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A randomized, double-blind, positive-controlled, prospective, dose-response clinical study to evaluate the efficacy and tolerability of an aqueous extract of Terminalia bellerica in lowering uric acid and creatinine levels in chronic kidney disease subjects with hyperuricemia
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Easy measuring: At 1.67 mg/mL, 1 unit = 0.01 mL 16.7 g on a U100 insulin syringe
Beyond 6 weeks: new baseline You are increasingly living without the pharmacological buffer
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