Does LUMATEPERONE Cause Wrong technique in product usage process? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Wrong technique in product usage process have been filed in association with LUMATEPERONE (CAPLYTA). This represents 0.1% of all adverse event reports for LUMATEPERONE.
7
Reports of Wrong technique in product usage process with LUMATEPERONE
0.1%
of all LUMATEPERONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From LUMATEPERONE?
Of the 7 reports.
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 LUMATEPERONE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does LUMATEPERONE Cause?
Dizziness (558)
Nausea (401)
Headache (358)
Somnolence (304)
Off label use (280)
Drug ineffective (241)
Mania (211)
Sedation (208)
Feeling abnormal (206)
Anxiety (183)
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 LUMATEPERONE Alternatives Have Lower Wrong technique in product usage process Risk?
LUMATEPERONE vs LUMIGAN
LUMATEPERONE vs LUPRON DEPOT
LUMATEPERONE vs LUPRON DEPOT-PED
LUMATEPERONE vs LURASIDONE
LUMATEPERONE vs LURBINECTEDIN