Does SPARSENTAN Cause Ill-defined disorder? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Ill-defined disorder have been filed in association with SPARSENTAN (FILSPARI). This represents 0.2% of all adverse event reports for SPARSENTAN.
8
Reports of Ill-defined disorder with SPARSENTAN
0.2%
of all SPARSENTAN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Ill-defined disorder From SPARSENTAN?
Of the 8 reports, 2 (25.0%) required hospitalization.
Is Ill-defined disorder Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SPARSENTAN. However, 8 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 Ill-defined disorder?
ACETAMINOPHEN\OXYCODONE (9,780)
ACETAMINOPHEN\HYDROCODONE (6,159)
TOCILIZUMAB (4,411)
RITUXIMAB (4,220)
ETANERCEPT (4,202)
METHOTREXATE (4,063)
ABATACEPT (3,630)
LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN (3,600)
LEFLUNOMIDE (3,570)
CERTOLIZUMAB PEGOL (3,273)
Which SPARSENTAN Alternatives Have Lower Ill-defined disorder Risk?
SPARSENTAN vs SPESOLIMAB-SBZO
SPARSENTAN vs SPIRAMYCIN
SPARSENTAN vs SPIRIVA
SPARSENTAN vs SPIRONOLACTONE
SPARSENTAN vs SPRYCEL