Does LEVODOPA Cause Product storage error? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Product storage error have been filed in association with LEVODOPA (L-Dopa). This represents 0.4% of all adverse event reports for LEVODOPA.
28
Reports of Product storage error with LEVODOPA
0.4%
of all LEVODOPA reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product storage error From LEVODOPA?
Of the 28 reports.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVODOPA. However, 28 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which LEVODOPA Alternatives Have Lower Product storage error Risk?
LEVODOPA vs LEVOFLOXACIN
LEVODOPA vs LEVOKETOCONAZOLE
LEVODOPA vs LEVOLEUCOVORIN
LEVODOPA vs LEVOMEPROMAZINE
LEVODOPA vs LEVOMETHADONE