Does SECUKINUMAB Cause Product administration error? 225 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 225 reports of Product administration error have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.2% of all adverse event reports for SECUKINUMAB.
225
Reports of Product administration error with SECUKINUMAB
0.2%
of all SECUKINUMAB reports
1
Deaths
5
Hospitalizations
How Dangerous Is Product administration error From SECUKINUMAB?
Of the 225 reports, 1 (0.4%) resulted in death, 5 (2.2%) required hospitalization, and 1 (0.4%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 225 reports have been filed with the FAERS database.
What Other Side Effects Does SECUKINUMAB Cause?
Drug ineffective (27,434)
Psoriasis (21,976)
Pain (15,244)
Arthralgia (13,769)
Fatigue (9,406)
Psoriatic arthropathy (8,900)
Pruritus (8,755)
Malaise (8,570)
Rash (8,023)
Condition aggravated (7,536)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
HYDROCHLOROTHIAZIDE\OLMESARTAN MEDOXOMIL (222)
Which SECUKINUMAB Alternatives Have Lower Product administration error Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG