Does ARTICAINE\EPINEPHRINE Cause Hypersensitivity? 49 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 49 reports of Hypersensitivity have been filed in association with ARTICAINE\EPINEPHRINE. This represents 3.2% of all adverse event reports for ARTICAINE\EPINEPHRINE.
49
Reports of Hypersensitivity with ARTICAINE\EPINEPHRINE
3.2%
of all ARTICAINE\EPINEPHRINE reports
0
Deaths
27
Hospitalizations
How Dangerous Is Hypersensitivity From ARTICAINE\EPINEPHRINE?
Of the 49 reports, 27 (55.1%) required hospitalization, and 8 (16.3%) were considered life-threatening.
Is Hypersensitivity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ARTICAINE\EPINEPHRINE. However, 49 reports have been filed with the FAERS database.
What Other Side Effects Does ARTICAINE\EPINEPHRINE Cause?
Drug ineffective (719)
Dyspnoea (79)
Hypoaesthesia (73)
Dizziness (65)
Paraesthesia (65)
Hypoaesthesia oral (56)
Loss of consciousness (50)
Nausea (46)
Pain (46)
Injection site pain (40)
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 ARTICAINE\EPINEPHRINE Alternatives Have Lower Hypersensitivity Risk?
ARTICAINE\EPINEPHRINE vs ASCIMINIB
ARTICAINE\EPINEPHRINE vs ASCORBIC ACID
ARTICAINE\EPINEPHRINE vs ASCORBIC ACID\FERROUS
ARTICAINE\EPINEPHRINE vs ASCORBIC ACID\FERROUS\FOLIC ACID
ARTICAINE\EPINEPHRINE vs ASCORBIC ACID\POLYETHYLENE GLYCOL 3350\POTASSIUM\SODIUM ASCORBATE\SODIUM\SODIUM