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 progestin presented as an oral formulation for oral use. It is employed to stimulate appetite and as hormone therapy in certain cancers, particularly in patients experiencing severe weight loss or tumor‑related hormone‑responsive disease.

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

Manufacturer / TM Owner

Bausch Health Ireland Limited

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Indications & Clinical Uses

Megace is a progestin that acts on hormonal pathways to address cachexia and hormone‑sensitive cancers.

  • Cachexia associated with AIDS or cancer: helps increase appetite and promote weight gain.
  • Loss of appetite / weight loss: stimulates hunger and improves nutritional status.
  • Endometrial cancer: provides anti‑neoplastic activity by modulating progesterone receptors.
  • Breast cancer: used as hormone therapy in selected progesterone‑receptor positive cases.

How It Works

  • Megestrol acetate binds to progesterone receptors, acting as an agonist that exerts antigonadotropic effects and modest glucocorticoid activity. This receptor activation reduces catabolic signaling, enhances appetite, and can inhibit tumor growth in hormone‑sensitive cancers by altering cell proliferation pathways.

Side Effects

Megace may cause a range of adverse reactions, ranging from mild to serious.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Vomiting: occasional episodes, especially at treatment initiation.
  • Diarrhea: loose stools that may affect hydration.
  • Edema: peripheral swelling due to fluid retention.
  • Weight gain: excessive increase beyond therapeutic goal.
  • Fatigue: generalized tiredness.

Serious or Rare Side Effects

  • Thromboembolic events: deep vein thrombosis or pulmonary embolism.
  • Adrenal insufficiency: signs of cortisol deficiency.
  • Cushing‑like syndrome: hyperglycemia, hypertension, and moon‑face appearance.
  • Severe infection: opportunistic infections due to immunosuppression.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.

Precautions & Warnings

When prescribing Megace, clinicians should consider several safety measures.

  • Monitor weight: assess for appropriate gain and avoid excessive accumulation.
  • Assess blood glucose: watch for hyperglycemia, especially in diabetic patients.
  • Evaluate thromboembolic risk: consider prophylaxis in high‑risk individuals.
  • Review liver function: periodic tests to detect hepatic toxicity.
  • Use caution in pregnancy: potential fetal risk requires risk‑benefit analysis.
  • Store at ambient temperature: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Megace can interact with other medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase megestrol levels.
  • Anticoagulants (e.g., warfarin): heightened risk of bleeding.
  • Antidiabetic agents (e.g., insulin, sulfonylureas): may require dose reduction due to hyperglycemia.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, phenytoin): may reduce therapeutic effect.
  • Systemic glucocorticoids: additive glucocorticoid activity.
  • NSAIDs: increased risk of gastrointestinal irritation.

Frequently Asked Questions

Megace (megestrol acetate) is prescribed to stimulate appetite in patients with severe weight loss due to AIDS‑related or cancer‑related cachexia, and as hormone therapy for certain hormone‑sensitive cancers such as endometrial and selected breast cancers.

Megestrol acetate binds to progesterone receptors, acting as an agonist that reduces catabolic signaling, increases appetite, and exerts anti‑neoplastic effects in hormone‑responsive tumors by modulating cell growth pathways and providing mild glucocorticoid activity.

The dosage of Megace is individualized; the prescribing clinician determines the appropriate amount based on the patient’s condition, response, and overall treatment plan. Specific dosing regimens should be obtained from a qualified healthcare professional.

Megace is classified as a pregnancy‑category drug with potential fetal risk, and its safety during breastfeeding has not been established. Use only if the potential benefit justifies the possible risk, and discuss alternatives with a healthcare provider.

To order Megace, submit an enquiry on the product page at gnhindia.com, specifying 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.

Compared with other appetite stimulants such as corticosteroids or mirtazapine, Megace offers a dual benefit of appetite stimulation and anti‑neoplastic activity in hormone‑sensitive cancers. Its progestin profile may be preferred when a hormonal mechanism is desired, though side‑effect profiles differ.

Megace should be stored at ambient 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, usually as a tablet, with or without food as directed by the prescriber. The exact administration schedule should follow the healthcare professional’s instructions.

Serious risks include thromboembolic events, adrenal insufficiency, Cushing‑like syndrome, severe infections, and hepatic dysfunction. Patients should be monitored regularly for signs of these conditions, and therapy should be adjusted or discontinued if they occur.

Megace is contraindicated in patients with known hypersensitivity to megestrol acetate or any formulation components, and it should be used with caution in individuals with uncontrolled diabetes, active thromboembolic disease, severe liver impairment, or those who are pregnant unless clearly indicated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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