eprosartan mesylate
eprosartan mesylate
Pharmacologic class: Angiotensin II receptor antagonist
Therapeutic class: Antihypertensive
Pregnancy risk category C (first trimester), D (second and third trimesters)
Action
Blocks aldosterone-stimulating and vasoconstrictive effects of angiotensin II at receptor sites in vascular smooth muscles and adrenal glands, decreasing vascular resistance
Availability
Tablets: 400 mg, 600 mg
Indications and dosages
➣ Hypertension
Adults: 600 mg P.O. once daily or in divided doses b.i.d. Total daily dosage range is 400 to 800 mg.
Contraindications
• Hypersensitivity to drug or its components
• Pregnancy or breastfeeding
Precautions
Use cautiously in:
• hypotension, heart failure, renal or hepatic impairment, obstructive biliary disorders, volume or sodium depletion
• concurrent high-dose diuretic therapy
• females of childbearing age
• children younger than age 18 (safety not established).
Administration
• Give initial dose in supervised medical setting, and monitor blood pressure for 2 hours after administration.
• Know that drug may be given alone or with other antihypertensives.
• Be aware that black patients have a higher risk of angioedema.
• Be prepared to treat transient hypotension by placing patient in supine position and giving I.V. normal saline infusion as needed.
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Adverse reactions
CNS: dizziness, fatigue, headache, syncope
CV: hypotension, chest pain, peripheral edema
EENT: sinus disorders
GI: nausea, diarrhea, constipation, abdominal pain, dry mouth
GU: albuminuria, renal failure
Hepatic: hepatitis
Metabolic: gout, hyperkalemia
Musculoskeletal: joint pain, back pain, muscle weakness
Respiratory: upper respiratory tract infection, cough, bronchitis
Skin: angioedema
Other: dental pain, fever, facial edema
Interactions
Drug-drug. Antihypertensives, diuretics: increased risk of hypotension
Nonsteroidal anti-inflammatory drugs: decreased antihypertensive effect of eprosartan
Potassium-sparing diuretics, potassium supplements: increased risk of hyperkalemia
Drug-diagnostic tests. Absolute neutrophil count, hemoglobin, platelets, white blood cells: decreased
Albumin, creatinine, liver function tests, serum BUN: elevated levels
Drug-food. Salt substitutes containing potassium: increased risk of hyperkalemia
Drug-herbs. Ephedra (ma huang): antagonism of eprosartan action
Drug-behaviors. Alcohol use: increased CNS depression
Patient monitoring
• Monitor vital signs, particularly for hypotension after administration.
• Assess cardiovascular status, especially for chest pain, syncope, and edema.
• Monitor liver and kidney function test results, watching for drug-induced hepatitis or renal failure.
• Assess respiratory status. Stay alert for dry, persistent cough and signs and symptoms of respiratory infections.
• Monitor electrolyte levels, and watch for signs and symptoms of hyperkalemia.
Patient teaching
• Instruct patient to take drug at same time each day, with or without food.
See Inform patient that drug may cause angioedema. Instruct him to immediately report facial or lip swelling, fever, or sore throat.
See Advise patient to immediately report chest pain, fainting, decreased urine output, unusual tiredness, yellowing of skin or eyes, or swelling.
See Tell female patient to contact prescriber right away if she suspects she's pregnant.
• Caution female not to breastfeed while taking drug.
• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs, tests, foods, herbs, and behaviors mentioned above.