Does SPARSENTAN Cause Intentional dose omission? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Intentional dose omission have been filed in association with SPARSENTAN (FILSPARI). This represents 0.3% of all adverse event reports for SPARSENTAN.
10
Reports of Intentional dose omission with SPARSENTAN
0.3%
of all SPARSENTAN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intentional dose omission From SPARSENTAN?
Of the 10 reports.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SPARSENTAN. However, 10 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 Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which SPARSENTAN Alternatives Have Lower Intentional dose omission Risk?
SPARSENTAN vs SPESOLIMAB-SBZO
SPARSENTAN vs SPIRAMYCIN
SPARSENTAN vs SPIRIVA
SPARSENTAN vs SPIRONOLACTONE
SPARSENTAN vs SPRYCEL