Does LEVODOPA Cause Device use issue? 443 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 443 reports of Device use issue have been filed in association with LEVODOPA (L-Dopa). This represents 6.7% of all adverse event reports for LEVODOPA.
443
Reports of Device use issue with LEVODOPA
6.7%
of all LEVODOPA reports
6
Deaths
18
Hospitalizations
How Dangerous Is Device use issue From LEVODOPA?
Of the 443 reports, 6 (1.4%) resulted in death, 18 (4.1%) required hospitalization.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVODOPA. However, 443 reports have been filed with the FAERS database.
What Other Side Effects Does LEVODOPA Cause?
Cough (2,142)
Drug ineffective (1,036)
Parkinson's disease (761)
Device issue (565)
Product residue present (534)
Device difficult to use (466)
Condition aggravated (463)
Dyskinesia (411)
Death (335)
Therapeutic product effect variable (298)
What Other Drugs Cause Device use issue?
SOMATROPIN (2,571)
LEVONORGESTREL (2,489)
COPPER (1,318)
BUDESONIDE\FORMOTEROL (1,236)
EXENATIDE (992)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
DUPILUMAB (528)
ALIROCUMAB (471)
INSULIN GLARGINE (469)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
Which LEVODOPA Alternatives Have Lower Device use issue Risk?
LEVODOPA vs LEVOFLOXACIN
LEVODOPA vs LEVOKETOCONAZOLE
LEVODOPA vs LEVOLEUCOVORIN
LEVODOPA vs LEVOMEPROMAZINE
LEVODOPA vs LEVOMETHADONE