Comparison of Generic-to-Brand Switchback Rates Between Generic and Authorized Generic Drugs

被引:19
|
作者
Hansen, Richard A. [1 ]
Qian, Jingjing [1 ]
Berg, Richard [2 ]
Linneman, James [2 ]
Seoane-Vazquez, Enrique [3 ]
Dutcher, Sarah K. [4 ]
Raofi, Saeid [4 ]
Page, C. David [5 ,6 ]
Peissig, Peggy [2 ]
机构
[1] Auburn Univ, Harrison Sch Pharm, Dept Hlth Outcomes Res & Policy, 020 Foy Hall, Auburn, AL 36849 USA
[2] Marshfield Clin Res Fdn, Biomed Informat Res Ctr, Marshfield, WI USA
[3] Massachusetts Coll Pharm & Hlth Sci, Int Ctr Pharmaceut Econ & Policy, Boston, MA USA
[4] US FDA, Off Gener Drugs, Silver Spring, MD USA
[5] Univ Wisconsin, Sch Med & Publ Hlth, Dept Biostat & Med Informat, Madison, WI USA
[6] Univ Wisconsin, Dept Comp Sci, Sch Med & Publ Hlth, 1210 W Dayton St, Madison, WI 53706 USA
来源
PHARMACOTHERAPY | 2017年 / 37卷 / 04期
关键词
generic; authorized generic; utilization; switchback; SUBSTITUTION; IMPACT; NAME; PATIENT; SAFETY;
D O I
10.1002/phar.1908
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Study ObjectiveGeneric drugs contain identical active ingredients as their corresponding brand drugs and are pharmaceutically equivalent and bioequivalent, whereas authorized generic drugs (AGs) contain both identical active and inactive ingredients as their corresponding brand drugs but are marketed as generics. This study compares generic-to-brand switchback rates between generic and AGs. DesignRetrospective cohort study. Data SourceClaims and electronic health record data from a regional U.S. health care system. PatientsThe full cohort consisted of 5542 unique patients who received select branded drugs during the 6 months prior to their generic drug market availability (between 1999 and 2014) and then were switched to an AG or generic drug within 30 months of generic drug entry. For these patients, 5929 unique patient-drug combinations (867 with AGs and 5062 with generic drugs) were evaluated. Measurements and Main ResultsTen drugs with AGs and generics marketed between 1999 and 2014 were evaluated. The date of the first generic prescription was considered the index date for each drug, and it marked the beginning of follow-up to evaluate the occurrence of generic-to-brand switchback patterns over the subsequent 30 months. Switchback rates were compared between patients receiving AGs versus those receiving generics using multivariable Cox proportional hazards models, controlling for individual drug effects, age, sex, Charlson Comorbidity Score, pre-index drug use characteristics, and pre-index health care utilization. Among the 5542 unique patients who switched from brand to generic or brand to AG, 264 (4.8%) switched back to the brand drug. Overall switchback rates were similar for AGs compared with generics (hazard ratio [HR] 0.86, 95% confidence interval [CI] 0.65-1.15). The likelihood of switchback was higher for alendronate (HR 1.64, 95% CI 1.20-2.23) and simvastatin (HR 1.81, 95% CI 1.30-2.54) and lower for amlodipine (HR 0.27, 95% CI 0.17-0.42) compared with the other drugs evaluated. ConclusionOverall switchback rates were similar between AG and generic drug users, indirectly supporting similar efficacy and tolerability profiles for brand and generic drugs. Reasons for differences in switchback rates among specific products need to be explored further.
引用
收藏
页码:429 / 437
页数:9
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