Does FOSCARBIDOPA\FOSLEVODOPA Cause Device power source issue? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Device power source issue have been filed in association with FOSCARBIDOPA\FOSLEVODOPA. This represents 0.4% of all adverse event reports for FOSCARBIDOPA\FOSLEVODOPA.
14
Reports of Device power source issue with FOSCARBIDOPA\FOSLEVODOPA
0.4%
of all FOSCARBIDOPA\FOSLEVODOPA reports
0
Deaths
9
Hospitalizations
How Dangerous Is Device power source issue From FOSCARBIDOPA\FOSLEVODOPA?
Of the 14 reports, 9 (64.3%) required hospitalization.
Is Device power source issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FOSCARBIDOPA\FOSLEVODOPA. However, 14 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 power source issue?
SOMATROPIN (1,219)
PEGFILGRASTIM (486)
TREPROSTINIL (299)
CARBIDOPA\LEVODOPA (62)
ETANERCEPT (54)
BACLOFEN (50)
GLYCOPYRROLATE (39)
DEVICE (20)
INTERFERON BETA-1B (13)
LECITHIN\POLOXAMER 407 (11)
Which FOSCARBIDOPA\FOSLEVODOPA Alternatives Have Lower Device power source issue Risk?
FOSCARBIDOPA\FOSLEVODOPA vs FOSCARNET
FOSCARBIDOPA\FOSLEVODOPA vs FOSFOMYCIN
FOSCARBIDOPA\FOSLEVODOPA vs FOSFOMYCIN TROMETHAMINE
FOSCARBIDOPA\FOSLEVODOPA vs FOSINOPRIL
FOSCARBIDOPA\FOSLEVODOPA vs FOSPHENYTOIN