Does DULERA Cause Device malfunction? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device malfunction have been filed in association with DULERA. This represents 1.5% of all adverse event reports for DULERA.
8
Reports of Device malfunction with DULERA
1.5%
of all DULERA reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device malfunction From DULERA?
Of the 8 reports.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULERA. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does DULERA Cause?
Product quality issue (287)
Drug dose omission (227)
No adverse event (187)
Dyspnoea (66)
Underdose (53)
Incorrect dose administered (42)
Drug ineffective (35)
Cough (29)
Asthma (28)
Product container issue (24)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which DULERA Alternatives Have Lower Device malfunction Risk?
DULERA vs DULOXETINE
DULERA vs DUPILUMAB
DULERA vs DURAGESIC
DULERA vs DUROGESIC
DULERA vs DUROTEP MT