Does DULERA Cause Product quality issue? 287 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 287 reports of Product quality issue have been filed in association with DULERA. This represents 54.6% of all adverse event reports for DULERA.
287
Reports of Product quality issue with DULERA
54.6%
of all DULERA reports
0
Deaths
7
Hospitalizations
How Dangerous Is Product quality issue From DULERA?
Of the 287 reports, 7 (2.4%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULERA. However, 287 reports have been filed with the FAERS database.
What Other Side Effects Does DULERA Cause?
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)
Dysphonia (19)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which DULERA Alternatives Have Lower Product quality issue Risk?
DULERA vs DULOXETINE
DULERA vs DUPILUMAB
DULERA vs DURAGESIC
DULERA vs DUROGESIC
DULERA vs DUROTEP MT