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|Fludrocortisone Acetate |
Drugs search, click the first letter of a drug name: | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | 1 | 2 | 3 | 4 | 5 | 6 | 8 | 9 Home Fludrocortisone AcetatePronouncation: (flew-droe-CORE-tih-sone ASS-uh-TATE)Class: Mineralocorticoid Trade Names: Mechanism of ActionPharmacologyExerts salt-retaining (mineralocorticoid) activity by acting on renal distal tubules to enhance reabsorption of sodium and increasing urinary excretion of potassium, hydrogen, and magnesium ions. PharmacokineticsAbsorptionFludrocortisone is rapidly absorbed from the GI tract. T max is 1.7 hr. EliminationThe plasma t 1/ 2 is about 3.5 hr. The biological t 1/ 2 is 18 to 36 hr. Indications and UsagePartial replacement therapy for primary and secondary adrenocortical insufficiency in Addison disease; treatment of salt-losing adrenogenital syndrome. Unlabeled UsesTreatment of severe orthostatic hypotension. ContraindicationsSystemic fungal infections. Dosage and AdministrationAddison DiseaseAdults PO 0.05 to 0.1 mg/day (range, 0.1 mg 3 times/wk to 0.2 mg/day). Salt-Losing Adrenogenital SyndromeAdults PO 0.1 to 0.2 mg/day. Drug InteractionsAmphotericin, potassium-losing diureticsMay increase potassium loss. Anticholinesterase agents (eg, neostigmine)May antagonize the effects of anticholinesterase agents in myasthenia gravis. Anticoagulants (eg, warfarin)Dose requirement of anticoagulant may be reduced or effect opposed. Barbiturates, hydantoins (eg, phenytoin), rifampinDecreased fludrocortisone activity. SalicylatesSerum levels may be reduced by corticosteroids, decreasing the effectiveness; in addition, the ulcerogenic effects of both agents may be increased. Laboratory Test InteractionsNone well documented. Adverse ReactionsCardiovascularEdema; hypertension; CHF; heart enlargement. DermatologicBruising; increased sweating; hives; rash. MiscellaneousHypokalemic alkalosis. May also cause adverse reactions associated with glucocorticoids (eg, dexamethasone). PrecautionsPregnancyCategory C . LactationExcreted in breast milk. ChildrenSafety and efficacy not established. Addison diseasePatients with Addison disease may exhibit exaggerated side effects; monitor closely for development of edema, significant weight gain, or increases in BP. Adrenal insufficiencyAdrenal insufficiency may occur. Increased doses may be needed before, during, or after stressful situations. Electrolyte disturbancesSodium retention and potassium loss are increased by high sodium intake. Sodium restriction and potassium supplementation may be necessary. GIUse with caution in patients with nonspecific ulcerative colitis if there is a possibility of impending perforation, abscess or other pyogenic infection, diverticulitis, fresh intestinal anastomoses, or peptic ulcer. InfectionsDrug may mask signs of infection and may decrease host-defense mechanisms to prevent dissemination of infection. ImmunizationsBecause of possible hazards of neurological complications and a lack of antibody response, do not vaccinate patients against smallpox while receiving corticosteroid therapy or undertake other immunization procedures. Ocular effectsProlonged use may produce posterior subcapsular cataracts and glaucoma with possible damage to the optic nerves and may enhance the establishment of secondary ocular infections caused by fungi or viruses. Supplemental measuresPatients receiving fludrocortisone may need supplemental measures (eg, glucocorticoids, electrolyte control) for optimal control of symptoms. OverdosageSymptomsHypertension, edema, hypokalemia, excessive weight gain, increase in heart size. Patient Information
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