Azacitidine Injection 100mg Citaza

What is the purpose of the medicine Azacitidine Injection?

Azacitidine Injection is also known by its brand name Vidaza, is a cancer medication. It is a treatment for those who are unable to get high-dose stem cell transplant treatment for the following conditions: Chronic myelomonocytic leukaemia is a type of leukaemia that affects the blood cells (CMML) Acute myeloid leukaemia (AML) is a kind of leukaemia that affects (AML)

What is the best way to administer Citaza?

Azacitidine is administered by a doctor or nurse at a medical office or hospital outpatient department as a powder that is mixed with water and injected subcutaneously (under the skin) or intravenously (into a vein). It’s normally given once a day for seven days.

How quickly does azacitidine start working?

VIDAZA is a long-term therapy. Treatment cycles are administered every 28 days for as long as your doctor prescribes. Your doctor may not notice a difference for several cycles (approximately 4 to 6 months). Your symptoms may reappear if you stop taking treatment.

What are the azacitidine chemotherapy side effects?

• Fatigue.
• Hair loss is a very prevalent problem.
• Bruising and bleeding are extremely prevalent.
• Infection.
• Anaemia is a condition in which a person’s blood levels are low (low red blood cell counts)
• The most frequent negative effects are nausea and vomiting. Appetites shift with the passage of time.
• Constipation. For more details Click Here.

Can you live with azacitidine for a long time?

Patients should be treated with azacitidine for at least 6 months, and treatment should be continued in patients who achieve a documented response or stable disease (sd) until disease progression or unacceptable toxicity occurs.

Is there a distinction between azacitidine and decitabine?

Decitabine medication is substantially related with a greater ORR (P = 0.026) and longer PFS (P = 0.037) when compared to azacitidine treatment, according to multivariate analyses. In response to the two HMAs, there were no significant differences in the occurrence of grade 3 or higher hematologic adverse events.

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