Does BUDESONIDE\FORMOTEROL Cause Device misuse? 121 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 121 reports of Device misuse have been filed in association with BUDESONIDE\FORMOTEROL. This represents 0.3% of all adverse event reports for BUDESONIDE\FORMOTEROL.
121
Reports of Device misuse with BUDESONIDE\FORMOTEROL
0.3%
of all BUDESONIDE\FORMOTEROL reports
0
Deaths
11
Hospitalizations
How Dangerous Is Device misuse From BUDESONIDE\FORMOTEROL?
Of the 121 reports, 11 (9.1%) required hospitalization, and 1 (0.8%) were considered life-threatening.
Is Device misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 121 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 misuse?
LEVONORGESTREL (279)
MIRENA (155)
ALBUTEROL (89)
EXENATIDE (54)
FLUTICASONE\SALMETEROL (44)
SYMBICORT (27)
BUDESONIDE (23)
GOLIMUMAB (20)
LISINOPRIL (15)
FLUTICASONE (14)
Which BUDESONIDE\FORMOTEROL Alternatives Have Lower Device misuse 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