Does ABOBOTULINUMTOXINA Cause Product use issue? 45 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Product use issue have been filed in association with ABOBOTULINUMTOXINA. This represents 0.8% of all adverse event reports for ABOBOTULINUMTOXINA.
45
Reports of Product use issue with ABOBOTULINUMTOXINA
0.8%
of all ABOBOTULINUMTOXINA reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product use issue From ABOBOTULINUMTOXINA?
Of the 45 reports, 1 (2.2%) required hospitalization.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABOBOTULINUMTOXINA. However, 45 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ABOBOTULINUMTOXINA Alternatives Have Lower Product use issue Risk?
ABOBOTULINUMTOXINA vs ABRAXANE
ABOBOTULINUMTOXINA vs ABROCITINIB
ABOBOTULINUMTOXINA vs ACALABRUTINIB
ABOBOTULINUMTOXINA vs ACAMPROSATE
ABOBOTULINUMTOXINA vs ACARBOSE