Article Contents ::
- 1 Details About Generic Salt :: Fludroco
- 2 Main Medicine Class:: Mineralocorticoid
- 3 (flew-droe-CORE-tih-sone ASS-uh-TATE) Florinef Acetate Class: Mineralocorticoid
- 4 Drugs Class ::
- 5 Disclaimer ::
- 6 The Information available on this site is for only Informational Purpose , before any use of this information please consult your Doctor .Price of the drugs indicated above may not match to real price due to many possible reasons may , including local taxes etc.. These are only approximate indicative prices of the drug.
Details About Generic Salt :: Fludroco
Main Medicine Class:: Mineralocorticoid
(flew-droe-CORE-tih-sone ASS-uh-TATE)
Florinef Acetate
Class: Mineralocorticoid
Drugs Class ::
Action Exerts 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.
Indications for Drugs ::
Indications Partial replacement therapy for primary and secondary adrenocortical insufficiency in Addison’s disease; treatment of salt-losing adrenogenital syndrome. unlabeled use(s): Treatment of severe orthostatic hypotension.
Drug Dose ::
Route/Dosage
Addison’s Disease
ADULTS & CHILDREN: PO 0.05 to 0.1 mg/day (range 0.1 mg 3 times/wk to 0.2 mg/day). INFANTS: PO 0.1 to 0.2 mg/day.
Salt-Losing Adrenogenital Syndrome
ADULTS & CHILDREN: PO 0.1 to 0.2 mg/day.
Severe Orthostatic Hypotension
ADULTS: PO 0.1 to 0.4 mg/day.
Contraindication ::
Contraindications Systemic fungal infections.
Drug Precautions ::
Precautions
Pregnancy: Category C. Lactation: Excreted in breast milk. Children: Safety and efficacy not established. Addison’s disease: Patients with Addison’s disease may exhibit exaggerated side effects; monitor closely for development of edema, significant weight gain, or increases in BP. Adrenal insufficiency: May occur. Increased doses may be needed before, during, or after stressful situations. Electrolyte disturbances: Sodium retention and potassium loss are increased by high sodium intake. Sodium restriction and potassium supplementation may be necessary. Supplemental measures: Patients receiving fludrocortisone may need supplemental measures (eg, glucocorticoids, electrolyte control) for optimal control of symptoms.
PATIENT CARE CONSIDERATIONS |
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Drug Side Effects ::
Adverse Reactions
CV: Edema; hypertension; CHF; heart enlargement. DERM: Bruising; increased sweating; hives; rash. OTHER: Hypokalemic alkalosis. May also cause adverse reactions associated with glucocorticoids (eg, dexamethasone).
Drug Mode of Action ::
Action Exerts 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.
Drug Interactions ::
Interactions
Amphotericin, potassium-losing diuretics: May increase potassium loss. Hydantoins (eg, phenytoin), rifampin: Decreased fludrocortisone activity.
Drug Assesment ::
Assessment/Interventions
- Obtain patient history, including drug history and any known allergies. Note cardiovascular disorders and recent or present fungal infection or other systemic infections.
- Assess baseline psychological status before beginning therapy.
- Take pulse and BP and monitor daily during therapy.
- Ensure that chest x-ray and serum electrolyte levels have been obtained before beginning therapy, and monitor frequently during treatment.
- Monitor weight gain and I&O during therapy.
- If signs of concurrent infection, significant increase in weight or BP, signs of hypokalemic alkalosis, dizziness, or severe headache occur, notify physician.
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Drug Storage/Management ::
Administration/Storage
- Store in tightly closed container at room temperature. Protect from light.
Drug Notes ::
Patient/Family Education
- Instruct patient to take medication exactly as prescribed. If dose is missed, it should be taken as soon as possible. Do not double up if within several hours of next dose. Caution patient not to stop medication abruptly. Instruct patient to notify physician if more than one dose is missed or a dosage cannot be taken due to nausea and/or vomiting.
- Advise patient to reduce dietary sodium, which accelerates potassium loss, and to eat foods rich in potassium.
- Tell patient to notify physician when experiencing a stressful situation (eg, emotional upheavals, dental extractions, trauma, surgery, or illness) as increased dosage may be needed.
- Instruct patient to report the following symptoms to physician: Increased or irregular heart beat, high BP, fluid retention, joint pain, muscle weakness, headache, dizziness, fever, or unusual weight gain.
- Instruct patient to report euphoria, depression, or other changes in mental status.
- Tell patient to be alert for spontaneous fractures and impaired wound healing.
- Advise patient of the importance of keeping follow-up visits.