Table 1.
Characteristics of the DRESS syndrome case | Total sample (n = 1534) |
---|---|
Age (years), median (Q1–Q3) | 41.0 (29.0–54.0) |
Sex (females), n (%) | 642 (41.9) |
BMI (kg/m2), median (Q1–Q3) | 23.9 (21.3–28.4) |
Dose (PDD/DDD), median (Q1–Q3) | 0.7 (0.2–1.3) |
AP treatment duration (days), median (Q1–Q3) | 22.0 (12.0–52.0) |
DRESS symptoms duration (days), median (Q1–Q3) | 11.0 (5.0–25.0) |
Lethal, n (%) | 164 (10.7) |
More than one AP, n (%) | 670 (43.7) |
Administration route, n (%) | |
Oral | 998 (65.1) |
Unknown | 177 (11.5) |
Intramuscular | 29 (1.9) |
Intravenous | 12 (0.8) |
Other | 17 (1.1) |
Reported co-medication with DRESS-related potential, n (%) | |
Anticonvulsants | 547 (35.7) |
Antibiotics | 91 (5.9) |
Miscellaneous | 53 (3.5) |
Country, n (%) | |
United States | 391 (25.5) |
United Kingdom | 214 (14.0) |
Germany | 148 (9.6) |
France | 143 (9.3) |
Australia | 138 (9.0) |
Japan | 92 (6.0) |
Canada | 91 (5.9) |
Other (40 countries) | 261 (17) |
Reporter, n (%) | |
Physician | 698 (45.5) |
Other health professional | 170 (11.1) |
Pharmacist | 132 (8.6) |
Consumer/non-health professional | 39 (2.5) |
Lawyer | 6 (0.4) |
AP antipsychotic, BMI body mass index, DDD defined daily dose, DRESS drug reaction with eosinophilia and systemic symptoms, PDD prescribed daily dose, Q1 first quartile, Q3 third quartile