Does PRABOTULINUMTOXINA-XVFS Cause Hypersensitivity? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Hypersensitivity have been filed in association with PRABOTULINUMTOXINA-XVFS. This represents 0.4% of all adverse event reports for PRABOTULINUMTOXINA-XVFS.
14
Reports of Hypersensitivity with PRABOTULINUMTOXINA-XVFS
0.4%
of all PRABOTULINUMTOXINA-XVFS reports
0
Deaths
2
Hospitalizations
How Dangerous Is Hypersensitivity From PRABOTULINUMTOXINA-XVFS?
Of the 14 reports, 2 (14.3%) required hospitalization.
Is Hypersensitivity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRABOTULINUMTOXINA-XVFS. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does PRABOTULINUMTOXINA-XVFS Cause?
Drug ineffective (1,332)
Off label use (1,088)
Therapeutic product effect decreased (714)
Drug effect less than expected (354)
Headache (153)
Injection site pain (99)
Patient dissatisfaction with treatment (90)
Injection site swelling (89)
Inappropriate schedule of product administration (72)
Injection site erythema (62)
What Other Drugs Cause Hypersensitivity?
ETANERCEPT (10,846)
ADALIMUMAB (10,641)
METHOTREXATE (9,799)
TOCILIZUMAB (9,076)
ABATACEPT (8,945)
INFLIXIMAB (8,519)
RITUXIMAB (8,408)
ADAPALENE (8,356)
LEFLUNOMIDE (7,926)
CERTOLIZUMAB PEGOL (7,353)
Which PRABOTULINUMTOXINA-XVFS Alternatives Have Lower Hypersensitivity Risk?
PRABOTULINUMTOXINA-XVFS vs PRADAXA
PRABOTULINUMTOXINA-XVFS vs PRALATREXATE
PRABOTULINUMTOXINA-XVFS vs PRALSETINIB
PRABOTULINUMTOXINA-XVFS vs PRAMIPEXOLE
PRABOTULINUMTOXINA-XVFS vs PRAMIPEXOLE\PRAMIPEXOLE