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 52 mg intrauterine system for intrauterine use. It provides long‑acting reversible contraception and prevents pregnancy 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 hormonal contraceptive delivered via an intrauterine system, is indicated for:

  • Long‑acting reversible contraception: provides up to five years of reliable pregnancy prevention.
  • Prevention of unintended pregnancy: suitable for women seeking a non‑daily, highly effective method.
  • Management of menstrual bleeding patterns: may reduce heavy or irregular bleeding in many users.

How It Works

  • Levonorgestrel released from the intrauterine system acts locally on the cervical mucus, endometrium and sperm. It thickens cervical mucus, impairs sperm motility and function, suppresses endometrial proliferation, and may inhibit ovulation, thereby preventing fertilisation and implantation.

Side Effects

Levosert may cause a range of adverse reactions. Most are mild and resolve with time.

Common Side Effects

  • Irregular bleeding or spotting, especially during the first months.
  • Amenorrhea (absence of periods) after continued use.
  • Pelvic or uterine cramping.
  • Breast tenderness or mild hormonal symptoms.
  • Headache or mild nausea.

Serious or Rare Side Effects

  • Uterine perforation during insertion.
  • Expulsion of the device.
  • Pelvic infection (e.g., PID) following placement.
  • Ectopic pregnancy if contraception fails.
  • Rare systemic hormonal effects such as thrombosis.

Precautions & Warnings

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

  • Screen for contraindications: ensure the patient has no active pelvic infection, unexplained vaginal bleeding, or known hypersensitivity to levonorgestrel.
  • Assess uterine anatomy: appropriate for a normal uterine cavity size and shape.
  • Confirm non‑pregnancy: a negative pregnancy test is required prior to placement.
  • Monitor device position: schedule follow‑up visits to check for displacement or expulsion.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levosert may interact with medications that affect levonorgestrel metabolism or hormone levels.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine, phenytoin): may significantly reduce contraceptive efficacy.
  • Certain antiretroviral protease inhibitors: can alter hormone concentrations and compromise effectiveness.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inducers (e.g., St. John’s wort, efavirenz): may modestly lower levonorgestrel levels.
  • Antifungal azoles and some antibiotics (e.g., griseofulvin): could affect hormone metabolism and require additional contraceptive measures.
  • Concurrent hormonal therapies (e.g., estrogen‑containing contraceptives): may increase overall hormonal exposure and warrant clinical review.

Frequently Asked Questions

Levosert is an intrauterine system that delivers levonorgestrel directly to the uterus. It is used as a long‑acting reversible contraceptive to prevent pregnancy for up to five years and can also help regulate menstrual bleeding patterns.

Levonorgestrel released from the device thickens cervical mucus, reduces sperm motility, suppresses the growth of the uterine lining, and may inhibit ovulation. These combined actions prevent fertilisation and implantation, providing effective contraception.

Levosert is supplied as a pre‑loaded 52 mg intrauterine system. The exact dosing regimen, including insertion timing and follow‑up schedule, is determined by the prescribing healthcare professional based on individual patient needs.

Levosert must not be used during pregnancy; a negative pregnancy test is required before insertion. Women who become pregnant while the device is in place should have it removed promptly. Limited data exist for breastfeeding, and clinicians should weigh benefits against potential risks.

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 oral progestin pills, Levosert offers continuous, low‑dose hormone delivery without daily adherence, providing up to five years of protection. Unlike copper IUDs, it may reduce menstrual bleeding. Its efficacy is comparable to other levonorgestrel‑based IUS devices but with a distinct 52 mg dose and duration.

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

Levosert is inserted by a trained healthcare professional into the uterine cavity through the cervix. The procedure is performed in a clinical setting using a sterile inserter. Once placed, the device remains in situ for up to five years, after which it can be removed or replaced.

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

Levosert is contraindicated in women with active pelvic infections, unexplained vaginal bleeding, known or suspected pregnancy, uterine anomalies that prevent proper placement, or hypersensitivity to levonorgestrel. Women with certain cancers or severe liver disease should also avoid its use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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