Does ADALIMUMAB-AATY Cause Intentional dose omission? 338 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 338 reports of Intentional dose omission have been filed in association with ADALIMUMAB-AATY (Yuflyma). This represents 20.1% of all adverse event reports for ADALIMUMAB-AATY.
338
Reports of Intentional dose omission with ADALIMUMAB-AATY
20.1%
of all ADALIMUMAB-AATY reports
7
Deaths
112
Hospitalizations
How Dangerous Is Intentional dose omission From ADALIMUMAB-AATY?
Of the 338 reports, 7 (2.1%) resulted in death, 112 (33.1%) required hospitalization, and 4 (1.2%) were considered life-threatening.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ADALIMUMAB-AATY. However, 338 reports have been filed with the FAERS database.
What Other Side Effects Does ADALIMUMAB-AATY Cause?
Drug ineffective (151)
Intentional product use issue (151)
Death (132)
Arthralgia (96)
Rheumatoid arthritis (94)
Fatigue (92)
Therapy interrupted (88)
Crohn's disease (87)
Headache (86)
Accidental exposure to product (85)
What Other Drugs Cause Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which ADALIMUMAB-AATY Alternatives Have Lower Intentional dose omission Risk?
ADALIMUMAB-AATY vs ADALIMUMAB-ADAZ
ADALIMUMAB-AATY vs ADALIMUMAB-ADBM
ADALIMUMAB-AATY vs ADALIMUMAB-AFZB
ADALIMUMAB-AATY vs ADALIMUMAB-ATTO
ADALIMUMAB-AATY vs ADALIMUMAB-BWWD