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Cortexone M

Cortexone M - General Information

Cortexone M is a mineralocorticoid hormone and an analog of desoxycorticosterone. It is white, odorless, and stable in air. It is practically insoluble in water, sparingly soluble in acetone, slightly soluble in methanol, ether and vegetable oils. Federal (U.S.A.) law restricts this drug to use by or on the order of a licensed veterinarian.

 

Pharmacology of Cortexone M

Used to treat adrenocortical insufficiency, desoxycorticosterone pivalate is a mineralocorticoid hormone and an analogue of desoxycorticosterone. It primarily acts on the metabolism of sodium, potassium and water. When the drug is given, there is decreased excretion of sodium accompanied by increased excretion of potassium; the concentration of sodium in the blood is thereby increased whereas that of potassium is decreased. There is a concomitant increase in the volume of blood and extracellular fluids, with a fall in hematocrit. It increases the rate of renal tubular absorption of sodium.

 

Cortexone M for patients

 

Cortexone M Interactions

 

Cortexone M Contraindications

Desoxycorticosterone Pivalate is contraindicated in patients with systemic fungal infections and in those with a history of possible or known hypersensitivity to this agent.

 

Additional information about Cortexone M

Cortexone M Indication: For treatment of adrenocortical insufficiency especially in multiple sclerosis, congenital cerebral palsy, polyarteritis nodosa, and rheumatoid arthritis.
Mechanism Of Action: Cortexone M binds to the mineralocorticoid receptor. Mineralocorticoids are a family of steroids, secreted by the adrenal cortex, necessary for the regulation of a number of metabolic processes including electrolyte regulation. Desoxycorticosterone pivalate exerts its effect through its interaction with the mineralocorticoid receptor (MR), whereby it reacts with the receptor proteins to form a steroid-receptor complex. This complex moves into the nucleus, where it binds to chromatin which results in genetic transcription of cellular DNA to messenger RNA. The steroid hormones appear to induce transcription and synthesis of specific proteins, which produce the physiological effects seen after administration.
Drug Interactions: Not Available
Food Interactions: Not Available
Generic Name: Desoxycorticosterone Pivalate
Synonyms: DOCP; Desoxycortone Pivalate; Desoxycorticosterone Trimethylacetate; Deoxycortone Trimethylacetate; Deoxycortone Pivalate; Deoxycortolone Pivalate; Deoxycorticosterone Trimethylacetate; Deoxycorticosterone Pivalate; DTMA
Drug Category: Diuretics; Anti-Addison Agents
Drug Type: Small Molecule; Approved
Other Brand Names containing Desoxycorticosterone Pivalate: Cortexone M; Neodin-Depositum; Percorten; Percorten M; Percorten Pivalate;
Absorption: Not Available
Toxicity (Overdose): Symptoms of overdose include polyuria, polydipsia, increased blood volume, edema, and cardiac enlargement.
Protein Binding: 90%
Biotransformation: Not Available
Half Life: Not Available
Dosage Forms of Cortexone M: Not Available
Chemical IUPAC Name: [2-(10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl)-2-oxoethyl] 2,2-dimethylpropanoate
Chemical Formula: C26H38O4
Desoxycorticosterone Pivalate on Wikipedia: Not Available
Organisms Affected: Humans and other mammals