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Probable fenofibrate-induced acute generalized exanthematous pustulosis
Anna E Power1, Linda V Graudins1, Catriona A McLean1
1Anna E. Power is a medical student, Monash University, Melbourne, Australia, and Summer Vacation Scholar, Centre of Cardiovascular Research & Education (CCRE) in Therapeutics, School of Public Health and Preventive Medicine, Alfred Centre, Melbourne. Linda V. Graudins, B.Pharm., Dip.HospPharm., PGrad.Clinepid., FSHP, is Senior Pharmacist, Pharmacy Department, Alfred Health, Melbourne. Catriona A. McLean, B.Sc., M.B.B.S., FRACPA, M.D., FFSc, is Pathologist, Department of Anatomical Pathology, Alfred Hospital, Melbourne. Ingrid Hopper, M.B.B.S., B.Med.SC., FRACP, is Clinical Pharmacologist, Alfred Health, and National Health and Medical Research Council Postgraduate Scholar, CCRE in Therapeutics, School of Public Health and Preventive Medicine, Alfred Centre.
A woman with type 1 diabetes developed a severe skin reaction, acute generalized exanthematous pustulosis (AGEP), after a single dose of fenofibrate. This case highlights a rare but serious adverse drug reaction potentially linked to fenofibrate.
Area of Science:
- Pharmacology
- Dermatology
- Toxicology
Background:
- Fenofibrate is a commonly prescribed lipid-lowering agent.
- Adverse drug reactions (ADRs) can range from mild to life-threatening.
- Acute Generalized Exanthematous Pustulosis (AGEP) is a severe cutaneous adverse reaction typically drug-induced.
Observation:
- A 58-year-old woman with type 1 diabetes presented with a severe blistering rash, fever, hypotension, and elevated liver enzymes.
- Symptoms began four hours after the first dose of fenofibrate (145 mg).
- Histopathology confirmed AGEP, a condition not commonly associated with fenofibrate.
Findings:
- The patient required intensive care, including vasopressor support and broad-spectrum antibiotics.
- Discontinuation of fenofibrate and treatment with topical steroids led to gradual resolution of AGEP.
- Naranjo scale analysis indicated a probable association between fenofibrate and AGEP development.
Implications:
- This case expands the known spectrum of fenofibrate-induced adverse drug reactions.
- Highlights the importance of considering rare ADRs even with common medications.
- Emphasizes prompt recognition and management of severe cutaneous reactions to medications.
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