Does LURASIDONE Cause Product administration interrupted? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product administration interrupted have been filed in association with LURASIDONE (lurasidone hydrochloride). This represents 0.1% of all adverse event reports for LURASIDONE.
11
Reports of Product administration interrupted with LURASIDONE
0.1%
of all LURASIDONE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product administration interrupted From LURASIDONE?
Of the 11 reports, 4 (36.4%) required hospitalization.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LURASIDONE. However, 11 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 interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which LURASIDONE Alternatives Have Lower Product administration interrupted Risk?
LURASIDONE vs LURBINECTEDIN
LURASIDONE vs LUSPATERCEPT
LURASIDONE vs LUSPATERCEPT-AAMT
LURASIDONE vs LUTEIN
LURASIDONE vs LUTETIUM LU-177