Does LEVODOPA Cause Product prescribing error? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product prescribing error have been filed in association with LEVODOPA (L-Dopa). This represents 0.2% of all adverse event reports for LEVODOPA.
16
Reports of Product prescribing error with LEVODOPA
0.2%
of all LEVODOPA reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product prescribing error From LEVODOPA?
Of the 16 reports, 1 (6.3%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVODOPA. However, 16 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)
Device use issue (443)
Dyskinesia (411)
Death (335)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which LEVODOPA Alternatives Have Lower Product prescribing error Risk?
LEVODOPA vs LEVOFLOXACIN
LEVODOPA vs LEVOKETOCONAZOLE
LEVODOPA vs LEVOLEUCOVORIN
LEVODOPA vs LEVOMEPROMAZINE
LEVODOPA vs LEVOMETHADONE