Does BENSERAZIDE\LEVODOPA Cause Product prescribing error? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Product prescribing error have been filed in association with BENSERAZIDE\LEVODOPA. This represents 2.6% of all adverse event reports for BENSERAZIDE\LEVODOPA.
52
Reports of Product prescribing error with BENSERAZIDE\LEVODOPA
2.6%
of all BENSERAZIDE\LEVODOPA reports
0
Deaths
44
Hospitalizations
How Dangerous Is Product prescribing error From BENSERAZIDE\LEVODOPA?
Of the 52 reports, 44 (84.6%) required hospitalization, and 5 (9.6%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BENSERAZIDE\LEVODOPA. However, 52 reports have been filed with the FAERS database.
What Other Side Effects Does BENSERAZIDE\LEVODOPA Cause?
Fall (282)
Dizziness (151)
Hallucination (136)
Dyskinesia (127)
General physical health deterioration (127)
Parkinson's disease (126)
Drug ineffective (119)
Confusional state (117)
Off label use (112)
Somnolence (110)
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 BENSERAZIDE\LEVODOPA Alternatives Have Lower Product prescribing error Risk?
BENSERAZIDE\LEVODOPA vs BENZALKONIUM
BENSERAZIDE\LEVODOPA vs BENZOCAINE
BENSERAZIDE\LEVODOPA vs BENZODIAZEPINE
BENSERAZIDE\LEVODOPA vs BENZONATATE
BENSERAZIDE\LEVODOPA vs BENZOYL PEROXIDE