Does SECUKINUMAB Cause Incorrect dose administered by device? 996 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 996 reports of Incorrect dose administered by device have been filed in association with SECUKINUMAB (COSENTYX). This represents 0.7% of all adverse event reports for SECUKINUMAB.
996
Reports of Incorrect dose administered by device with SECUKINUMAB
0.7%
of all SECUKINUMAB reports
2
Deaths
25
Hospitalizations
How Dangerous Is Incorrect dose administered by device From SECUKINUMAB?
Of the 996 reports, 2 (0.2%) resulted in death, 25 (2.5%) required hospitalization, and 6 (0.6%) were considered life-threatening.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SECUKINUMAB. However, 996 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 Incorrect dose administered by device?
EXENATIDE (3,332)
EVOLOCUMAB (2,840)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
PEGFILGRASTIM (487)
Which SECUKINUMAB Alternatives Have Lower Incorrect dose administered by device Risk?
SECUKINUMAB vs SELADELPAR LYSINE
SECUKINUMAB vs SELEGILINE
SECUKINUMAB vs SELENIUM
SECUKINUMAB vs SELENIUM SULFIDE
SECUKINUMAB vs SELEXIPAG