Does APREMILAST Cause Product administration interrupted? 314 Reports in FDA Database
Visibly Younger Skin in Weeks
Synevra Lift & Lock — Swiss peptide serum + nutrients. 60-day money-back guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 314 reports of Product administration interrupted have been filed in association with APREMILAST (Otezla). This represents 0.2% of all adverse event reports for APREMILAST.
314
Reports of Product administration interrupted with APREMILAST
0.2%
of all APREMILAST reports
0
Deaths
10
Hospitalizations
How Dangerous Is Product administration interrupted From APREMILAST?
Of the 314 reports, 10 (3.2%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for APREMILAST. However, 314 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 administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
ADALIMUMAB (86)
Which APREMILAST Alternatives Have Lower Product administration interrupted Risk?
APREMILAST vs APREPITANT
APREMILAST vs APROTININ
APREMILAST vs ARANESP
APREMILAST vs ARAVA
APREMILAST vs AREDIA