AMLODIPINE, VALSARTAN, HYDROCHLOROTHIAZIDE- amlodipine besylate valsartan hydrochlorothiazide tablet, film coated United States - English - NLM (National Library of Medicine)

amlodipine, valsartan, hydrochlorothiazide- amlodipine besylate valsartan hydrochlorothiazide tablet, film coated

par pharmaceutical, inc. - amlodipine besylate (unii: 864v2q084h) (amlodipine - unii:1j444qc288), valsartan (unii: 80m03yxj7i) (valsartan - unii:80m03yxj7i), hydrochlorothiazide (unii: 0j48lph2th) (hydrochlorothiazide - unii:0j48lph2th) - amlodipine 5 mg - amlodipine/valsartan/hydrochlorothiazide is indicated for the treatment of hypertension, to lower blood pressure. lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. these benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes, including amlodipine, hydrochlorothiazide, and the arb class to which valsartan principally belongs. there are no controlled trials demonstrating risk reduction with amlodipine/valsartan/hydrochlorothiazide. control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. many patients will require more than 1 drug to achieve blood pressure goals. for specific advice on goals and management, see published guidelines, such as those of the national high blood pressure education p

AMLODIPINE, VALSARTAN, HYDROCHLOROTHIAZIDE- amlodipine valsartan and hydrochlorothiazide tablet, film coated United States - English - NLM (National Library of Medicine)

amlodipine, valsartan, hydrochlorothiazide- amlodipine valsartan and hydrochlorothiazide tablet, film coated

sandoz inc - amlodipine besylate (unii: 864v2q084h) (amlodipine - unii:1j444qc288), valsartan (unii: 80m03yxj7i) (valsartan - unii:80m03yxj7i), hydrochlorothiazide (unii: 0j48lph2th) (hydrochlorothiazide - unii:0j48lph2th) - amlodipine 5 mg - numerous antihypertensive drugs, from a variety of pharmacologic classes and with different mechanisms of action, have been shown in randomized controlled trials to reduce cardiovascular morbidity and mortality, and it can be concluded that it is blood pressure reduction, and not some other pharmacologic property of the drugs, that is largely responsible for those benefits. the largest and most consistent cardiovascular outcome benefit has been a reduction in the risk of stroke, but reductions in myocardial infarction and cardiovascular mortality also have been seen regularly. elevated systolic or diastolic pressure causes increased cardiovascular risk, and the absolute risk increase per mmhg is greater at higher blood pressures, so that even modest reductions of severe hypertension can provide substantial benefit. relative risk reduction from blood pressure reduction is similar across populations with varying absolute risk, so the absolute benefit is greater in patients who are at higher risk independent of

Amlodipine/Valsartan/Hydrochlorothiazide Krka 10 mg/160 mg/12.5 mg film-coated tablets Ireland - English - HPRA (Health Products Regulatory Authority)

amlodipine/valsartan/hydrochlorothiazide krka 10 mg/160 mg/12.5 mg film-coated tablets

krka, d.d., novo mesto - amlodipine; valsartan; hydrochlorothiazide - film-coated tablet - 10/160/12.5 milligram(s) - valsartan, amlodipine and hydrochlorothiazide

Amlodipine/Valsartan/Hydrochlorothiazide Krka 10 mg/160 mg/25 mg film-coated tablets Ireland - English - HPRA (Health Products Regulatory Authority)

amlodipine/valsartan/hydrochlorothiazide krka 10 mg/160 mg/25 mg film-coated tablets

krka, d.d., novo mesto - amlodipine; valsartan; hydrochlorothiazide - film-coated tablet - 10/160/25 milligram(s) - valsartan, amlodipine and hydrochlorothiazide

Amlodipine/Valsartan/Hydrochlorothiazide Krka 10 mg/320 mg/25 mg film-coated tablets Ireland - English - HPRA (Health Products Regulatory Authority)

amlodipine/valsartan/hydrochlorothiazide krka 10 mg/320 mg/25 mg film-coated tablets

krka, d.d., novo mesto - amlodipine; valsartan; hydrochlorothiazide - film-coated tablet - 10/320/25 milligram(s) - valsartan, amlodipine and hydrochlorothiazide

Amlodipine/Valsartan/Hydrochlorothiazide Krka 5 mg/160 mg/12.5 mg film-coated tablets Ireland - English - HPRA (Health Products Regulatory Authority)

amlodipine/valsartan/hydrochlorothiazide krka 5 mg/160 mg/12.5 mg film-coated tablets

krka, d.d., novo mesto - amlodipine; valsartan; hydrochlorothiazide - film-coated tablet - 5/160/12.5 milligram(s) - valsartan, amlodipine and hydrochlorothiazide

Amlodipine/Valsartan/Hydrochlorothiazide Krka 5 mg/160 mg/25 mg film-coated tablets Ireland - English - HPRA (Health Products Regulatory Authority)

amlodipine/valsartan/hydrochlorothiazide krka 5 mg/160 mg/25 mg film-coated tablets

krka, d.d., novo mesto - amlodipine; valsartan; hydrochlorothiazide - film-coated tablet - 5/160/25 milligram(s) - valsartan, amlodipine and hydrochlorothiazide

AMLODIPINE/VALSARTAN/HCT NOVARTIS 10/320/25  amlodipine/valsartan/hydrochlorothiazide tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

amlodipine/valsartan/hct novartis 10/320/25 amlodipine/valsartan/hydrochlorothiazide tablet blister pack

novartis pharmaceuticals australia pty ltd - valsartan, quantity: 320 mg; hydrochlorothiazide, quantity: 25 mg; amlodipine besilate, quantity: 13.87 mg (equivalent: amlodipine, qty 10 mg) - tablet, film coated - excipient ingredients: magnesium stearate; colloidal anhydrous silica; crospovidone; microcrystalline cellulose; hypromellose; purified talc; macrogol 4000; iron oxide yellow - amlodipine/valsartan/hct novartis is indicated only as substitution therapy for the treatment of hypertension in patients whose blood pressure is already adequately controlled on the triple combination of amlodipine, valsartan and hydrochlorothiazide taken either as three single component formulations or as dual-component formulation with a single component formulation, all components at the same dose level. treatment should not be initiated with these fixed-dose combinations (see dosage and administration).

AMLODIPINE/VALSARTAN/HCT NOVARTIS 10/160/25  amlodipine/valsartan/hydrochlorothiazide tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

amlodipine/valsartan/hct novartis 10/160/25 amlodipine/valsartan/hydrochlorothiazide tablet blister pack

novartis pharmaceuticals australia pty ltd - amlodipine besilate, quantity: 13.87 mg (equivalent: amlodipine, qty 10 mg); hydrochlorothiazide, quantity: 25 mg; valsartan, quantity: 160 mg - tablet, film coated - excipient ingredients: colloidal anhydrous silica; magnesium stearate; crospovidone; microcrystalline cellulose; hypromellose; purified talc; macrogol 4000; iron oxide yellow - amlodipine/valsartan/hct novartis is indicated only as substitution therapy for the treatment of hypertension in patients whose blood pressure is already adequately controlled on the triple combination of amlodipine, valsartan and hydrochlorothiazide taken either as three single component formulations or as dual-component formulation with a single component formulation, all components at the same dose level. treatment should not be initiated with these fixed-dose combinations (see dosage and administration).

AMLODIPINE/VALSARTAN/HCT NOVARTIS 10/160/12.5 amlodipine/valsartan/hydrochlorothiazide tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

amlodipine/valsartan/hct novartis 10/160/12.5 amlodipine/valsartan/hydrochlorothiazide tablet blister pack

novartis pharmaceuticals australia pty ltd - valsartan, quantity: 160 mg; amlodipine besilate, quantity: 13.87 mg (equivalent: amlodipine, qty 10 mg); hydrochlorothiazide, quantity: 12.5 mg - tablet, film coated - excipient ingredients: microcrystalline cellulose; colloidal anhydrous silica; crospovidone; magnesium stearate; hypromellose; purified talc; macrogol 4000; iron oxide red; iron oxide yellow; titanium dioxide - amlodipine/valsartan/hct novartis is indicated only as substitution therapy for the treatment of hypertension in patients whose blood pressure is already adequately controlled on the triple combination of amlodipine, valsartan and hydrochlorothiazide taken either as three single component formulations or as dual-component formulation with a single component formulation, all components at the same dose level. treatment should not be initiated with these fixed-dose combinations (see dosage and administration).