Does BUDESONIDE\FORMOTEROL Cause Complication associated with device? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Complication associated with device have been filed in association with BUDESONIDE\FORMOTEROL. This represents 0.0% of all adverse event reports for BUDESONIDE\FORMOTEROL.
10
Reports of Complication associated with device with BUDESONIDE\FORMOTEROL
0.0%
of all BUDESONIDE\FORMOTEROL reports
0
Deaths
3
Hospitalizations
How Dangerous Is Complication associated with device From BUDESONIDE\FORMOTEROL?
Of the 10 reports, 3 (30.0%) required hospitalization.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 10 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)
Intentional product misuse (3,399)
Loss of personal independence in daily activities (3,397)
Off label use (3,269)
Device malfunction (2,771)
What Other Drugs Cause Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
Which BUDESONIDE\FORMOTEROL Alternatives Have Lower Complication associated with device Risk?
BUDESONIDE\FORMOTEROL vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE\FORMOTEROL vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE\FORMOTEROL vs BUMETANIDE
BUDESONIDE\FORMOTEROL vs BUPIVACAINE
BUDESONIDE\FORMOTEROL vs BUPIVACAINE\BUPIVACAINE ANHYDROUS