Archives of Medical Research
Volume 37, Issue 7 , Pages 899-902, October 2006

Epidemiology of Adverse Cutaneous Drug Reactions. A Prospective Study in Hospitalized Patients

  • Amparo Hernandez-Salazar

      Affiliations

    • Department of Dermatology Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City, Mexico
  • ,
  • Samuel Ponce de Leon-Rosales

      Affiliations

    • Subdivision of Hospital Epidemiology and Patient Care Quality Control Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City, Mexico
  • ,
  • Sigfrido Rangel-Frausto

      Affiliations

    • Pharmacy Department, Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City, Mexico
  • ,
  • Elia Criollo

      Affiliations

    • Pharmacy Department, Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City, Mexico
  • ,
  • Carla Archer-Dubon

      Affiliations

    • Department of Dermatology Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City, Mexico
  • ,
  • Rocio Orozco-Topete

      Affiliations

    • Department of Dermatology Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City, Mexico
    • Corresponding Author InformationAddress reprint requests to: Rocio Orozco-Topete, MD, Dermatology Department, Vasco de Quiroga 15, sección XVI, Tlalpan, 14000, México, D.F., México

Received 2 June 2005; accepted 20 March 2006.

(ARCMED-D-05-00211).

Background

Drug reactions are commonly present in the skin; however, their frequency in our setting is unknown.

Methods

A 10-month prospective cohort study including all hospitalized patients was designed. Those with adverse cutaneous drug reactions (ACDR) were clinically identified.

Results

Thirty five drug reactions (prevalence of 0.7%) were seen among 4785 (2713 females, 2072 males) discharged patients. According to Begaud's imputability criteria, the reactions were most likely attributed to a drug in 4.87%, likely in 41.46% and possible in 53.65%. The most commonly seen dermatoses were morbilliform rash 51.2%, urticaria 12.2% and erythema multiforme 4.9%. Drugs most frequently associated with ACDR were amoxicillin clavulanate (8), amphotericin B (2) and metamizole (4). Expressed as risk by 1000 day-doses (Dd: the risk a patient has of developing an ACDR after receiving 1 day of treatment with the drug): amoxicillin clavulanate Dd 7.7, amphotericin B Dd 4.8 and metamizole Dd 3.7. Immunosuppressed patients were most frequently affected. Notably, patients with systemic lupus erythematosus (SLE) had a 4.68 higher risk (CI 95% 1.794–12.186 p <0.001) of developing an ACDR. AIDS patients showed a risk of 8.68 (CI 95% 2.18–33.19 p <0.001). Non-Hodgkin's lymphoma patients also had an increased risk of developing an ACDR. Six of the 35 identified cases were patients who had been hospitalized due to a severe drug reaction (1.3/1000 patients); one died from complications directly related to the ACDR, representing a 16.6% mortality rate among those admitted for an ACDR and 0.02% among the global mortality.

Conclusions

We have a low prevalence of drug reactions compared to data reported in the literature. Pharmacovigilance with special attention to immunosuppressed SLE or AIDS patients is stressed.

Key Words: Drugs, Prevalence, Adverse effects

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PII: S0188-4409(06)00168-8

doi:10.1016/j.arcmed.2006.03.010

Archives of Medical Research
Volume 37, Issue 7 , Pages 899-902, October 2006