Does UPADACITINIB Cause Post procedural complication? 241 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 241 reports of Post procedural complication have been filed in association with UPADACITINIB (Rinvoq). This represents 0.4% of all adverse event reports for UPADACITINIB.
241
Reports of Post procedural complication with UPADACITINIB
0.4%
of all UPADACITINIB reports
6
Deaths
80
Hospitalizations
How Dangerous Is Post procedural complication From UPADACITINIB?
Of the 241 reports, 6 (2.5%) resulted in death, 80 (33.2%) required hospitalization, and 4 (1.7%) were considered life-threatening.
Is Post procedural complication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UPADACITINIB. However, 241 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 Post procedural complication?
ADALIMUMAB (2,494)
ETANERCEPT (318)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (244)
RISANKIZUMAB-RZAA (232)
INFLIXIMAB (217)
METHOTREXATE (188)
TREPROSTINIL (174)
HUMAN IMMUNOGLOBULIN G (159)
PREDNISONE (157)
CARBIDOPA\LEVODOPA (156)
Which UPADACITINIB Alternatives Have Lower Post procedural complication Risk?
UPADACITINIB vs URAPIDIL
UPADACITINIB vs UREA
UPADACITINIB vs URIDINE TRIACETATE
UPADACITINIB vs UROFOLLITROPIN
UPADACITINIB vs URSODIOL