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Amifostine Injection

Amifostine Injection Specification

Packaging Type
Vial

Indication
Prevention of nephrotoxicity and xerostomia during cancer therapy

Life Span
24 months

Brand Name
Amifostine Injection

Dosage Form
Liquid for injection

Pacakaging (Quantity Per Box)
1 vial per box

Origin of Medicine
India

Salt Composition
Amifostine 500 mg

Drug Type
Allopathic

Ingredients
Amifostine

Physical Form
Injection

Function
Cytoprotective agent, reduces side effects of cancer treatment

Recommended For
Cancer patients undergoing chemotherapy or radiotherapy

Dosage
As directed by physician

Dosage Guidelines
Administer intravenously prior to chemotherapy or radiotherapy

Suitable For
Adults

Quantity
500 mg/vial

Storage Instructions
Store below 25C, protect from light and moisture

Side Effects
May include hypotension, nausea, vomiting, mild rash

Prescription/Non Prescription
Prescription

Color
White to off-white powder (to be reconstituted)

Reconstitution Solvent
Sterile water for injection

Warning
To be used under medical supervision only

Therapeutic Class
Chemo-protectant agent

Administration Route
Intravenous (IV)

Amifostine Injection Trade Information

Minimum Order Quantity
300 Boxes

Supply Ability
500000 Boxes Per Month

Delivery Time
7 Days

Main Export Market(s)
Asia

Main Domestic Market
All India

Certifications
WHO, GMP, ISO

About Amifostine Injection

Product Name: Amifostine Injection

Protects normal tissues - ensures full theraphy

Composition

Each vial contains amifostine:

500mg Amifostine

Strength / Packing

Vial of 500 mg Amifostine

How Amifostine Injection Works

Amifostine Injection functions as a chemo-protectant agent, reducing the toxic effects cancer treatments can have on healthy tissues. Administered intravenously before chemotherapy or radiotherapy, it offers critical protection for organs like the kidneys and glands, enhancing patient tolerance to aggressive treatments.

Safe Storage and Handling

Store Amifostine Injection below 25C in a cool, dry place, away from light and moisture. The powder should be reconstituted with sterile water for injection just prior to use, and handled only by qualified medical professionals to ensure efficacy and safety.

Who Can Benefit from Amifostine Injection?

This injection is recommended for adult cancer patients undergoing chemotherapy or radiotherapy, particularly for those at risk of nephrotoxicity or xerostomia. The medicine is prescribed by physicians and tailored according to individual treatment regimens.

FAQ's of Amifostine Injection:

Q: How is Amifostine Injection administered?

A: Amifostine Injection is administered intravenously. The powder is first reconstituted with sterile water for injection and then given as an IV infusion under medical supervision, usually before chemotherapy or radiotherapy sessions.

Q: What is the main benefit of using Amifostine Injection during cancer treatment?

A: The primary benefit of Amifostine Injection is its ability to protect normal tissues, particularly the kidneys and salivary glands, from the toxic effects of chemotherapy and radiotherapy, thereby reducing associated side effects such as nephrotoxicity and dry mouth (xerostomia).

Q: When should Amifostine Injection be given?

A: Amifostine Injection is typically administered immediately before chemotherapy or radiotherapy, according to the physician's specific dosage and timing recommendations.

Q: What are the possible side effects of Amifostine Injection?

A: Possible side effects include hypotension (low blood pressure), nausea, vomiting, and mild rash. Side effects should be reported to your healthcare provider promptly for appropriate management.

Q: Where should Amifostine Injection be stored?

A: Store Amifostine Injection in a cool, dry place below 25C, protected from light and moisture. The vial should only be reconstituted and used by healthcare professionals in a clinical setting.

Q: Who should use Amifostine Injection?

A: This medication is suitable for adult cancer patients undergoing chemotherapy or radiotherapy who are at risk of treatment-related kidney damage or dry mouth. It must be prescribed and supervised by a physician.

Q: What process should be followed for reconstituting and administering Amifostine Injection?

A: The powder should be mixed with sterile water for injection immediately before use, and then administered intravenously by a qualified healthcare provider following the prescribed dosage guidelines.

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