Does LUTETIUM OXODOTREOTIDE LU-177 Cause Liver function test increased? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Liver function test increased have been filed in association with LUTETIUM OXODOTREOTIDE LU-177 (Lutathera). This represents 0.1% of all adverse event reports for LUTETIUM OXODOTREOTIDE LU-177.
7
Reports of Liver function test increased with LUTETIUM OXODOTREOTIDE LU-177
0.1%
of all LUTETIUM OXODOTREOTIDE LU-177 reports
0
Deaths
0
Hospitalizations
How Dangerous Is Liver function test increased From LUTETIUM OXODOTREOTIDE LU-177?
Of the 7 reports.
Is Liver function test increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LUTETIUM OXODOTREOTIDE LU-177. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does LUTETIUM OXODOTREOTIDE LU-177 Cause?
Ill-defined disorder (1,538)
General physical health deterioration (906)
Death (431)
Malignant neoplasm progression (338)
Platelet count decreased (220)
Nausea (214)
Covid-19 (193)
Fatigue (185)
Diarrhoea (169)
Disease progression (169)
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 LUTETIUM OXODOTREOTIDE LU-177 Alternatives Have Lower Liver function test increased Risk?
LUTETIUM OXODOTREOTIDE LU-177 vs LUTROPIN ALFA
LUTETIUM OXODOTREOTIDE LU-177 vs LYMECYCLINE
LUTETIUM OXODOTREOTIDE LU-177 vs LYRICA
LUTETIUM OXODOTREOTIDE LU-177 vs LYSERGIDE
LUTETIUM OXODOTREOTIDE LU-177 vs MABTHERA