AI Article Synopsis

  • The study investigates the safety of etoricoxib, a cyclooxygenase-2 inhibitor, for patients who have adverse reactions to traditional NSAIDs.
  • A trial with 37 NSAID-sensitive patients revealed that 34 tolerated etoricoxib without issues, while 3 (8%) experienced a generalized urticarial rash.
  • The findings suggest that etoricoxib is generally well-tolerated in these patients, but recommend conducting a preliminary challenge test in a controlled setting before prescribing the medication.

Article Abstract

Background: The use of cyclooxygenase-2 inhibitors, a new class of analgesic drugs, is suggested in patients with hypersensitivity to nonsteroidal anti-inflammatory drugs (NSAIDs).

Objective: To evaluate tolerance to etoricoxib, a new cyclooxygenase-2 inhibitor, in NSAID-sensitive patients with urticaria-type adverse reactions.

Patients: Thirty-seven patients with adverse reactions to NSAIDs.

Methods: Single-blind, placebo-controlled oral challenge with increasing doses of etoricoxib.

Results: Thirty-four patients tolerated etoricoxib treatment without adverse reactions, but a generalized urticarial rash developed in 3 patients (8%).

Conclusions: Etoricoxib, like other cyclooxygenase-2 inhibitors, is a well-tolerated drug in most NSAID-sensitive patients. However, according to our experience, a previous challenge test in a safe environment may be necessary before prescribing the drug to such patients.

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http://dx.doi.org/10.1016/S1081-1206(10)60691-6DOI Listing

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Etoricoxib is a non-steroidal anti-inflammatory drug with high selectivity for cyclooxygenase 2 (COX-2), exerting a pronounced anti-inflammatory effect with fewer adverse events when compared to COX-1 inhibitors. The present study aimed to evaluate the bioequivalence between two etoricoxib-coated tablet formulations to meet regulatory requirements for a branded generic product registration in Brazil. A crossover study with an open-label, randomized design and a single-dose regimen with two treatments and two periods was conducted on healthy Brazilians of both genders.

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