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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ERDAFITINIB Cause Hyperphosphataemia? 39 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of Hyperphosphataemia have been filed in association with ERDAFITINIB (BALVERSA). This represents 3.5% of all adverse event reports for ERDAFITINIB.

39
Reports of Hyperphosphataemia with ERDAFITINIB
3.5%
of all ERDAFITINIB reports
4
Deaths
11
Hospitalizations

How Dangerous Is Hyperphosphataemia From ERDAFITINIB?

Of the 39 reports, 4 (10.3%) resulted in death, 11 (28.2%) required hospitalization, and 1 (2.6%) were considered life-threatening.

Is Hyperphosphataemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ERDAFITINIB. However, 39 reports have been filed with the FAERS database.

What Other Side Effects Does ERDAFITINIB Cause?

Death (255) Off label use (86) Diarrhoea (75) Stomatitis (58) Fatigue (45) Onycholysis (44) Disease progression (41) Dry mouth (41) Nail disorder (40) Dry eye (38)

What Other Drugs Cause Hyperphosphataemia?

ALLOPURINOL (139) LANSOPRAZOLE (138) ACETAMINOPHEN (132) SEVELAMER (129) ONDANSETRON (127) CALCITRIOL (125) IPRATROPIUM (123) ALBUTEROL (122) METRONIDAZOLE (120) HYDROMORPHONE (118)

Which ERDAFITINIB Alternatives Have Lower Hyperphosphataemia Risk?

ERDAFITINIB vs ERENUMAB ERDAFITINIB vs ERENUMAB-AOOE ERDAFITINIB vs ERENUMAB\ERENUMAB-AOOE ERDAFITINIB vs ERGOCALCIFEROL ERDAFITINIB vs ERGOCALCIFEROL\PHYTONADIONE\RETINOL\TOCOPHEROL

Related Pages

ERDAFITINIB Full Profile All Hyperphosphataemia Reports All Drugs Causing Hyperphosphataemia ERDAFITINIB Demographics