Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Gemtuzumab ozogamicin
Drug ID BADD_D01015
Description Gemtuzumab ozogamicin is a recombinant humanized IgG4 kappa antibody which is conjugated with calicheamicin derivative, a cytotoxic antitumor antibiotic isolated from fermentation of Micromonospora echinospora ssp. calichensis. Gemtuzumab ozogamicin has approximately 50% of the antibody loaded with 4-6 moles calicheamicin per mole of antibody [FDA Label]. The antibody is specifically directed against the CD33 antigen present on leukemic myeloblasts in most patients with acute myeloid leukemia (AML). By binding to the CD33 antigen on tumors, the cytotoxic agent blocks the growth of cancerous cells and causes cell death. Marketing approval of gemtuzumab ozogamicin was granted on May 17, 2000 by FDA as a treatment for patients with CD33-positive AML in first relapse who are 60 years of age or older and who are not considered candidates for cytotoxic chemotherapy [A98]. However, it was voluntarily withdrawn from the market in 2010 due to safety concerns, increased patient deaths and insufficient evidence of clinical benefit during confirmatory trials [L941]. On September 1 2017, gemtuzumab ozogamicin was again approved for the treatment of adults with newly diagnosed CD33-positive acute myeloid leukemia but with a lower dosing regimen and a different schedule in combination with chemotherapy or on its own [L941]. It is also indicated for the treatment of patients aged 2 years and older with CD33-positive AML who have experienced a relapse or who have not responded to initial treatment (refractory) [L941].
Indications and Usage Indicated for the treatment of patients with CD33 positive acute myeloid leukemia in first relapse who are 60 years of age or older and who are not considered candidates for other cytotoxic chemotherapy. Indicated for the treatment of patients aged 2 years and older with CD33-positive AML who have experienced a relapse or who have not responded to initial treatment (refractory).
Marketing Status approved; investigational
ATC Code L01FX02
DrugBank ID DB00056
KEGG ID D03259
MeSH ID D000079982
PubChem ID Not Available
TTD Drug ID D06EWO
NDC Product Code 0008-4510
UNII 8GZG754X6M
Synonyms Gemtuzumab | Mylotarg | Gemtuzumab Ozogamicin | Gemtuzumab-Ozogamicin | CMA 676 | CMA-676 | CMA676
Chemical Information
Molecular Formula Not Available
CAS Registry Number 220578-59-6
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)
Abdominal pain07.01.05.002--
Activated partial thromboplastin time abnormal13.01.02.019---
Alanine aminotransferase13.03.04.002---
Alanine aminotransferase abnormal13.03.04.003---
Anaemia01.03.02.001--
Anaphylactic reaction10.01.07.001; 24.06.03.006--
Anxiety19.06.02.002--
Aspartate aminotransferase13.03.04.008---
Aspartate aminotransferase abnormal13.03.04.009---
Asthenia08.01.01.001---
Back pain15.03.04.005--
Blood alkaline phosphatase13.04.02.010---
Blood bilirubin13.03.04.015---
Blood creatinine13.13.01.020---
Blood lactate dehydrogenase increased13.04.02.002--
Bradycardia02.03.02.002---
Budd-Chiari syndrome09.01.06.001; 24.01.03.001--
Cerebral haemorrhage17.08.01.003; 24.07.04.001---
Chills08.01.09.001; 15.05.03.016--
Constipation07.02.02.001--
Cough22.02.03.001--
Depression19.15.01.001--
Diarrhoea07.02.01.001--
Disseminated intravascular coagulation01.01.02.002; 24.01.01.010--
Dizziness02.11.04.006; 17.02.05.003; 24.06.02.007--
Dyspepsia07.01.02.001--
Dyspnoea02.11.05.003; 22.02.01.004--
Ecchymosis01.01.03.001; 23.06.01.001; 24.07.06.002---
Epistaxis22.04.03.001; 24.07.01.005--
Febrile neutropenia01.02.03.002; 08.05.02.004--
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