Does LEVODOPA Cause Product dose omission? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product dose omission have been filed in association with LEVODOPA (L-Dopa). This represents 0.1% of all adverse event reports for LEVODOPA.
7
Reports of Product dose omission with LEVODOPA
0.1%
of all LEVODOPA reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission From LEVODOPA?
Of the 7 reports.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVODOPA. However, 7 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which LEVODOPA Alternatives Have Lower Product dose omission Risk?
LEVODOPA vs LEVOFLOXACIN
LEVODOPA vs LEVOKETOCONAZOLE
LEVODOPA vs LEVOLEUCOVORIN
LEVODOPA vs LEVOMEPROMAZINE
LEVODOPA vs LEVOMETHADONE