A study was conducted to determine the cost and patient adher- ence rates of lipid-lowering therapy with an extended-release niacin and lovastatin (ERNL) combination agent versus a separate extended-release niacin and statin (ERN-S) combination or statin monotherapy.
METHODS The study methods were as follows:
CONCLUSIONS
Editors' Note: This study was originally presented as a poster at the Academy of Managed Care Pharmacy (AMCP) Educational Conference, October 13–16, 2004, in Baltimore, Md.
Dr LaFleur is an outcomes fellow at the Pharmacotherapy Outcomes Research Center at the University of Utah College of Pharmacy, Salt Lake City, Utah. Dr LaFleur can be reached at joanne.lafleur@pharm.utah.edu
. Mr Thompson is a research assistant at the Department of Family and Preventive Medicine, School of Public Health, University of Utah. Dr Ho is a Medco Outcomes fellow at the Pharmacotherapy Outcomes Research Center at the University of Utah College of Pharmacy. Mr Stockdale is a research assistant professor in the Pharmacotherapy Outcomes Research Center, University of Utah. Dr Charland is associate director of Health Economics and Outcomes, Kos Pharmaceuticals, and an adjunct associate professor at the University of Colorado in Denver, Colo. Dr Oderda is director of the Pharmacotherapy Outcomes Research Center and a professor at the University of Utah College of Pharmacy. Dr Brixner is an associate professor and chair of the Department of Pharmacotherapy at the University of Utah and executive director of the Pharmacotherapy Outcomes Research Center at the University of Utah College of Pharmacy.
REFERENCES 1. Blandford L, Dans PE, Ober JD, Wheelock C. Analyzing variations in medication compliance related to individual drug, drug class, and prescribing physician. J Managed Care Pharm. 1999;5:47–51.
2. Benner JS, Glynn RJ, Mogun H, et al. Long-term persistence in use of statin therapy in elderly patients. JAMA. 2002;288:455–461.
3. Diggle PJ, Heagerty P, Liang KY, Zeger SJ. Analysis of Longitudinal Data. 2nd ed. Oxford, England: Oxford University Press; 2002.
FDA Approves Neffy 1 mg Nasal Spray for Pediatric Patients
March 6th 2025Neffy 1 mg is now approved by the FDA to treat pediatric patients who weigh 33 to 65 lbs. Neffy was first FDA-approved as a 2 mg dose in August 2024 for the emergency treatment of anaphylaxis in children and adults weighing at least 66 lbs.
Read More
David Calabrese of OptumRx Talks Top Three Drugs in Pipeline, Industry Trends in Q2
July 1st 2020In this week's episode of Tuning Into The C-Suite podcast, MHE's Briana Contreras chatted with David Calabrese, R.Ph, MHP, who is senior vice president and chief pharmacy officer of pharmacy care services company, OptumRx. David is also a member of Managed Healthcare Executives’ Editorial Advisory Board. During the discussion, he shared the OptumRx Quarter 2 Drug Pipeline Insights Report of 2020. Some of the information shared includes the three notable drugs currently being reviewed or those that have been recently approved by the FDA. Also discussed were any interesting industry trends to watch for.
Listen
Trelegy and Breo Offer Incremental Improvement Over Generics
March 3rd 2025The Institute for Clinical and Economic Review has prepared a special report on Trelegy and Breo, two therapies that treat patients with chronic obstructive pulmonary disease that are part of CMS's drug price negotiation program.
Read More