Does LURASIDONE Cause Product dose omission issue? 67 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 67 reports of Product dose omission issue have been filed in association with LURASIDONE (lurasidone hydrochloride). This represents 0.4% of all adverse event reports for LURASIDONE.
67
Reports of Product dose omission issue with LURASIDONE
0.4%
of all LURASIDONE reports
0
Deaths
15
Hospitalizations
How Dangerous Is Product dose omission issue From LURASIDONE?
Of the 67 reports, 15 (22.4%) required hospitalization, and 1 (1.5%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LURASIDONE. However, 67 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 issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which LURASIDONE Alternatives Have Lower Product dose omission issue Risk?
LURASIDONE vs LURBINECTEDIN
LURASIDONE vs LUSPATERCEPT
LURASIDONE vs LUSPATERCEPT-AAMT
LURASIDONE vs LUTEIN
LURASIDONE vs LUTETIUM LU-177