Azacitidinum [INN-Latin] en es it fr

Azacitidinum [INN-Latin] Brand names, Azacitidinum [INN-Latin] Analogs

Azacitidinum [INN-Latin] Brand Names Mixture

  • No information avaliable

Azacitidinum [INN-Latin] Chemical_Formula


Azacitidinum [INN-Latin] RX_link

Azacitidinum [INN-Latin] fda sheet

Azacitidinum_[INN-Latin] FDA

Azacitidinum [INN-Latin] msds (material safety sheet)

Azacitidinum_[INN-Latin] MSDS

Azacitidinum [INN-Latin] Synthesis Reference

No information avaliable

Azacitidinum [INN-Latin] Molecular Weight

244.205 g/mol

Azacitidinum [INN-Latin] Melting Point

229 oC

Azacitidinum [INN-Latin] H2O Solubility

8.9E+004 mg/L

Azacitidinum [INN-Latin] State


Azacitidinum [INN-Latin] LogP


Azacitidinum [INN-Latin] Dosage Forms

Azacitidine for injectable suspension is supplied as a lyophilized powder in 100 mg single-use vials packaged in cartons of 1 vial.

Azacitidinum [INN-Latin] Indication

For treatment of patients with the following myelodysplastic syndrome subtypes: refractory anemia or refractory anemia with ringed sideroblasts (if accompanied by neutropenia or thrombocytopenia or requiring transfusions), refractory anemia with excess blasts, refractory anemia with excess blasts in transformation, and chronic myelomonocytic leukemia.

Azacitidinum [INN-Latin] Pharmacology

Azacitidine is believed to exert its antineoplastic effects by causing hypomethylation of DNA and direct cytotoxicity on abnormal hematopoietic cells in the bone marrow. The concentration of azacitidine required for maximum inhibition of DNA methylation in vitro does not cause major suppression of DNA synthesis. Hypomethylation may restore normal function to genes that are critical for differentiation and proliferation. The cytotoxic effects of azacitidine cause the death of rapidly dividing cells, including cancer cells that are no longer responsive to normal growth control mechanisms. Non-proliferating cells are relatively insensitive to azacitidine.

Azacitidinum [INN-Latin] Absorption

Azacitidine is rapidly absorbed after subcutaneous administration. The bioavailability of subcutaneous azacitidine relative to IV azacitidine is approximately 89%, based on area under the curve.

Azacitidinum [INN-Latin] side effects and Toxicity

One case of overdose with azacitidine was reported during clinical trials. A patient experienced diarrhea, nausea, and vomiting after receiving a single IV dose of approximately 290 mg/m2, almost 4 times the recommended starting dose.

Azacitidinum [INN-Latin] Patient Information

Azacitidinum [INN-Latin] Organisms Affected

Humans and other mammals