Does BUDESONIDE Cause Expired product administered? 50 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Expired product administered have been filed in association with BUDESONIDE (BREYNA). This represents 0.2% of all adverse event reports for BUDESONIDE.
50
Reports of Expired product administered with BUDESONIDE
0.2%
of all BUDESONIDE reports
0
Deaths
8
Hospitalizations
How Dangerous Is Expired product administered From BUDESONIDE?
Of the 50 reports, 8 (16.0%) required hospitalization.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 50 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
Which BUDESONIDE Alternatives Have Lower Expired product administered Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE