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 an intrauterine system (IUS) for intrauterine use. The device releases levonorgestrel locally over several years to provide reliable, reversible contraception for women of reproductive age.

GNH India supplies Levosert as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, including both public and private healthcare providers.

Manufacturer / TM Owner

Gedeon Richter Plc.

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Indications & Clinical Uses

  • Levosert, containing levonorgestrel, is used within the hormonal contraceptive pathway for long‑acting reversible contraception.
  • Contraception: provides highly effective, reversible birth control for up to five years.
  • Long‑acting reversible contraception (LARC): offers a low‑maintenance option that does not require daily dosing.
  • Prevention of unintended pregnancy: reduces the risk of pregnancy in women seeking a dependable method.

How It Works

  • Levosert releases levonorgestrel directly into the uterine cavity, where the progestogen binds to progesterone receptors in the endometrium and cervical mucus. This action thickens cervical mucus, suppresses ovulation in many cycles, and induces endometrial changes that inhibit implantation, resulting in effective 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)
  • Menstrual cramps or pelvic discomfort
  • Headache
  • Breast tenderness or enlargement
  • Mood changes

Serious or Rare Side Effects

  • Pelvic inflammatory disease (PID)
  • Uterine perforation during insertion
  • Ectopic pregnancy if contraception fails
  • Severe allergic reaction (anaphylaxis)
  • Device expulsion or migration

Precautions & Warnings

  • Before insertion and during use, certain precautions should be observed to ensure safety and effectiveness.
  • Screening: confirm the patient is not pregnant and has no active pelvic infection.
  • Medical history: assess for contraindications such as unexplained vaginal bleeding, uterine anomalies, or hormone‑sensitive cancers.
  • Follow‑up: schedule a post‑insertion visit to verify correct placement and address any concerns.
  • Bleeding patterns: counsel users about possible changes in menstrual flow, including prolonged spotting.
  • Interaction with hormonal therapies: avoid concurrent systemic estrogen therapy unless medically indicated.
  • Store at ambient temperature: keep the device in its original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Concurrent systemic estrogen therapy: may increase the risk of thromboembolic events.
  • Recent uterine surgery (within 6 weeks): raises the chance of device displacement or perforation.

Moderate Interactions (Monitor Closely)

  • Rifampin, griseofulvin, or other enzyme‑inducing antibiotics: can lower levonorgestrel levels.
  • Anticonvulsants such as carbamazepine or phenytoin: may reduce contraceptive efficacy.
  • St. John’s wort or other herbal inducers: possible decreased hormonal effect.

Frequently Asked Questions

Levosert is an intrauterine system that delivers levonorgestrel to provide long‑acting reversible contraception. It is intended for women who want a highly effective, low‑maintenance birth control method that can remain in place for several years.

Levonorgestrel released from Levosert acts locally on the cervix and endometrium. It thickens cervical mucus, suppresses ovulation in many cycles, and creates endometrial changes that prevent implantation, thereby preventing pregnancy.

The dose of levonorgestrel in Levosert is fixed by the manufacturer and is not adjusted by the patient. The prescribing clinician determines the appropriate device based on the patient’s clinical needs and regulatory guidelines.

Levosert is not intended for use during pregnancy; it must be inserted only after confirming the patient is not pregnant. Women who become pregnant while the device is in place should consult a healthcare professional. Limited data are available for breastfeeding, and clinicians should evaluate risks and benefits individually.

To order Levosert, submit an enquiry on the product page at gnhindia.com with 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, low‑maintenance hormone delivery without the need for daily adherence. Unlike injectable progestins, it provides a longer duration of action (up to five years) and allows for rapid return of fertility after removal.

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 aseptic technique, and the device remains in place for the approved duration without further dosing.

Serious risks, though rare, include uterine perforation during insertion, pelvic inflammatory disease, and ectopic pregnancy if the device fails. Users should seek immediate medical attention for severe abdominal pain, abnormal bleeding or signs of infection.

Levosert is contraindicated in women with current pregnancy, active pelvic infection, unexplained vaginal bleeding, known or suspected uterine anomalies, or hormone‑sensitive cancers. It should also be avoided in individuals with a history of severe allergic reaction to levonorgestrel or any component of the device.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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