Does CARBIDOPA\LEVODOPA Cause Device dislocation? 2,937 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,937 reports of Device dislocation have been filed in association with CARBIDOPA\LEVODOPA. This represents 5.0% of all adverse event reports for CARBIDOPA\LEVODOPA.
2,937
Reports of Device dislocation with CARBIDOPA\LEVODOPA
5.0%
of all CARBIDOPA\LEVODOPA reports
246
Deaths
2,054
Hospitalizations
How Dangerous Is Device dislocation From CARBIDOPA\LEVODOPA?
Of the 2,937 reports, 246 (8.4%) resulted in death, 2,054 (69.9%) required hospitalization, and 50 (1.7%) were considered life-threatening.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CARBIDOPA\LEVODOPA. However, 2,937 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)
Weight decreased (2,772)
What Other Drugs Cause Device dislocation?
LEVONORGESTREL (13,757)
COPPER (6,955)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
DEXAMETHASONE (290)
Which CARBIDOPA\LEVODOPA Alternatives Have Lower Device dislocation Risk?
CARBIDOPA\LEVODOPA vs CARBIMAZOLE
CARBIDOPA\LEVODOPA vs CARBOCYSTEINE
CARBIDOPA\LEVODOPA vs CARBOMER
CARBIDOPA\LEVODOPA vs CARBON DIOXIDE
CARBIDOPA\LEVODOPA vs CARBON MONOXIDE