Does BUDESONIDE\FORMOTEROL Cause Condition aggravated? 1,242 Reports in FDA Database

Q: Does BUDESONIDE\FORMOTEROL cause Condition aggravated?

1,242 reports of Condition aggravated have been filed with the FDA for BUDESONIDE\FORMOTEROL, representing 3.4% of all BUDESONIDE\FORMOTEROL adverse event reports.

Q: How dangerous is Condition aggravated from BUDESONIDE\FORMOTEROL?

Of 1,242 reports, 63 (5.1%) resulted in death and 621 required hospitalization.

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According to the FDA Adverse Event Reporting System (FAERS), 1,242 reports of Condition aggravated have been filed in association with BUDESONIDE\FORMOTEROL. This represents 3.4% of all adverse event reports for BUDESONIDE\FORMOTEROL.

1,242

Reports of Condition aggravated with BUDESONIDE\FORMOTEROL

3.4%

of all BUDESONIDE\FORMOTEROL reports

Deaths

621

Hospitalizations

How Dangerous Is Condition aggravated From BUDESONIDE\FORMOTEROL?

Of the 1,242 reports, 63 (5.1%) resulted in death, 621 (50.0%) required hospitalization, and 95 (7.6%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 1,242 reports have been filed with the FAERS database.

What Other Side Effects Does BUDESONIDE\FORMOTEROL Cause?

Dyspnoea (11,158) Asthma (10,045) Wheezing (5,632) Cough (4,466) Therapeutic product effect incomplete (4,392) Drug ineffective (3,469)