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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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Propofol
短效性靜脈注射全身麻醉劑。 使用於成人及一個月以上之兒童作為誘導或維持麻醉之用。 使用於成人病人診斷及外科手術過程中之鎮靜之用，可單獨使用或與其他局部麻醉劑或全身麻醉劑合併使用。 已住在加護病房中使用人工呼吸器之超過16歲成人病人作為鎮靜之用。
注射劑 1% 20ml, 50ml
衛署藥輸字第022868號，請點擊下列按鈕前往網站查詢。
SODIUM CHLORIDE, POLY(O-2 HYDROXYETHYL)STARCH (MOLAR SUBS 0.38-0.45; AVERAGE MOLECULAR WEIGHT 130000)
單獨使用晶質輸注液無法治療之急性出血導致之低血容積病人，本品無法取代紅血球及血漿中的凝血因子。
500ml
衛署藥輸字第024260號，請點擊下列按鈕前往網站查詢。
Metronidazole
厭氧性菌引起之感染症
注射劑 5mg/ml, 100ml
衛署藥輸字第017835號，請點擊下列按鈕前往網站查詢。
Rocuronium Bromide
全身麻醉的輔佐藥，以幫助支氣管內插管、提供手術需快速麻醉誘導時骨骼肌肉鬆弛狀態、加護病房中需插管及使用人工呼吸器時。
10mg/ml
衛部藥輸字第026336號，請點擊下列按鈕前往網站查詢。
CISATRACURIUM BESYLATE
本品為一高選擇性及競爭性的非去極化神經肌肉阻斷劑。可作為全身麻醉之輔助劑或加護病房使用，用以鬆弛骨骼肌，幫助氣管插管及與人工呼吸器的協調。
注射劑 2mg/ml
衛部藥輸字第026541號，請點擊下列按鈕前往網站查詢。
Fluconazole
抗黴菌劑
注射劑 2mg/ml, 100ml
衛署藥輸字第024844號，請點擊下列按鈕前往網站查詢。
MEROPENEM TRIHYDRATE
對Meropenem具有感受性之細菌引起之感染症。
乾粉注射劑 500mg/vial, 1g/vial
衛部藥輸字第026737號，請點擊下列按鈕前往網站查詢。
CEFTRIAXONE SODIUM
葡萄球菌、鏈球菌、肺炎隻球菌、腦膜炎球菌及其他具有感受性細菌引起感染症
乾粉注射劑, 1g
衛部藥輸字第026347號，請點擊下列按鈕前往網站查詢。
CEFTAZIDIME 5H2O
Ceftazidime是殺菌性頭孢子菌抗生素、對多種乙內醯胺酶有抵抗力、並對廣範圍的革蘭氏陽性及陰性細菌有效。
乾粉注射劑, 2g
衛部藥輸字第026703號，請點擊下列按鈕前往網站查詢。
