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Q3/2025: Strong organic revenue and excellent EPS growth; EBIT growth guidance raised
Explore how biosimilars drive smarter healthcare investment and global access with Fresenius Kabi’s support for Biosimilars Week 2025.
Recognized by Vizient for supply assurance and strategic collaboration, Fresenius Kabi earns two major awards.
Dr. Hannah Wozniak receives €250,000 JUMPstart Clinical Nutrition research award for a personalized nutrition and early mobilization trial in ventilated patients.
Fresenius continues to reduce complexity and increase efficiency in its global network. In line with #FutureFresenius, the company announces the divestment of Fresenius Kabi’s Calea homecare business in Canada.
Fresenius is collaborating with other companies and academic institutions with the goals of accelerating the manufacturing of CAR-T cell therapy, making it more cost-effective, and improving patient access across Europe.
Q2/2025: Ongoing strong revenue and EPS growth, guidance for organic revenue growth raised
Fresenius Kabi will exclusively commercialize Polpharma Biologics’ vedolizumab biosimilar candidate PB016 globally (except in the Middle East and North Africa).
Fresenius announced that the European Commission has granted approval for their denosumab biosimilars Conexxence®* and Bomyntra®* in Europe.
Dr. Wan Daud from Malaysia receives €100,000 research support through the JUMPstart Renal Nutrition Therapy Program to conduct her CKD nutrition study.
Recognized for service and innovation, Fresenius Kabi earns its 5th Premier award. Discover how we help hospitals improve care and reduce costs.
NutriKabina by Fresenius Kabi is a telehealth innovation that enables fast, accessible nutrition screening for oncology patients in hospitals across Argentina.
Fresenius Kabi advances responsible antibiotic manufacturing with AMR certification at its Portugal site: protecting public health for future generations.
mAbxience, a Fresenius Kabi majority-owned group with partial ownership from Insud Pharma, is pleased to announce that the European Commission has granted approval for its denosumab biosimilars Denbrayce® and Izamby®.
Fresenius Kabi’s fifth and sixth biosimilars Conexxence® (denosumab-bnht) and Bomyntra® (denosumab-bnht) are now available in the U.S. for all approved indications for their respective reference products, Prolia® (denosumab) and Xgeva® (denosumab).
Discover how Fresenius Kabi is expanding global R&D centers for Nutrition. Explore the new locations driving excellence.
Fresenius announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) issued a positive opinion for the marketing authorization of its biosimilar candidates to Prolia® (denosumab) and Xgeva® (denosumab).
Q1/2025: Strong top line and excellent EPS growth, outlook confirmed
Discover best practices in perioperative nutrition from leading surgical experts. Four podcast episodes on surgery and nutrition management.
Lizl Veldsman from South Africa wins the award for her study on preventing muscle loss in ICU patients, supported by Fresenius Kabi's research grant.
Fresenius Kabi optimizes production network: Fresenius Kabi and EMS have signed an agreement to transfer the ownership of Fresenius Kabi's production site in Anápolis, Brazil, to EMS.
Fresenius announced that the Biologics License Application (BLA) for the denosumab biosimilars Conexxence®** (denosumab-bnht) and Bomyntra®** (denosumab-bnht) of its operating company Fresenius Kabi has been approved by the FDA.
We were honored to welcome over 100 healthcare professionals from 33 countries to our headquarters for the FRANC2024 Oncology – the Fresenius Kabi Advanced Nutrition Conference.
Learn more about chronic kidney disease and how health care professionals play a crucial role in early detection and patient education.
Fresenius Kabi’s ustekinumab biosimilar Otulfi® (ustekinumab-aauz), developed by Formycon AG, is now available in the United States and European Union.
FY/24: Upgraded outlook achieved, consistent financial performance with profitable growth.
With this mentoring program, Fresenius Kabi supports early-career clinicians and researchers through education, networking, and funding opportunities.
To further advance research and medical education in the field of intensive care medicine, Fresenius Kabi continues its collaboration with ESICM in 2025.
