Does PALIPERIDONE Cause Product dose omission? 426 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 426 reports of Product dose omission have been filed in association with PALIPERIDONE (paliperidone). This represents 1.0% of all adverse event reports for PALIPERIDONE.
426
Reports of Product dose omission with PALIPERIDONE
1.0%
of all PALIPERIDONE reports
2
Deaths
69
Hospitalizations
How Dangerous Is Product dose omission From PALIPERIDONE?
Of the 426 reports, 2 (0.5%) resulted in death, 69 (16.2%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PALIPERIDONE. However, 426 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)
Product dose omission issue (1,304)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which PALIPERIDONE Alternatives Have Lower Product dose omission Risk?
PALIPERIDONE vs PALIVIZUMAB
PALIPERIDONE vs PALONOSETRON
PALIPERIDONE vs PAMIDRONATE
PALIPERIDONE vs PAMIDRONIC ACID
PALIPERIDONE vs PANCRELIPASE