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These studies suggest Diovan 160 mg is effective and well-tolerated for reducing arterial blood pressure in patients with mild to moderate hypertension, and it is comparable in efficacy and safety to other formulations and combinations.
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Several studies have assessed the bioequivalence of Diovan 160 mg tablets with other valsartan formulations. One study compared the pharmacokinetic parameters of Valzan® 160 mg tablets with Diovan® 160 mg tablets in a randomized, two-way crossover study involving 24 healthy male volunteers. The results showed no significant differences in pharmacokinetic parameters such as AUC and Cmax between the two formulations, indicating that Valzan® is bioequivalent to Diovan®.
Another study evaluated the bioequivalence of a new 320 mg valsartan tablet with two 160 mg valsartan capsules. The study, conducted in 40 healthy volunteers, found that the pharmacokinetic parameters of the new tablet formulation were within the acceptable range for bioequivalence when compared to the marketed capsules.
Diovan 160 mg has been extensively studied for its efficacy in managing hypertension. In a study involving 20 patients with mild to moderate hypertension, Diovan 160 mg/day significantly reduced both systolic and diastolic blood pressure over an 8-week period. The study concluded that Diovan is effective and well-tolerated in this patient population.
Another study focused on patients with severe arterial hypertension who were treated with Diovan 80-160 mg/day in combination with other antihypertensive agents. The results showed that Diovan effectively lowered arterial pressure in 80% of the patients, with minimal side effects.
Diovan is often used in combination with other antihypertensive agents to achieve better blood pressure control. A study on the fixed combination of valsartan and hydrochlorothiazide (HCT) found that this combination is more effective in controlling blood pressure compared to monotherapy. The combination therapy was well-tolerated and provided additional benefits by blocking the effects of angiotensin II, which is responsible for cardiovascular remodeling.
Long-term studies have also demonstrated the efficacy of Diovan in reducing left ventricular hypertrophy (LVH), a condition associated with increased cardiovascular risk. In a randomized, double-blind study, valsartan significantly reduced left ventricular mass index in patients with essential hypertension and LVH over an 8-month period.
Diovan 160 mg is a highly effective and well-tolerated option for the treatment of hypertension. Its bioequivalence with other valsartan formulations has been well-established, and it has shown significant efficacy in both monotherapy and combination therapy settings. Long-term use of Diovan also offers benefits in reducing cardiovascular risks associated with conditions like left ventricular hypertrophy.
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