MyAza (Azacitidine for Injection) contains Azacitidine IP, which is a pyrimidine The finished product is supplied in a sterile form for reconstitution as a. No formal clinical drug interaction studies with azacitidine have been conducted. The printed package leaflet of the medicinal product must state the name. Drug: Azacitidine – Vidaza® Oncology – Intravenous Dilution Data. (, ) – [ SEE PACKAGE INSERT FOR ADDITIONAL DETAILS]].

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When suppressor gene activity is blocked, cell division becomes unregulated, leading to the formation of neoplastic cells. This suppressed reactivity can persist for up to 6 weeks after treatment discontinuation. Send the page ” ” to a friend, relative, colleague or yourself.

Recipient’s Email Separate multiple email address with a comma Please enter valid email address Recipient’s email is required. Moderate Immunosuppressives may decrease the immunological response to tuberculin purified protein derivative, PPD.

Rotate sites for each injection thigh, abdomen, or upper arm. Hypermethylation is thought to be an early step in malignant transformation of cells.

Among those patients, overall survival was Monitor liver function tests prior to starting azacitidine and before each cycle of therapy. The solution is stable at room temperature 25 degrees C or 77 degrees F for up to 1 hour after reconstitution. Bone marrow suppression, neutropenia, thrombocytopenia. Your Name Your name is required. If the dose requires using more than one mg vial, divide the dose equally between 2 syringes; due to retention in the vial and needle, it may not be feasible to withdraw all of the contents from the vial.


All patients should receive antiemetics prior to each azacitidine dose. Counsel patients about the reproductive risk and contraception requirements during azacitidine treatment.

Shake or roll the vial vigorously until all powder is dissolved; the solution should be clear.

Administer the total dose over a period of 10 — 40 minutes. The following symptoms require medical attention, but are not an emergency. Your email has been sent.

Azacitidine – Vidaza® – GlobalRPH

Azacitidine is contraindicated in patients with advanced hepatic malignancies. Chemotherapy and biotherapy guidelines and recommendations for practice 2nd. Rotate sites for each injection thigh, abdomen, or upper arm. The primary route of elimination is urinary excretion. Once incorporated into tRNA, azacitidine inhibits tRNA methyltransferases and interferes with tRNA methylation and azacitkdine, which leads to inhibition of protein synthesis.

Azacitidine (Vidaza) | – A Hematology Oncology Wiki

Do not filter the suspension after reconstitution as this may remove the active substance. Major Do not use penicillamine with antineoplastic agents due to the increased risk of developing severe hematologic and renal toxicity. If it comes into contact with mucous membranes, flush thoroughly azscitidine water.


Azacitidine inhibition of DNA methyltransferase is dose- azacitivine time-dependent. Elevated BUN or serum creatinine level during therapy: Shake or roll the vial vigorously until a uniform suspension occurs; the suspension will be cloudy.

Azacitidine (Vidaza)

Hepatotoxicity may occur in patients with severe hepatic impairment. The reconstituted product may be kept in the vial or drawn into a syringe.

Doses greater than 4 mL should be divided equally into 2 syringes and injected into 2 separate sites.

Methylation usually suppresses gene transcription and gene deletion. However, you should always inform your health care provider if you experience any unusual symptoms.