2006
DOI: 10.1258/jrsm.99.3.132
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Risk of cardiovascular events and celecoxib: a systematic review and meta-analysis

Abstract: The available data indicate an increased risk of myocardial infarction with celecoxib therapy, consistent with a class effect for COX-2 specific inhibitors.

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Cited by 174 publications
(101 citation statements)
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“…After the withdrawal of rofecoxib and valdecoxib, celecoxib remained on the market in the United States, and research surrounding the safety of NSAIDs continued. 65,66 Many experts were not convinced that the cardiovascular effects of rofecoxib represented a class effect. 54,67 In addition, the debate continued regarding the association between COX-1 and COX-2 selectivity and risks, as well as factors that modulate drug response.…”
Section: Nsaids: Cox-2 Versus Cox-1 Selectivitymentioning
confidence: 99%
“…After the withdrawal of rofecoxib and valdecoxib, celecoxib remained on the market in the United States, and research surrounding the safety of NSAIDs continued. 65,66 Many experts were not convinced that the cardiovascular effects of rofecoxib represented a class effect. 54,67 In addition, the debate continued regarding the association between COX-1 and COX-2 selectivity and risks, as well as factors that modulate drug response.…”
Section: Nsaids: Cox-2 Versus Cox-1 Selectivitymentioning
confidence: 99%
“…De fleste som har undersøkt mulige sammenhenger mellom dose ikke-steroid antiinflammatorisk middel og økt risiko for kardiovaskulaere hendelser, har påvist en dose-effektsammenheng (7,13,17,18,31). Unntaket er naproksen, hvor risikoøkningen har vaert fravaerende (tab 2), og en metaanalyse (6) der man ikke kunne påvise at den vaskulaere risikoen til verken selektive COX-2-hemmere eller tradisjonelle ikke-steroide antiinflammatoriske midler var doseavhengig.…”
Section: Er Risikoen Avhengig Av Dose Behandlingsvarighet Eller Andrunclassified
“…Nonsteroidal anti-inflammatory drugs are associated with well-known risks of gastrointestinal (Boers et al, 2007;Gabriel et al, 1991;, cardiovascular (Antman et al, 2007;Caldwell et al, 2006;Juni et al, 2004;Kearney et al, 2006;Motsko et al, 2006), and renal (Barkin & Buvanendran, 2004;Evans et al, 1995) adverse events. Hepatic adverse events have been reported infrequently (Rostom et al, 2005;Rubenstein & Laine, 2004), and are certainly less common than with acetaminophen.…”
Section: Nonsteroidal Anti-inflammatory Drugsmentioning
confidence: 99%
“…Acetaminophen is a welltolerated first-line pharmacotherapy but has limited efficacy (Zhang et al, 2010) and highdose, long-term use is associated with hepatic toxicity (Watkins et al, 2006). NSAIDs have better efficacy than acetaminophen but have well-known risks of gastrointestinal (Boers et al, 2007;Gabriel et al, 1991;, cardiovascular (Antman et al, 2007;Caldwell et al, 2006;Kearney et al, 2006;Motsko et al, 2006), and other systemic adverse effects that increase with age, dose, and duration of use.…”
Section: Introductionmentioning
confidence: 99%