Short-term and long-term tolerability of rofecoxib in patients with prior reactions to nonsteroidal anti-inflammatory drugs

被引:14
作者
Nettis, E [1 ]
Colanardi, MC [1 ]
Ferrannini, A [1 ]
Tursi, A [1 ]
机构
[1] Univ Bari, Div Clin Immunol & Allergy, Dept Med Clin Immunol & Infect Dis, Bari, Italy
关键词
D O I
10.1016/S1081-1206(10)61281-1
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Rofecoxib is a selective cyclooxygenase 2 (COX-2) inhibitor and is well tolerated as an alternative to nonsteroidal anti-inflammatory drugs (NSAIDs) in patients with a previous adverse reaction to other classes of NSAIDs. Until now, there has not been information in the literature about its long-term tolerability. Objective: To provide follow-up data on patients with a history of adverse cutaneous reactions to NSAIDs who underwent and tolerated a challenge test with rofecoxib. Methods: Study patients had historically experienced cutaneous adverse reactions to aspirin and NSAIDs and had undergone single-blind challenges with rofecoxib, 25 mg. A questionnaire was distributed to all participants. In particular, they were asked to clarify any reactive symptoms they had developed after ingestion of the drug. All patients were reexamined 1 to 3 years after testing. At reexamination, they were carefully and personally interviewed using the previously distributed questionnaire. Results: Of the 182 patients who participated in the study, none reacted to rofecoxib during single-blind challenges. Fifty-one (28%) never received rofecoxib again, whereas 131 (72%) were exposed to rofecoxib, often on multiple occasions. Only 7 (5%) of the 131 patients reported cutaneous reactions to rofecoxib during the 3 years of follow-up. Conclusions: Rofecoxib appears to be a safe alternative drug among atopic individuals, antibiotic-hypersensitive individuals, and individuals who experienced adverse cutaneous reactions to more than 1 class of NSAIDs, but it is less safe among chronic urticaria patients. Further investigations that include a larger sample are required to confirm our results especially among chronic urticaria patients.
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页码:29 / 33
页数:5
相关论文
共 26 条
[1]  
ANDRI L, 1994, ANN ALLERGY, V72, P29
[2]   Detection of patients with multiple drug allergy syndrome by elective tolerance tests [J].
Asero, R .
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 1998, 80 (02) :185-188
[3]   Rofecoxib safe in NSAID hypersensitivity [J].
Berges-Gimeno, MP ;
Camacho-Garrido, E ;
García-Rodriguez, RM ;
Alfaya, T ;
García, CM ;
Hinojosa, M .
ALLERGY, 2001, 56 (10) :1017-1018
[4]  
Block SH, 2002, J ALLERGY CLIN IMMUN, V109, P373, DOI 10.1067/mai.2002.121531
[5]   The selective cyclooxygenase-2 inhibitor rofecoxib may improve the treatment of chronic idiopathic urticaria [J].
Boehncke, WH ;
Ludwig, RJ ;
Zollner, TM ;
Ochsendorf, F ;
Kaufmann, R ;
Gibbs, BF .
BRITISH JOURNAL OF DERMATOLOGY, 2003, 148 (03) :604-606
[6]   Comparison of upper gastrointestinal toxicity of rofecoxib and naproxen in patients with rheumatoid arthritis. [J].
Bombardier, C ;
Laine, L ;
Reicin, A ;
Shapiro, D ;
Burgos-Vargas, R ;
Davis, B ;
Day, R ;
Ferraz, MB ;
Hawkey, CJ ;
Hochberg, MC ;
Kvien, TK ;
Schnitzer, TJ ;
Weaver, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (21) :1520-1528
[7]   Aseptic meningitis associated with rofecoxib [J].
Bonnel, RA ;
Villalba, ML ;
Karwoski, CB ;
Beitz, J .
ARCHIVES OF INTERNAL MEDICINE, 2002, 162 (06) :713-715
[8]   Rofecoxib-induced instant aquagenic wrinkling of the palms [J].
Carder, KR ;
Weston, WL .
PEDIATRIC DERMATOLOGY, 2002, 19 (04) :353-355
[9]  
CHARANDEEP K, 2001, DERMATOLOGY, V203, P351
[10]   Urticaria and angioedema induced by COX-2 inhibitors [J].
Grimm, V ;
Rakoski, J ;
Ring, J .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 109 (02) :370-370