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Gastric ulcer in a child treated with deferasirox
Tiene Bauters1, Veerle Mondelaers, Hugo Robays
1Department of Pharmacy, Ghent University Hospital, De Pintelaan 185, 9000, Ghent, Belgium. tiene.bauters@uzgent.be
Insights
Deferasirox, a medication for thalassemia major, may cause gastric ulcers, an infrequent but severe adverse event. This case report highlights a potential risk associated with deferasirox treatment in patients with thalassemia.
Area of Science:
- Gastroenterology
- Hematology
- Pharmacology
Background:
- Thalassemia major is a severe inherited blood disorder requiring lifelong treatment.
- Deferasirox is a widely used iron chelator for managing iron overload in thalassemia patients.
- Iron overload in thalassemia can lead to various complications, necessitating effective chelation therapy.
Observation:
- A patient with thalassemia major developed a gastric ulcer during treatment with deferasirox.
- The gastric ulcer was suspected to be an adverse drug reaction to deferasirox.
- While gastric ulcers are listed as infrequent, this case emphasizes their potential severity.
Findings:
- This report details the first known case of a gastric ulcer attributed to deferasirox in a thalassemia major patient.
- The adverse event highlights a potentially underreported complication of deferasirox therapy.
- The severity of the gastric ulcer necessitated reporting this specific adverse drug reaction.
Implications:
- Clinicians should be vigilant for gastrointestinal adverse events, including gastric ulcers, in patients treated with deferasirox.
- This case may prompt further investigation into the gastrointestinal safety profile of deferasirox.
- Enhanced monitoring and patient counseling regarding potential deferasirox side effects are warranted.
Abstract:
We present a patient with thalassemia major who developed a gastric ulcer, probably related to the use of deferasirox. Although gastric ulcer is mentioned as infrequent adverse event in the scientific product information of deferasirox, in our current knowledge, this is the first case-report on this adverse drug reaction. The severity of this event justifies the reporting of this case.
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