Does PALIPERIDONE Cause Product administration error? 133 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 133 reports of Product administration error have been filed in association with PALIPERIDONE (paliperidone). This represents 0.3% of all adverse event reports for PALIPERIDONE.
133
Reports of Product administration error with PALIPERIDONE
0.3%
of all PALIPERIDONE reports
1
Deaths
47
Hospitalizations
How Dangerous Is Product administration error From PALIPERIDONE?
Of the 133 reports, 1 (0.8%) resulted in death, 47 (35.3%) required hospitalization, and 5 (3.8%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PALIPERIDONE. However, 133 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which PALIPERIDONE Alternatives Have Lower Product administration error Risk?
PALIPERIDONE vs PALIVIZUMAB
PALIPERIDONE vs PALONOSETRON
PALIPERIDONE vs PAMIDRONATE
PALIPERIDONE vs PAMIDRONIC ACID
PALIPERIDONE vs PANCRELIPASE