Medically reviewed by Drugs.com. Last updated on June 25, 2019.
Generic name: BEVACIZUMAB 100mg in 4mL
Dosage form: injection, solution
Important Administration Information
Do not administer MVASI until at least 28 days following surgery and the wound is fully healed.
Metastatic Colorectal Cancer
The recommended dosage when MVASI is administered in combination with intravenous fluorouracil-based chemotherapy is:
- 5 mg/kg intravenously every 2 weeks in combination with bolus-IFL.
- 10 mg/kg intravenously every 2 weeks in combination with FOLFOX4.
- 5 mg/kg intravenously every 2 weeks or 7.5 mg/kg intravenously every 3 weeks in combination with fluoropyrimidine-irinotecan- or fluoropyrimidine-oxaliplatin-based chemotherapy in patients who have progressed on a first-line bevacizumab product-containing regimen.
First-Line Non-Squamous Non-Small Cell Lung Cancer
The recommended dosage is 15 mg/kg intravenously every 3 weeks in combination with carboplatin and paclitaxel.
Metastatic Renal Cell Carcinoma
The recommended dosage is 10 mg/kg intravenously every 2 weeks in combination with interferon-alfa.
Persistent, Recurrent, or Metastatic Cervical Cancer
The recommended dosage is 15 mg/kg intravenously every 3 weeks in combination with paclitaxel and cisplatin, or in combination with paclitaxel and topotecan.
Dosage Modifications for Adverse Reactions
Table 1 describes dosage modifications for specific adverse reactions [see Warnings and Precautions (5)]. No dose reductions for MVASI are recommended.
|Adverse Reaction||Severity||Dosage Modification|
|Gastrointestinal Perforations and Fistulae [see Warnings and Precautions (5.1)]||
|Wound Healing Complications [see Warnings and Precautions (5.2)]||
|Hemorrhage [see Warnings and Precautions (5.3)]||
|Thromboembolic Events [see Warnings and Precautions (5.4, 5.5)]||
|Hypertension [see Warnings and Precautions (5.6)]||
||Withhold MVASI until controlled with medical management; resume once controlled|
|Posterior Reversible Encephalopathy Syndrome (PRES) [see Warnings and Precautions (5.7)]||
|Renal Injury and Proteinuria [see Warnings and Precautions (5.8)]||
||Withhold MVASI until proteinuria less than 2 grams per 24 hours|
|Infusion-Related Reactions [see Warnings and Precautions (5.9)]||
||Interrupt infusion; resume at a decreased rate of infusion after symptoms resolve|
||Decrease infusion rate|
|Congestive Heart Failure [see Warnings and Precautions (5.12)]||Any||Discontinue MVASI|
Preparation and Administration
- Use appropriate aseptic technique.
- Visually inspect vial for particulate matter and discoloration prior to preparation and administration. Discard vial if solution is cloudy, discolored or contains particulate matter.
- Withdraw necessary amount of MVASI and dilute in a total volume of 100 mL of 0.9% Sodium Chloride Injection, USP. DO NOT ADMINISTER OR MIX WITH DEXTROSE SOLUTION.
- Discard any unused portion left in a vial, as the product contains no preservatives.
- Store diluted MVASI solution at 2°C to 8°C (36°F to 46°F) for up to 8 hours.
- No incompatibilities between MVASI and polyvinylchloride or polyolefin bags have been observed.
- Administer as an intravenous infusion.
- First infusion: Administer infusion over 90 minutes.
- Subsequent infusions: Administer second infusion over 60 minutes if first infusion is tolerated. Administer all subsequent infusions over 30 minutes if second infusion over 60 minutes is tolerated.
Frequently asked questions
- How many biosimilars have been approved in the United States?
- What is the difference between Mvasi and Avastin?
More about Mvasi (bevacizumab)
- Side Effects
- During Pregnancy or Breastfeeding
- Drug Interactions
- Pricing & Coupons
- En Español
- Drug class: VEGF/VEGFR inhibitors
- FDA Alerts (6)
- FDA Approval History
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Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.