Generic Name and Formulations:
Losartan potassium 25mg, 50mg, 100mg; tabs.
Company:
Merck & Co., Inc.
Treatment of diabetic nephropathy in type 2 diabetes with hypertension.
Initially 50mg once daily; may increase to 100mg once daily.
Not established.
Angiotensin II receptor blocker.
Concomitant aliskiren in patients with diabetes.
Fetal toxicity; discontinue as soon as pregnancy is detected. Correct salt/volume depletion before starting therapy, or reduce initial dose. Renal impairment: monitor for worsening renal function. Hepatic impairment. Severe CHF. Renal artery stenosis. Pregnancy (Cat.C in 1st trimester, Cat.D in 2nd and 3rd trimesters). Nursing mothers: not recommended.
Hyperkalemia with K+ supplements, K+ sparing diuretics, K+ containing salt substitutes. May be antagonized by, and renal toxicity potentiated by NSAIDs, including selective COX-2 inhibitors (monitor renal function periodically in elderly and/or volume-depleted). Monitor lithium. Dual inhibition of the renin-angiotensin system with ARBs, ACEIs, or aliskiren may increase risk of hypotension, hyperkalemia, renal function changes; monitor closely. Concomitant aliskiren in renal impairment (CrCl <60mL/min): not recommended.
Dizziness, insomnia, muscle cramps, leg pain, hyperkalemia, angioedema, orthostatic hypotension, rhabdomyolysis (rare).
Hepatic (CYP2C9, 3A4).
Fecal, renal.
YES
Tabs 25mg—90, 1000; 50mg, 100mg—30, 90, 1000
Hypertension (HTN). To reduce stroke risk in hypertensive patients with left ventricular hypertrophy (LVH); this benefit may not apply to black patients.
Hypovolemia or hepatic insufficiency: initially 25mg once daily. HTN: initially 50mg once daily; range 25–100mg/day; max 100mg/day in 1 or 2 divided doses. HTN with LVH: initially 50mg once daily; then add hydrochlorothiazide (HCTZ) 12.5mg/day and/or increase losartan to 100mg/day, then may increase HCTZ to 25mg/day.
<6yrs or CrCl <30mL/min: not established. ≥6yrs: initially 0.7mg/kg (max 50mg) once daily; usual max 1.4mg/kg (100mg) once daily.
Angiotensin II receptor blocker.
Concomitant aliskiren in patients with diabetes.
Fetal toxicity; discontinue as soon as pregnancy is detected. Correct salt/volume depletion before starting therapy, or reduce initial dose. Renal impairment: monitor for worsening renal function. Hepatic impairment. Severe CHF. Renal artery stenosis. Pregnancy (Cat.C in 1st trimester, Cat.D in 2nd and 3rd trimesters). Nursing mothers: not recommended.
Hyperkalemia with K+ supplements, K+ sparing diuretics, K+ containing salt substitutes. May be antagonized by, and renal toxicity potentiated by NSAIDs, including selective COX-2 inhibitors (monitor renal function periodically in elderly and/or volume-depleted). Monitor lithium. Dual inhibition of the renin-angiotensin system with ARBs, ACEIs, or aliskiren may increase risk of hypotension, hyperkalemia, renal function changes; monitor closely. Concomitant aliskiren in renal impairment (CrCl <60mL/min): not recommended.
Dizziness, insomnia, muscle cramps, leg pain, hyperkalemia, angioedema, rhabdomyolysis (rare).
Hepatic (CYP2C9, 3A4).
Fecal, renal.
YES
Tabs 25mg—90, 1000; 50mg, 100mg—30, 90, 1000