Does ARIPIPRAZOLE LAUROXIL Cause Product preparation error? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product preparation error have been filed in association with ARIPIPRAZOLE LAUROXIL (ARISTADA). This represents 0.2% of all adverse event reports for ARIPIPRAZOLE LAUROXIL.
10
Reports of Product preparation error with ARIPIPRAZOLE LAUROXIL
0.2%
of all ARIPIPRAZOLE LAUROXIL reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product preparation error From ARIPIPRAZOLE LAUROXIL?
Of the 10 reports, 1 (10.0%) required hospitalization.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ARIPIPRAZOLE LAUROXIL. However, 10 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 preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
Which ARIPIPRAZOLE LAUROXIL Alternatives Have Lower Product preparation error Risk?
ARIPIPRAZOLE LAUROXIL vs ARIXTRA
ARIPIPRAZOLE LAUROXIL vs ARMODAFINIL
ARIPIPRAZOLE LAUROXIL vs AROMASIN
ARIPIPRAZOLE LAUROXIL vs ARSENIC TRIOXIDE
ARIPIPRAZOLE LAUROXIL vs ARTEMETHER\LUMEFANTRINE