Does SECUKINUMAB Cause Wrong technique in device usage process? 505 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 505 reports of Wrong technique in device usage process have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.3% of all adverse event reports for SECUKINUMAB.
505
Reports of Wrong technique in device usage process with SECUKINUMAB
0.3%
of all SECUKINUMAB reports
5
Deaths
55
Hospitalizations
How Dangerous Is Wrong technique in device usage process From SECUKINUMAB?
Of the 505 reports, 5 (1.0%) resulted in death, 55 (10.9%) required hospitalization, and 2 (0.4%) were considered life-threatening.
Is Wrong technique in device usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 505 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 device usage process?
ALBUTEROL (5,380)
SOMATROPIN (4,746)
EXENATIDE (3,255)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,673)
FLUTICASONE\SALMETEROL (2,259)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (2,197)
INSULIN GLARGINE (1,749)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,531)
BUDESONIDE\FORMOTEROL (1,481)
BELIMUMAB (1,347)
Which SECUKINUMAB Alternatives Have Lower Wrong technique in device usage process Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG