Does LEVODOPA Cause Wrong technique in product usage process? 196 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 196 reports of Wrong technique in product usage process have been filed in association with LEVODOPA (L-Dopa). This represents 3.0% of all adverse event reports for LEVODOPA.
196
Reports of Wrong technique in product usage process with LEVODOPA
3.0%
of all LEVODOPA reports
0
Deaths
6
Hospitalizations
How Dangerous Is Wrong technique in product usage process From LEVODOPA?
Of the 196 reports, 6 (3.1%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LEVODOPA. However, 196 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which LEVODOPA Alternatives Have Lower Wrong technique in product usage process Risk?
LEVODOPA vs LEVOFLOXACIN
LEVODOPA vs LEVOKETOCONAZOLE
LEVODOPA vs LEVOLEUCOVORIN
LEVODOPA vs LEVOMEPROMAZINE
LEVODOPA vs LEVOMETHADONE