irbesartan and hydrochlorothiazide tablet
1 INDICATIONS AND USAGE Irbesartan and hydrochlorothiazide tablets are indicated for the treatment of hypertension. Irbesartan and hydrochlorothiazide may be used in patients whose blood pressure is not adequately controlled on monotherapy. Irbesartan and hydrochlorothiazide may also be used as initial therapy in patients who are likely to need multiple drugs to achieve their blood pressure goals. The choice of irbesartan and hydrochlorothiazide as initial therapy for hypertension should be based on an assessment of potential benefits and risks. Patients with stage 2 (moderate or severe) hypertension are at relatively high risk for cardiovascular events (such as strokes, heart attacks, and heart failure), kidney failure, and vision problems, so prompt treatment is clinically relevant. The decision to use a combination as initial therapy should be individualized and may be shaped by considerations such as the baseline blood pressure, the target goal, and the incremental likelihood of achieving goal with a combination compared with monotherapy. Data from Studies V and VI [see Clinical Studies ( 14.2 )] provide estimates of the probability of reaching a blood pressure goal with irbesartan and hydrochlorothiazide compared to irbesartan or hydrochlorothiazide (HCTZ) monotherapy. The relationship between baseline blood pressure and achievement of a SeSBP <140 or <130 mmHg or SeDBP <90 or <80 mmHg in patients treated with irbesartan and hydrochlorothiazide compared to patients treated with irbesartan or HCTZ monotherapy are shown in Figures 1a through 2b. Figure 1a: Probability of Achieving SBP <140 mmHg in Patients from Initial Therapy Studies V (Week 8) and VI (Week 7)* Figure 1b: Probability of Achieving SBP <130 mmHg in Patients from Initial Therapy Studies V (Week 8) and VI (Week 7)* Figure 2a: Probability of Achieving DBP <90 mmHg in Patients from Initial Therapy Studies V (Week 8) and VI (Week 7)* Figure 2b: Probability of Achieving DBP <80 mmHg in Patients from Initial Therapy Studies V (Week 8) and VI (Week 7)* *For all probability curves, patients without blood pressure measurements at Week 7 (Study VI) and Week 8 (Study V) were counted as not reaching goal (intent-to-treat analysis). The above graphs provide a rough approximation of the likelihood of reaching a targeted blood pressure goal (e.g., Week 8 sitting systolic blood pressure β€140 mmHg) for the treatment groups. The curve of each treatment group in each study was estimated by logistic regression modeling from all available data of that treatment group. The estimated likelihood at the right tail of each curve is less reliable due to small numbers of subjects with high baseline blood pressures. For example, a patient with a blood pressure of 180/105 mmHg has about a 25% likelihood of achieving a goal of <140 mmHg (systolic) and 50% likelihood of achieving <90 mmHg (diastolic) on irbesartan alone (and lower still likelihoods on HCTZ alone). The likelihood of achieving these goals on irbesartan and hydrochlorothiazide rises to about 40% (systolic) or 70% (diastolic). Irbesartan and hydrochlorothiazide is a combination of irbesartan, an angiotensin II receptor antagonist, and hydrochlorothiazide, a thiazide diuretic, indicated for hypertension: β’ In patients not adequately controlled with monotherapy. ( 1 ) β’ As initial therapy in patients likely to need multiple drugs to achieve their blood pressure goals. ( 1 ) figure1a.jpg figure1b.jpg figure2a.jpg figure2b.jpg
west-ward pharmaceuticals corp.
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irbesartan and hydrochlorothiazide tablet
west-ward pharmaceuticals corp.
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16 HOW SUPPLIED/STORAGE AND HANDLING 16.1 How Supplied
IRBESARtan AND HYDROCHLOROTHIAZIDE Tablets, USP The 150 mg/12.5 mg tablets are light red speckled, round biconvex tablets, debossed with product identification β54β over β857β on one side and plain on the other side. NDC 0054-0254-13: Bottle of 30 Tablets NDC 0054-0254-22: Bottle of 90 Tablets NDC 0054-0254-29: Bottle of 500 Tablets The 300 mg/12.5 mg tablets are light yellow speckled, modified oval biconvex tablets, debossed with product identification β54 948β on one side and plain on the other side. NDC 0054-0255-13: Bottle of 30 Tablets NDC 0054-0255-22: Bottle of 90 Tablets NDC 0054-0255-29: Bottle of 500 Tablets The 300 mg/25 mg tablets are light red speckled, modified oval biconvex tablets, debossed with product identification β54 268β on one side and plain on the other side. NDC 0054-0256-13: Bottle of 30 Tablets NDC 0054-0256-22: Bottle of 90 Tablets NDC 0054-0256-29: Bottle of 500 Tablets 16.2 Storage Store at 20ΒΊ to 25Β°C (68ΒΊ to 77Β°F). [See USP Controlled Room Temperature.]
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