Does LUSPATERCEPT-AAMT Cause Condition aggravated? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Condition aggravated have been filed in association with LUSPATERCEPT-AAMT. This represents 0.6% of all adverse event reports for LUSPATERCEPT-AAMT.
10
Reports of Condition aggravated with LUSPATERCEPT-AAMT
0.6%
of all LUSPATERCEPT-AAMT reports
1
Deaths
4
Hospitalizations
How Dangerous Is Condition aggravated From LUSPATERCEPT-AAMT?
Of the 10 reports, 1 (10.0%) resulted in death, 4 (40.0%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LUSPATERCEPT-AAMT. However, 10 reports have been filed with the FAERS database.
What Other Side Effects Does LUSPATERCEPT-AAMT Cause?
Death (162)
Haemoglobin decreased (98)
Fatigue (86)
Off label use (85)
Weight decreased (76)
Dizziness (64)
Product storage error (64)
Drug ineffective (58)
Dyspnoea (52)
Fall (51)
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 LUSPATERCEPT-AAMT Alternatives Have Lower Condition aggravated Risk?
LUSPATERCEPT-AAMT vs LUTEIN
LUSPATERCEPT-AAMT vs LUTETIUM LU-177
LUSPATERCEPT-AAMT vs LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN
LUSPATERCEPT-AAMT vs LUTETIUM OXODOTREOTIDE LU-177
LUSPATERCEPT-AAMT vs LUTROPIN ALFA