Does ALEMTUZUMAB Cause Laboratory test abnormal? 166 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 166 reports of Laboratory test abnormal have been filed in association with ALEMTUZUMAB (Campath). This represents 1.2% of all adverse event reports for ALEMTUZUMAB.
166
Reports of Laboratory test abnormal with ALEMTUZUMAB
1.2%
of all ALEMTUZUMAB reports
6
Deaths
91
Hospitalizations
How Dangerous Is Laboratory test abnormal From ALEMTUZUMAB?
Of the 166 reports, 6 (3.6%) resulted in death, 91 (54.8%) required hospitalization, and 9 (5.4%) were considered life-threatening.
Is Laboratory test abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALEMTUZUMAB. However, 166 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 Laboratory test abnormal?
LENALIDOMIDE (4,215)
CINACALCET (4,210)
POMALIDOMIDE (1,218)
ADALIMUMAB (845)
ETANERCEPT (753)
DALFAMPRIDINE (650)
PALBOCICLIB (550)
NIRAPARIB (536)
METHOTREXATE (507)
ECULIZUMAB (441)
Which ALEMTUZUMAB Alternatives Have Lower Laboratory test abnormal Risk?
ALEMTUZUMAB vs ALENDRONATE
ALEMTUZUMAB vs ALENDRONATE\CHOLECALCIFEROL
ALEMTUZUMAB vs ALENDRONIC ACID
ALEMTUZUMAB vs ALEVE
ALEMTUZUMAB vs ALEVE CAPLET