GNH USA

Europe — EMA

Kyleena

GNH USA supplies Kyleena (Levonorgestrel), a progestin contraceptive for long‑acting intrauterine contraception. Request a quote for global supply.

Levonorgestrel

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What is Levonorgestrel?

Levonorgestrel, the active ingredient in Kyleena, is a progestin presented as an intrauterine system for intrauterine use. The device releases levonorgestrel locally to provide continuous contraception, preventing pregnancy in women of reproductive age for up to five years.

GNH USA supplies Kyleena as a licensed, GDP‑compliant international pharmaceutical supplier, providing the intrauterine system to hospitals, pharmacies and clinics worldwide, and supporting global procurement with regulatory expertise and reliable logistics. Our network ensures timely delivery and compliance with local health authority requirements, and we also offer technical assistance for device insertion and patient counseling.

What is Levonorgestrel used for?

Kyleena, containing levonorgestrel, is used in the hormonal contraceptive pathway to prevent pregnancy.

Contraception: provides continuous prevention of pregnancy for up to five years. LARC (Long‑acting reversible contraception): offers a reversible, hormone‑based intrauterine method. Family planning: enables women to plan pregnancies with a single insertion and minimal maintenance.

What are the side effects of Levonorgestrel?

Side effects are reported by some users of the intrauterine system.

Common Side Effects: - Irregular bleeding or spotting - Amenorrhea (absence of periods) - Pelvic or cramping pain - Breast tenderness - Headache - Acne or oily skin

Serious or Rare Side Effects: - Uterine perforation - Device expulsion - Pelvic inflammatory infection - Ectopic pregnancy - Ovarian cyst formation - Severe allergic reaction (anaphylaxis)

What precautions apply to Levonorgestrel?

Before insertion, several precautions should be observed.

Screen for pregnancy: confirm the patient is not pregnant prior to device placement. Assess uterine anatomy: avoid use in women with known uterine anomalies or fibroids that distort the cavity. Check for active infection: postpone insertion if pelvic infection or sexually transmitted disease is present. Consider hormonal contraindications: do not use in patients with estrogen‑dependent tumours or severe liver disease. Monitor device position: schedule follow‑up examinations to detect displacement or expulsion. Store at ambient temperature: keep in original packaging, protect from moisture and direct sunlight.

What does Levonorgestrel interact with?

Levonorgestrel may interact with other medicines that affect hormone metabolism.

Major Interactions (Avoid): - Enzyme inducers (e.g., rifampin, carbamazepine, phenytoin): may markedly reduce levonorgestrel efficacy. - Antifungal azoles (e.g., ketoconazole, itraconazole): can increase levonorgestrel levels and risk of side effects. - HIV protease inhibitors (e.g., ritonavir): may alter hormone concentrations.

Moderate Interactions (Monitor Closely): - Certain antibiotics (e.g., rifampicin, griseofulvin): may modestly decrease contraceptive effectiveness. - Antiepileptic drugs with mixed enzyme activity: require clinical monitoring of contraceptive reliability.

Frequently asked questions

What is Kyleena used for?+
Kyleena is a hormonal intrauterine system that provides long‑acting reversible contraception, preventing pregnancy for up to five years after a single insertion by releasing levonorgestrel directly into the uterus.
How does levonorgestrel work in Kyleena?+
Levonorgestrel released from the device binds to progesterone receptors in the cervical mucus and endometrium, thickening the mucus, inhibiting sperm motility, and suppressing the growth of the uterine lining, which together block fertilisation and implantation.
What is the usual dose of Kyleena?+
The dosage regimen of Kyleena is determined by the prescribing healthcare professional; the device contains a fixed amount of levonorgestrel that provides continuous release for up to five years and is not adjusted by the patient.
Is Kyleena safe to use during pregnancy or breastfeeding?+
Kyleena must not be inserted in a woman who is already pregnant. Women who become pregnant after insertion should have the device removed. Limited data are available for breastfeeding; clinicians should evaluate risks and benefits on an individual basis.
How do I order Kyleena from GNH USA?+
To place an order, submit an enquiry on the Kyleena product page at gnh-usa.com, specifying the required quantity. GNH USA 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.
How does Kyleena compare with other intrauterine contraceptives?+
Compared with copper IUDs, Kyleena releases a progestin rather than copper, resulting in fewer menstrual bleeding changes and a lower incidence of dysmenorrhoea. Compared with Mirena, Kyleena contains a lower levonorgestrel dose and is slightly smaller, making it suitable for women who have not previously given birth.
What are the storage and handling requirements for Kyleena?+
Kyleena should be stored at ambient temperature, below 25 °C, in its original sealed packaging, protected from moisture and direct sunlight. The device should be handled only by trained healthcare professionals during insertion.
How is Kyleena administered?+
Kyleena is inserted by a qualified clinician into the uterine cavity through the cervical canal using a specialised inserter. The procedure is performed in a clinical setting under aseptic conditions and does not require anesthesia in most cases.
What are the most serious risks associated with Kyleena?+
The most serious complications include uterine perforation during insertion, device expulsion, pelvic inflammatory infection, and the rare possibility of ectopic pregnancy if fertilisation occurs despite the device.
Who should not use Kyleena?+
Kyleena is contraindicated in women who are currently pregnant, have active pelvic infection, unexplained vaginal bleeding, known or suspected uterine anomalies, estrogen‑dependent tumours, severe liver disease, or who are allergic to levonorgestrel or any component of the device.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Levonorgestrel
Route
Intrauterine Use
Manufacturer
Bayer Ab
Origin
EU

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