Does ALEMTUZUMAB Cause Fibrin d dimer increased? 39 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of Fibrin d dimer increased have been filed in association with ALEMTUZUMAB (Campath). This represents 0.3% of all adverse event reports for ALEMTUZUMAB.
39
Reports of Fibrin d dimer increased with ALEMTUZUMAB
0.3%
of all ALEMTUZUMAB reports
1
Deaths
29
Hospitalizations
How Dangerous Is Fibrin d dimer increased From ALEMTUZUMAB?
Of the 39 reports, 1 (2.6%) resulted in death, 29 (74.4%) required hospitalization, and 2 (5.1%) were considered life-threatening.
Is Fibrin d dimer increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALEMTUZUMAB. However, 39 reports have been filed with the FAERS database.
What Other Side Effects Does ALEMTUZUMAB Cause?
Headache (1,808)
Fatigue (1,744)
Pyrexia (1,441)
Off label use (1,259)
Rash (1,094)
Nausea (1,053)
Dyspnoea (855)
Lymphocyte count decreased (852)
Asthenia (841)
Multiple sclerosis relapse (836)
What Other Drugs Cause Fibrin d dimer increased?
ADALIMUMAB (97)
RIVAROXABAN (91)
PREDNISONE (69)
RITUXIMAB (63)
APIXABAN (59)
ASPIRIN (54)
ACETAMINOPHEN (53)
LENALIDOMIDE (53)
METHOTREXATE (52)
BAMLANIVIMAB (49)
Which ALEMTUZUMAB Alternatives Have Lower Fibrin d dimer increased Risk?
ALEMTUZUMAB vs ALENDRONATE
ALEMTUZUMAB vs ALENDRONATE\CHOLECALCIFEROL
ALEMTUZUMAB vs ALENDRONIC ACID
ALEMTUZUMAB vs ALEVE
ALEMTUZUMAB vs ALEVE CAPLET