Does BUDESONIDE\FORMOTEROL Cause Device breakage? 117 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 117 reports of Device breakage have been filed in association with BUDESONIDE\FORMOTEROL. This represents 0.3% of all adverse event reports for BUDESONIDE\FORMOTEROL.
117
Reports of Device breakage with BUDESONIDE\FORMOTEROL
0.3%
of all BUDESONIDE\FORMOTEROL reports
0
Deaths
14
Hospitalizations
How Dangerous Is Device breakage From BUDESONIDE\FORMOTEROL?
Of the 117 reports, 14 (12.0%) required hospitalization, and 4 (3.4%) were considered life-threatening.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 117 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 breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which BUDESONIDE\FORMOTEROL Alternatives Have Lower Device breakage 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