erdafitinib (Balversa)
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Indications
- treatment of advanced bladder cancer with an FGFR3 or FGFR2 aberration failing platinum-based chemotherapy
Dosage
- starting dose of 8 mg once daily
- increase to 9 mg daily if serum phosphate < 5.5 mg/dL, between days 14 & 17.
Tabs: 3 mg, 4 mg, 5 mg
Monitor
Adverse effects
- central serous retinopathy or retinal pigment epithelial detachment resulting in visual field defect (25%)[3]
- increased serum phosphate, increased serum creatinine
- increased serum ALT, increased serum alkaline phosphatase
- decreased serum sodium
- stomatitis, fatigue, diarrhea, dry mouth, onycholysis
Laboratory
Mechanism of action
- inhibits FGF receptor
More general terms
References
- ↑ PubChem: 67462786
- ↑ Wikipedia: Erdafitinib https://en.wikipedia.org/wiki/Erdafitinib
- ↑ 3.0 3.1 FDA News Release. April 12, 2019 FDA grants accelerated approval to erdafitinib for metastatic urothelial carcinoma. https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-accelerated-approval-erdafitinib-metastatic-urothelial-carcinoma