Does BUDESONIDE\FORMOTEROL Cause Device issue? 1,411 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,411 reports of Device issue have been filed in association with BUDESONIDE\FORMOTEROL. This represents 3.9% of all adverse event reports for BUDESONIDE\FORMOTEROL.
1,411
Reports of Device issue with BUDESONIDE\FORMOTEROL
3.9%
of all BUDESONIDE\FORMOTEROL reports
5
Deaths
207
Hospitalizations
How Dangerous Is Device issue From BUDESONIDE\FORMOTEROL?
Of the 1,411 reports, 5 (0.4%) resulted in death, 207 (14.7%) required hospitalization, and 13 (0.9%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE\FORMOTEROL. However, 1,411 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which BUDESONIDE\FORMOTEROL Alternatives Have Lower Device 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