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position statements

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December 25, 2017

A Statement Regarding Media Coverage of Gleostine® (lomustine)

November 15, 2017

Gleostine® Pricing

About Gleostine
  • History of Lomustine
  • How Gleostine Works
  • NextSource Pharmaceuticals
Treatment
  • Brain Tumor & Hodgkin’s Lymphoma
  • Dosing & Administration
  • Effectiveness & Safety
Resources
  • Tips for Caregivers
  • Patient Assistance Program  
  • Contact Us
  • Privacy & Security
  • Terms & Conditions

Copyright© NextSource Biotechnology, LLC 2017 All rights reserved.

 

IMPORTANT SAFETY INFORMATION

DOWNLOAD PRESCRIBING INFORMATION

Gleostine® (lomustine) should be administered under the supervision of a qualified physician experienced in the use of cancer chemotherapeutic agents.

Bone marrow suppression, notably thrombocytopenia and leukopenia, which may contribute to bleeding and overwhelming infections in an already compromised patient, is the most common and severe of the toxic effects of Gleostine® (see WARNINGS and ADVERSE REACTIONS).

Since the major toxicity is delayed bone marrow suppression, blood counts should be monitored weekly for at least 6 weeks after a dose (see ADVERSE REACTIONS). At the recommended dosage, courses of Gleostine® should not be given more frequently than every 6 weeks.

The bone marrow toxicity of Gleostine® is cumulative and therefore dosage adjustment must be considered on the basis of nadir blood counts from prior dose (see dosage adjustment table under DOSAGE AND ADMINISTRATION)

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