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Adverse event reporting can be found at the bottom of the page

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What are BiosimilarsManufacturing BiosimilarsPfizer's Heritage & ExpertiseOncology Biosimilar Portfolio

Prescribing information for relevant Pfizer oncology biosimilars and Adverse Event reporting information can be found at the bottom of the page. 

Oncology Biosimilars

Biological therapy provides a targeted and individualised approach that has revolutionised oncology treatment.1 The introduction of biosimilars has increased the number of therapeutic options available to healthcare professionals, providing cost-effective treatment options with a range of additional benefits and features.

In oncology, a number of biosimilars have demonstrated safety and efficacy comparable to their reference products, based on clinical trial data, real-world evidence, and the product’s physical and chemical properties. Taken together, the evidence supports the use of these biosimilars as equivalent therapeutic options to reference products when considering treatment options for people with certain cancers.2

Manufacturing Biosimilars

Pfizer is committed to ensuring high standards for biosimilar quality, regulatory compliance, and supplying fast, flexible solutions across the full manufacturing and supply chain spectrum.
 

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Biosimilars Portfolio

Pfizer has a portfolio of biosimilars on the market, including both cancer therapies and other biosimilar medicines, to give patients various treatment options.



 

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Heritage & Expertise

Pfizer's biosimilars are produced to meet the same high-quality standards as Pfizer’s other biologics – using the same robust protocols for monitoring quality throughout every stage of the manufacturing process.
 

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Prescribing Information for Great Britain and Northern Ireland:
 
Trazimera® (trastuzumab) Nivestim® (filgrastim)
Ruxience® (rituximab) Retacrit® (epoetin zeta)
Zirabev® (bevacizumab)  
References:​​​​​​​Falzone L, et al. Frontiers in Pharmacology 2018; 9: 1300.Peeters M, et al. Future Oncology 2021; 17(29): 3881-3892. 
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PP-RIT-GBR-0075. October 2023

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search 

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Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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