Does BUDESONIDE Cause Eosinophil count increased? 493 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 493 reports of Eosinophil count increased have been filed in association with BUDESONIDE (BREYNA). This represents 2.0% of all adverse event reports for BUDESONIDE.
493
Reports of Eosinophil count increased with BUDESONIDE
2.0%
of all BUDESONIDE reports
0
Deaths
213
Hospitalizations
How Dangerous Is Eosinophil count increased From BUDESONIDE?
Of the 493 reports, 213 (43.2%) required hospitalization, and 26 (5.3%) were considered life-threatening.
Is Eosinophil count increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 493 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 Eosinophil count increased?
ALBUTEROL (1,359)
PREDNISONE (846)
BUDESONIDE\FORMOTEROL (719)
DUPILUMAB (712)
TIOTROPIUM (682)
MEPOLIZUMAB (670)
MONTELUKAST (504)
CLOZAPINE (475)
FLUTICASONE\SALMETEROL (416)
OMALIZUMAB (329)
Which BUDESONIDE Alternatives Have Lower Eosinophil count increased Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE