Does BUDESONIDE\FORMOTEROL Cause Poor quality device used? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Poor quality device used have been filed in association with BUDESONIDE\FORMOTEROL. This represents 0.1% of all adverse event reports for BUDESONIDE\FORMOTEROL.
28
Reports of Poor quality device used with BUDESONIDE\FORMOTEROL
0.1%
of all BUDESONIDE\FORMOTEROL reports
0
Deaths
4
Hospitalizations
How Dangerous Is Poor quality device used From BUDESONIDE\FORMOTEROL?
Of the 28 reports, 4 (14.3%) required hospitalization, and 1 (3.6%) were considered life-threatening.
Is Poor quality device used Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 28 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 Poor quality device used?
SOMATROPIN (3,162)
MOMETASONE FUROATE (2,159)
ALBUTEROL (1,251)
FORMOTEROL\MOMETASONE FUROATE (1,091)
MEDROXYPROGESTERONE (80)
ETHINYL ESTRADIOL\ETONOGESTREL (77)
FOLLITROPIN (58)
ETONOGESTREL (55)
ETANERCEPT (46)
ESTRADIOL (41)
Which BUDESONIDE\FORMOTEROL Alternatives Have Lower Poor quality device used 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