Eprosartan Mesylate
A to Z Drug Facts
(eh-pro-SAHR-tan MAL-ee-ate) |
Teveten |
Tablets: 400 mg |
Tablets: 600 mg |
Class: Antihypertensive, Angiotensin II antagonist |
Action Antagonizes the effect of angiotensin II (vasoconstriction and aldosterone secretion) by blocking the angiotensin II receptor (AT1 receptor) in vascular smooth muscle and the adrenal gland, producing decreased BP.
Indications Treatment of hypertension.
Contraindications Standard considerations.
Route/Dosage
Adults: PO 400 to 800 mg/day; usual starting dose 600 mg/day.
Interactions None well documented.
Lab Test Interferences
Lithium
Plasma concentrations may be increased by eprosartan, resulting in an increase in the pharmacologic and adverse effects of lithium.
Adverse Reactions
CARDIOVASCULAR: Abnormal ECG; extrasystoles; atrial fibrillation. CNS: Fatigue; depression. GI: Abdominal pain. GU: UTI. METABOLIC: Hypertriglyceridemia; hyperkalemia; hypokalemia. RESPIRATORY: Upper respiratory tract infection; rhinitis; pharyngitis; coughing. OTHER: Arthralgia.
Precautions
Pregnancy: Category C (first trimester); category D (second and third trimesters). Lactation: Undetermined. CHILDREN: Safety and efficacy not established. Renal function impairment: Use with caution in patients whose renal function may depend on the activity of the renin-angiotensin-aldosterone system (eg, patients with severe CHF), use may be associated with oliguria, progressive azotemia, acute renal failure, and death.
PATIENT CARE CONSIDERATIONS |
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Administration/Storage
- Store at room temperature in a tightly closed container.
- Administer alone or in combination with other antihypertensives such as diuretic and calcium channel blocker.
- Assess patient status and do not administer to patients with intravascular volume depletion until the condition has been corrected.
Assessment/Interventions
- Obtain patient history, including drug history and any known allergies.
- Monitor BP and pulse.
- Should hypotension, tachycardia, or bradycardia occur, withhold the medication and notify the health care provider.
- Monitor patient for signs of hypersensitivity including angioedema involving swelling of the face, lips, and tongue, or difficulty breathing.
Patient/Family Education
- Instruct patient to take the medication as prescribed at the same time each day.
- Inform patient that eprosartan controls but does not cure hypertension.
- Caution patient to take the dose exactly as prescribed and not to stop taking the medication even if feeling better.
- Instruct patient not to increase or decrease the dosage.
- Instruct patient that achievement of maximum BP reduction will usually take about 2 to 3 wk.
- Instruct family and patient in BP and pulse measurement skills.
- Caution patient to call primary health care provider should abnormal measurements occur.
- Instruct patient in methods of fall prevention including rising slowly and sitting on the side of the bed before standing, especially early in therapy.
- Inform patient of the importance of adjunct therapies such as dietary planning, regular exercise program, weight reduction, low sodium diet, alcohol reduction, smoking cessation, and stress management.
- Instruct patient to report symptoms of weakness, fatigue, dizziness, or lightheadedness to health care provider.
- Caution patient to notify health care provider or dentist of eprosartan use prior to surgery or treatment.
- Advise women to contact health care provider if pregnant, planning on becomming pregnant, or breastfeeding.
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Copyright © 2003 Facts and Comparisons
David S. Tatro
A to Z Drug Facts