Does BUDESONIDE Cause Incorrect dose administered by device? 115 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 115 reports of Incorrect dose administered by device have been filed in association with BUDESONIDE (BREYNA). This represents 0.5% of all adverse event reports for BUDESONIDE.
115
Reports of Incorrect dose administered by device with BUDESONIDE
0.5%
of all BUDESONIDE reports
0
Deaths
9
Hospitalizations
How Dangerous Is Incorrect dose administered by device From BUDESONIDE?
Of the 115 reports, 9 (7.8%) required hospitalization, and 1 (0.9%) were considered life-threatening.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 115 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 Incorrect dose administered by device?
EXENATIDE (3,332)
EVOLOCUMAB (2,840)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
SECUKINUMAB (996)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
Which BUDESONIDE Alternatives Have Lower Incorrect dose administered by device Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE