Does UPADACITINIB Cause Intentional dose omission? 232 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 232 reports of Intentional dose omission have been filed in association with UPADACITINIB (Rinvoq). This represents 0.4% of all adverse event reports for UPADACITINIB.
232
Reports of Intentional dose omission with UPADACITINIB
0.4%
of all UPADACITINIB reports
2
Deaths
8
Hospitalizations
How Dangerous Is Intentional dose omission From UPADACITINIB?
Of the 232 reports, 2 (0.9%) resulted in death, 8 (3.4%) required hospitalization, and 2 (0.9%) 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 UPADACITINIB. However, 232 reports have been filed with the FAERS database.
What Other Side Effects Does UPADACITINIB Cause?
Pain (4,444)
Arthralgia (3,815)
Drug ineffective (3,384)
Covid-19 (2,978)
Rheumatoid arthritis (2,730)
Pain in extremity (2,353)
Fatigue (2,153)
Fall (2,081)
Surgery (2,037)
Therapy interrupted (1,741)
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 UPADACITINIB Alternatives Have Lower Intentional dose omission Risk?
UPADACITINIB vs URAPIDIL
UPADACITINIB vs UREA
UPADACITINIB vs URIDINE TRIACETATE
UPADACITINIB vs UROFOLLITROPIN
UPADACITINIB vs URSODIOL