Does ABOBOTULINUMTOXINA Cause Product preparation error? 751 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 751 reports of Product preparation error have been filed in association with ABOBOTULINUMTOXINA. This represents 13.0% of all adverse event reports for ABOBOTULINUMTOXINA.
751
Reports of Product preparation error with ABOBOTULINUMTOXINA
13.0%
of all ABOBOTULINUMTOXINA reports
2
Deaths
9
Hospitalizations
How Dangerous Is Product preparation error From ABOBOTULINUMTOXINA?
Of the 751 reports, 2 (0.3%) resulted in death, 9 (1.2%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABOBOTULINUMTOXINA. However, 751 reports have been filed with the FAERS database.
What Other Side Effects Does ABOBOTULINUMTOXINA Cause?
Off label use (2,271)
Drug ineffective (1,677)
Headache (379)
Overdose (344)
Inappropriate schedule of drug administration (318)
Therapeutic response shortened (313)
Eyelid ptosis (301)
Injection site pain (278)
Muscular weakness (272)
Intentional product misuse (259)
What Other Drugs Cause Product preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
SODIUM OXYBATE (222)
Which ABOBOTULINUMTOXINA Alternatives Have Lower Product preparation error Risk?
ABOBOTULINUMTOXINA vs ABRAXANE
ABOBOTULINUMTOXINA vs ABROCITINIB
ABOBOTULINUMTOXINA vs ACALABRUTINIB
ABOBOTULINUMTOXINA vs ACAMPROSATE
ABOBOTULINUMTOXINA vs ACARBOSE