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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 ALEMTUZUMAB Cause Product use issue? 95 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 95 reports of Product use issue have been filed in association with ALEMTUZUMAB (Campath). This represents 0.7% of all adverse event reports for ALEMTUZUMAB.

95
Reports of Product use issue with ALEMTUZUMAB
0.7%
of all ALEMTUZUMAB reports
6
Deaths
27
Hospitalizations

How Dangerous Is Product use issue From ALEMTUZUMAB?

Of the 95 reports, 6 (6.3%) resulted in death, 27 (28.4%) required hospitalization, and 4 (4.2%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALEMTUZUMAB. However, 95 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 Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which ALEMTUZUMAB Alternatives Have Lower Product use issue Risk?

ALEMTUZUMAB vs ALENDRONATE ALEMTUZUMAB vs ALENDRONATE\CHOLECALCIFEROL ALEMTUZUMAB vs ALENDRONIC ACID ALEMTUZUMAB vs ALEVE ALEMTUZUMAB vs ALEVE CAPLET

Related Pages

ALEMTUZUMAB Full Profile All Product use issue Reports All Drugs Causing Product use issue ALEMTUZUMAB Demographics