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MOZOBIL® (plerixafor) injection, for subcutaneous use

Mozobil (plerixafor) injection is a sterile, preservative-free, clear, colorless to pale-yellow, isotonic solution for subcutaneous injection. Each mL of the sterile solution contains 20 mg of plerixafor. Each single-dose vial is filled to deliver 1.2 mL of the sterile solution that contains 24 mg of plerixafor and 5.9 mg of sodium chloride in

http://products.sanofi.us/Mozobil/mozobil.html

HIGHLIGHTS OF PRESCRIBING INFORMATION

HIGHLIGHTS OF PRESCRIBING INFORMATION These highlights do not include all the information needed to use MOZOBIL safely and effectively. See full prescribing information for MOZOBIL. MOZOBIL (plerixafor injection), Solution for Subcutaneous use Initial U.S. Approval: 2008 -----INDICATIONS AND USAGE-----

https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/022311s001lbl.pdf

Mozobil (plerixafor injection) | Official Patient Site

Welcome to the official patient site for Mozobil (plerixafor injection), an FDA-approved medication for patients living with non‐Hodgkin's lymphoma (NHL) or multiple myeloma (MM). See Important Safety Information.

https://www.mozobil.com/

Mozobil® (plerixafor)

Mozobil™injection [package insert]. Cambridge, MA: Genzyme Corporation 2. Referenced with permission from the NCCN Drugs & Biologics Compendium (NCCN Compendium®) plerixafor. National Comprehensive Cancer Network, 2019. The NCCN Compendium® is a derivative. Mozobil® (plerixafor)

https://secured.connecticare.com/providers/PDFs/MedicareDrug/Mozobil® (plerixafor).pdf

Mozobil® (plerixafor) - Magellan Provider

Begin treatment with Mozobil after the patient has received G-CSF once daily for 4 days Administer daily morning doses of G-CSF 10 mcg/kg for 4 days prior to the first evening dose of Mozobil and on each day prior to apheresis Administer Mozobil approximately 11 hours prior to initiation of each

https://specialtydrug.magellanprovider.com/media/32349/mozobil.pdf

Mozobil (Sanofi-aventis U.S. LLC): FDA Package Insert, Page 2

Patients were primarily treated with Mozobil at daily doses of 0.24 mg/kg SC. Median exposure to Mozobil in these studies was 2 days (range 1 to 7 days). In the two randomized studies in patients with NHL and MM, a total of 301 patients were treated in the Mozobil and G-CSF group and 292 patients were treated in the placebo and G-CSF group.

https://medlibrary.org/lib/rx/meds/mozobil-1/page/2/

Mozobil - FDA prescribing information, side effects and uses

Mozobil is indicated in combination with granulocyte-colony stimulating factor (G-CSF) to mobilize hematopoietic stem cells (HSCs) to the peripheral blood for collection and subsequent autologous transplantation in patients with non-Hodgkin's lymphoma (NHL) and multiple myeloma (MM).

https://www.drugs.com/pro/mozobil.html

Package Insert - Immunosuppression Thymoglobulin

Reconstitution After calculating the number of vials needed, using aseptic technique, reconstitute each vial of THYMOGLOBULIN with 5 mL of Sterile Water for Injection, USP (SWFI).

https://www.fda.gov/media/74641/download

PANHEMATIN® (hemin for injection) │ Clinical Data

Panhematin ® is a hemin for injection indicated for the amelioration of recurrent attacks of acute intermittent porphyria (AIP) temporally related to the menstrual cycle in susceptible women, after initial carbohydrate therapy is known or suspected to be inadequate. Limitations of Use

https://www.panhematin.com/healthcare-professionals/about-panhematin

Clinical Policy: Plerixafor (Mozobil) - Envolve Health

1. Mozobil [package insert]. Cambridge, MA: Genzyme Corporation; August 2009. Important Reminder This clinical policy has been developed by appropriately experienced and licensed health care professionals based on a review and consideration of currently available generally accepted standards of

https://acariahealth.envolvehealth.com/content/dam/centene/envolve-pharmacy-solutions/pdfs/pa-guidelines-specialty/ERX.SPMN.236 Plerixafor (Mozobil) - Q4 2016.pdf

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