Does UPADACITINIB Cause Intentional product misuse? 155 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 155 reports of Intentional product misuse have been filed in association with UPADACITINIB (Rinvoq). This represents 0.2% of all adverse event reports for UPADACITINIB.
155
Reports of Intentional product misuse with UPADACITINIB
0.2%
of all UPADACITINIB reports
3
Deaths
39
Hospitalizations
How Dangerous Is Intentional product misuse From UPADACITINIB?
Of the 155 reports, 3 (1.9%) resulted in death, 39 (25.2%) required hospitalization, and 2 (1.3%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UPADACITINIB. However, 155 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 product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which UPADACITINIB Alternatives Have Lower Intentional product misuse Risk?
UPADACITINIB vs URAPIDIL
UPADACITINIB vs UREA
UPADACITINIB vs URIDINE TRIACETATE
UPADACITINIB vs UROFOLLITROPIN
UPADACITINIB vs URSODIOL