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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does LUTETIUM LU-177 Cause Condition aggravated? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Condition aggravated have been filed in association with LUTETIUM LU-177. This represents 5.3% of all adverse event reports for LUTETIUM LU-177.

6
Reports of Condition aggravated with LUTETIUM LU-177
5.3%
of all LUTETIUM LU-177 reports
0
Deaths
1
Hospitalizations

How Dangerous Is Condition aggravated From LUTETIUM LU-177?

Of the 6 reports, 1 (16.7%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LUTETIUM LU-177. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does LUTETIUM LU-177 Cause?

Malignant neoplasm progression (39) Fatigue (35) Diarrhoea (29) Abdominal pain (19) Asthenia (19) Vomiting (19) Blood pressure increased (18) Body temperature decreased (18) Drug ineffective (18) Blood pressure systolic increased (17)

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 LUTETIUM LU-177 Alternatives Have Lower Condition aggravated Risk?

LUTETIUM LU-177 vs LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN LUTETIUM LU-177 vs LUTETIUM OXODOTREOTIDE LU-177 LUTETIUM LU-177 vs LUTROPIN ALFA LUTETIUM LU-177 vs LYMECYCLINE LUTETIUM LU-177 vs LYRICA

Related Pages

LUTETIUM LU-177 Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated LUTETIUM LU-177 Demographics