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 may be used to manage 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 Ab

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Indications & Clinical Uses

Jaydess, a levonorgestrel‑releasing intrauterine system, is used within the hormonal contraceptive pathway for the following clinical indications:

  • Contraception: provides highly effective, long‑term prevention of pregnancy for up to three years.
  • Heavy menstrual bleeding: reduces menstrual blood loss and can improve anemia in women with dysfunctional uterine bleeding (off‑label in some regions).

How It Works

  • Levonorgestrel released from the intrauterine system acts locally on the endometrium and cervical mucus. The steady low‑dose release (~20 µg/day) suppresses ovulation in some cycles, thickens cervical mucus to impede sperm penetration, and induces endometrial atrophy, creating an environment unsuitable for implantation while minimizing systemic hormone exposure.

Side Effects

Levonorgestrel IUS may be associated with a range of adverse reactions, most of which are mild and resolve spontaneously.

Common Side Effects

  • Irregular bleeding: spotting or breakthrough bleeding during the first months.
  • Amenorrhea: absence of menstrual periods after initial adjustment.
  • Pelvic pain or cramping: mild discomfort around the uterus.

Serious or Rare Side Effects

  • Uterine perforation: possible during insertion, may need surgical management.
  • Expulsion: device may be partially or fully expelled, requiring re‑insertion.
  • Infection: pelvic inflammatory disease or endometritis associated with the procedure.

Precautions & Warnings

Before prescribing Jaydess, clinicians should consider several safety measures.

  • Patient selection: confirm no current pregnancy and assess uterine size and shape.
  • Contraindications: avoid in women with active pelvic infection, unexplained vaginal bleeding, or known hypersensitivity to levonorgestrel.
  • Insertion timing: place within 5 days of menstrual onset or after confirmed negative pregnancy test.
  • Follow‑up: schedule pelvic exam 4–6 weeks post‑insertion to verify placement.
  • Device removal: plan removal after approved duration (up to 3 years) or earlier if complications arise.
  • Store at ambient temperature: keep below 25 °C in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levonorgestrel IUS may interact with other medicines that affect hormone metabolism.

Major Interactions (Avoid)

  • CYP3A4 inducers: drugs such as rifampicin, carbamazepine, or phenytoin may reduce levonorgestrel effectiveness.
  • Strong CYP3A4 inhibitors: agents like ketoconazole can increase systemic exposure, though clinical relevance is low for intrauterine delivery.

Moderate Interactions (Monitor Closely)

  • Antiretroviral therapy: certain protease inhibitors may alter hormone levels; monitor for breakthrough bleeding.
  • Herbal supplements: St. John’s wort may decrease efficacy; advise patients to discuss use.
  • Prolonged broad‑spectrum antibiotics: generally safe, but review if therapy exceeds several weeks.

Frequently Asked Questions

Jaydess is a levonorgestrel‑releasing intrauterine system indicated for highly effective contraception and, in some regions, for the management of heavy menstrual bleeding. It provides continuous hormone release directly within the uterus, offering long‑term birth control without daily dosing.

Levonorgestrel from the IUS is released at about 20 µg per day. It thickens cervical mucus, suppresses ovulation in many cycles, and creates an atrophic endometrium, all of which prevent sperm penetration and implantation, thereby averting pregnancy.

The dose is set by the prescriber through device selection. Jaydess contains 13.5 mg of levonorgestrel that releases approximately 20 µg daily for up to three years. No patient‑initiated dosing adjustments are required.

Jaydess is contraindicated in pregnancy (Category X) and should not be inserted in a pregnant woman. Women who become pregnant while the device is in place should seek immediate medical advice. Limited data exist for breastfeeding; clinicians usually consider alternative methods until lactation is established.

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 any necessary import documentation.

Both Jaydess and Mirena are levonorgestrel‑releasing intrauterine systems, but Jaydess contains a lower total hormone load (13.5 mg) and is approved for up to three years, whereas Mirena contains 52 mg and is approved for five years. The lower dose may result in fewer systemic effects for some users.

Jaydess should be stored at ambient temperature, below 25 °C, in its original sealed packaging. Protect the device from moisture, direct sunlight and physical damage. Do not attempt to open or manipulate the system before insertion by a qualified healthcare professional.

Jaydess is inserted by a trained clinician into the uterine cavity using a specialized inserter. The procedure is performed in a clinical setting, typically during the first few days of the menstrual cycle or after a negative pregnancy test, and does not require anesthesia in most cases.

Serious risks include uterine perforation during insertion, device expulsion, and pelvic infection. Although rare, these complications may require surgical intervention or device removal. Prompt medical evaluation is essential if severe abdominal pain, fever, or abnormal bleeding occurs.

Women with current pregnancy, active pelvic infection, unexplained vaginal bleeding, known hypersensitivity to levonorgestrel, or uterine anomalies that preclude proper placement should avoid Jaydess. Additionally, those with a history of breast cancer or thromboembolic disorders should discuss alternative contraception with their clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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