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Components:
Megestrol
Method of action:
Endocrine Therapy
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Medically reviewed by Militian Inessa Mesropovna, PharmD. Last updated on 2019.09.18

Name of the medicinal product

Acestrol

Qualitative and quantitative composition

Megestrol

Pharmaceutical form

Granules

Therapeutic indications

The information provided in Therapeutic indications of Acestrol is based on data of another medicine with exactly the same composition as the Acestrol of the medicine (Megestrol). Be careful and be sure to specify the information on the section Therapeutic indications in the instructions to the drug Acestrol directly from the package or from the pharmacist at the pharmacy.
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Megace is a progestational agent, indicated for the treatment of certain hormone dependent neoplasms, such as breast cancer.

Dosage (Posology) and method of administration

The information provided in Dosage (Posology) and method of administration of Acestrol is based on data of another medicine with exactly the same composition as the Acestrol of the medicine (Megestrol). Be careful and be sure to specify the information on the section Dosage (Posology) and method of administration in the instructions to the drug Acestrol directly from the package or from the pharmacist at the pharmacy.
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Breast cancer:

160 mg/day taken once daily.

At least two months of continuous treatment is considered an adequate period for determining the efficacy of Megace.

Children:

Safety and effectiveness in paediatric patients have not been established.

Megace is not recommended for use in children.

Elderly:

In general, use in elderly patients should be cautious, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.

Special warnings and precautions for use

The information provided in Special warnings and precautions for use of Acestrol is based on data of another medicine with exactly the same composition as the Acestrol of the medicine (Megestrol). Be careful and be sure to specify the information on the section Special warnings and precautions for use in the instructions to the drug Acestrol directly from the package or from the pharmacist at the pharmacy.
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Precautions:

Megace should be used with caution in patients with a history of thrombophlebitis and in patients with severe impaired liver function.

This product should be used under the supervision of a specialist and the patients kept under regular surveillance. This product can exert adrenocortical effects. This should be borne in mind in patient surveillance.

Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine.

Insufficient data from clinical studies of megesterol acetate are available for patients 65 years of age and older to determine whether they respond differently than younger patients. Other reported clinical experience has not identified differences in responses between elderly and younger patients. In general, use in elderly patients should be cautious, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy. Megestrol acetate is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken during treatment with megestrol acetate, and it may be useful to monitor renal function.

Effects on ability to drive and use machines

The information provided in Effects on ability to drive and use machines of Acestrol is based on data of another medicine with exactly the same composition as the Acestrol of the medicine (Megestrol). Be careful and be sure to specify the information on the section Effects on ability to drive and use machines in the instructions to the drug Acestrol directly from the package or from the pharmacist at the pharmacy.
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There are no known effects of megestrol acetate on the ability to drive or operate machinery.

Undesirable effects

The information provided in Undesirable effects of Acestrol is based on data of another medicine with exactly the same composition as the Acestrol of the medicine (Megestrol). Be careful and be sure to specify the information on the section Undesirable effects in the instructions to the drug Acestrol directly from the package or from the pharmacist at the pharmacy.
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The main side-effect experienced by patients while taking megestrol acetate, particularly at high doses, is weight gain, which is usually not associated with water retention, but which is secondary to an increased appetite and food intake. Weight gain is associated with an increase in fat and body cell mass.

Constipation and urinary frequency have also been reported in patients who received high doses of megestrol acetate in clinical trials.

A rarely encountered side effect of prolonged administration of megestrol acetate is urticaria, presumably an idiosyncratic reaction to the drug. The drug is devoid of the myelosuppressive activity characteristic of many cytotoxic drugs and it causes no significant changes in haematology, blood chemistry or urinalysis.

Pituitary adrenal axis abnormalities including glucose intolerance, new onset diabetes, exacerbation of pre-existing diabetes with decreased glucose tolerance and Cushing's syndrome have been reported with the use of megestrol acetate. Clinically apparent adrenal insufficiency has been rarely reported in patients shortly after discontinuing megestrol acetate. The possibility of adrenal suppression should be considered in all patients taking or withdrawing from chronic megestrol acetate therapy. Replacement stress doses of glucocorticoids may be indicated.

The list is presented by system organ class, MedDRA preferred term, and frequency using the following frequency categories: very common (>1/10), common (>1/100, < 1/10), uncommon (>1/1000, <1/100), rare (>1/10000, <1/1000), very rare (< 1/10000), and not known (cannot be estimated from the available data).

System Organ Class

Frequency

MedDRA Term

Neoplasms benign, malignant, and unspecified (including cysts and polyps)

Common

Tumour flare #

Endocrine disorders

Very common

Adrenal insufficiency, cushingoid, Cushing's syndrome

Metabolism and nutrition disorders

Very common

Diabetes mellitus, glucose tolerance impaired, hyperglycaemia, increased appetite

Psychiatric disorders

Common

Mood altered

Nervous system disorders

Common

Carpal tunnel syndrome, lethargy

Cardiac disorders

Common

Cardiac failure

Vascular disorders

Very common

Thrombophlebitis, pulmonary embolism*, hypertension, hot flush

Respiratory, thoracic and mediastinal disorders

Very common

Dyspnoea

Gastrointestinal disorders

Common

Nausea, vomiting, diarrhoea, flatulence

Very common

Constipation

Skin and subcutaneous tissue disorders

Common

Rash, alopecia

Renal and urinary disorders

Common

Pollakiuria

Reproductive system and breast disorders

Common

Menrorrhagia, erectile dysfunction

General disorders and administration site condition

Common

Asthenia, pain, oedema

Investigations

Very common

Weight increased

†Source of frequencies: Megestrol Acetate Oral, Corporate Product Labeling Profile (CPLP) dated 12 November 1996.

