Does SUTIMLIMAB-JOME Cause Condition aggravated? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Condition aggravated have been filed in association with SUTIMLIMAB-JOME. This represents 5.7% of all adverse event reports for SUTIMLIMAB-JOME.
12
Reports of Condition aggravated with SUTIMLIMAB-JOME
5.7%
of all SUTIMLIMAB-JOME reports
4
Deaths
4
Hospitalizations
How Dangerous Is Condition aggravated From SUTIMLIMAB-JOME?
Of the 12 reports, 4 (33.3%) resulted in death, 4 (33.3%) required hospitalization, and 1 (8.3%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUTIMLIMAB-JOME. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does SUTIMLIMAB-JOME Cause?
Off label use (18)
Arthralgia (15)
Haemoglobin decreased (15)
Drug ineffective (10)
Fatigue (10)
Haemolysis (10)
Headache (9)
Inappropriate schedule of product administration (8)
Covid-19 (7)
Cyanosis (7)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which SUTIMLIMAB-JOME Alternatives Have Lower Condition aggravated Risk?
SUTIMLIMAB-JOME vs SUVOREXANT
SUTIMLIMAB-JOME vs SUZETRIGINE
SUTIMLIMAB-JOME vs SYMBICORT
SUTIMLIMAB-JOME vs SYNAGIS
SUTIMLIMAB-JOME vs SYNTHROID