Trastuzumab Lyophilized Powder Solution For Infusion Vivitra 440
Trastuzumab Lyophilized Powder Solution For Infusion Vivitra 440

Trastuzumab Lyophilized Powder Solution For Infusion Vivitra 440

MOQ : 10 Pieces

Trastuzumab Lyophilized Powder Solution For Infusion Vivitra 440 Specification

  • Dosage Form
  • Lyophilized Powder for Solution for Infusion
  • Indication
  • Treatment of HER2-positive breast cancer and gastric cancer
  • Salt Composition
  • Trastuzumab 440 mg
  • Feature
  • Biosimilar to Herceptin; Ready to reconstitute and infuse
  • Ingredients
  • Trastuzumab (active), Excipients (inactive)
  • Application
  • Intravenous infusion for cancer therapy
  • Physical Color/Texture
  • White to off-white lyophilized powder
  • Fermentation Smell
  • Odorless
  • Storage Instructions
  • Store at 2C-8C (Refrigerate, Do not freeze)
  • Shelf Life
  • 24 months from the date of manufacture
  • Contraindications
  • Known hypersensitivity to trastuzumab or excipients
  • Administration Route
  • Intravenous (IV) only
  • International Approvals
  • Available in US, EU, UK, Canada, Australia
  • Reconstitution Volume
  • 20 mL bacteriostatic water for injection
  • Infusion Time
  • Typically 30 to 90 minutes per protocol
  • Intended Patient Population
  • Adults with HER2-positive cancers
  • Pack Size
  • Single use vial containing 440 mg trastuzumab
  • Precautions
  • Monitor cardiac function before and during treatment
  • Prescription Status
  • Prescription only (Rx)
 
 

Trastuzumab Lyophilized Powder Solution For Infusion Vivitra 440 About



Discover the crackerjack deal on Vivitra 440, the celebrated biosimilar of trastuzumab, now trending among advanced cancer therapies. This immaculate lyophilized powder solution is designed for infusion, indicated for adults with HER2-positive breast and gastric cancers. Each single-use vial offers 440 mg trastuzumab, reconstituted with 20 mL bacteriostatic water, delivering a tailored treatment by IV infusion-usually within 30 to 90 minutes as per protocol. International approvals-including US, EU, UK, Canada, and Australia-substantiate its global trust. Vivitra 440 ensures optimal efficacy and safety under specialist prescription, following strict cardiac monitoring guidelines. Offer valid for hospitals, clinics, and healthcare providers seeking superior therapeutic value.

Immaculate Usage and Distinctive Features

Vivitra 440 is strictly for prescription use in adults with HER2-positive cancers. Its celebrated design as a lyophilized powder ensures rapid and reliable reconstitution. The immaculate biosimilar to Herceptin offers a ready-to-infuse formulation, paving the way for shorter infusion times between 30 and 90 minutes. Its extra features include international approvals and comprehensive compatibility with standard IV administration sets, facilitating seamless integration into oncology protocols and enhancing patient care outcomes in clinical practice.


Packaging, Payment, and Handover Details

Vivitra 440 arrives in a single-use vial, securely packaged to maintain product integrity and safety. Handover is conducted under strictly controlled conditions to ensure uninterrupted cold chain compliance. Goods transport is organized with premium carriers to guarantee optimal storage temperatures, especially for longer distances. List price quotations are provided upon inquiry, with flexible payment terms to accommodate various healthcare procurement processes. Standard delivery time typically ranges between 3 to 7 working days, subject to location and demand.


FAQ's of Trastuzumab Lyophilized Powder Solution For Infusion Vivitra 440:


Q: How should Vivitra 440 be correctly stored before use?

A: Vivitra 440 must be refrigerated at temperatures between 2C-8C and should never be frozen. Follow local protocols for secure storage in a healthcare environment.

Q: What is the process for reconstituting and administering Vivitra 440?

A: The powder should be reconstituted using 20 mL of bacteriostatic water for injection, then gently swirled until fully dissolved. It is administered via intravenous infusion over 30 to 90 minutes, as recommended by the healthcare provider.

Q: When is Vivitra 440 indicated for use?

A: Vivitra 440 is intended for adults diagnosed with HER2-positive breast cancer or gastric cancer, as directed by a specialized healthcare professional.

Q: Where can Vivitra 440 be sourced internationally?

A: Vivitra 440 is available in the US, EU, UK, Canada, Australia, and various other countries through approved medical suppliers and authorized distributors.

Q: What are the key benefits of using Vivitra 440 over other treatments?

A: Vivitra 440, as a biosimilar to Herceptin, offers celebrated efficacy with comparable safety. Its ready-to-use formulation and global approvals make it an accessible and reliable option for HER2-positive cancer therapy.

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