Does CARBIDOPA\LEVODOPA Cause Device breakage? 634 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 634 reports of Device breakage have been filed in association with CARBIDOPA\LEVODOPA. This represents 1.1% of all adverse event reports for CARBIDOPA\LEVODOPA.
634
Reports of Device breakage with CARBIDOPA\LEVODOPA
1.1%
of all CARBIDOPA\LEVODOPA reports
43
Deaths
427
Hospitalizations
How Dangerous Is Device breakage From CARBIDOPA\LEVODOPA?
Of the 634 reports, 43 (6.8%) resulted in death, 427 (67.4%) required hospitalization, and 12 (1.9%) were considered life-threatening.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CARBIDOPA\LEVODOPA. However, 634 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 breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
INSULIN GLARGINE (237)
Which CARBIDOPA\LEVODOPA Alternatives Have Lower Device breakage Risk?
CARBIDOPA\LEVODOPA vs CARBIMAZOLE
CARBIDOPA\LEVODOPA vs CARBOCYSTEINE
CARBIDOPA\LEVODOPA vs CARBOMER
CARBIDOPA\LEVODOPA vs CARBON DIOXIDE
CARBIDOPA\LEVODOPA vs CARBON MONOXIDE