Does IBREXAFUNGERP Cause Recalled product administered? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Recalled product administered have been filed in association with IBREXAFUNGERP. This represents 15.5% of all adverse event reports for IBREXAFUNGERP.
20
Reports of Recalled product administered with IBREXAFUNGERP
15.5%
of all IBREXAFUNGERP reports
0
Deaths
1
Hospitalizations
How Dangerous Is Recalled product administered From IBREXAFUNGERP?
Of the 20 reports, 1 (5.0%) required hospitalization.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for IBREXAFUNGERP. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does IBREXAFUNGERP Cause?
Drug ineffective (31)
Diarrhoea (26)
Nausea (22)
Vomiting (13)
Therapeutic product effect incomplete (10)
Dizziness (9)
Product dispensing error (9)
Abdominal pain (7)
Off label use (7)
Abdominal pain upper (6)
What Other Drugs Cause Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which IBREXAFUNGERP Alternatives Have Lower Recalled product administered Risk?
IBREXAFUNGERP vs IBRITUMOMAB TIUXETAN
IBREXAFUNGERP vs IBRUTINIB
IBREXAFUNGERP vs IBUPROFEN
IBREXAFUNGERP vs IBUPROFEN LYSINE
IBREXAFUNGERP vs IBUPROFEN UNKNOWN PRODUCT