Does SECUKINUMAB Cause Product prescribing error? 821 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), 821 reports of Product prescribing error have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.5% of all adverse event reports for SECUKINUMAB.
821
Reports of Product prescribing error with SECUKINUMAB
0.5%
of all SECUKINUMAB reports
9
Deaths
152
Hospitalizations
How Dangerous Is Product prescribing error From SECUKINUMAB?
Of the 821 reports, 9 (1.1%) resulted in death, 152 (18.5%) required hospitalization, and 22 (2.7%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 821 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
RAMIPRIL (322)
Which SECUKINUMAB Alternatives Have Lower Product prescribing error Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG