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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 storage error? 10 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product storage error have been filed in association with ALEMTUZUMAB (Campath). This represents 0.1% of all adverse event reports for ALEMTUZUMAB.

10
Reports of Product storage error with ALEMTUZUMAB
0.1%
of all ALEMTUZUMAB reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product storage error From ALEMTUZUMAB?

Of the 10 reports, 1 (10.0%) required hospitalization.

Is Product storage error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALEMTUZUMAB. However, 10 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 storage error?

INSULIN GLARGINE (7,743) EVOLOCUMAB (6,606) ETANERCEPT (3,653) DENOSUMAB (3,621) ERENUMAB-AOOE (2,958) DUPILUMAB (2,631) ALBUTEROL (2,474) ABATACEPT (2,101) DARBEPOETIN ALFA (1,619) INSULIN LISPRO (1,448)

Which ALEMTUZUMAB Alternatives Have Lower Product storage error 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 storage error Reports All Drugs Causing Product storage error ALEMTUZUMAB Demographics