PLERIXAFOR - INJECTION
PHONETIC PRONUNCIATION: (pler-IX-a-for)
COMMON BRAND NAME(S): Mozobil
GENERIC NAME(S): plerixafor
Uses
USES: Plerixafor is used by patients with certain types of cancer (non-Hodgkin's lymphoma-NHL, multiple myeloma-MM) to prepare them for stem cell transplant. Stem cells, which are found mainly in the bone marrow, turn into red blood cells, white blood cells, and platelets. Plerixafor is used to help stem cells move from the bone marrow to the bloodstream so that the cells can be collected and stored. The stem cells are then infused back into the patient after chemotherapy or radiation.
How to use PLERIXAFOR - INJECTION
HOW TO USE: Before using, check this product visually for particles or discoloration. If either is present, do not use the liquid. Before injecting each dose, clean the injection site with rubbing alcohol. Change the injection site each time to lessen injury under the skin. Inject this medication under the skin as directed by your doctor, usually about 11 hours before the blood filtering procedure. The dosage is based on your medical condition and weight. Your doctor will also direct you to use another medication (G-CSF) to prepare for the procedure. Carefully follow your doctor's instructions on how to use both medications correctly.
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Faq for PLERIXAFOR - INJECTION
Plerixafor injection is used in combination with other medications to help increase the number of hematopoietic stem cells in the blood for autologous stem cell transplant in patients with multiple myeloma or non-Hodgkin lymphoma.
Plerixafor works by blocking a protein called CXCR4, which helps stem cells stay in the bone marrow. By blocking CXCR4, plerixafor allows stem cells to be released into the bloodstream, making them available for collection for transplant.
Plerixafor is given as an injection under the skin (subcutaneously) about 11 hours before the scheduled stem cell collection. The exact dosage and timing will be determined by your healthcare provider.
The most common side effects of plerixafor injection include diarrhea, nausea, vomiting, injection site reactions (redness, swelling, pain), fatigue, dizziness, headache, and decreased white blood cell count. It is essential to inform your doctor about any bothersome or severe side effects.
Plerixafor can interfere with the effectiveness of certain medications, including G-CSF, St. John's wort, and drugs that affect liver enzymes. It is crucial to inform your healthcare provider about all the medications you are taking before starting plerixafor.
Plerixafor is classified as a pregnancy category D drug, indicating a potential risk to the fetus. It should only be used if the potential benefits outweigh the potential risks. It is essential to discuss the risks and benefits with your doctor if you are pregnant or planning to become pregnant.
It is unknown whether plerixafor passes into breast milk. Due to the lack of data, it is recommended to avoid breastfeeding while on plerixafor.
Plerixafor vials should be stored at controlled room temperature between 20°C to 25°C (68°F to 77°F). They should be protected from light and kept out of reach of children.
If you miss a dose of plerixafor, consult your healthcare provider immediately. They will provide guidance on whether the dose can be rescheduled or if any adjustments need to be made.
Disclaimer
IMPORTANT: HOW TO USE THIS INFORMATION: This is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate for you. This information is not individual medical advice and does not substitute for the advice of your health care professional. Always ask your health care professional for complete information about this product and your specific health needs.
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