Does DULERA Cause Product container issue? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Product container issue have been filed in association with DULERA. This represents 4.6% of all adverse event reports for DULERA.
24
Reports of Product container issue with DULERA
4.6%
of all DULERA reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product container issue From DULERA?
Of the 24 reports, 1 (4.2%) required hospitalization, and 1 (4.2%) were considered life-threatening.
Is Product container issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DULERA. However, 24 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)
Dysphonia (19)
What Other Drugs Cause Product container issue?
CYCLOSPORINE (910)
MINOXIDIL (556)
MOMETASONE FUROATE (450)
FORMOTEROL\MOMETASONE FUROATE (375)
LIFITEGRAST (244)
ALBUTEROL (192)
LATANOPROST (158)
CARBOXYMETHYLCELLULOSE\GLYCERIN (123)
BRIMONIDINE (121)
ACETAMINOPHEN (118)
Which DULERA Alternatives Have Lower Product container issue Risk?
DULERA vs DULOXETINE
DULERA vs DUPILUMAB
DULERA vs DURAGESIC
DULERA vs DUROGESIC
DULERA vs DUROTEP MT