Article Contents ::
- 1 Details About Generic Salt :: Amilorid
- 2 Main Medicine Class:: Potassium-sparing diuretic
- 3 (uh-MILL-oh-ride HIGH-droe-KLORide) Midamor Class: Potassium-sparing diuretic
- 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 :: Amilorid
Main Medicine Class:: Potassium-sparing diuretic
(uh-MILL-oh-ride HIGH-droe-KLORide)
Midamor
Class: Potassium-sparing diuretic
Drugs Class ::
Action Interferes with sodium reabsorption at distal tubule, resulting in increased excretion of water and sodium and decreased excretion of potassium.
Indications for Drugs ::
Indications Treatment of CHF or hypertension (in combination with thiazide or loop diuretics) and diuretic-induced hypokalemia. Unlabeled use(s): Reduction of lithium-induced polyuria. Aerosol form: Slowed reduction of pulmonary function in patients with cystic fibrosis.
Drug Dose ::
Route/Dosage
ADULTS: PO 5 to 10 mg daily. LITHIUM-INDUCED POLYURIA: PO 10 to 20 mg daily. CYSTIC FIBROSIS: Dissolve in 0.3% saline and deliver by nebulizer.
Contraindication ::
Contraindications Serum potassium > 5.5 mEq/L; potassium supplementation; impaired renal function: spironolactone or triamterene therapy.
Drug Precautions ::
Precautions
Pregnancy: Category B. Lactation: Undetermined. Children: Safety and efficacy not established. Diabetes mellitus: Hyperkalemia may occur. Electrolyte imbalances and BUN increase: Hyperkalemia, hyponatremia, hypochloremia, and increases in BUN may occur. Hepatic impairment: With severe liver disease, hepatic encephalopathy (eg, tremors, confusion, coma, jaundice) may occur. Renal impairment: Use cautiously in patients with this condition.
PATIENT CARE CONSIDERATIONS |
|
Drug Side Effects ::
Adverse Reactions
CV: Angina pectoris; orthostatic hypotension; arrhythmia. CNS: Headache; dizziness; encephalopathy; paresthesia; tremors; vertigo; nervousness; mental confusion; insomnia; decreased libido; depression. DERM: Skin rash; itching; pruritus. EENT: Visual disturbances; tinnitus; nasal congestion. GI: Nausea; anorexia; diarrhea; vomiting; abdominal pain; gas pain; appetite changes; constipation; GI bleeding; abdominal fullness; thirst; dry mouth; heartburn; flatulence. GU: Impotence; polyuria; dysuria; urinary frequency. HEMA: Aplastic anemia; neutropenia. HEPA: Jaundice. META: Increased serum potassium levels. RESP: Cough; dyspnea. OTHER: Musculoskeletal (weakness; fatigue; muscle cramps; joint/back/chest pain; neck or shoulder ache).
Drug Mode of Action ::
Action Interferes with sodium reabsorption at distal tubule, resulting in increased excretion of water and sodium and decreased excretion of potassium.
Drug Interactions ::
Interactions
Angiotensin-converting enzyme inhibitors: May result in severely elevated serum potassium levels. Potassium preparations: May severely increase serum potassium levels, possibly resulting in cardiac arrhythmias or cardiac arrest. Do not administer to patients taking potassium preparations.
Drug Assesment ::
Assessment/Interventions
- Obtain patient history, including drug history and any known allergies. Note BP and renal disease or history of potassium supplement use.
- Monitor potassium, BUN, and creatinine levels.
- If sudden elevation in serum potassium level (> 5.5 mEq/L) occurs, withhold dose and notify physician.
- Monitor fluid and electrolyte balance during therapy (eg, I&O, daily weight, edema).
- If drug is given in combination with another antihypertensive, monitor BP throughout administration.
- If hypokalemia is suspected, obtain periodic ECG during therapy.
- If ECG changes occur (eg, peaked T waves, abnormal S or P waves), withhold dose and notify physician.
- Monitor for signs of hyperkalemia (eg, fatigue, muscle weakness, cardiac irregularities).
- Monitor for signs of hyponatremia.
- Monitor renal function.
Drug Storage/Management ::
Administration/Storage
- Administer medication with food, preferably in the morning.
- Store in tightly closed container in cool location.
Drug Notes ::
Patient/Family Education
- Explain that dietary considerations are very important while taking this medication. Advise patient to avoid the following: Eating excessive amounts of potassium-rich foods (bananas, citrus fruits, raisins, nuts), using salt substitutes, taking medications high in potassium and eating foods high in sodium (tomatoes, pickled foods, canned foods, luncheon meats).
- Teach patient to monitor BP daily.
- Instruct patient to take medication as directed, even if feeling well.
- Encourage patient to avoid sudden changes in position to prevent orthostatic hypotension.
- Advise patient that drug may cause dizziness and blurred vision, and to use caution while driving or performing other tasks requiring mental alertness.
- Inform patient that this medication causes increased urine output.
- Teach patient signs and symptoms of hyperkalemia and hyponatremia.
- Caution patient to notify any physician or dentist seen about taking this medication and notify physician of cramps or chronic fatigue and weakness, which are serious side effects.