Does BENSERAZIDE\LEVODOPA Cause Device issue? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Device issue have been filed in association with BENSERAZIDE\LEVODOPA. This represents 0.9% of all adverse event reports for BENSERAZIDE\LEVODOPA.
18
Reports of Device issue with BENSERAZIDE\LEVODOPA
0.9%
of all BENSERAZIDE\LEVODOPA reports
1
Deaths
17
Hospitalizations
How Dangerous Is Device issue From BENSERAZIDE\LEVODOPA?
Of the 18 reports, 1 (5.6%) resulted in death, 17 (94.4%) required hospitalization, and 4 (22.2%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BENSERAZIDE\LEVODOPA. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does BENSERAZIDE\LEVODOPA Cause?
Fall (282)
Dizziness (151)
Hallucination (136)
Dyskinesia (127)
General physical health deterioration (127)
Parkinson's disease (126)
Drug ineffective (119)
Confusional state (117)
Off label use (112)
Somnolence (110)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which BENSERAZIDE\LEVODOPA Alternatives Have Lower Device issue Risk?
BENSERAZIDE\LEVODOPA vs BENZALKONIUM
BENSERAZIDE\LEVODOPA vs BENZOCAINE
BENSERAZIDE\LEVODOPA vs BENZODIAZEPINE
BENSERAZIDE\LEVODOPA vs BENZONATATE
BENSERAZIDE\LEVODOPA vs BENZOYL PEROXIDE