Does BUDESONIDE Cause Product quality issue? 361 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 361 reports of Product quality issue have been filed in association with BUDESONIDE (BREYNA). This represents 1.4% of all adverse event reports for BUDESONIDE.
361
Reports of Product quality issue with BUDESONIDE
1.4%
of all BUDESONIDE reports
1
Deaths
25
Hospitalizations
How Dangerous Is Product quality issue From BUDESONIDE?
Of the 361 reports, 1 (0.3%) resulted in death, 25 (6.9%) required hospitalization, and 4 (1.1%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 361 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which BUDESONIDE Alternatives Have Lower Product quality issue Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE