Does BUDESONIDE Cause Product dose omission issue? 777 Reports in FDA Database

Q: Does BUDESONIDE cause Product dose omission issue?

777 reports of Product dose omission issue have been filed with the FDA for BUDESONIDE, representing 3.1% of all BUDESONIDE adverse event reports.

Q: How dangerous is Product dose omission issue from BUDESONIDE?

Of 777 reports, 33 (4.2%) resulted in death and 208 required hospitalization.

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According to the FDA Adverse Event Reporting System (FAERS), 777 reports of Product dose omission issue have been filed in association with BUDESONIDE (BREYNA). This represents 3.1% of all adverse event reports for BUDESONIDE.

777

Reports of Product dose omission issue with BUDESONIDE

3.1%

of all BUDESONIDE reports

Deaths

208

Hospitalizations

How Dangerous Is Product dose omission issue From BUDESONIDE?

Of the 777 reports, 33 (4.2%) resulted in death, 208 (26.8%) required hospitalization, and 37 (4.8%) were considered life-threatening.

Is Product dose omission issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 777 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)