Does SUTIMLIMAB-JOME Cause Inappropriate schedule of product administration? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Inappropriate schedule of product administration have been filed in association with SUTIMLIMAB-JOME. This represents 3.8% of all adverse event reports for SUTIMLIMAB-JOME.
8
Reports of Inappropriate schedule of product administration with SUTIMLIMAB-JOME
3.8%
of all SUTIMLIMAB-JOME reports
0
Deaths
0
Hospitalizations
How Dangerous Is Inappropriate schedule of product administration From SUTIMLIMAB-JOME?
Of the 8 reports.
Is Inappropriate schedule of product administration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUTIMLIMAB-JOME. However, 8 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)
Condition aggravated (12)
Drug ineffective (10)
Fatigue (10)
Haemolysis (10)
Headache (9)
Covid-19 (7)
Cyanosis (7)
What Other Drugs Cause Inappropriate schedule of product administration?
ADAPALENE (16,473)
DUPILUMAB (14,927)
AVOBENZONE\OCTISALATE\OCTOCRYLENE (12,546)
INSULIN GLARGINE (8,982)
INFLIXIMAB (6,847)
INFLIXIMAB-DYYB (5,977)
SECUKINUMAB (4,817)
DULAGLUTIDE (3,606)
VEDOLIZUMAB (3,259)
SACUBITRIL\VALSARTAN (2,870)
Which SUTIMLIMAB-JOME Alternatives Have Lower Inappropriate schedule of product administration Risk?
SUTIMLIMAB-JOME vs SUVOREXANT
SUTIMLIMAB-JOME vs SUZETRIGINE
SUTIMLIMAB-JOME vs SYMBICORT
SUTIMLIMAB-JOME vs SYNAGIS
SUTIMLIMAB-JOME vs SYNTHROID