Does LUSPATERCEPT-AAMT Cause Haemoglobin decreased? 98 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 98 reports of Haemoglobin decreased have been filed in association with LUSPATERCEPT-AAMT. This represents 5.8% of all adverse event reports for LUSPATERCEPT-AAMT.
98
Reports of Haemoglobin decreased with LUSPATERCEPT-AAMT
5.8%
of all LUSPATERCEPT-AAMT reports
3
Deaths
15
Hospitalizations
How Dangerous Is Haemoglobin decreased From LUSPATERCEPT-AAMT?
Of the 98 reports, 3 (3.1%) resulted in death, 15 (15.3%) required hospitalization, and 2 (2.0%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LUSPATERCEPT-AAMT. However, 98 reports have been filed with the FAERS database.
What Other Side Effects Does LUSPATERCEPT-AAMT Cause?
Death (162)
Fatigue (86)
Off label use (85)
Weight decreased (76)
Dizziness (64)
Product storage error (64)
Drug ineffective (58)
Dyspnoea (52)
Fall (51)
Weight increased (44)
What Other Drugs Cause Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which LUSPATERCEPT-AAMT Alternatives Have Lower Haemoglobin decreased 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