GNH USA

Europe — EMA

Nexplanon (Etonogestrel)

GNH USA supplies Nexplanon (Etonogestrel), a progestin contraceptive for prevention of pregnancy in women of reproductive age.

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What is Etonogestrel?

Etonogestrel, the active ingredient in Nexplanon, is a progestin presented as a 68 mg subdermal implant for subcutaneous use. It provides long‑acting reversible contraception by preventing ovulation and altering cervical mucus, offering up to three years of pregnancy protection for women of reproductive age.

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

What is Etonogestrel used for?

Etonogestrel is a progestin used in hormonal contraception to prevent pregnancy.

- Prevention of pregnancy (contraception): provides highly effective, reversible contraception for up to three years. - Family planning: enables women to plan and space pregnancies with a single, low‑maintenance device. - Long‑acting reversible contraception: offers a convenient alternative to daily oral pills or monthly injectables.

What are the side effects of Etonogestrel?

Nexplanon 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) - Headache - Weight gain - Acne or skin changes - Breast tenderness

Serious or Rare Side Effects: - Deep vein thrombosis or pulmonary embolism - Severe allergic reaction (anaphylaxis, rash, swelling) - Infection at the insertion site - Implant migration or extrusion - Hormonal imbalance causing mood changes - Significant hypertension

What precautions apply to Etonogestrel?

Before initiating Nexplanon therapy, several safety considerations should be reviewed.

- Pregnancy testing: confirm the patient is not pregnant prior to insertion. - Smoking: advise women over 35 who smoke to consider alternative methods. - Thromboembolic history: assess for prior clotting disorders or risk factors. - Medication review: evaluate concomitant drugs that may reduce efficacy. - Follow‑up schedule: plan removal or replacement at the three‑year mark. - Store at ambient temperature: keep in the original packaging, protect from moisture and direct sunlight.

What does Etonogestrel interact with?

Etonogestrel can interact with other medicines that affect its metabolism or hormonal activity.

Major Interactions (Avoid): - Rifampin, carbamazepine, phenytoin: strong enzyme inducers that markedly lower implant effectiveness. - St. John's wort: herbal inducer that may reduce plasma levels. - Certain antiretrovirals (e.g., efavirenz): can compromise contraceptive reliability.

Moderate Interactions (Monitor Closely): - Griseofulvin: moderate enzyme inducer, may require additional contraceptive measures. - Antifungal azoles (ketoconazole, itraconazole): may increase hormone levels, monitor for side effects. - Antiepileptic drugs with moderate inducing potential (e.g., phenobarbital): assess efficacy periodically.

Frequently asked questions

What is Nexplanon used for?+
Nexplanon is a subdermal implant that delivers the progestin etonogestrel to provide long‑acting reversible contraception. It is indicated for the prevention of pregnancy in women of reproductive age and offers up to three years of continuous protection.
How does etonogestrel work to prevent pregnancy?+
Etonogestrel released from the implant suppresses the luteinizing hormone surge, which blocks ovulation. It also thickens cervical mucus, making it difficult for sperm to travel, and alters the endometrium, creating an environment unsuitable for implantation.
What is the usual dose of Nexplanon?+
Nexplanon is supplied as a single 68 mg subdermal implant. The exact dosing schedule, including insertion and removal timing, is determined by the prescribing healthcare professional based on clinical guidelines.
Is Nexplanon safe to use during pregnancy or breastfeeding?+
Nexplanon is classified as pregnancy category X, meaning it must not be used by women who are pregnant. Women should use an alternative method if they become pregnant. Limited data exist for breastfeeding, and a healthcare provider should assess risks versus benefits.
How do I order Nexplanon from GNH USA?+
To place an order, submit an enquiry on the 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 necessary import documentation.
How does Nexplanon compare with other contraceptive methods?+
Compared with daily oral pills, Nexplanon offers higher typical‑use effectiveness and eliminates the need for daily adherence. Unlike injectable progestins, it requires only a single insertion for up to three years, providing greater convenience and consistent hormone levels.
What are the storage and handling requirements for Nexplanon?+
Nexplanon should be stored at ambient temperature, below 25 °C, in its original sealed packaging. Protect the device from moisture, direct sunlight and extreme temperatures to maintain its stability until the time of insertion.
How is Nexplanon administered?+
A qualified healthcare professional inserts the Nexplanon implant subdermally in the inner side of the upper arm using a sterile applicator. The procedure is minimally invasive, performed in an outpatient setting, and the implant remains in place for up to three years before removal or replacement.
What are the most serious risks associated with Nexplanon?+
Serious risks include rare but potentially life‑threatening events such as deep vein thrombosis, pulmonary embolism, severe allergic reactions, and infection at the insertion site. Users should seek immediate medical attention if they experience unexplained swelling, severe pain, shortness of breath, or signs of an allergic response.
Who should not use Nexplanon?+
Nexplanon is contraindicated in women who are pregnant, have a known hypersensitivity to etonogestrel or any component of the device, have active breast cancer, or have a history of thromboembolic disorders without appropriate medical evaluation. A thorough medical assessment is required before insertion.
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
Etonogestrel
Route
Subcutaneous Use
Manufacturer
Organon France
Origin
EU

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