Does ABOBOTULINUMTOXINA Cause Condition aggravated? 60 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 60 reports of Condition aggravated have been filed in association with ABOBOTULINUMTOXINA. This represents 1.0% of all adverse event reports for ABOBOTULINUMTOXINA.
60
Reports of Condition aggravated with ABOBOTULINUMTOXINA
1.0%
of all ABOBOTULINUMTOXINA reports
2
Deaths
17
Hospitalizations
How Dangerous Is Condition aggravated From ABOBOTULINUMTOXINA?
Of the 60 reports, 2 (3.3%) resulted in death, 17 (28.3%) required hospitalization, and 4 (6.7%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABOBOTULINUMTOXINA. However, 60 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ABOBOTULINUMTOXINA Alternatives Have Lower Condition aggravated Risk?
ABOBOTULINUMTOXINA vs ABRAXANE
ABOBOTULINUMTOXINA vs ABROCITINIB
ABOBOTULINUMTOXINA vs ACALABRUTINIB
ABOBOTULINUMTOXINA vs ACAMPROSATE
ABOBOTULINUMTOXINA vs ACARBOSE