  • Levonorgestrel released from the intrauterine system binds to progesterone receptors in the hypothalamus and pituitary, suppressing the luteinising hormone surge and thereby inhibiting ovulation. It also thickens cervical mucus, creating a barrier to sperm, and induces endometrial changes that reduce the likelihood of implantation.

Side Effects

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

Common Side Effects

  • Irregular vaginal bleeding: spotting or breakthrough bleeding, especially during the first months.
  • Amenorrhoea: absence of menstrual periods after initial adjustment.
  • Pelvic or abdominal pain: cramping associated with insertion or hormonal effects.
  • Headache: mild to moderate intensity.
  • Breast tenderness: hormonal‑related discomfort.
  • Nausea: occasional gastrointestinal upset.

Serious or Rare Side Effects

  • Uterine perforation: risk during insertion, requiring medical intervention.
  • Expulsion of the device: partial or complete loss of the IUS.
  • Pelvic infection: possible post‑insertion infection requiring antibiotics.
  • Ectopic pregnancy: rare but serious if pregnancy occurs.
  • Allergic reaction: rash, itching, or swelling at the insertion site.
  • Hormone‑related thromboembolic events: extremely rare clotting disorders.

Precautions & Warnings

Before using Levosert, certain precautions should be observed to ensure safety and effectiveness.

  • Screen for pregnancy: confirm the patient is not pregnant prior to insertion.
  • Assess uterine anatomy: ensure the uterus is suitable for an intrauterine system.
  • Check contraindications: avoid use in active pelvic infection, known or suspected malignancy, or unexplained vaginal bleeding.
  • Monitor for device displacement: schedule follow‑up visits to verify correct positioning.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Enzyme‑inducing anticonvulsants (e.g., carbamazepine, phenytoin): may reduce levonorgestrel levels.
  • Rifampicin: can decrease hormonal effectiveness.
  • Certain antiretrovirals (e.g., efavirenz): may lower contraceptive efficacy.

Moderate Interactions (Monitor Closely)

  • Broad‑spectrum antibiotics (e.g., tetracycline): possible slight reduction in hormone levels.
  • Herbal supplements such as St. John’s wort: may affect levonorgestrel metabolism.

Frequently Asked Questions

Levosert is a levonorgestrel‑releasing intrauterine system indicated for the prevention of pregnancy. It provides a long‑acting, reversible contraceptive effect for up to five years, eliminating the need for daily pills or frequent clinic visits.

Levonorgestrel released from the device binds to progesterone receptors, suppressing the luteinising hormone surge and preventing ovulation. It also thickens cervical mucus and alters the endometrial lining, creating multiple barriers to fertilisation and implantation.

Levosert is supplied as a pre‑loaded intrauterine system that releases approximately 20 µg of levonorgestrel per day. The exact dosing regimen, including insertion timing and duration of use, is determined by the prescribing clinician.

Levosert must not be used in women who are pregnant; it is intended for contraception in non‑pregnant individuals. Limited data suggest it is compatible with breastfeeding, but clinicians should evaluate each case and discuss potential risks with the patient.

To order Levosert, 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 provides hormonal regulation, reducing menstrual bleeding and dysmenorrhoea. Unlike oral contraceptives, it requires no daily adherence and offers up to five years of protection. Its efficacy is comparable to other levonorgestrel‑based IUS devices.

Levosert should be stored at room 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 inserted into the uterine cavity by a trained clinician using a specialized inserter. The procedure is performed in a clinical setting under aseptic conditions, and the device remains in place to release levonorgestrel continuously for the approved duration.

Serious risks include uterine perforation during insertion, expulsion of the device, pelvic infection, and the rare possibility of ectopic pregnancy if contraception fails. Prompt medical evaluation is required if severe abdominal pain, abnormal bleeding or signs of infection occur.

Levosert is contraindicated in women who are pregnant, have active pelvic infections, unexplained vaginal bleeding, known or suspected uterine malignancy, or significant uterine anomalies that prevent proper placement. Patients with a history of thromboembolic disorders should discuss alternatives with their clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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