Does ABOBOTULINUMTOXINA Cause Intentional product misuse? 259 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 259 reports of Intentional product misuse have been filed in association with ABOBOTULINUMTOXINA. This represents 4.5% of all adverse event reports for ABOBOTULINUMTOXINA.
259
Reports of Intentional product misuse with ABOBOTULINUMTOXINA
4.5%
of all ABOBOTULINUMTOXINA reports
0
Deaths
4
Hospitalizations
How Dangerous Is Intentional product misuse From ABOBOTULINUMTOXINA?
Of the 259 reports, 4 (1.5%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABOBOTULINUMTOXINA. However, 259 reports have been filed with the FAERS database.
What Other Side Effects Does ABOBOTULINUMTOXINA Cause?
Off label use (2,271)
Drug ineffective (1,677)
Product preparation error (751)
Headache (379)
Overdose (344)
Inappropriate schedule of drug administration (318)
Therapeutic response shortened (313)
Eyelid ptosis (301)
Injection site pain (278)
Muscular weakness (272)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which ABOBOTULINUMTOXINA Alternatives Have Lower Intentional product misuse Risk?
ABOBOTULINUMTOXINA vs ABRAXANE
ABOBOTULINUMTOXINA vs ABROCITINIB
ABOBOTULINUMTOXINA vs ACALABRUTINIB
ABOBOTULINUMTOXINA vs ACAMPROSATE
ABOBOTULINUMTOXINA vs ACARBOSE