Does BUDESONIDE\FORMOTEROL Cause Device mechanical issue? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Device mechanical issue have been filed in association with BUDESONIDE\FORMOTEROL. This represents 0.1% of all adverse event reports for BUDESONIDE\FORMOTEROL.
35
Reports of Device mechanical issue with BUDESONIDE\FORMOTEROL
0.1%
of all BUDESONIDE\FORMOTEROL reports
0
Deaths
3
Hospitalizations
How Dangerous Is Device mechanical issue From BUDESONIDE\FORMOTEROL?
Of the 35 reports, 3 (8.6%) required hospitalization.
Is Device mechanical issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 35 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 Device mechanical issue?
SOMATROPIN (6,411)
INSULIN GLARGINE-YFGN (853)
INSULIN GLARGINE (725)
ALBUTEROL (455)
DEVICE (226)
ETANERCEPT (145)
FLUTICASONE\SALMETEROL (127)
GLATIRAMER (124)
EXENATIDE (108)
MEDROXYPROGESTERONE (99)
Which BUDESONIDE\FORMOTEROL Alternatives Have Lower Device mechanical issue 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