STUDY IN HYPERURICEMIC PATIENTS TO KNOW THE FENOFIBRATE SAFETY AND ITS EFFICACY

Journal Title: Indo American Journal of Pharmaceutical Sciences - Year 2018, Vol 5, Issue 5

Abstract

Background: Allopurinol is commonly used as antihypertensive medicine. Fenofibrate, a fibric acid derivative, is widely used in hyperlipidemia treatment. Fenofibrate reduce serum uric acid levels effectively. Objective: This study was performed to evaluate the safety and efficacy of fenofibrate in patients with hyperuricemia. Study Design: Interventional Study Place and Duration: The study was performed in the Out Patient Department of Nephrology Unit of Nishter Hospital, Multan for the period of six months from January 2017 to July 2017. Materials and methods: Sixty hyperuricemic patients with serum uric acid levels of desil- lary or higher of 7.0 mg were enrolled and assigned to receive 300 mg allofurinol or 200 mg fenofibrate for 12 weeks. The efficacy of the drug was measured in percentage of patients successfully controlling serum uric acid levels of less than 6 mg P. Dl at 90 days. The efficacy of the drug was also checked by measuring the percentage of serum uric acid levels changes at day 1 to 90 days. Safety was checked by observing side effects (AE) and laboratory investigations. Findings: The percentage comparison of cases in which uric acid level in serum was lower than 6.5 mg at 90th day in both groups was statically significant (P = 0.14). However, the percentage difference in uric acid level between 0 and 90 days was significantly highly among the two groups (p = 0.001). Although the proportion of individuals experiencing any side effects was greater in the fenofibrate group, the side effects that caused the allopurinol group to discontinue treatment were found to be higher. Conclusion: Fenofibrate 200 mg is an effective antihypertensive agent once a day. Key words: Uric acid, Fenofibrate, hyperuricemia.

Authors and Affiliations

Keywords

Related Articles

FORMULAITON AND PHARMACOKINETIC EVALUATION OF NAPROXEN SODIUM MODIFIED RELEASE TABLET

The objective of the study was to develop naproxen sodium SR tablets were prepared by direct compression method using hydroxy propyl methyl cellulose (HPMC K 100). To know the effect of polymer concentration invitro stud...

EVALUATION OF FREQUENCY AND SEVERITY OF ANXIETY AND MOOD DISORDERS AMONG PATIENTS WITH GRAVES' DISEASE

Objective: Graves' disease has been associated with an increased psychiatric morbidity. It is unclarified whether this relates to Graves' disease or chronic disease per se. The aim of our study was to evaluate the freque...

PRELIMINARY PHYTOCHEMICAL SCREENING OF VARIOUS EXTRACTS OF ANISOMELES MALABARICA

Traditional systems thus contain beliefs and practices in order to avoid, prevent, or avert ailments, which constitute traditional preventive medicine. The use of medicinal herbs and herbal medicine is an age-old traditi...

FORMULATION DEVELOPMENT OF CR OFLAXACIN MATRIX TABLET AND THEIR IN-VITRO EVALUATION

Among the all sophisticated drug deliveries oral drug delivery is known as safest and most convenient rout of administration. DDS are formulated for rapid release, for CDD (Controlled Drug delivery and release) and for t...

HEPATITIS C VIRUS INFECTION: PREVENTION AND CONTROL - A MINI REVIEW

It is estimated that around more than 2% of the population of world is suffering with hepatitis C virus and death cases because of cirrhosis and liver cancer is more than 350000.The load and epidemiology of HCV infection...

Download PDF file
  • EP ID EP287778
  • DOI -
  • Views 245
  • Downloads 0

How To Cite

(2018). STUDY IN HYPERURICEMIC PATIENTS TO KNOW THE FENOFIBRATE SAFETY AND ITS EFFICACY. Indo American Journal of Pharmaceutical Sciences, 5(5), 3880-3883. https://europub.co.uk/articles/-A-287778