Does ARIPIPRAZOLE LAUROXIL Cause Product administration error? 77 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 77 reports of Product administration error have been filed in association with ARIPIPRAZOLE LAUROXIL (ARISTADA). This represents 1.8% of all adverse event reports for ARIPIPRAZOLE LAUROXIL.
77
Reports of Product administration error with ARIPIPRAZOLE LAUROXIL
1.8%
of all ARIPIPRAZOLE LAUROXIL reports
0
Deaths
11
Hospitalizations
How Dangerous Is Product administration error From ARIPIPRAZOLE LAUROXIL?
Of the 77 reports, 11 (14.3%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ARIPIPRAZOLE LAUROXIL. However, 77 reports have been filed with the FAERS database.
What Other Side Effects Does ARIPIPRAZOLE LAUROXIL Cause?
Off label use (1,024)
Needle issue (567)
Injection site pain (426)
Drug ineffective (262)
Weight increased (207)
Product administered at inappropriate site (198)
Hallucination, auditory (172)
Therapeutic response shortened (172)
Underdose (169)
Incorrect dose administered (162)
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 ARIPIPRAZOLE LAUROXIL Alternatives Have Lower Product administration error Risk?
ARIPIPRAZOLE LAUROXIL vs ARIXTRA
ARIPIPRAZOLE LAUROXIL vs ARMODAFINIL
ARIPIPRAZOLE LAUROXIL vs AROMASIN
ARIPIPRAZOLE LAUROXIL vs ARSENIC TRIOXIDE
ARIPIPRAZOLE LAUROXIL vs ARTEMETHER\LUMEFANTRINE