Product image of Levosert Two (Levonorgestrel) supplied by GNH India

Levosert Two

Active Ingredient:
Levonorgestrel
Origin:
EU

Levosert Two (Levonorgestrel)

Levonorgestrel, the active ingredient in Levosert Two, is a progestogen presented as an intrauterine system for intrauterine use. It delivers a continuous low dose of hormone to the uterine cavity, providing highly effective, reversible contraception for women of reproductive age.

GNH India supplies Levosert Two as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation to support global distribution. Levosert Two is manufactured under EU guidelines and is available for export to multiple regions.

Manufacturer / TM Owner

Gedeon Richter Plc.

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Indications & Clinical Uses

  • Levosert Two, containing levonorgestrel, is used in the hormonal contraceptive pathway to prevent pregnancy.
  • Contraception (prevention of pregnancy): provides highly effective reversible birth control for women of reproductive age.
  • Hormonal intrauterine device: maintains low local levonorgestrel concentrations to inhibit ovulation and alter cervical mucus.
  • Long‑acting reversible contraception: eliminates the need for daily dosing and offers up to several years of protection.

How It Works

  • Levonorgestrel released from the intrauterine system acts locally on the endometrium, cervical mucus and hypothalamic‑pituitary axis. It suppresses ovulation, thickens cervical mucus to impede sperm passage, and induces endometrial changes that prevent implantation, thereby delivering sustained contraceptive effect without significant systemic exposure.

Side Effects

Levosert Two may be associated with a range of adverse reactions.

Common Side Effects

  • Irregular vaginal bleeding or spotting
  • Amenorrhea (absence of periods)
  • Pelvic or uterine cramping
  • Breast tenderness or mild pain
  • Headache or mild migraine
  • Mild abdominal discomfort

Serious or Rare Side Effects

  • Uterine perforation during insertion
  • Pelvic inflammatory infection
  • Expulsion of the intrauterine system
  • Ectopic pregnancy if contraception fails
  • Severe allergic reaction to levonorgestrel

Precautions & Warnings

  • Prior to insertion, clinicians should evaluate patient suitability and counsel on potential risks.
  • Screen for contraindications: ensure no active pelvic infection, unexplained vaginal bleeding, or known hypersensitivity to levonorgestrel.
  • Pregnancy testing: confirm the patient is not pregnant before device placement.
  • Follow‑up visit: schedule a post‑insertion check to verify correct positioning.
  • Avoid use in women with known uterine anomalies or severe fibroids.
  • Store at room temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levosert Two may interact with other medicines that affect hormone metabolism.

Major Interactions (Avoid)

  • Enzyme‑inducing anticonvulsants (e.g., carbamazepine) may reduce levonorgestrel efficacy.
  • Rifampin therapy can lower hormone levels and increase risk of contraceptive failure.
  • Certain antiretroviral protease inhibitors may alter levonorgestrel metabolism.

Moderate Interactions (Monitor Closely)

  • Broad‑spectrum antibiotics such as tetracycline may slightly affect contraceptive reliability.
  • Herbal supplements like St. John’s wort can reduce hormone concentrations.
  • Antifungal azoles (e.g., ketoconazole) may increase levonorgestrel levels, requiring monitoring.

Frequently Asked Questions

Levosert Two is an intrauterine system that delivers levonorgestrel to provide long‑acting reversible contraception. It is prescribed to prevent pregnancy in women of reproductive age and is a highly effective alternative to daily oral hormonal methods.

Levonorgestrel released from the intrauterine device suppresses ovulation, thickens cervical mucus to block sperm entry, and creates endometrial changes that prevent implantation. These actions together provide continuous contraceptive protection without systemic hormone spikes.

The dosing regimen for Levosert Two is determined by the prescribing clinician based on the product’s specifications and the patient’s clinical profile. The device is inserted once and provides contraception for several years without the need for daily dosing.

Levosert Two is intended for use in women who are not pregnant. It should not be inserted in a confirmed pregnancy. Safety during breastfeeding has not been established for this intrauterine system, and clinicians should discuss alternatives with nursing mothers.

To order Levosert Two, 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 contraceptive pills, Levosert Two offers continuous hormone release, eliminating daily adherence issues. Unlike copper IUDs, it uses a progestogen to reduce menstrual bleeding. Its efficacy is comparable to other hormonal IUS devices, providing up to several years of protection with a single insertion.

Levosert Two 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 insertion.

Levosert Two is a sterile intrauterine system that 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 typically takes only a few minutes.

Serious risks, although rare, include uterine perforation during insertion, pelvic inflammatory infection, expulsion of the device, and ectopic pregnancy if contraception fails. Patients should be monitored for signs of infection, abnormal bleeding, or device displacement.

Levosert Two is contraindicated in women with active pelvic infection, unexplained vaginal bleeding, known hypersensitivity to levonorgestrel, uterine anomalies that preclude proper placement, or current pregnancy. Clinicians should assess each patient’s medical history before recommending the device.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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