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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 Unresponsive to stimuli? 42 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Unresponsive to stimuli have been filed in association with ALEMTUZUMAB (Campath). This represents 0.3% of all adverse event reports for ALEMTUZUMAB.

42
Reports of Unresponsive to stimuli with ALEMTUZUMAB
0.3%
of all ALEMTUZUMAB reports
9
Deaths
30
Hospitalizations

How Dangerous Is Unresponsive to stimuli From ALEMTUZUMAB?

Of the 42 reports, 9 (21.4%) resulted in death, 30 (71.4%) required hospitalization, and 2 (4.8%) were considered life-threatening.

Is Unresponsive to stimuli Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALEMTUZUMAB. However, 42 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 Unresponsive to stimuli?

OXYCODONE (738) FENTANYL (662) QUETIAPINE (542) MORPHINE (483) BACLOFEN (464) CARBIDOPA\LEVODOPA (417) ACETAMINOPHEN (406) CLONAZEPAM (385) METFORMIN (360) OLANZAPINE (353)

Which ALEMTUZUMAB Alternatives Have Lower Unresponsive to stimuli 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 Unresponsive to stimuli Reports All Drugs Causing Unresponsive to stimuli ALEMTUZUMAB Demographics