Article Contents ::
- 1 Details About Generic Salt :: Filgrast
- 2 Main Medicine Class:: Colony-stimulating factor
- 3 (fill-GRAH-stim) Neupogen Class: Colony-stimulating factor
- 4 Drugs Class ::
- 5 Disclaimer ::
- 6 The Information available on this site is for only Informational Purpose , before any use of this information please consult your Doctor .Price of the drugs indicated above may not match to real price due to many possible reasons may , including local taxes etc.. These are only approximate indicative prices of the drug.
Details About Generic Salt :: Filgrast
Main Medicine Class:: Colony-stimulating factor
(fill-GRAH-stim)
Neupogen
Class: Colony-stimulating factor
Drugs Class ::
Action Stimulates neutrophil production within bone marrow.
Indications for Drugs ::
Indications Decrease incidence of infection, manifested by febrile neutropenia, in patients with nonmyeloid malignancies receiving myelosuppressive anticancer drugs; cancer patients receiving myelosuppressive chemotherapy; cancer patients receiving bone-marrow transplant; patients with severe chronic neutropenia (SCN); peripheral blood progenitor cell (PBPC) collection and therapy in cancer patients. unlabeled use(s): Filgrastim may be beneficial in AIDS, drug-induced and congenital agranulocytosis, alloimmune neonatal neutropenia.
Drug Dose ::
Route/Dosage
Myelosuppressive chemotherapy
IV/SC: 5 mcg/kg/day as single daily injection; may increase in increments of 5 mcg/kg for each chemotherapy cycle.
Bone marrow transplant
IV/SC: 10 mcg/kg/day given as an IV infusion of 4 or 24 hr or as a continuous 24 hr SC infusion.
Severe chronic neutropenia
Congenital neutropenia: Starting dose: 6 mcg/kg twice daily SC qd.
Idiopathic or cyclic neutropenia: Starting dose: 5 mcg/kg as a single injection SC qd. Dose adjustments–Chronic daily administration is required to maintain clinical benefit. ANC should not be used as the sole indication of efficacy. Individually adjust the dose based on the patients’ clinical course as well as ANC. In the Phase III study, the target ANC was 1,500 to 10,000/mm3. However, patients may experience clinical benefit with ANCs below this target range. Reduce the dose if the ANC is persistently more than 10,000/mm3.
Contraindication ::
Contraindications Hypersensitivity to Escherichia coli-derived proteins.
Drug Precautions ::
Precautions
Pregnancy: Category C. Lactation: Undetermined. Cardiac events: Monitoring patients with preexisting cardiac conditions is recommended. Chronic administration: Safety and efficacy not established. Hematologic effects: Regular monitoring of hematocrit and platelet count recommended due to possible increased risk of thrombocytopenia or anemia.
PATIENT CARE CONSIDERATIONS |
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Drug Side Effects ::
Adverse Reactions
HEMA: Leukocytosis. OTHER: Bone pain; reversible elevations in uric acid, LDH, and alkaline phosphatase.
Drug Mode of Action ::
Action Stimulates neutrophil production within bone marrow.
Drug Interactions ::
Interactions
Drugs that may potentiate the release of neutrophils, such as lithium, should be used with caution. INCOMPATIBILITIES: Precipitate may form if diluted with saline.
Drug Assesment ::
Assessment/Interventions
- Obtain complete patient history, including drug history and any known allergies.
- Monitor hematocrit, CBC, and platelet count 2 to 3 times weekly.
- Document any hypotensive effects.
- Document CBC and platelet counts prior to chemotherapy and twice per week during therapy.
- Inform physician and discontinue dose if absolute neutrophil count > 10,000/mm3.
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Drug Storage/Management ::
Administration/Storage
- Do not give filgrastim 24 hr before or 24 hr after cytotoxic chemotherapy.
- Do not shake medication.
- Warm to room temperature before injection. Use within 24 hr.
- Use only 1 dose per vial, and do not reenter vial.
- Do not dilute with saline.
- Give IV injection, diluted in D5W, over 15 to 30 min.
- Store in refrigerator, but do not freeze. Discard any unused vial left at room temperature > 6 hr.
Drug Notes ::
Patient/Family Education
- Instruct in proper techniques for administration and storage.
- Explain that most common adverse effect is bone pain.
- Explain importance of follow-up laboratory work as directed.
- Counsel patient on signs of thrombocytopenia (eg, bruising, petechiae, ecchymosis, epistaxis, bleeding from mucus membranes) and ways to avoid infection.