Does BUDESONIDE\FORMOTEROL Cause Device use issue? 1,236 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,236 reports of Device use issue have been filed in association with BUDESONIDE\FORMOTEROL. This represents 3.4% of all adverse event reports for BUDESONIDE\FORMOTEROL.
1,236
Reports of Device use issue with BUDESONIDE\FORMOTEROL
3.4%
of all BUDESONIDE\FORMOTEROL reports
4
Deaths
102
Hospitalizations
How Dangerous Is Device use issue From BUDESONIDE\FORMOTEROL?
Of the 1,236 reports, 4 (0.3%) resulted in death, 102 (8.3%) required hospitalization, and 20 (1.6%) were considered life-threatening.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 1,236 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 use issue?
SOMATROPIN (2,571)
LEVONORGESTREL (2,489)
COPPER (1,318)
EXENATIDE (992)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
DUPILUMAB (528)
ALIROCUMAB (471)
INSULIN GLARGINE (469)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
LEVODOPA (443)
Which BUDESONIDE\FORMOTEROL Alternatives Have Lower Device use 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