What is the dosing for Granix (tbo-filgrastim)?

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From the FDA Drug Label

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From the Research

Granix (tbo-filgrastim) is typically dosed at 5 mcg/kg body weight once daily as a subcutaneous injection for patients receiving myelosuppressive chemotherapy. Treatment should begin at least 24 hours after chemotherapy administration and continue daily until the expected neutrophil nadir has passed and neutrophil count has recovered to normal range, usually for up to 14 days per chemotherapy cycle. The medication comes in prefilled syringes of 300 mcg/0.5 mL and 480 mcg/0.8 mL. Patients or caregivers should be properly trained on administration technique, including proper disposal of needles. Common side effects include bone pain, which can be managed with non-narcotic analgesics. Granix works by stimulating the bone marrow to produce neutrophils, helping to reduce the risk of infection in patients whose neutrophil counts are decreased due to chemotherapy. Blood counts should be monitored regularly during therapy to assess response and determine when treatment can be discontinued.

According to the most recent study 1, tbo-filgrastim has demonstrated bioequivalence to reference filgrastim in terms of its pharmacokinetic and pharmacodynamic profiles, and has been shown to be effective in ameliorating severe neutropenia in patients receiving chemotherapy for various types of cancer. The study also notes that tbo-filgrastim is generally well tolerated, with a similar safety profile to that of reference filgrastim.

Key points to consider when prescribing Granix (tbo-filgrastim) include:

  • Starting treatment at least 24 hours after chemotherapy administration
  • Continuing treatment daily until the expected neutrophil nadir has passed and neutrophil count has recovered to normal range
  • Monitoring blood counts regularly to assess response and determine when treatment can be discontinued
  • Proper training on administration technique, including proper disposal of needles
  • Management of common side effects, such as bone pain, with non-narcotic analgesics.

It's also important to note that the dosing and administration of Granix (tbo-filgrastim) may vary depending on the specific clinical context and patient population, and that the medication should be used in accordance with established guidelines and recommendations 2, 3, 4, 5.

References

Research

Tbo-Filgrastim: A Review in Neutropenic Conditions.

BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 2016

Research

Refining the role of pegfilgrastim (a long-acting G-CSF) for prevention of chemotherapy-induced febrile neutropenia: consensus guidance recommendations.

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2017

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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