Product image of Nomegestrol Eg (Nomegestrol Acetate) supplied by GNH India

Nomegestrol Eg

Active Ingredient:
Nomegestrol Acetate
Origin:
EU

Nomegestrol Eg (Nomegestrol Acetate)

Nomegestrol Acetate, the active ingredient in Nomegestrol Eg, is a progestin (synthetic progestogen) presented as an oral tablet for systemic use. It is employed as a progestogen‑only contraceptive and for hormone replacement therapy in menopausal women.

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

Manufacturer / TM Owner

Eg Labo Laboratoires Eurogenerics

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Indications & Clinical Uses

  • Nomegestrol Eg is a synthetic progestogen used in hormonal pathways related to contraception and menopause management.
  • Contraception: prevents pregnancy by suppressing ovulation and inducing endometrial changes that inhibit implantation.
  • Hormone replacement therapy: relieves menopausal symptoms such as hot flashes and prevents endometrial hyperplasia in estrogen‑treated women.

How It Works

  • Nomegestrol Acetate acts as an agonist at progesterone receptors, binding with high affinity to the intracellular receptor complex. This activation suppresses the hypothalamic‑pituitary‑gonadal axis, inhibiting the luteinizing hormone surge and thereby preventing ovulation. In the uterus, it induces secretory transformation of the endometrium, creating an environment unsuitable for implantation.

Side Effects

Nomegestrol Eg may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Nausea: occasional upset stomach.
  • Breast tenderness: transient discomfort.
  • Weight gain: modest increase in body weight.
  • Mood changes: irritability or mild depression.
  • Irregular bleeding: spotting or breakthrough bleeding.

Serious or Rare Side Effects

  • Venous thromboembolism: deep vein thrombosis or pulmonary embolism.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.
  • Depression: severe or persistent mood disorder.
  • Hypertension: new‑onset high blood pressure.
  • Uterine rupture: extremely rare, usually associated with uterine surgery.

Precautions & Warnings

  • Before initiating therapy with Nomegestrol Eg, clinicians should evaluate individual risk factors and counsel patients on safe use.
  • Assess thrombotic risk: avoid in patients with a history of venous thromboembolism.
  • Evaluate liver function: monitor in patients with hepatic impairment.
  • Monitor blood pressure: check regularly during treatment.
  • Counsel on smoking cessation: smoking increases cardiovascular risk.
  • Avoid use in pregnancy: contraindicated due to teratogenic potential.
  • Store at room temperature: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Nomegestrol Eg can interact with other medicines that affect its metabolism or pharmacodynamic profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce contraceptive efficacy.
  • Anticoagulants (e.g., warfarin): may alter anticoagulant control.
  • HIV protease inhibitors: potential for reduced hormonal activity.

Moderate Interactions (Monitor Closely)

  • Antifungals (e.g., ketoconazole, itraconazole): may increase plasma levels.
  • Macrolide antibiotics (e.g., erythromycin): possible modest increase in hormone exposure.
  • Antiepileptic drugs (e.g., phenytoin): may modestly decrease effectiveness.

Frequently Asked Questions

Nomegestrol Eg contains the progestin nomegestrol acetate and is indicated as a progestogen‑only oral contraceptive and as hormone replacement therapy to relieve menopausal symptoms such as hot flashes.

Nomegestrol acetate binds to progesterone receptors, suppressing the luteinizing hormone surge and preventing ovulation. In the uterus it induces a secretory endometrium that is not receptive to implantation.

The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s clinical situation and local regulatory guidance.

Nomegestrol Eg is classified as pregnancy category X; it is contraindicated in pregnancy because it may cause fetal harm. Safety during breastfeeding has not been established, and use is generally avoided.

Enquiries are submitted via the product page on gnhindia.com, where you specify the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Nomegestrol acetate offers a high affinity for progesterone receptors and a favorable bleeding profile compared with some older progestins. Its once‑daily oral dosing is similar to other progestogen‑only pills, but individual tolerability and risk factors may influence product choice.

Store the tablets at room temperature, below 25 °C, in the original packaging. Protect them from moisture, excessive heat and direct sunlight to maintain potency.

Nomegestrol Eg is taken orally, usually once daily at the same time each day, as directed by the prescriber. Swallow the tablet whole with water; do not split or chew unless instructed otherwise.

Serious risks include venous thromboembolism, hepatic dysfunction, severe allergic reactions, and hypertension. Patients should seek immediate medical attention if they experience symptoms such as unexplained leg pain, jaundice, rash with swelling, or a sudden rise in blood pressure.

Contraindications include women who are pregnant, have a history of thromboembolic disorders, active liver disease, known or suspected breast cancer, uncontrolled hypertension, or who are smokers over the age of 35.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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