Does BENSERAZIDE\LEVODOPA Cause Product administration error? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product administration error have been filed in association with BENSERAZIDE\LEVODOPA. This represents 0.7% of all adverse event reports for BENSERAZIDE\LEVODOPA.
14
Reports of Product administration error with BENSERAZIDE\LEVODOPA
0.7%
of all BENSERAZIDE\LEVODOPA reports
4
Deaths
13
Hospitalizations
How Dangerous Is Product administration error From BENSERAZIDE\LEVODOPA?
Of the 14 reports, 4 (28.6%) resulted in death, 13 (92.9%) required hospitalization, and 1 (7.1%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BENSERAZIDE\LEVODOPA. However, 14 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which BENSERAZIDE\LEVODOPA Alternatives Have Lower Product administration error Risk?
BENSERAZIDE\LEVODOPA vs BENZALKONIUM
BENSERAZIDE\LEVODOPA vs BENZOCAINE
BENSERAZIDE\LEVODOPA vs BENZODIAZEPINE
BENSERAZIDE\LEVODOPA vs BENZONATATE
BENSERAZIDE\LEVODOPA vs BENZOYL PEROXIDE