Does APREMILAST Cause Intentional dose omission? 151 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 151 reports of Intentional dose omission have been filed in association with APREMILAST (Otezla). This represents 0.1% of all adverse event reports for APREMILAST.
151
Reports of Intentional dose omission with APREMILAST
0.1%
of all APREMILAST reports
3
Deaths
18
Hospitalizations
How Dangerous Is Intentional dose omission From APREMILAST?
Of the 151 reports, 3 (2.0%) resulted in death, 18 (11.9%) required hospitalization, and 4 (2.6%) were considered life-threatening.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for APREMILAST. However, 151 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 Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which APREMILAST Alternatives Have Lower Intentional dose omission Risk?
APREMILAST vs APREPITANT
APREMILAST vs APROTININ
APREMILAST vs ARANESP
APREMILAST vs ARAVA
APREMILAST vs AREDIA