A COMPARATIVE STUDY TO EVALUATE THE EFFICACY AND SAFETY OF ROSUVASTATIN 5MG VERSUS ATORVASTATIN 20MG IN PATIENTS WITH DYSLIPIDAEMIA
AbstractDyslipidemia is a known risk factor for Atherosclerotic Cardiovascular Diseases (ASCVD). Statins are first choice drug for the treatment of dyslipidemia. The FDA advises a low starting dose of rosuvastatin at 5 mg/day in Asians. The present study is a randomized, open labelled study done at Victoria Hospital, Bangalore to compare the efficacy and safety of rosuvastatin 5mg versus atorvastatin 20mg in patients with dyslipidemia. A total of 60 treatment naïve adult patients with dyslipidemia were randomized into two arms of 30 each in 1:1 ratio to receive either rosuvastatin 5mg or atorvastatin 20mg. Lipid profiles at baseline and at 6th week follow-up visit was recorded. Efficacy was assessed by mean change in lipid parameters at the end of 6 weeks and safety by recording the number and severity of adverse events reported by the patient at any time during the study. Among the 60 patients the mean difference at 6th week from baseline for Total cholesterol, LDL, HDL and Triglyceride for the rosuvastatin and atorvastatin group were (mg/dl) -48.7, -38.6, +4.7, -20.1 and -56.6, -46.6, +4.8, -19 respectively. In both the arms, the mean differences were significant. However, no significant difference (p˃0.05) was seen in any lipid parameter between the two arms at the 6th week. Five patients reported myalgia in the atorvastatin arm and one patient reported myalgia in the rosuvastatin arm. Hence, this study concludes that rosuvastatin at a dose of 5mg OD was found to be as efficacious as atorvastatin 20mg OD with relatively less side effects in patients with dyslipidemia.
Article Information
24
1978-1984
565 KB
15
English
IJPSR
A. P. Venkataraman, P. Sushma, Laxminarayana Kamath * and K. R. Raveendra
Department of Pharmacology, Bangalore Medical College and Research Institute, Bangalore, Karnataka, India.
drlnkamath@gmail.com
06 February 2025
19 February 2025
21 February 2025
10.13040/IJPSR.0975-8232.16(7).1978-84
01 July 2025