Does SECUKINUMAB Cause Wrong technique in product usage process? 797 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 797 reports of Wrong technique in product usage process have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.5% of all adverse event reports for SECUKINUMAB.
797
Reports of Wrong technique in product usage process with SECUKINUMAB
0.5%
of all SECUKINUMAB reports
2
Deaths
41
Hospitalizations
How Dangerous Is Wrong technique in product usage process From SECUKINUMAB?
Of the 797 reports, 2 (0.3%) resulted in death, 41 (5.1%) required hospitalization, and 10 (1.3%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 797 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which SECUKINUMAB Alternatives Have Lower Wrong technique in product usage process Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG