Does CARBIDOPA\LEVODOPA Cause Device material issue? 68 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Device material issue have been filed in association with CARBIDOPA\LEVODOPA. This represents 0.1% of all adverse event reports for CARBIDOPA\LEVODOPA.
68
Reports of Device material issue with CARBIDOPA\LEVODOPA
0.1%
of all CARBIDOPA\LEVODOPA reports
8
Deaths
34
Hospitalizations
How Dangerous Is Device material issue From CARBIDOPA\LEVODOPA?
Of the 68 reports, 8 (11.8%) resulted in death, 34 (50.0%) required hospitalization.
Is Device material issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CARBIDOPA\LEVODOPA. However, 68 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 Device material issue?
COPPER (603)
SOMATROPIN (472)
ADALIMUMAB (62)
ESTRADIOL (51)
PEGFILGRASTIM (33)
ESTRADIOL\LEVONORGESTREL (24)
ABATACEPT (14)
LEVONORGESTREL (13)
BACLOFEN (11)
METHOTREXATE (9)
Which CARBIDOPA\LEVODOPA Alternatives Have Lower Device material issue Risk?
CARBIDOPA\LEVODOPA vs CARBIMAZOLE
CARBIDOPA\LEVODOPA vs CARBOCYSTEINE
CARBIDOPA\LEVODOPA vs CARBOMER
CARBIDOPA\LEVODOPA vs CARBON DIOXIDE
CARBIDOPA\LEVODOPA vs CARBON MONOXIDE