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Filgrastim
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Product Information
Filgrastim's primary mechanism of action is to stimulate the production and release of neutrophils, a type of white blood cell, from the bone marrow. It is a recombinant form of human granulocyte colony-stimulating factor (G-CSF), a naturally occurring protein that regulates the production and maturation of neutrophils. Filgrastim binds to specific G-CSF receptors on hematopoietic stem cells, primarily located in the bone marrow. This binding triggers a cascade of intracellular signals that promote the proliferation, differentiation, and maturation of neutrophil precursors. The result is an increased production of neutrophils, which are essential for fighting infections, particularly in individuals with neutropenia or those undergoing chemotherapy, as it helps to restore neutrophil counts and enhance immune function.
Filgrastim
Granulocyte colony-stimulating factor.
Injection
The following are the uses of Filgrastim Injection:
In the case of an overdose of Filgrastim Injection, prompt medical attention is required. Symptoms may include bone pain, severe headache, shortness of breath, and allergic reactions such as rash or itching. Seek emergency care if you suspect an overdose, as medical professionals can provide necessary interventions to manage symptoms and prevent potential complications. It is crucial to act swiftly and inform healthcare providers of the situation.
In the case of a missed dose of Filgrastim Injection, it is important to administer the medication as soon as you remember. However, if it is almost time for the next scheduled dose, it is recommended to skip the missed dose and continue with the regular dosing schedule. Do not administer a double dose to make up for a missed one, as this may increase the risk of side effects. If you miss multiple doses, contact your healthcare provider for guidance on how to adjust your dosing schedule and ensure the medication's effectiveness.
To administer the Filgrastim injection, clean the injection site with an alcohol swab, insert the needle at a 45-degree angle, inject the medication slowly, and then gently remove the needle while applying pressure to the site with a sterile cotton ball for a few seconds.
Following are the conditions when Filgrastim Injection should not be used:
The side effects of Filgrastim Injection may include:
Following are the precautions and warnings for Filgrastim Injection:
Following are the drug interactions for Filgrastim Injection:
Following are the food interactions for Filgrastim Injection:
Filgrastim Injection should be stored in a refrigerator at a temperature between 2°C to 8°C (36°F to 46°F). It is crucial to keep the injection in its original packaging to protect it from light and moisture. Do not freeze the medication as it may affect its potency. If the injection has been stored at room temperature, it must be used within a specified time frame as directed by the manufacturer, typically within a few days. Once the injection is removed from the refrigerator, it should be allowed to reach room temperature before administration. After use, any remaining medication should be properly disposed of according to local guidelines for pharmaceutical waste disposal. This ensures the safe and effective management of the medication and minimizes environmental impact. It is important to keep Filgrastim Injection out of the reach of children and pets to prevent accidental exposure.
Following are the quick tips for Filgrastim Injection:
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