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Drug-induced Sweet's syndrome: A case/non-case study in the French pharmacovigilance database.
Martin, Salomé; Trenque, Thierry; Herlem, Emmanuelle; Boulay, Charlène; Pizzoglio, Véronique; Azzouz, Brahim.
Afiliación
  • Martin S; Regional Centre of Pharmacovigilance and Pharmacoepidemiology, Reims University Hospital, 51100, Reims, France.
  • Trenque T; Regional Centre of Pharmacovigilance and Pharmacoepidemiology, Reims University Hospital, 51100, Reims, France.
  • Herlem E; Regional Centre of Pharmacovigilance and Pharmacoepidemiology, Reims University Hospital, 51100, Reims, France.
  • Boulay C; Regional Centre of Pharmacovigilance and Pharmacoepidemiology, Rouen University Hospital, 76000, Rouen, France.
  • Pizzoglio V; Regional Centre of Pharmacovigilance and Pharmacoepidemiology, Lyon University Hospital, 69495, Lyon, France.
  • Azzouz B; Regional Centre of Pharmacovigilance and Pharmacoepidemiology, Reims University Hospital, 51100, Reims, France.
Br J Clin Pharmacol ; 2023 Aug 09.
Article en En | MEDLINE | ID: mdl-37555568
AIMS: Sweet's syndrome is an acute febrile neutrophilic dermatosis first described in 1964 by Robert Douglas Sweet. The pathophysiological mechanism is not fully established; however, several cases of Sweet's syndrome have been reported following drug administration. METHODS: To investigate the existence of pharmacovigilance signals between drugs and the occurrence of Sweet's syndrome, we performed a case/non-case study on reports of 'acute febrile neutrophilic dermatosis' registered in the French pharmacovigilance database. Reporting odds ratio (ROR) with its 95% confidence interval were calculated. RESULTS: Amongthe 994 789 reports recorded in the database, 136 were Sweet's syndrome, of which 50.7% were men and the median age was 59 years (range 15-91). A total of 224 drugs were mentioned as suspects: 21.0% were antibacterials, 19.2% were antineoplastics and 12.1% were immunosuppressants. Median time to onset from drug initiation to the development of Sweet's syndrome was 15 days (range 1-1095). The highest RORs were observed with bortezomib (74.04 [40.8-134.2]), azacitidine (72.14 [29.4-176.9]), perfilgrastim (67.05 [21.2-211.6]), azathioprine (55.46 [34.8-88.4]) and bendamustine (35.84 [11.4-112.8]). CONCLUSIONS: Pharmacovigilance signals have been observed between the occurrence of Sweet's syndrome and colony-stimulating factors, immunosuppressants, antineoplastics and antibiotics. Clinicians should be aware of the potential associations with these drugs and should be encouraged to report any case of drug-induced Sweet's syndrome.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Br J Clin Pharmacol Año: 2023 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Br J Clin Pharmacol Año: 2023 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido