Does SECUKINUMAB Cause Product storage error? 1,274 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,274 reports of Product storage error have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.8% of all adverse event reports for SECUKINUMAB.
1,274
Reports of Product storage error with SECUKINUMAB
0.8%
of all SECUKINUMAB reports
6
Deaths
62
Hospitalizations
How Dangerous Is Product storage error From SECUKINUMAB?
Of the 1,274 reports, 6 (0.5%) resulted in death, 62 (4.9%) required hospitalization, and 23 (1.8%) were considered life-threatening.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 1,274 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which SECUKINUMAB Alternatives Have Lower Product storage error Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG