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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 SPARSENTAN Cause Blood uric acid increased? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Blood uric acid increased have been filed in association with SPARSENTAN (FILSPARI). This represents 0.3% of all adverse event reports for SPARSENTAN.

9
Reports of Blood uric acid increased with SPARSENTAN
0.3%
of all SPARSENTAN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Blood uric acid increased From SPARSENTAN?

Of the 9 reports.

Is Blood uric acid increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SPARSENTAN. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does SPARSENTAN Cause?

Dizziness (521) Fatigue (448) Hypotension (377) Product use in unapproved indication (262) Nausea (231) Peripheral swelling (197) Headache (186) Pruritus (171) Blood creatinine increased (145) Glomerular filtration rate decreased (141)

What Other Drugs Cause Blood uric acid increased?

PEGLOTICASE (359) ALLOPURINOL (194) ALBUTEROL (170) LANSOPRAZOLE (144) RUXOLITINIB (143) WARFARIN (143) ACETAMINOPHEN (137) SIMVASTATIN (137) GABAPENTIN (136) CALCITRIOL (135)

Which SPARSENTAN Alternatives Have Lower Blood uric acid increased Risk?

SPARSENTAN vs SPESOLIMAB-SBZO SPARSENTAN vs SPIRAMYCIN SPARSENTAN vs SPIRIVA SPARSENTAN vs SPIRONOLACTONE SPARSENTAN vs SPRYCEL

Related Pages

SPARSENTAN Full Profile All Blood uric acid increased Reports All Drugs Causing Blood uric acid increased SPARSENTAN Demographics