Does CARBIDOPA\LEVODOPA Cause Device leakage? 627 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 627 reports of Device leakage have been filed in association with CARBIDOPA\LEVODOPA. This represents 1.1% of all adverse event reports for CARBIDOPA\LEVODOPA.
627
Reports of Device leakage with CARBIDOPA\LEVODOPA
1.1%
of all CARBIDOPA\LEVODOPA reports
37
Deaths
370
Hospitalizations
How Dangerous Is Device leakage From CARBIDOPA\LEVODOPA?
Of the 627 reports, 37 (5.9%) resulted in death, 370 (59.0%) required hospitalization, and 14 (2.2%) were considered life-threatening.
Is Device leakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CARBIDOPA\LEVODOPA. However, 627 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 leakage?
SOMATROPIN (9,113)
LEUPROLIDE (5,861)
EXENATIDE (5,115)
PEGFILGRASTIM (1,380)
ALBIGLUTIDE (1,195)
SECUKINUMAB (910)
RISPERIDONE (878)
TREPROSTINIL (874)
DEVICE (795)
GUSELKUMAB (712)
Which CARBIDOPA\LEVODOPA Alternatives Have Lower Device leakage Risk?
CARBIDOPA\LEVODOPA vs CARBIMAZOLE
CARBIDOPA\LEVODOPA vs CARBOCYSTEINE
CARBIDOPA\LEVODOPA vs CARBOMER
CARBIDOPA\LEVODOPA vs CARBON DIOXIDE
CARBIDOPA\LEVODOPA vs CARBON MONOXIDE