Does INVESTIGATIONAL PRODUCT Cause Liver function test increased? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Liver function test increased have been filed in association with INVESTIGATIONAL PRODUCT. This represents 0.3% of all adverse event reports for INVESTIGATIONAL PRODUCT.
14
Reports of Liver function test increased with INVESTIGATIONAL PRODUCT
0.3%
of all INVESTIGATIONAL PRODUCT reports
0
Deaths
5
Hospitalizations
How Dangerous Is Liver function test increased From INVESTIGATIONAL PRODUCT?
Of the 14 reports, 5 (35.7%) required hospitalization, and 2 (14.3%) were considered life-threatening.
Is Liver function test increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for INVESTIGATIONAL PRODUCT. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does INVESTIGATIONAL PRODUCT Cause?
Febrile neutropenia (241)
Pneumonia (229)
Acute kidney injury (198)
Pyrexia (189)
Anaemia (176)
Diarrhoea (170)
Sepsis (168)
Dyspnoea (156)
Nausea (134)
Hypotension (130)
What Other Drugs Cause Liver function test increased?
METHOTREXATE (3,839)
ADALIMUMAB (2,070)
ETANERCEPT (1,829)
LEFLUNOMIDE (1,521)
ABATACEPT (1,415)
TOCILIZUMAB (1,406)
RITUXIMAB (1,325)
SULFASALAZINE (1,263)
HYDROXYCHLOROQUINE (1,259)
TOFACITINIB (1,221)
Which INVESTIGATIONAL PRODUCT Alternatives Have Lower Liver function test increased Risk?
INVESTIGATIONAL PRODUCT vs INVOKANA
INVESTIGATIONAL PRODUCT vs IOBENGUANE I-131
INVESTIGATIONAL PRODUCT vs IOBITRIDOL
INVESTIGATIONAL PRODUCT vs IODINE
INVESTIGATIONAL PRODUCT vs IODINE\IOFLUPANE I-123