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 However, it was voluntarily withdrawn from the market in 2010 due to safety concerns, increased patient deaths and insufficient evidence of clinical benefit during confirmatory trials [L941].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 Prescription; Discontinued
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
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
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Nausea07.01.07.001--
Neutropenia01.02.03.004--Not Available
Neutrophil count13.01.06.046--Not Available
Oedema peripheral02.05.04.007; 08.01.07.007; 14.05.06.011--
Pain08.01.08.004--
Petechiae24.07.06.004; 23.06.01.003; 01.01.03.002--Not Available
Pharyngitis22.07.03.004; 11.01.13.003; 07.05.07.004--
Platelet count13.01.04.011--Not Available
Pneumonia22.07.01.003; 11.01.09.003--Not Available
Portal vein thrombosis24.01.03.003; 09.01.06.007--
Prothrombin time13.01.02.038--Not Available
Pruritus23.03.12.001--
Pulmonary haemorrhage22.02.04.003; 24.07.01.016--
Pyrexia08.05.02.003--
Rash23.03.13.001--Not Available
Renal disorder20.01.02.002--Not Available
Renal failure20.01.03.005--Not Available
Rhinitis22.07.03.006; 11.01.13.004--
Sepsis11.01.11.003--
Shock24.06.02.002--Not Available
Stomatitis07.05.06.005--
Tachycardia02.03.02.007--Not Available
Thrombocytopenia01.08.01.002--Not Available
Vaginal haemorrhage24.07.03.005; 21.08.01.001--
Vomiting07.01.07.003--
White blood cell count13.01.06.027--Not Available
Neutropenic sepsis11.01.11.006; 01.02.03.007--Not Available
Infusion related reaction12.02.05.009; 10.01.01.017; 08.01.03.002--
Haemorrhage24.07.01.002--Not Available
Blood alkaline phosphatase increased13.04.02.004--
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