Indications |
Subcutaneous Chemotherapy-induced neutropenia Adult: 5-10 mcg/kg (60,000-110,000 IU/kg) daily starting 24 hr after last dose of chemotherapy and continued for 7-10 days. Max: 10 mcg/kg (110,000 IU/kg) daily. Subcutaneous Ganciclovir-induced neutropenia Adult: 5 mcg/kg (60,000 IU/kg) daily. After the 5th dose, adjust dose according to neutrophil count. Max: 10 mcg/kg (110,000 IU/kg) daily. Intravenous Bone marrow transplantation Adult: 10 mcg/kg (110,000 IU/kg) daily by infusion over 4-6 hr beginning on the day after the procedure and continued for 30 days depending on the neutrophil count. Max: 10 mcg/kg (110,000 IU/kg) daily. Reconstitution: Reconstitute the lyophilised powder with 1 ml of sterile water for inj. Further dilute the reconstituted solution in 25, 50 or 100 ml infusion bags or bottles of either normal saline solution or 5% dextrose in water. Infusion admixture solution should contain a final concentration of not <7 mcg> | |||||
Overdosage | Symptoms: Tachycardia, hypotension, flu-like syndrome. Treatment: Symptomatic. | |||||
Contraindications | Myeloid malignancies. Lactation. | |||||
Special Precautions | Patients with any pre-malignant or malignant myeloid condition, pre-existing pulmonary disease. Discontinue use in patients who develop signs of pulmonary infiltrates. Patients with fluid retention or heart failure. Regularly monitor CBC during therapy. Pregnancy. | |||||
Adverse Drug Reactions | Fever and chills, nausea, dyspnoea, diarrhoea, rash, rigors, inj site reaction (SC admin), vomiting, fatigue, anorexia, bone and musculoskeletal pain, asthenia, transient hypotension, non-specific chest pain, stomatitis, headache, increased sweating, abdominal pain, pruritus, dizziness, peripheral oedema, paraesthesia and myalgia. Antibodies can develop. Potentially Fatal: Anaphylactic reactions, pleural and pericardial effusion, cardiac arrhythmias. | |||||
Drug Interactions | May increase occurrence of bleomycin-induced pulmonary toxicity. Potentially Fatal: Increased risk of myelosuppression when given simultaneously with myelosuppressive cytotoxic antineoplastics. Do not use within 24 hr of cytotoxic chemotherapy. See Below for More molgramostim Drug Interactions | |||||
Storage | Intravenous: Store at 2-8°C. Do not freeze. Protect from light. Subcutaneous: Store at 2-8°C. Do not freeze. Protect from light. | |||||
Mechanism of Action | Molgramostim is a granulocyte-macrophage colony-stimulating factor (GM-CSF) that influences the growth, differentiation and function of the granulocytes, macrophages and eosinophils. It helps in the separation of granulocyte and macrophage pathways and also enhances cell function. | |||||
CIMS Class | Haematopoietic Agents | |||||
ATC Classification | L03AA03 - molgramostim ; Belongs to the class of colony stimulating factors. Used as immunostimulants. | |||||
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Contraindications |
Myeloid malignancies. Lactation. | |||||
Warnings / Precautions |
Patients with any pre-malignant or malignant myeloid condition, pre-existing pulmonary disease. Discontinue use in patients who develop signs of pulmonary infiltrates. Patients with fluid retention or heart failure. Regularly monitor CBC during therapy. Pregnancy. | |||||
Adverse Reactions |
Fever and chills, nausea, dyspnoea, diarrhoea, rash, rigors, inj site reaction (SC admin), vomiting, fatigue, anorexia, bone and musculoskeletal pain, asthenia, transient hypotension, non-specific chest pain, stomatitis, headache, increased sweating, abdominal pain, pruritus, dizziness, peripheral oedema, paraesthesia and myalgia. Antibodies can develop. Potentially Fatal: Anaphylactic reactions, pleural and pericardial effusion, cardiac arrhythmias. |
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Overdose Reactions |
Symptoms: Tachycardia, hypotension, flu-like syndrome. Treatment: Symptomatic. | |||||
Drug Interactions |
May increase occurrence of bleomycin-induced pulmonary toxicity. Potentially Fatal: Increased risk of myelosuppression when given simultaneously with myelosuppressive cytotoxic antineoplastics. Do not use within 24 hr of cytotoxic chemotherapy. See Below for More molgramostim Drug Interactions |
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Mechanism of Actions |
Molgramostim is a granulocyte-macrophage colony-stimulating factor (GM-CSF) that influences the growth, differentiation and function of the granulocytes, macrophages and eosinophils. It helps in the separation of granulocyte and macrophage pathways and also enhances cell function. | |||||
Storage Conditions |
Intravenous: Store at 2-8°C. Do not freeze. Protect from light. Subcutaneous: Store at 2-8°C. Do not freeze. Protect from light. | |||||
ATC Classification |
L03AA03 - molgramostim ; Belongs to the class of colony stimulating factors. Used as immunostimulants. | |||||
Storage |
Intravenous: Store at 2-8°C. Do not freeze. Protect from light. Subcutaneous: Store at 2-8°C. Do not freeze. Protect from light. | |||||
Available As |
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Molgramostin
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Molgramostin Containing Brands
Molgramostin is used in following diseases
Drug - Drug Interactions of Molgramostin
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