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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does LEVODOPA Cause Device defective? 51 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 51 reports of Device defective have been filed in association with LEVODOPA (L-Dopa). This represents 0.8% of all adverse event reports for LEVODOPA.

51
Reports of Device defective with LEVODOPA
0.8%
of all LEVODOPA reports
0
Deaths
1
Hospitalizations

How Dangerous Is Device defective From LEVODOPA?

Of the 51 reports, 1 (2.0%) required hospitalization.

Is Device defective Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LEVODOPA. However, 51 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 Device defective?

SOMATROPIN (1,719) USTEKINUMAB (1,071) SECUKINUMAB (666) GUSELKUMAB (574) GOLIMUMAB (539) ABATACEPT (458) ALBUTEROL (445) TOCILIZUMAB (400) INSULIN GLARGINE (397) EXENATIDE (387)

Which LEVODOPA Alternatives Have Lower Device defective Risk?

LEVODOPA vs LEVOFLOXACIN LEVODOPA vs LEVOKETOCONAZOLE LEVODOPA vs LEVOLEUCOVORIN LEVODOPA vs LEVOMEPROMAZINE LEVODOPA vs LEVOMETHADONE

Related Pages

LEVODOPA Full Profile All Device defective Reports All Drugs Causing Device defective LEVODOPA Demographics