Does APREMILAST Cause Incorrect product administration duration? 59 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 59 reports of Incorrect product administration duration have been filed in association with APREMILAST (Otezla). This represents 0.0% of all adverse event reports for APREMILAST.
59
Reports of Incorrect product administration duration with APREMILAST
0.0%
of all APREMILAST reports
55
Deaths
54
Hospitalizations
How Dangerous Is Incorrect product administration duration From APREMILAST?
Of the 59 reports, 55 (93.2%) resulted in death, 54 (91.5%) required hospitalization, and 54 (91.5%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for APREMILAST. However, 59 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which APREMILAST Alternatives Have Lower Incorrect product administration duration Risk?
APREMILAST vs APREPITANT
APREMILAST vs APROTININ
APREMILAST vs ARANESP
APREMILAST vs ARAVA
APREMILAST vs AREDIA