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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 Product distribution issue? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product distribution issue have been filed in association with SPARSENTAN (FILSPARI). This represents 0.2% of all adverse event reports for SPARSENTAN.

6
Reports of Product distribution issue with SPARSENTAN
0.2%
of all SPARSENTAN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product distribution issue From SPARSENTAN?

Of the 6 reports.

Is Product distribution issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SPARSENTAN. However, 6 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 distribution issue?

LENALIDOMIDE (858) CERTOLIZUMAB PEGOL (403) SECUKINUMAB (340) RUXOLITINIB (301) HUMAN IMMUNOGLOBULIN G (279) POMALIDOMIDE (254) RELUGOLIX (243) VEDOLIZUMAB (150) PIMAVANSERIN (134) TEDUGLUTIDE (132)

Which SPARSENTAN Alternatives Have Lower Product distribution issue Risk?

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

Related Pages

SPARSENTAN Full Profile All Product distribution issue Reports All Drugs Causing Product distribution issue SPARSENTAN Demographics