Does BUDESONIDE Cause Product prescribing issue? 110 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 110 reports of Product prescribing issue have been filed in association with BUDESONIDE (BREYNA). This represents 0.4% of all adverse event reports for BUDESONIDE.
110
Reports of Product prescribing issue with BUDESONIDE
0.4%
of all BUDESONIDE reports
1
Deaths
12
Hospitalizations
How Dangerous Is Product prescribing issue From BUDESONIDE?
Of the 110 reports, 1 (0.9%) resulted in death, 12 (10.9%) required hospitalization, and 1 (0.9%) were considered life-threatening.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 110 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 prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which BUDESONIDE Alternatives Have Lower Product prescribing issue Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE