Biotechnology has brought about the discovery and development of a new generation of human therapeutics. Dyspnea was reported in patients treated with KYPROLIS.

The most common adverse reactions in the combination therapy trials: anemia, neutropenia, diarrhea, dyspnea, fatigue, thrombocytopenia, pyrexia, insomnia, muscle spasm, cough, upper respiratory tract infection, hypokalemia. Stop KYPROLIS for Grade 3 or 4 dyspnea until resolved or returned to baseline. Protein engineers are using the building blocks nature provides to design an ever-expanding toolkit of new drug formats to fight disease. return d.getFullYear(); Amgen has developed a collection of online resources available to help you learn more about areas of interest. Previous: These products provide significant clinical benefits, and in many cases, provide therapies where no effective treatment existed.
Caregivers should wear protective gloves when assisting patients in applying or changing occlusive dressings and observe safety precautions for disposal of used dressings, gloves, and cleaning materials. Advances in human genetics are pinpointing genes that cause disease and providing a new way to identify highly relevant drug targets. The safety of reinitiating KYPROLIS is not known. Monitor blood pressure regularly in all patients.

Withhold KYPROLIS for PAH until resolved or returned to baseline and consider whether to restart based on a benefit/risk assessment. Signs and symptoms include fever, chills, arthralgia, myalgia, facial flushing, facial edema, laryngeal edema, vomiting, weakness, shortness of breath, hypotension, syncope, chest tightness, or angina. YOU ARE NOW LEAVING AMGEN'S WEB SITE. Amgen has built an organization distinguished by world-class scientists with a talent for applying novel approaches to treat disease. Amgen is one of the world’s leading biotechnology companies. At Amgen, we are driven by our commitment to transform the lives of cancer patients and keep them at the center of everything we do. The length of time that it takes for us to complete clinical trials and obtain regulatory approval for product marketing has in the past varied and we expect similar variability in the future. Our business may be impacted by government investigations, litigation and product liability claims. The 3 Most Important Drugs in Amgen's Pipeline Amgen has been a late-stage juggernaut lately, but it's these experimental drugs within its pipeline that you … Patients or close contacts have the option of follow-up testing for further characterization of the infection. Further, while we routinely obtain patents for our products and technology, the protection offered by our patents and patent applications may be challenged, invalidated or circumvented by our competitors, or we may fail to prevail in present and future intellectual property litigation. Monitor for evidence of TLS during treatment and manage promptly, and withhold until resolved.
Access to Medicines Initiatives Outside the U.S. Non-Healthcare Donations and Sponsorships, http://www.prnewswire.com/news-releases/amgen-showcases-oncology-pipeline-at-asco-2020-301058857.html, Amgen Showcases Oncology Pipeline At ASCO 2020, In combination with dexamethasone or with lenalidomide plus dexamethasone for the treatment of patients with relapsed or refractory multiple myeloma who have received one to three lines of therapy, As a single agent for the treatment of patients with relapsed or refractory multiple myeloma who have received one or more lines of therapy. About IMLYGIC® (talimogene laherparepvec) IMLYGIC is a genetically modified herpes simplex type 1 virus that is injected directly into tumors. While adequate hydration is required prior to each dose in Cycle 1, monitor all patients for evidence of volume overload, especially patients at risk for cardiac failure. Do you want to link to this External Site and leave Amgen.com?


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