Does SPARSENTAN Cause Product availability issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product availability issue have been filed in association with SPARSENTAN (FILSPARI). This represents 0.2% of all adverse event reports for SPARSENTAN.
7
Reports of Product availability issue with SPARSENTAN
0.2%
of all SPARSENTAN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product availability issue From SPARSENTAN?
Of the 7 reports.
Is Product availability issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SPARSENTAN. However, 7 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 Product availability issue?
RUXOLITINIB (2,142)
LISDEXAMFETAMINE DIMESYLATE (1,530)
CERTOLIZUMAB PEGOL (1,381)
VEDOLIZUMAB (636)
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (610)
METHYLPHENIDATE (444)
SECUKINUMAB (399)
BIMEKIZUMAB-BKZX (364)
LACOSAMIDE (359)
BRIVARACETAM (324)
Which SPARSENTAN Alternatives Have Lower Product availability issue Risk?
SPARSENTAN vs SPESOLIMAB-SBZO
SPARSENTAN vs SPIRAMYCIN
SPARSENTAN vs SPIRIVA
SPARSENTAN vs SPIRONOLACTONE
SPARSENTAN vs SPRYCEL