Does IBREXAFUNGERP Cause Condition aggravated? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Condition aggravated have been filed in association with IBREXAFUNGERP. This represents 3.9% of all adverse event reports for IBREXAFUNGERP.
5
Reports of Condition aggravated with IBREXAFUNGERP
3.9%
of all IBREXAFUNGERP reports
0
Deaths
0
Hospitalizations
How Dangerous Is Condition aggravated From IBREXAFUNGERP?
Of the 5 reports.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBREXAFUNGERP. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does IBREXAFUNGERP Cause?
Drug ineffective (31)
Diarrhoea (26)
Nausea (22)
Recalled product administered (20)
Vomiting (13)
Therapeutic product effect incomplete (10)
Dizziness (9)
Product dispensing error (9)
Abdominal pain (7)
Off label use (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 IBREXAFUNGERP Alternatives Have Lower Condition aggravated Risk?
IBREXAFUNGERP vs IBRITUMOMAB TIUXETAN
IBREXAFUNGERP vs IBRUTINIB
IBREXAFUNGERP vs IBUPROFEN
IBREXAFUNGERP vs IBUPROFEN LYSINE
IBREXAFUNGERP vs IBUPROFEN UNKNOWN PRODUCT