Does BUDESONIDE Cause Intentional product use issue? 298 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 298 reports of Intentional product use issue have been filed in association with BUDESONIDE (BREYNA). This represents 1.2% of all adverse event reports for BUDESONIDE.
298
Reports of Intentional product use issue with BUDESONIDE
1.2%
of all BUDESONIDE reports
11
Deaths
54
Hospitalizations
How Dangerous Is Intentional product use issue From BUDESONIDE?
Of the 298 reports, 11 (3.7%) resulted in death, 54 (18.1%) required hospitalization, and 3 (1.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 298 reports have been filed with the FAERS database.
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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which BUDESONIDE Alternatives Have Lower Intentional product use issue Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE