Does BUDESONIDE Cause Product use in unapproved indication? 1,214 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,214 reports of Product use in unapproved indication have been filed in association with BUDESONIDE (BREYNA). This represents 4.8% of all adverse event reports for BUDESONIDE.
1,214
Reports of Product use in unapproved indication with BUDESONIDE
4.8%
of all BUDESONIDE reports
100
Deaths
325
Hospitalizations
How Dangerous Is Product use in unapproved indication From BUDESONIDE?
Of the 1,214 reports, 100 (8.2%) resulted in death, 325 (26.8%) required hospitalization, and 84 (6.9%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 1,214 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 Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which BUDESONIDE Alternatives Have Lower Product use in unapproved indication Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE