Product image of Jaydess (Levonorgestrel) supplied by GNH India

Jaydess

Active Ingredient:
Levonorgestrel
Origin:
EU

Jaydess (Levonorgestrel)

Levonorgestrel, the active ingredient in Jaydess, is a progestin presented as a 13.5 mg intrauterine system for intrauterine use. It prevents pregnancy and can be used to treat heavy menstrual bleeding in women of reproductive age.

GNH India supplies Jaydess as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Bayer Spa

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Indications & Clinical Uses

  • Jaydess is a hormonal intrauterine system that acts on the reproductive endocrine pathway to provide contraception and manage menstrual disorders.
  • Contraception: offers highly effective, reversible birth control for up to three years.
  • Heavy menstrual bleeding: reduces menstrual blood loss and improves bleeding patterns.
  • Endometrial protection: maintains a thin, stable endometrium, decreasing the risk of hyperplasia.

How It Works

  • Levonorgestrel released from the intrauterine system binds to progesterone receptors in the cervical mucus, endometrium, and hypothalamic‑pituitary axis. This thickens cervical mucus, inhibits endometrial proliferation, and suppresses ovulation, creating a local environment that prevents sperm penetration and implantation, thereby averting pregnancy.

Side Effects

Jaydess 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)
  • Pelvic or abdominal discomfort
  • Headache or breast tenderness
  • Mood changes or acne
  • Weight gain or fluid retention

Serious or Rare Side Effects

  • Uterine perforation during insertion
  • Device expulsion or displacement
  • Pelvic inflammatory infection
  • Ectopic pregnancy if contraception fails
  • Severe allergic reaction (anaphylaxis)
  • Hormone‑dependent tumor growth (rare)

Precautions & Warnings

  • Before prescribing Jaydess, clinicians should consider several safety measures.
  • Screen for pregnancy: product is contraindicated in confirmed or suspected pregnancy (Category X).
  • Assess uterine position: ensure appropriate placement and uterine size.
  • Monitor for infection: watch for signs of pelvic infection after insertion.
  • Check for uterine abnormalities: avoid in bicornuate or septate uterus.
  • Store at room temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levonorgestrel released from an intrauterine system can be affected by certain medications that alter hormone metabolism.

Major Interactions (Avoid)

  • Rifampin or other strong enzyme inducers: may reduce levonorgestrel effectiveness.
  • Certain antiepileptic drugs (e.g., carbamazepine, phenytoin): can lower hormone levels.
  • St. John's wort: may decrease contraceptive efficacy.

Moderate Interactions (Monitor Closely)

  • Antiretroviral agents (e.g., efavirenz): may modestly reduce hormone exposure.
  • Antifungal azoles (e.g., ketoconazole): could increase levonorgestrel levels.
  • Herbal supplements affecting CYP3A4: monitor for breakthrough bleeding.

Frequently Asked Questions

Jaydess is an intrauterine system that releases levonorgestrel to provide highly effective, reversible contraception for up to three years and to treat heavy menstrual bleeding by reducing menstrual blood loss.

Levonorgestrel binds to progesterone receptors, thickening cervical mucus, suppressing ovulation, and thinning the endometrial lining. These actions together create an environment that prevents sperm penetration and implantation, thereby avoiding pregnancy.

The intrauterine system contains 13.5 mg of levonorgestrel, delivering approximately 20 µg per day. The exact dosing regimen, including insertion timing and follow‑up, is determined by the prescribing clinician.

Jaydess is contraindicated in pregnancy (Category X) and should not be inserted in a pregnant woman. Women may breastfeed while using Jaydess; levonorgestrel exposure through breast milk is minimal, but clinicians should assess individual risk.

Enquiries are submitted via the product page at gnhindia.com, where you specify 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 required import documentation.

Compared with oral progestin pills, Jaydess offers continuous low‑dose hormone release, eliminating daily adherence requirements and providing up to three years of protection. Unlike copper IUDs, it reduces menstrual bleeding and may improve dysmenorrhea.

Store the device at room temperature, below 25 °C, in its original sealed packaging. Protect it from moisture, direct sunlight, and extreme temperatures to maintain the integrity of the hormone reservoir.

Jaydess 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 the device remains in place for up to three years.

Serious risks include uterine perforation during insertion, device expulsion, pelvic inflammatory infection, and the rare possibility of ectopic pregnancy if contraceptive failure occurs. Prompt medical evaluation is required if any of these events are suspected.

Jaydess is contraindicated in women who are pregnant, have active pelvic infection, unexplained vaginal bleeding, known or suspected breast cancer, or uterine anomalies such as bicornuate or septate uterus. It should also be avoided in women with a history of severe allergic reaction to levonorgestrel.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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