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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 Contraindicated product administered? 60 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 60 reports of Contraindicated product administered have been filed in association with SPARSENTAN (FILSPARI). This represents 1.8% of all adverse event reports for SPARSENTAN.

60
Reports of Contraindicated product administered with SPARSENTAN
1.8%
of all SPARSENTAN reports
0
Deaths
7
Hospitalizations

How Dangerous Is Contraindicated product administered From SPARSENTAN?

Of the 60 reports, 7 (11.7%) required hospitalization.

Is Contraindicated product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SPARSENTAN. However, 60 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 Contraindicated product administered?

ABATACEPT (13,559) METHOTREXATE (13,121) ETANERCEPT (12,062) TOCILIZUMAB (11,547) ADALIMUMAB (11,270) LEFLUNOMIDE (11,206) HYDROXYCHLOROQUINE (10,557) RITUXIMAB (10,479) INFLIXIMAB (9,618) SULFASALAZINE (8,698)

Which SPARSENTAN Alternatives Have Lower Contraindicated product administered Risk?

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

Related Pages

SPARSENTAN Full Profile All Contraindicated product administered Reports All Drugs Causing Contraindicated product administered SPARSENTAN Demographics