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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 Mobility decreased? 229 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 229 reports of Mobility decreased have been filed in association with ALEMTUZUMAB (Campath). This represents 1.6% of all adverse event reports for ALEMTUZUMAB.

229
Reports of Mobility decreased with ALEMTUZUMAB
1.6%
of all ALEMTUZUMAB reports
7
Deaths
130
Hospitalizations

How Dangerous Is Mobility decreased From ALEMTUZUMAB?

Of the 229 reports, 7 (3.1%) resulted in death, 130 (56.8%) required hospitalization, and 9 (3.9%) were considered life-threatening.

Is Mobility decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALEMTUZUMAB. However, 229 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 Mobility decreased?

ADALIMUMAB (8,829) ETANERCEPT (8,321) METHOTREXATE (5,936) ABATACEPT (4,519) TOCILIZUMAB (4,403) LEFLUNOMIDE (4,354) HYDROXYCHLOROQUINE (4,105) RITUXIMAB (4,067) INFLIXIMAB (3,784) TOFACITINIB (3,734)

Which ALEMTUZUMAB Alternatives Have Lower Mobility decreased 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 Mobility decreased Reports All Drugs Causing Mobility decreased ALEMTUZUMAB Demographics