Does BUDESONIDE\FORMOTEROL Cause Device malfunction? 2,771 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,771 reports of Device malfunction have been filed in association with BUDESONIDE\FORMOTEROL. This represents 7.6% of all adverse event reports for BUDESONIDE\FORMOTEROL.
2,771
Reports of Device malfunction with BUDESONIDE\FORMOTEROL
7.6%
of all BUDESONIDE\FORMOTEROL reports
9
Deaths
399
Hospitalizations
How Dangerous Is Device malfunction From BUDESONIDE\FORMOTEROL?
Of the 2,771 reports, 9 (0.3%) resulted in death, 399 (14.4%) required hospitalization, and 44 (1.6%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 2,771 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)
Sleep disorder due to a general medical condition (2,742)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
ACLIDINIUM (1,325)
Which BUDESONIDE\FORMOTEROL Alternatives Have Lower Device malfunction 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