Does PALIPERIDONE Cause Product dose omission issue? 1,304 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,304 reports of Product dose omission issue have been filed in association with PALIPERIDONE (paliperidone). This represents 3.2% of all adverse event reports for PALIPERIDONE.
1,304
Reports of Product dose omission issue with PALIPERIDONE
3.2%
of all PALIPERIDONE reports
8
Deaths
218
Hospitalizations
How Dangerous Is Product dose omission issue From PALIPERIDONE?
Of the 1,304 reports, 8 (0.6%) resulted in death, 218 (16.7%) required hospitalization, and 4 (0.3%) 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 PALIPERIDONE. However, 1,304 reports have been filed with the FAERS database.
What Other Side Effects Does PALIPERIDONE Cause?
Injury (4,348)
Gynaecomastia (4,155)
Off label use (4,041)
Drug ineffective (2,812)
Weight increased (2,136)
Hospitalisation (2,066)
Abnormal weight gain (1,816)
Hyperprolactinaemia (1,427)
Schizophrenia (1,361)
Galactorrhoea (1,277)
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 PALIPERIDONE Alternatives Have Lower Product dose omission issue Risk?
PALIPERIDONE vs PALIVIZUMAB
PALIPERIDONE vs PALONOSETRON
PALIPERIDONE vs PAMIDRONATE
PALIPERIDONE vs PAMIDRONIC ACID
PALIPERIDONE vs PANCRELIPASE