GNH USA

Europe — EMA

Levosert

GNH USA supplies Levosert (Levonorgestrel), a progestogen hormonal contraceptive for long‑acting reversible contraception. Request a quote for global supply.

Levonorgestrel

Request sourcing

1
Pack/s

What is Levonorgestrel?

Levonorgestrel, the active ingredient in Levosert, is a progestogen presented as a 52 mg intrauterine system (IUS) for intrauterine use. It delivers a steady low dose of levonorgestrel to provide long‑acting reversible contraception for women of reproductive age, through a single device placed by a qualified clinician.

GNH USA supplies Levosert as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable access to this intrauterine contraceptive system. Our distribution network ensures compliance with local regulatory requirements and timely delivery.

What is Levonorgestrel used for?

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

Contraception: provides continuous birth control for up to five years. Heavy menstrual bleeding: reduces menstrual blood loss and may improve dysmenorrhea. Endometrial protection: maintains a thin endometrium, lowering the risk of endometrial hyperplasia.

What are the side effects of Levonorgestrel?

Levosert may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects: - Irregular bleeding or spotting - Amenorrhea (absence of periods) - Cervical discharge - Pelvic or abdominal cramping - Headache

Serious or Rare Side Effects: - Uterine perforation during insertion or removal - Expulsion of the intrauterine system - Pelvic inflammatory disease or infection - Ectopic pregnancy if contraception fails - Severe allergic reaction (anaphylaxis)

What precautions apply to Levonorgestrel?

Before insertion, clinicians should evaluate patients for contraindications and counsel on expected changes.

Screening: confirm absence of active pelvic infection, uterine anomalies, or malignancy. Pregnancy testing: ensure the patient is not pregnant at the time of insertion. Follow‑up: schedule a post‑insertion visit to verify correct placement. Bleeding patterns: advise that menstrual bleeding may become irregular, lighter, or cease. Removal: device should be removed by a qualified provider after the intended duration or if complications arise. Store at ambient temperature: keep in the original packaging, protect from moisture and direct sunlight.

What does Levonorgestrel interact with?

Levonorgestrel levels can be altered by other medicines, requiring attention to potential efficacy changes.

Major Interactions (Avoid): - Enzyme inducers such as rifampicin that markedly reduce levonorgestrel concentrations. - Antiepileptic drugs (e.g., carbamazepine, phenytoin) that may compromise contraceptive effectiveness.

Moderate Interactions (Monitor Closely): - Antifungal azoles (e.g., ketoconazole) that can increase levonorgestrel exposure. - Certain antiretrovirals (e.g., efavirenz) that may lower hormone levels. - Herbal supplements like St. John’s wort that may affect hormonal metabolism.

Frequently asked questions

What is Levosert used for?+
Levosert is a levonorgestrel‑releasing intrauterine system indicated for long‑acting reversible contraception. It provides continuous birth control for up to five years and can also be used to reduce heavy menstrual bleeding and improve menstrual regularity in women of reproductive age.
How does levonorgestrel work in Levosert?+
Levonorgestrel released from the IUS binds to progesterone receptors in the endometrium, cervical mucus, and the hypothalamic‑pituitary axis. This suppresses ovulation, thickens cervical mucus to block sperm, and creates an atrophic endometrium, together preventing implantation.
What is the usual dose of Levosert?+
Levosert is supplied as a single 52 mg intrauterine system that releases approximately 20 µg of levonorgestrel per day. The exact dosing regimen, including insertion timing and duration of use, is determined by the prescribing clinician based on individual patient needs.
Is Levosert safe during pregnancy or breastfeeding?+
Levosert is contraindicated in women who are pregnant; it should be inserted only after confirming a negative pregnancy test. Limited data are available for breastfeeding, and clinicians should weigh potential risks and benefits before use in lactating women.
How do I order Levosert from GNH USA?+
To order Levosert, submit an enquiry on the product page at gnh-usa.com specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.
How does Levosert compare with other hormonal contraceptives?+
Compared with oral progestin‑only pills, Levosert offers a once‑inserted, maintenance‑free option with higher typical‑use efficacy and no daily adherence. Unlike copper IUDs, it may reduce menstrual bleeding and cause fewer menstrual cramps, though copper devices have no hormonal side effects.
How should Levosert be stored and handled?+
Levosert should be stored at ambient temperature, below 25 °C, in its original sealed packaging. Protect the device from moisture, direct sunlight, and physical damage until it is inserted by a qualified healthcare professional.
How is Levosert administered?+
Levosert is inserted into the uterine cavity by a trained clinician using a sterile insertion kit. The procedure is performed in a clinical setting under aseptic conditions, and placement is confirmed by pelvic examination or ultrasound as needed.
What are the most serious risks associated with Levosert?+
Serious risks include uterine perforation during insertion or removal, infection such as pelvic inflammatory disease, expulsion of the device, and the rare possibility of ectopic pregnancy if contraceptive failure occurs. Prompt medical evaluation is required if any of these events are suspected.
Who should not use Levosert?+
Levosert is contraindicated in women with current pelvic infection, known or suspected uterine or cervical malignancy, unexplained vaginal bleeding, uterine anomalies that preclude proper placement, or a history of severe allergic reaction to levonorgestrel or device components.
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
Gedeon Richter Plc.
Origin
EU

Related products