Maximizing blood pressure lowering effects: a review of drug class comparisons and rationale for combination approaches. [PDF]
Yang Y, Wan F, Xu J, Mei Deng H, Pan P.
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Association Between Pre-hospital Medication Use and Outcomes in Patients Hospitalized for COVID-19 Pneumonia: A Multicenter Observational Study in the Netherlands. [PDF]
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Plasma aldosterone is low in patients hospitalized with COVID-19 and not associated with changes in serum potassium levels: <i>post hoc</i> observational analyses of clinical trial data. [PDF]
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Differences in clinical profiles and cancer incidence among patients with type 2 diabetes in primary care: Comparison between multidisciplinary and usual management. [PDF]
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Adherence, Switches, and Drug Spending After Angiotensin Receptor Blocker Recalls and Shortages.
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Unlocking Novel Therapeutic Potential of Angiotensin II Receptor Blockers. [PDF]
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Class- and Molecule-specific Differential Effects of Angiotensin II Type 1 Receptor Blockers
Current Pharmaceutical Design, 2013Angiotensin II (Ang II) type 1 (AT1) receptor is a member of the G protein-coupled receptor superfamily and contains 359 amino acids. AT1 receptor blockers (ARBs, e.g., eprosartan, losartan, candesartan, valsartan, telmisartan, olmesartan, irbesartan, and azilsartan) have been developed and are available for clinical use, and basic and clinical studies
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Acta Diabetologica, 2005Vascular protection is key to reducing the morbidity associated with diabetes. Angiotensin II is known to exert a variety of deleterious effects on the vasculature, and this is likely to be a major explanation of the protective benefits observed with blockade of the renin-angiotensin-aldosterone system (RAAS).
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