Does LURASIDONE Cause Product administration error? 130 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 130 reports of Product administration error have been filed in association with LURASIDONE (lurasidone hydrochloride). This represents 0.8% of all adverse event reports for LURASIDONE.
130
Reports of Product administration error with LURASIDONE
0.8%
of all LURASIDONE reports
0
Deaths
11
Hospitalizations
How Dangerous Is Product administration error From LURASIDONE?
Of the 130 reports, 11 (8.5%) required hospitalization, and 1 (0.8%) 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 LURASIDONE. However, 130 reports have been filed with the FAERS database.
What Other Side Effects Does LURASIDONE Cause?
Off label use (1,878)
Drug ineffective (1,715)
Feeling abnormal (1,025)
Anxiety (1,009)
Weight increased (959)
Somnolence (938)
Depression (908)
Insomnia (827)
Dyskinesia (791)
Nausea (790)
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 LURASIDONE Alternatives Have Lower Product administration error Risk?
LURASIDONE vs LURBINECTEDIN
LURASIDONE vs LUSPATERCEPT
LURASIDONE vs LUSPATERCEPT-AAMT
LURASIDONE vs LUTEIN
LURASIDONE vs LUTETIUM LU-177