#with or without hypercalcemia

* Pulmonary embolism (in some cases fatal)

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme. Website: www.mhra.gov.uk/yellowcard.

Overdose

The information provided in Overdose of Acestrol is based on data of another medicine with exactly the same composition as the Acestrol of the medicine (Megestrol). Be careful and be sure to specify the information on the section Overdose in the instructions to the drug Acestrol directly from the package or from the pharmacist at the pharmacy.
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No acute toxicological effects have resulted from studies involving Megace (megestrol acetate) administered in dosages as high as 1600 mg/day for six months or more.

Reports of overdose have also been received in the postmarketing setting. Signs and symptoms reported in the context of overdose included diarrhoea, nausea, abdominal pain, shortness of breath, cough, unsteady gait, listlessness, and chest pain. There is no specific antidote for overdose with Megace. In case of overdose, appropriate supportive measures should be taken.

Pharmacodynamic properties

The information provided in Pharmacodynamic properties of Acestrol is based on data of another medicine with exactly the same composition as the Acestrol of the medicine (Megestrol). Be careful and be sure to specify the information on the section Pharmacodynamic properties in the instructions to the drug Acestrol directly from the package or from the pharmacist at the pharmacy.
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Megace (megestrol acetate) possesses pharmacological properties similar to those of natural progesterone. Its progestational activity is slightly greater than that of medroxyprogesterone acetate, norethindrone, norethindrone acetate and norethynodrel; slightly less than that of chlormadinone acetate; and substantially less than that of norgestrel.

Megestrol acetate is a potent progestogen that exerts significant anti-oestrogenic effects. It has no androgenic or oestrogenic properties. It has anti-gonadotropic, anti-uterotropic and anti-androgenic/anti-myotropic actions. It has a slight but significant glucocorticoid effect and a very slight mineralocorticoid effect.

Pharmacokinetic properties

The information provided in Pharmacokinetic properties of Acestrol is based on data of another medicine with exactly the same composition as the Acestrol of the medicine (Megestrol). Be careful and be sure to specify the information on the section Pharmacokinetic properties in the instructions to the drug Acestrol directly from the package or from the pharmacist at the pharmacy.
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Peak plasma levels of tritiated megestrol acetate and metabolites occur one to three hours after oral administration. When 4 to 91mg of c-labelled megestrol acetate were administered orally to women, the major route of drug elimination was in the urine. The urinary and fecal recovery of total radioactivity within 10 days ranged from 56.6% to 78.4% (mean 66.4%) and 7.7% to 30.3% (mean 19.8%), respectively. The total recovered radioactivity varied between 83.1% and 94.7% (mean 86.2%).

Megestrol acetate metabolites, which were identified in the urine as glucuronide conjugates, were 17-alpha-acetoxy-2-alpha hydroxy-6-methylpregna-4, 6-diene-3, 20-dione; 17-alpha-acetoxy-6-hydroxymethylpregna-4, 6-diene-3, 20-dione; and 17-alpha-acetoxy-2 alpha-hydroxy-6-hydromethylpregna-4, 6-diene-3, 20-dione; these identified metabolites accounted for only 5-8% of the administered dose.

Serum concentrations were measured after the administration of single and multiple oral doses of megestrol acetate. Adult male and post-menopausal female volunteers, no more than 65 years of age participated in the study.

Megestrol acetate is readily absorbed following oral administration of 20, 40, 80 and 200 mg doses. Megestrol serum concentrations increase with increasing doses, the relationship between increasing dosage and increasing serum levels not being arithmetically proportional. Average peak serum concentrations for the four doses tested were 89, 190, 209 and 465 ng/ml.

Mean peak serum concentrations are found three hours after single-dose administration for all dosage levels studied. The serum concentration curve appears biphasic, and the beta-phase half-life is 15 to 20 hours long.

After multiple doses over a three-day period, serum levels increase each day and are estimated to reach 80% to 90% predicted steady-state levels on the third day.

Preclinical safety data

The information provided in Preclinical safety data of Acestrol is based on data of another medicine with exactly the same composition as the Acestrol of the medicine (Megestrol). Be careful and be sure to specify the information on the section Preclinical safety data in the instructions to the drug Acestrol directly from the package or from the pharmacist at the pharmacy.
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Administration of megestrol acetate to female dogs for up to 7 years was associated with an increased incidence of both benign and malignant tumors of the breast. Comparable studies in rats and studies in monkeys were not associated with an increased incidence of tumors. The relationship of megestrol acetate-associated dog tumors to humans is unknown, but should be considered in assessing the benefit-to-risk ratio when prescribing Megace, and in surveillance of patients on therapy

Fertility and reproduction studies with high doses of megestrol acetate have shown a reversible feminising effect on some male rat foetuses.

Incompatibilities

The information provided in Incompatibilities of Acestrol is based on data of another medicine with exactly the same composition as the Acestrol of the medicine (Megestrol). Be careful and be sure to specify the information on the section Incompatibilities in the instructions to the drug Acestrol directly from the package or from the pharmacist at the pharmacy.
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Not applicable

Special precautions for disposal and other handling

The information provided in Special precautions for disposal and other handling of Acestrol is based on data of another medicine with exactly the same composition as the Acestrol of the medicine (Megestrol). Be careful and be sure to specify the information on the section Special precautions for disposal and other handling in the instructions to the drug Acestrol directly from the package or from the pharmacist at the pharmacy.
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No special requirements.