Fresenius, via its operating company Fresenius Kabi, announced today that the U.S. FDA has granted 510(k) clearance to its Adaptive Nomogram.
Fresenius Kabi is a Top Employer in 2025, with twelve countries receiving certification from the Top Employers Institute.
Fresenius, through its operating company Fresenius Kabi, is broadening its growing biopharma portfolio through a new licensing agreement with South Korea’s SamChunDang Pharm (SCD).
Fresenius, through its operating company Fresenius Kabi, announced today that Epinephrine Injection, USP, is now available in the United States.
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搜尋
IRINOTECAN HYDROCHLORIDE TRIHYDRATE
晚期性大腸直腸癌之第一線治療藥物：與5-FU及folinic acid合併，使用於未曾接受過化學治療之患者。單獨使用於曾接受5-FU療程治療無效之患者。與cetuximab併用，治療曾接受含irinotecan之細胞毒性療法治療失敗且具有上皮生長因子接受體(EGFR)表現型KRAS野生型轉移性大腸直腸癌患者。與5-fluorouracil、folinic acid及bevacizumab合併治療，做為轉移性大腸癌或直腸癌患者的第一線治療藥物。與capecitabine合併治療，做為轉移性大腸直腸癌患者的第一線治療藥物。
2ml; 5ml小瓶
衛署藥輸字第024625號，請點擊下列按鈕前往網站查詢。
etoposide
抗癌症
5毫升小瓶
衛署藥輸字第024638號，請點擊下列按鈕前往網站查詢。
Paclitaxel
晚期卵巢癌, 腋下淋巴轉移之乳癌, 作為接續含杜薩魯比辛在內之輔助化學療法, 已使用合併療法失敗的轉移性乳癌, 非小細胞肺癌, 愛滋病相關卡波西氏肉瘤之第二線療法。與Cisplatin併用作為晚期卵巢癌之第一線療法
5、16.7、43.4、50毫升小瓶裝 25毫升小瓶裝
衛署藥輸字第024738號，請點擊下列按鈕前往網站查詢。
Carboplatin
卵巢癌
15毫升、45毫升小瓶
衛署藥輸字第024804號，請點擊下列按鈕前往網站查詢。
VINORELBINE TARTRATE
非小細胞肺癌、移轉性乳癌。
1毫升(充填入5mL玻璃小瓶)、5毫升玻璃小瓶裝
衛署藥輸字第025489號，請點擊下列按鈕前往網站查詢。
OXALIPLATIN
和5-fluorouracil (5-FU)及folinic acid (FA)併用，作為第三期結腸癌(Duke’s C)原發腫瘤完全切除手術後的輔助療法。治療轉移性結腸直腸癌。Oxaliplatin和fluoropyrimidine併用可用於局部晚期及復發/轉移性胃癌之治療。與5-fluorouracil、leucovorin及irinotecan合併治療(FOLFIRINOX)，作為轉移性胰臟癌之第一線治療藥物。
10毫升、20毫升玻璃小瓶裝
衛署藥輸字第025631號，請點擊下列按鈕前往網站查詢。
GEMCITABINE HYDROCHLORIDE
非小細胞肺癌、胰臟癌、膀胱癌。Gemcitabine與paclitaxel併用，可使用於曾經使用過anthracycline之局部復發且無法手術切除或轉移性之乳癌病患。用於曾經使用含鉑類藥物(platinum-based)治療後復發且間隔至少6個月之卵巢癌，作為第二線治療。膽道癌。
200毫克、1公克玻璃小瓶裝
衛署藥輸字第025681號，請點擊下列按鈕前往網站查詢。
Cisplatin
抗惡性腫瘍劑
10毫升、50毫升小瓶
衛署藥輸字第025744號，請點擊下列按鈕前往網站查詢。
Docetaxel
乳癌、非小細胞肺癌、前列腺癌、胃腺癌、頭頸癌
20毫克/毫升及80毫克/4毫升玻璃小瓶裝
衛署藥輸字第026334號，請點擊下列按鈕前往網站查詢。
