Generic versus brand-name drugs used in cardiovascular diseases

被引:68
作者
Manzoli, Lamberto [1 ,2 ]
Flacco, Maria Elena [1 ,2 ]
Boccia, Stefania [3 ]
D'Andrea, Elvira [4 ]
Panic, Nikola [3 ]
Marzuillo, Carolina [4 ]
Siliquini, Roberta [5 ]
Ricciardi, Walter [6 ]
Villari, Paolo [4 ]
Ioannidis, John P. A. [7 ,8 ,9 ,10 ]
机构
[1] Univ G dAnnunzio, Dept Med & Aging Sci, Via Vestini 5, I-66013 Chieti, Italy
[2] Reg Hlth Care Agcy Abruzzo, Via Attilio Monti 9, Pescara, Italy
[3] Univ Cattolica Sacro Cuore, Inst Publ Hlth, Largo Francesco Vito 1, I-00168 Rome, Italy
[4] Univ Roma La Sapienza, Dept Publ Hlth & Infect Dis, Viale Regina Elena 324, I-00161 Rome, Italy
[5] Univ Turin, Dept Publ Hlth Sci, Via Santena 5bis, I-10126 Turin, Italy
[6] Italian Natl Inst Hlth, Via Regina Elena 299, I-00161 Rome, Italy
[7] Stanford Univ, Sch Med, Stanford Prevent Res Ctr, Dept Med, Stanford, CA USA
[8] Stanford Univ, Sch Med, Dept Hlth Res & Policy, Stanford, CA USA
[9] Stanford Univ, Sch Humanities & Sci, Dept Stat, Stanford, CA USA
[10] Meta Res Innovat Ctr Stanford METRICS, Stanford, CA USA
关键词
Generic drug; Brand-name drug; Cardiovascular diseases; Meta-analysis; Efficacy; Safety; 2 TABLET FORMULATIONS; OPEN-LABEL; RANDOMIZED-SEQUENCE; 2-WAY CROSSOVER; BIOEQUIVALENCE EVALUATION; AMLODIPINE BESYLATE; PARALLEL-GROUP; KOREAN ADULTS; DOUBLE-BLIND; CLOPIDOGREL BISULFATE;
D O I
10.1007/s10654-015-0104-8
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
This meta-analysis aimed to compare the efficacy and adverse events, either serious or mild/moderate, of all generic versus brand-name cardiovascular medicines. We searched randomized trials in MEDLINE, Scopus, EMBASE, Cochrane Controlled Clinical Trial Register, and ClinicalTrials.gov (last update December 1, 2014). Attempts were made to contact the investigators of all potentially eligible trials. Two investigators independently extracted and analyzed soft (including systolic blood pressure, LDL cholesterol, and others) and hard efficacy outcomes (including major cardiovascular adverse events and death), minor/moderate and serious adverse events. We included 74 randomized trials; 53 reported a parts per thousand yen1 efficacy outcome (overall sample 3051), 32 measured mild/moderate adverse events (n = 2407), and 51 evaluated serious adverse events (n = 2892). We included trials assessing ACE inhibitors (n = 12), anticoagulants (n = 5), antiplatelet agents (n = 17), beta-blockers (n = 11), calcium channel blockers (n = 7); diuretics (n = 13); statins (n = 6); and others (n = 3). For both soft and hard efficacy outcomes, 100 % of the trials showed non-significant differences between generic and brand-name drugs. The aggregate effect size was 0.01 (95 % CI -0.05; 0.08) for soft outcomes; -0.06 (-0.71; 0.59) for hard outcomes. All but two trials showed non-significant differences in mild/moderate adverse events, and aggregate effect size was 0.07 (-0.06; 0.20). Comparable results were observed for each drug class and in each stratified meta-analysis. Overall, 8 serious possibly drug-related adverse events were reported: 5/2074 subjects on generics; 3/2076 subjects on brand-name drugs (OR 1.69; 95 % CI 0.40-7.20). This meta-analysis strengthens the evidence for clinical equivalence between brand-name and generic cardiovascular drugs. Physicians could be reassured about prescribing generic cardiovascular drugs, and health care organization about endorsing their wider use.
引用
收藏
页码:351 / 368
页数:18
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