Does UPADACITINIB Cause Product use complaint? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Product use complaint have been filed in association with UPADACITINIB (Rinvoq). This represents 0.0% of all adverse event reports for UPADACITINIB.
27
Reports of Product use complaint with UPADACITINIB
0.0%
of all UPADACITINIB reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product use complaint From UPADACITINIB?
Of the 27 reports, 5 (18.5%) required hospitalization, and 1 (3.7%) were considered life-threatening.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UPADACITINIB. However, 27 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 Product use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which UPADACITINIB Alternatives Have Lower Product use complaint Risk?
UPADACITINIB vs URAPIDIL
UPADACITINIB vs UREA
UPADACITINIB vs URIDINE TRIACETATE
UPADACITINIB vs UROFOLLITROPIN
UPADACITINIB vs URSODIOL