Does BUDESONIDE\FORMOTEROL Cause Hypersensitivity? 738 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 738 reports of Hypersensitivity have been filed in association with BUDESONIDE\FORMOTEROL. This represents 2.0% of all adverse event reports for BUDESONIDE\FORMOTEROL.
738
Reports of Hypersensitivity with BUDESONIDE\FORMOTEROL
2.0%
of all BUDESONIDE\FORMOTEROL reports
2
Deaths
211
Hospitalizations
How Dangerous Is Hypersensitivity From BUDESONIDE\FORMOTEROL?
Of the 738 reports, 2 (0.3%) resulted in death, 211 (28.6%) required hospitalization, and 20 (2.7%) 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 BUDESONIDE\FORMOTEROL. However, 738 reports have been filed with the FAERS database.
What Other Side Effects Does BUDESONIDE\FORMOTEROL Cause?
Dyspnoea (11,158)
Asthma (10,045)
Wheezing (5,632)
Cough (4,466)
Therapeutic product effect incomplete (4,392)
Drug ineffective (3,469)
Intentional product misuse (3,399)
Loss of personal independence in daily activities (3,397)
Off label use (3,269)
Device malfunction (2,771)
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 BUDESONIDE\FORMOTEROL Alternatives Have Lower Hypersensitivity Risk?
BUDESONIDE\FORMOTEROL vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE\FORMOTEROL vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE\FORMOTEROL vs BUMETANIDE
BUDESONIDE\FORMOTEROL vs BUPIVACAINE
BUDESONIDE\FORMOTEROL vs BUPIVACAINE\BUPIVACAINE ANHYDROUS