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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does BUDESONIDE Cause Hypersensitivity? 452 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 452 reports of Hypersensitivity have been filed in association with BUDESONIDE (BREYNA). This represents 1.8% of all adverse event reports for BUDESONIDE.

452
Reports of Hypersensitivity with BUDESONIDE
1.8%
of all BUDESONIDE reports
4
Deaths
176
Hospitalizations

How Dangerous Is Hypersensitivity From BUDESONIDE?

Of the 452 reports, 4 (0.9%) resulted in death, 176 (38.9%) required hospitalization, and 55 (12.2%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

Yes, Hypersensitivity is listed as a known adverse reaction in the official FDA drug label for BUDESONIDE.

What Other Side Effects Does BUDESONIDE Cause?

Asthma (4,544) Dyspnoea (4,441) Drug ineffective (4,384) Off label use (3,033) Wheezing (2,590) Cough (2,269) Therapeutic product effect incomplete (2,191) Loss of personal independence in daily activities (1,890) Condition aggravated (1,548) Fatigue (1,508)

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 Alternatives Have Lower Hypersensitivity Risk?

BUDESONIDE vs BUDESONIDE\FORMOTEROL BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM BUDESONIDE vs BUMETANIDE BUDESONIDE vs BUPIVACAINE

Related Pages

BUDESONIDE Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity BUDESONIDE Demographics