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Irbesartan and Hydrochlorothiazide - Pictures


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Irbesartan and Hydrochlorothiazide

Avalide 


Pictures

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Infants with histories of in utero exposure to an angiotensin II receptor antagonist should be closely observed for hypotension oliguria and hyperkalemia If oliguria occurs attention


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These adverse effects do not appear to have resulted from intrauterine drug exposure that has been limited to the first trimester Mothers whose embryos and fetuses are exposed to an


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Infants with histories of in utero exposure to an angiotensin II receptor antagonist should be closely observed for hypotension oliguria and hyperkalemia If oliguria occurs attention


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an overdose Other signs may include dry mouth excessive thirst muscle cramps weakness restlessness confusion and nausea If you suspect an overdose seek medical attention immediately


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DRUG INTERACTIONS No significant drug drug pharmacokinetic or pharmacodynamic interactions have been found in interaction studies with hydrochlorothiazide digoxin warfarin and nifedipine


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WARNINGS Fetal Neonatal Morbidity and Mortality


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th Avalide 12 5 mg 300 mg jpg

2776 LOGO HEART 12 5 mg 300 mg


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th Avalide 300 25 mg jpg

LOGO HEART 2788 25 mg 300 mg


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While Bristol Myers Squibb Sanofi Synthelabo Partnership uses reasonable efforts to include accurate and up to date information in the Site Bristol Myers Squibb Sanofi Synthelabo Partnership


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Avalide Hydrochlorothiazide and irbesartan hyde droe klor oh THYE a zide and ER beh sar tan Avalide


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this medication for conditions other than the ones listed in these drug information articles If you are unsure why you are taking this medication contact your doctor Avalide Irbesartan Hydrochlorothiazide Tablets


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Avalide Avalide Irbesartan Hydrochlorothiazide is a combination angiotensin II receptor blocker and


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8 weeks from irbesartan 150 to 300 mg day or from irbesartan 300 mg to irbesartan 300 mg plus hydrochlorothiazide HCTZ 12 5 mg day if their seated diastolic blood pressure SeDBP remained 90 mm Hg Trough blood pressures and safety assessments were measured at intervals during the study The primary end point was the comparison of the reduction in blood pressure at the end of


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November 28, 2009



Page Updated: June 1, 2005
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