Does CARBIDOPA\LEVODOPA Cause Complication associated with device? 169 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 169 reports of Complication associated with device have been filed in association with CARBIDOPA\LEVODOPA. This represents 0.3% of all adverse event reports for CARBIDOPA\LEVODOPA.
169
Reports of Complication associated with device with CARBIDOPA\LEVODOPA
0.3%
of all CARBIDOPA\LEVODOPA reports
14
Deaths
113
Hospitalizations
How Dangerous Is Complication associated with device From CARBIDOPA\LEVODOPA?
Of the 169 reports, 14 (8.3%) resulted in death, 113 (66.9%) required hospitalization, and 7 (4.1%) were considered life-threatening.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CARBIDOPA\LEVODOPA. However, 169 reports have been filed with the FAERS database.
What Other Side Effects Does CARBIDOPA\LEVODOPA Cause?
Fall (7,132)
Death (5,403)
Dyskinesia (5,368)
Tremor (3,689)
General physical health deterioration (3,636)
On and off phenomenon (3,509)
Hallucination (3,367)
Drug ineffective (3,205)
Parkinson's disease (3,140)
Device dislocation (2,937)
What Other Drugs Cause Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
MACITENTAN (169)
TEDUGLUTIDE (133)
AMBRISENTAN (125)
Which CARBIDOPA\LEVODOPA Alternatives Have Lower Complication associated with device Risk?
CARBIDOPA\LEVODOPA vs CARBIMAZOLE
CARBIDOPA\LEVODOPA vs CARBOCYSTEINE
CARBIDOPA\LEVODOPA vs CARBOMER
CARBIDOPA\LEVODOPA vs CARBON DIOXIDE
CARBIDOPA\LEVODOPA vs CARBON MONOXIDE