Does PALIPERIDONE Cause Wrong product administered? 59 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 59 reports of Wrong product administered have been filed in association with PALIPERIDONE (paliperidone). This represents 0.1% of all adverse event reports for PALIPERIDONE.
59
Reports of Wrong product administered with PALIPERIDONE
0.1%
of all PALIPERIDONE reports
0
Deaths
22
Hospitalizations
How Dangerous Is Wrong product administered From PALIPERIDONE?
Of the 59 reports, 22 (37.3%) required hospitalization, and 1 (1.7%) were considered life-threatening.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PALIPERIDONE. However, 59 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which PALIPERIDONE Alternatives Have Lower Wrong product administered Risk?
PALIPERIDONE vs PALIVIZUMAB
PALIPERIDONE vs PALONOSETRON
PALIPERIDONE vs PAMIDRONATE
PALIPERIDONE vs PAMIDRONIC ACID
PALIPERIDONE vs PANCRELIPASE