Does LURASIDONE Cause Wrong technique in product usage process? 346 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 346 reports of Wrong technique in product usage process have been filed in association with LURASIDONE (lurasidone hydrochloride). This represents 2.0% of all adverse event reports for LURASIDONE.
346
Reports of Wrong technique in product usage process with LURASIDONE
2.0%
of all LURASIDONE reports
0
Deaths
20
Hospitalizations
How Dangerous Is Wrong technique in product usage process From LURASIDONE?
Of the 346 reports, 20 (5.8%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LURASIDONE. However, 346 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which LURASIDONE Alternatives Have Lower Wrong technique in product usage process Risk?
LURASIDONE vs LURBINECTEDIN
LURASIDONE vs LUSPATERCEPT
LURASIDONE vs LUSPATERCEPT-AAMT
LURASIDONE vs LUTEIN
LURASIDONE vs LUTETIUM LU-177