Does FOSCARBIDOPA\FOSLEVODOPA Cause Device issue? 124 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 124 reports of Device issue have been filed in association with FOSCARBIDOPA\FOSLEVODOPA. This represents 3.9% of all adverse event reports for FOSCARBIDOPA\FOSLEVODOPA.
124
Reports of Device issue with FOSCARBIDOPA\FOSLEVODOPA
3.9%
of all FOSCARBIDOPA\FOSLEVODOPA reports
5
Deaths
76
Hospitalizations
How Dangerous Is Device issue From FOSCARBIDOPA\FOSLEVODOPA?
Of the 124 reports, 5 (4.0%) resulted in death, 76 (61.3%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FOSCARBIDOPA\FOSLEVODOPA. However, 124 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which FOSCARBIDOPA\FOSLEVODOPA Alternatives Have Lower Device issue Risk?
FOSCARBIDOPA\FOSLEVODOPA vs FOSCARNET
FOSCARBIDOPA\FOSLEVODOPA vs FOSFOMYCIN
FOSCARBIDOPA\FOSLEVODOPA vs FOSFOMYCIN TROMETHAMINE
FOSCARBIDOPA\FOSLEVODOPA vs FOSINOPRIL
FOSCARBIDOPA\FOSLEVODOPA vs FOSPHENYTOIN