Product image of Megace (Megestrol Acetate) supplied by GNH India

Megace

Active Ingredient:
Megestrol Acetate
Origin:
EU

Megace (Megestrol Acetate)

Megestrol acetate, the active ingredient in Megace, is a synthetic progestin presented as an oral tablet for oral use. It is employed to stimulate appetite in patients with cachexia related to AIDS or cancer and as hormone therapy for certain advanced breast and endometrial cancers, and is approved for use in the European Union market.

GNH India supplies Megace as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide, providing reliable sourcing and regulatory support for global health programs.

Manufacturer / TM Owner

Bausch Health Ireland Limited

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Indications & Clinical Uses

Megace (megestrol acetate) is used in clinical settings that involve hormone‑dependent disease pathways and severe weight loss.

  • Cachexia associated with AIDS or cancer: stimulates appetite and promotes weight gain in patients experiencing severe wasting.
  • Advanced breast cancer: provides hormonal therapy that can help slow tumor progression in estrogen‑responsive disease.
  • Endometrial cancer: used as a progestogenic agent to inhibit disease progression in selected cases.

How It Works

  • Megestrol acetate is a synthetic progestin that binds to intracellular progesterone receptors, producing anti‑estrogenic effects in hormone‑sensitive tissues. Its glucocorticoid‑like activity also modulates hypothalamic pathways that regulate appetite, leading to increased food intake and weight gain while influencing tumor growth in certain cancers.

Side Effects

Megace may cause a range of adverse reactions, which are grouped by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Vomiting: occasional emesis.
  • Weight gain: increase in body mass, sometimes fluid‑related.
  • Edema: peripheral swelling.
  • Fatigue: feeling of tiredness.
  • Hot flashes: transient warmth and sweating.

Serious or Rare Side Effects

  • Thromboembolic events: deep vein thrombosis or pulmonary embolism.
  • Adrenal insufficiency: signs of cortisol deficiency.
  • Severe infection: opportunistic bacterial or fungal infections.
  • Cushingoid appearance: facial rounding and skin changes.
  • Hyperglycemia: elevated blood glucose levels.
  • Hepatotoxicity: abnormal liver function tests.

Precautions & Warnings

Before initiating Megace, clinicians should consider several safety measures to minimize risk.

  • Monitor blood glucose: check for hyperglycemia, especially in diabetic patients.
  • Assess lipid profile: watch for increases in cholesterol and triglycerides.
  • Evaluate thromboembolic risk: avoid use in patients with history of clotting disorders.
  • Review adrenal function: consider potential suppression of cortisol production.
  • Use caution in hepatic impairment: adjust monitoring if liver disease is present.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Megace can interact with other medicines, requiring attention to the level of interaction.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased bleeding risk.
  • Antiretroviral protease inhibitors: altered metabolism leading to unpredictable levels.
  • CYP3A4 inducers (e.g., rifampin, phenytoin): reduced efficacy of megestrol acetate.
  • Systemic corticosteroids: additive glucocorticoid effects.
  • Hormonal contraceptives: decreased contraceptive effectiveness.

Moderate Interactions (Monitor Closely)

  • Antidiabetic agents: may require dose adjustment due to hyperglycemia.
  • Antihypertensives: potential fluid retention can affect blood pressure control.
  • Digoxin: monitor serum levels for possible increase.
  • Thyroid hormones: assess for altered thyroid function tests.

Frequently Asked Questions

Megace contains megestrol acetate and is prescribed to stimulate appetite in patients with severe wasting due to AIDS or cancer, and as hormone therapy for certain advanced breast and endometrial cancers.

Megestrol acetate binds to progesterone receptors, exerting anti‑estrogenic effects, while its glucocorticoid‑like activity influences hypothalamic pathways that increase appetite and can modulate tumor growth in hormone‑sensitive cancers.

The dosage of Megace is individualized by the prescribing clinician based on the patient’s condition, weight, and response. Specific dosing regimens are not provided here and should follow the prescriber’s instructions.

Safety data for Megace in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and decisions should be made by the treating physician.

To request Megace, submit an enquiry on the product page at gnhindia.com with 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 necessary import documentation.

Megace (megestrol acetate) is a synthetic progestin with both progestogenic and glucocorticoid‑like activity, distinguishing it from other appetite stimulants such as corticosteroids or ghrelin mimetics. Its dual mechanism can provide robust appetite stimulation but may carry a different side‑effect profile, especially regarding hormonal effects.

Megace should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and excessive heat to maintain stability.

Megace is taken orally, typically as a tablet swallowed with water. The exact administration schedule, including timing relative to meals, is determined by the prescribing healthcare professional.

Serious risks include thromboembolic events, adrenal insufficiency, severe infections, Cushingoid changes, hyperglycemia, and potential liver function abnormalities. Patients should be monitored regularly for these complications.

Megace is contraindicated in patients with known hypersensitivity to megestrol acetate, active uncontrolled thromboembolic disease, or severe uncontrolled diabetes. Caution is also advised for individuals with significant liver disease or adrenal insufficiency.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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