Product Description
Since last manyyears SaintroyLifescienceis leading manufacture, export and supplierofFulvestrant Injectionfrom Surat, Gujarat, India. Fulvestrant Injection used for the treatment of hormone receptor positive metastatic breast cancer or locally advanced unresectable disease in postmenopausal women; it is given by injection.
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ISO/GMP/cGMP/WHOGMP/NAFDAC approved, PPB Kenya approved/USFDA approved/EUGMP approved/MOH Iran approved manufacturingfacility in Gujarat, India.
Registration: Saintroy Lifescienceis interested inregistration of own brand or customer brands in ministryof health of clientscountry and we also provide the products samples, COA, COPP, ACTorCTD dossier, DMF, Manufacturing license, Free sales certificate and other required documents.
Export Country:Saintroy Lifescience Fulvestrant Injectionexport to USA, Canada, Germany, Europe, France, Ghana, Nigeria,Kenya, Senegal, Sudan,UAE, Kuwait, Dubai, Cameroon, Lebanon, Peru, Chile,Somalia, Philippines, Myanmar, Maldives, Thailand, Singapore, Malaysia, HongKong, China, Zimbabwe, Togo, Burkina Faso, Niger,Guinea Bissau, Congo,Democratic of republic, Ivory Costa, Oman, Guatemala, Nicaragua, Salvador,Qatar, Costa Rica, Panama, Cuba, Colombia, Bolivia, Argentine, Algeria, Guyana,Morocco, Jordan, Bahrain, Iran, Egypt, Kyrgyzstan, Uzbekistan, Kazakhstan.
Precise Dosage and AdministrationEach 5 ml prefilled syringe contains 250 mg of fulvestrant, designed for monthly intramuscular injections as per physician directives. The prefilled presentation with a safety needle ensures accurate dosing and reduces handling risk, making it suitable for use in healthcare facilities.
Therapeutic Indication and BenefitFulvestrant Injection is indicated for postmenopausal women with hormone receptor-positive metastatic breast cancer. Its mechanism targets estrogen receptors, providing a valuable treatment option in advanced cases where hormonal therapy is required.
Safety and Regulatory ComplianceThis preparation is available strictly on prescription and is for use only by healthcare professionals. Contraindications include hypersensitivity to fulvestrant or its excipients, as well as pregnancy and lactation. Regulatory controls ensure patient safety and quality.
Storage and StabilityThe injection must be stored in a cool, dry environment, away from direct sunlight, to maintain potency and safety. With a shelf life of up to two years, its stable formulation ensures efficacy throughout its intended use period.
FAQ's of Fulvestrant Injection:
Q: How should Fulvestrant Injection be administered and who is authorized to give it?
A: Fulvestrant Injection must be administered by a qualified healthcare professional via intramuscular injection, typically in the gluteal muscle. Patients should not attempt self-administration.
Q: What is the typical dosage and recommended administration schedule for this injection?
A: The recommended dosage is 250 mg (one 5 ml syringe) administered once a month, or as directed by a physician, following standard protocols for intramuscular injections.
Q: What is the primary medical use of Fulvestrant Injection?
A: This injection is used in postmenopausal women for the treatment of hormone receptor-positive metastatic breast cancer, helping to combat cancer growth dependent on estrogen receptors.
Q: Are there any specific contraindications or precautions associated with this medication?
A: Fulvestrant Injection is contraindicated in individuals with known hypersensitivity to fulvestrant or its excipients, and should not be used during pregnancy or lactation. It is for use by healthcare professionals only.
Q: Where should Fulvestrant Injection be stored to ensure quality?
A: The product should be kept in a cool, dry place to maintain its stability and efficacy, away from sunlight and moisture. Proper storage helps prevent degradation of the medication.
Q: What are the benefits of using a prefilled syringe with a safety needle for this product?
A: The prefilled glass syringe with a safety needle offers dose accuracy, improved safety for healthcare providers, and ease of use, reducing the risk of contamination or dosing errors.