Photosensitivity From Avapritinib: Pharamacovigilance Analysis
- PMID: 39475689
- PMCID: PMC10334909
- DOI: 10.2196/39229
Photosensitivity From Avapritinib: Pharamacovigilance Analysis
Abstract
Certain protein kinase inhibitors have been reported to cause photosensitivity. Avapritinib is a tyrosine kinase inhibitor that was approved in January 2020. The aim of this analysis was to determine if a statistically significant signal exists between Avapritinib and photosensitivity in the real-world population. A disproportionality analysis was conducted using the Food and Drug Administration Adverse Event Reporting System (FAERS) from January 1, 2020, to December 31, 2021. A literature review was also performed to identify case reports of Avapritinib-induced photosensitivity. A total of 13 adverse event reports with Avapritinib as the drug and photosensitivity as the reaction were identified in FAERS. Avapritinib was the suspect drug in all 13 reports, and in 12 of the 13 reports, Avapritinib was the only drug listed. Disproportionality analysis found a proportional reporting ratio of 11.0, χ21=107, reporting odds ratio of 11.0, and a lower limit of the 95% CI of the information component of 2.1. The literature review found 1 case report of Avapritinib-induced photosensitivity in a patient who had been taking Avapritinib 300 mg daily for 5 months. A statistically significant signal was found between Avapritinib use and photosensitivity. Clinicians should continue to balance the benefits and risks when prescribing Avapritinib to patients.
Keywords: Avapritinib; adverse event; adverse reaction; cancer; drug-induced; light; oncology; pharmaceutical; pharmacology; pharmacovigilance; photosensitive; photosensitivity; photosensitizer; photosensitizing; side effect; tumor.
©Ajit Venkatakrishnan, Brandon Chu, Pushkar Aggarwal. Originally published in JMIR Dermatology (http://derma.jmir.org), 10.08.2022.
Conflict of interest statement
Conflicts of Interest: None declared.
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References
-
- Juzeniene A, Moan J. Beneficial effects of UV radiation other than via vitamin D production. Dermatoendocrinol. 2012 Apr 01;4(2):109–17. doi: 10.4161/derm.20013. http://europepmc.org/abstract/MED/22928066 2012DE0169R - DOI - PMC - PubMed
-
- Ciccolini KT, Kim J, Chaudhari SP, Lucas AS, Benhuri B, Duran J, Wu S, Lacouture ME. Incidence and risk of developing photosensitivity with targeted anticancer therapies. J Am Acad Dermatol. 2019 Oct;81(4):1009–1011. doi: 10.1016/j.jaad.2019.01.077. http://europepmc.org/abstract/MED/30731178 S0190-9622(19)30188-4 - DOI - PMC - PubMed
-
- July - September 2021 | Potential signals of serious risks/new safety information identified by the FDA Adverse Event Reporting System (FAERS) US Food and Drug Administration. 2022. [2022-07-28]. https://tinyurl.com/34cazd5k .
-
- FDA Adverse Event Reporting System (FAERS) public dashboard. US Food and Drug Administration. [2022-07-28]. https://tinyurl.com/yh22mc2c .
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