Does SUTIMLIMAB-JOME Cause Haemoglobin decreased? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Haemoglobin decreased have been filed in association with SUTIMLIMAB-JOME. This represents 7.2% of all adverse event reports for SUTIMLIMAB-JOME.
15
Reports of Haemoglobin decreased with SUTIMLIMAB-JOME
7.2%
of all SUTIMLIMAB-JOME reports
0
Deaths
5
Hospitalizations
How Dangerous Is Haemoglobin decreased From SUTIMLIMAB-JOME?
Of the 15 reports, 5 (33.3%) required hospitalization, and 1 (6.7%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SUTIMLIMAB-JOME. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does SUTIMLIMAB-JOME Cause?
Off label use (18)
Arthralgia (15)
Condition aggravated (12)
Drug ineffective (10)
Fatigue (10)
Haemolysis (10)
Headache (9)
Inappropriate schedule of product administration (8)
Covid-19 (7)
Cyanosis (7)
What Other Drugs Cause Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which SUTIMLIMAB-JOME Alternatives Have Lower Haemoglobin decreased Risk?
SUTIMLIMAB-JOME vs SUVOREXANT
SUTIMLIMAB-JOME vs SUZETRIGINE
SUTIMLIMAB-JOME vs SYMBICORT
SUTIMLIMAB-JOME vs SYNAGIS
SUTIMLIMAB-JOME vs SYNTHROID