Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Alemtuzumab
Drug ID BADD_D00064
Description Humanized monoclonal antibody specific to lymphocyte antigens. It is a recombinant DNA-derived humanized monoclonal antibody (Campath-1H) that is directed against the 21-28 kD cell surface glycoprotein,CD52. The Campath-1H antibody is an IgG1 kappa with human variable framework and constant regions, and complementarity-determining regions from a murine (rat) monoclonal antibody (Campath-1G). Campath is produced in mammalian cell (Chinese hamster ovary) suspension culture in a medium containing neomycin.
Indications and Usage Alemtuzumab (Campath) is a monoclonal antibody therapy used for treatment of B-cell chronic lymphocytic leukemia.
Marketing Status approved; investigational
ATC Code L04AA34
DrugBank ID DB00087
KEGG ID D02802
MeSH ID D000074323
PubChem ID Not Available
TTD Drug ID D01ZYG
NDC Product Code 58468-0200; 58468-0357
UNII 3A189DH42V
Synonyms Alemtuzumab | Campath 1H | Monoclonal Antibody Campath-1H | Antibody Campath-1H, Monoclonal | Campath-1H, Monoclonal Antibody | Monoclonal Antibody Campath 1H | Campath-1H | Campath1H | Campath 1M | Campath-1M | MabCambath | Lemtrada | Campath 1G | Campath-1-G | Campath 1 G | Campath1G | Campath-1G | Campath
Chemical Information
Molecular Formula Not Available
CAS Registry Number 216503-57-0
SMILES Not Available
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice.
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Pain in extremity15.03.04.010--
Paraesthesia17.02.06.005; 23.03.03.094--
Parathyroid disorder05.04.03.001---
Progressive multifocal leukoencephalopathy11.05.05.001; 17.16.02.002---
Pruritus23.03.12.001--
Pyrexia08.05.02.003--
Rash23.03.13.001---
Respiratory arrest22.02.01.009---
Sepsis11.01.11.003--
Serum sickness10.01.03.004; 12.02.08.004--
Sinusitis11.01.13.005; 22.07.03.007--
Suicidal ideation19.12.01.003--
Syncope02.11.04.015; 17.02.04.008; 24.06.02.012--
Tachycardia02.03.02.007---
Thrombocytopenia01.08.01.002---
Transfusion reaction01.05.01.005; 10.02.04.001; 12.02.08.001---
Tremor17.01.06.002--
Tumour lysis syndrome14.05.01.004; 16.32.03.002--
Upper respiratory tract infection11.01.13.009; 22.07.03.011--
Urinary tract infection11.01.14.004; 20.08.02.001--
Urticaria10.01.06.001; 23.04.02.001--
Viral infection11.05.04.001---
Vomiting07.01.07.003--
Ejection fraction decreased13.14.02.003--
T-lymphocyte count decreased13.01.06.049---
Chronic inflammatory demyelinating polyradiculoneuropathy10.04.10.004; 17.09.04.004---
Cytomegalovirus viraemia11.05.01.003---
Lymphoproliferative disorder01.13.02.001; 16.21.02.001---
Optic neuropathy06.02.08.002; 17.04.05.005---
Antibody test positive13.06.03.001---
The 3th Page    First    Pre   3 4    Next   Last    Total 4 Pages