Does FOSCARBIDOPA\FOSLEVODOPA Cause Device use error? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Device use error have been filed in association with FOSCARBIDOPA\FOSLEVODOPA. This represents 0.5% of all adverse event reports for FOSCARBIDOPA\FOSLEVODOPA.
15
Reports of Device use error with FOSCARBIDOPA\FOSLEVODOPA
0.5%
of all FOSCARBIDOPA\FOSLEVODOPA reports
0
Deaths
13
Hospitalizations
How Dangerous Is Device use error From FOSCARBIDOPA\FOSLEVODOPA?
Of the 15 reports, 13 (86.7%) required hospitalization.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FOSCARBIDOPA\FOSLEVODOPA. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does FOSCARBIDOPA\FOSLEVODOPA Cause?
On and off phenomenon (391)
Fall (343)
Hallucination (293)
Dyskinesia (237)
Death (203)
General physical health deterioration (173)
Infusion site erythema (157)
Mobility decreased (154)
Infusion site pain (143)
Malaise (139)
What Other Drugs Cause Device use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
Which FOSCARBIDOPA\FOSLEVODOPA Alternatives Have Lower Device use error Risk?
FOSCARBIDOPA\FOSLEVODOPA vs FOSCARNET
FOSCARBIDOPA\FOSLEVODOPA vs FOSFOMYCIN
FOSCARBIDOPA\FOSLEVODOPA vs FOSFOMYCIN TROMETHAMINE
FOSCARBIDOPA\FOSLEVODOPA vs FOSINOPRIL
FOSCARBIDOPA\FOSLEVODOPA vs FOSPHENYTOIN