Does APREMILAST Cause Product dose omission? 4,567 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 4,567 reports of Product dose omission have been filed in association with APREMILAST (Otezla). This represents 3.3% of all adverse event reports for APREMILAST.
4,567
Reports of Product dose omission with APREMILAST
3.3%
of all APREMILAST reports
0
Deaths
133
Hospitalizations
How Dangerous Is Product dose omission From APREMILAST?
Of the 4,567 reports, 133 (2.9%) required hospitalization, and 1 (0.0%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for APREMILAST. However, 4,567 reports have been filed with the FAERS database.
What Other Side Effects Does APREMILAST Cause?
Diarrhoea (23,752)
Nausea (21,352)
Psoriasis (19,255)
Headache (17,024)
Drug ineffective (14,121)
Abdominal discomfort (7,653)
Psoriatic arthropathy (7,035)
Vomiting (5,959)
Rash (5,883)
Pain (5,676)
What Other Drugs Cause Product dose omission?
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
TOFACITINIB (1,104)
Which APREMILAST Alternatives Have Lower Product dose omission Risk?
APREMILAST vs APREPITANT
APREMILAST vs APROTININ
APREMILAST vs ARANESP
APREMILAST vs ARAVA
APREMILAST vs AREDIA