Trastuzumab injection
Price 12000.0 INR/ Bottle
Trastuzumab injection Specification
- Indication
- HER2-positive breast cancer, metastatic gastric cancer
- Salt Composition
- Trastuzumab
- Dosage Form
- Injection
- Enzyme Types
- Monoclonal Antibody (not an enzyme)
- Feature
- Targeted therapy for HER2-positive cancer
- Ingredients
- Trastuzumab lyophilized powder, excipients
- Application
- Intravenous administration
- Ph Level
- 6.0
- Temperature Needed For Fermentation
- Not applicable; manufacturing uses mammalian cell culture
- Physical Color/Texture
- White to pale yellow lyophilized powder
- Fermentation Smell
- Odorless
- Storage Instructions
- Store at 2C to 8C; do not freeze
- Shelf Life
- 24 months
- Contraindications
- Hypersensitivity to Trastuzumab or excipients
- Reconstitution
- Reconstitute with sterile water for injection
- Packaging Type
- Single-use vial
- Strength
- 440 mg/vial
- Route of Synthesis
- Recombinant DNA technology in mammalian cells
- Therapeutic Class
- Antineoplastic agent, Monoclonal antibody
- Diluent Required
- Sterile Water for Injection (SWFI)
- Administration Route
- Intravenous infusion only
- Precautions
- Monitor cardiac function before and during treatment
- Preservation Conditions After Reconstitution
- Use immediately or store refrigerated up to 24 hours
Trastuzumab injection Trade Information
- Minimum Order Quantity
- 100 Pieces
- FOB Port
- MUMBAI
- Payment Terms
- Paypal, Telegraphic Transfer (T/T)
- Supply Ability
- 100 Pieces Per Week
- Delivery Time
- 1 Week
- Sample Available
- No
- Sample Policy
- If order is confirmed we will reimburse the sample cost
- Packaging Details
- 1 VIAL
- Main Export Market(s)
- Asia, Middle East, Africa
- Certifications
- COA , GMP
About Trastuzumab injection
Targeted Therapy for HER2-Positive Cancers
Trastuzumab injection specifically targets the HER2 protein, providing effective treatment for HER2-positive breast and metastatic gastric cancer patients. Its action mechanism helps slow cancer progression, often improving patient outcomes.
Proper Reconstitution and Administration
The lyophilized powder must be reconstituted with sterile water for injection and administered exclusively as an intravenous infusion. Once prepared, the reconstituted solution should be used immediately or refrigerated for up to 24 hours to ensure efficacy and safety.
Handling and Storage Recommendations
Store the lyophilized vial at 2C to 8C and protect it from freezing. After reconstitution, any unused solution should be discarded after 24 hours. Always use under appropriate medical supervision to ensure patient safety.
FAQ's of Trastuzumab injection:
Q: How should Trastuzumab injection be prepared and administered?
A: Trastuzumab injection is supplied as a white to pale yellow lyophilized powder. It should be reconstituted with sterile water for injection, and the resulting solution administered intravenously as an infusion by a healthcare professional.Q: What conditions does Trastuzumab treat?
A: Trastuzumab is indicated for the treatment of HER2-positive breast cancer and metastatic gastric cancer, targeting tumors that overexpress the HER2 protein.Q: When should Trastuzumab injection be used after reconstitution?
A: It is best to use Trastuzumab immediately after reconstitution. If this is not possible, the solution can be stored under refrigeration (2C to 8C) and must be used within 24 hours.Q: Where should Trastuzumab vials be stored before and after preparation?
A: Unreconstituted vials should be stored in a refrigerator at 2C to 8C. After reconstitution, the solution should be kept refrigerated and used within 24 hours; do not freeze at any stage.Q: What monitoring is required during Trastuzumab treatment?
A: Cardiac function should be assessed before starting therapy and monitored periodically throughout treatment, as Trastuzumab can affect heart function in some patients.Q: What are the benefits of using Trastuzumab for cancer treatment?
A: Trastuzumab is a targeted therapy that offers improved outcomes for patients with HER2-positive cancers, lowering the risk of disease progression compared to non-targeted treatments.

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