Does LURASIDONE Cause Product dose omission? 210 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 210 reports of Product dose omission have been filed in association with LURASIDONE (lurasidone hydrochloride). This represents 1.2% of all adverse event reports for LURASIDONE.
210
Reports of Product dose omission with LURASIDONE
1.2%
of all LURASIDONE reports
1
Deaths
14
Hospitalizations
How Dangerous Is Product dose omission From LURASIDONE?
Of the 210 reports, 1 (0.5%) resulted in death, 14 (6.7%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LURASIDONE. However, 210 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which LURASIDONE Alternatives Have Lower Product dose omission Risk?
LURASIDONE vs LURBINECTEDIN
LURASIDONE vs LUSPATERCEPT
LURASIDONE vs LUSPATERCEPT-AAMT
LURASIDONE vs LUTEIN
LURASIDONE vs LUTETIUM LU-177