Myelosuppressive chemotherapy drugs

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Actual: Myelosuppression occurs with chemotherapy because chemotherapy agents kill or slow down rapidly dividing cells. Although this treatment targets cancer cells, it also affects healthy bone marrow cells.
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The chemotherapy regimens were classified into four grades based on the persistency of myelosuppression induced by chemotherapy. Mild myelosuppressive chemotherapies were classified as grade A, moderate ones as grade B, severe ones as grade C, and chemotherapies that caused severe myelosuppression and persistent immunodeficiency (known as

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G-CSF tbo-filgrastim (Granix) is indicated for the following: Patients with Cancer Receiving Myelosuppressive Chemotherapy and/or Immunotherapy: to reduce

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A CDK4 and CDK6 inhibitor to reduce the risk of chemotherapy induced myelosuppression. Drugs Drug Targets. Drug, Target, Type. Trilaciclib Solute carrier

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Myelosuppressive Chemotherapy Treatment. Neupogen, Granix, Zarxio, Releuko, Nivestym, Nypozi. Indicated to decrease infection incidence as manifested by febrile neutropenia in patients with nonmyeloid malignancies receiving myelosuppressive anticancer drugs associated with a significant incidence of severe neutropenia with fever

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chemotherapy-related anemia. [Pg.983] Myelosuppression is one of the most common dose-limiting side effects of cancer drugs that cause myelosuppression.

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Causes of Myelosuppression The majority of chemotherapy drugs have been associated with myelosuppression. However, different chemo agents affect blood cell

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Epogen, Procrit, Retacrit Treatment of anemia in patients with nonmyeloid malignancies where anemia is due to effect of concomitant myelosuppressive chemotherapy, and upon initiation, there is a minimum of 2 additional months of planned chemotherapy

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For prophylaxis of febrile neutropenia (FN) caused by myelosuppressive chemotherapy and request for Neulasta/Neulasta Onpro, Nyvepria, Udenyca

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A semimechanistic pharmacokinetic-pharmacodynamic model describing chemotherapy-induced myelosuppression through drug-specific parameters and system-related

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