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Mashup Score: 0Tofacitinib exhibits shorter timeline to initial clinical response in PsA vs. placebo - 2 year(s) ago
Tofacitinib for psoriatic arthritis is efficacious in most patient-reported and clinical endpoints over time, and shows shorter initial and meaningful response times versus switching from placebo to the drug at month 3, noted researchers. “The efficacy and safety of oral tofacitinib 5 mg or 10mg twice daily (BID) or adalimumab (40mg administered subcutaneously once every 2weeks [Q2W]) have
Source: www.healio.comCategories: Latest Headlines, RheumatologyTweet
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Mashup Score: 0
Patients with rheumatoid arthritis who received tofacitinib demonstrated a greater risk for major adverse cardiovascular events and cancer than those treated with TNF inhibitors, according to data in The New England Journal of Medicine. In the study — a safety trial ordered by the FDA following reports of increased lipid levels and cancer incidence associated with tofacitinib (Xeljanz,
Source: www.healio.comCategories: Latest Headlines, RheumatologyTweet
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Mashup Score: 3FDA approves Xeljanz for active ankylosing spondylitis - 2 year(s) ago
The FDA has approved Xeljanz for the treatment of adults with active ankylosing spondylitis who have had an inadequate response, or intolerance to, TNF inhibitors, according to a Pfizer press release.The announcement marks the fifth indication for the drug, making it the first and only oral JAK inhibitor approved in the United States for five diseases, according to Pfizer. Xeljanz (tofacitinib)
Source: www.healio.comCategories: Latest Headlines, RheumatologyTweet
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Mashup Score: 0High-Dose Tofacitinib Cuts Colectomy Rates For Acute Severe UC - 2 year(s) ago
A regimen of three daily doses of tofacitinib (Xeljanz, Pfizer) slashed rates of colectomy by nearly 90% in patients admitted to the hospital for acute severe ulcerative colitis, researchers have found.
Source: www.gastroendonews.comCategories: Gastroenterology, Latest HeadlinesTweet
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Mashup Score: 0High-Dose Tofacitinib Cuts Colectomy Rates For Acute Severe UC - 2 year(s) ago
A regimen of three daily doses of tofacitinib (Xeljanz, Pfizer) slashed rates of colectomy by nearly 90% in patients admitted to the hospital for acute severe ulcerative colitis, researchers have found.
Source: www.gastroendonews.comCategories: Gastroenterology, Latest HeadlinesTweet
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Mashup Score: 2FDA adds black box warning to JAK inhibitors; cites heart-related issues, cancer, death - 3 year(s) ago
The FDA has called for additional warning labels on janus kinase inhibitors after a safety review found this class of medications was associated with an excess risk for serious heart-related events, cancer, blood clots and death. An alert was previously issued by the FDA in February about the risk for serious health-related problems and cancer linked to tofacitinib (Xeljanz, Pfizer) compared with
Source: www.healio.comCategories: Latest Headlines, RheumatologyTweet-
Despite #FDA black box warnings against #Xeljanz , #Olumiant and #Rinvoq Dr. Stanley Cohen @UTSWNews noted that these drugs "should still be an option with proper discussion of the benefits and risk" for young healthy patients at low risk for complications https://t.co/VQfVnVweqO https://t.co/zXRMsBfoFK
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Mashup Score: 2FDA adds black box warning to JAK inhibitors; cites heart-related issues, cancer, death - 3 year(s) ago
The FDA has called for additional warning labels on janus kinase inhibitors after a safety review found this class of medications was associated with an excess risk for serious heart-related events, cancer, blood clots and death. An alert was previously issued by the FDA in February about the risk for serious health-related problems and cancer linked to tofacitinib (Xeljanz, Pfizer) compared with
Source: www.healio.comCategories: Latest Headlines, RheumatologyTweet
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Mashup Score: 0'We need to see the data': FDA's Xeljanz safety warning stirs concerns for JAK inhibitors - 3 year(s) ago
For Pfizer and its JAK inhibitor, Xeljanz, February rang in with the sound of alarm bells, as the FDA issued its third warning about the drug in 2 years. In this latest alert regarding tofacitinib, the FDA warned providers of an increased risk for serious heart-related issues and cancer among older patients, compared with TNF inhibitors.This has left many experts anxious to dig into the full
Source: www.healio.comCategories: Latest Headlines, RheumatologyTweet
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Mashup Score: 0
The FDA issued an alert concerning an increased risk for serious cardiovascular events and malignancies with the JAK inhibitor, tofacitinib, compared with TNF inhibitors.
Source: www.clinicaloncology.comCategories: Hem/Onc News and Journals, Latest HeadlinesTweet
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Mashup Score: 0'We need to see the data': FDA's Xeljanz safety warning stirs concerns for JAK inhibitors - 3 year(s) ago
For Pfizer and its JAK inhibitor, Xeljanz, February rang in with the sound of alarm bells, as the FDA issued its third warning about the drug in 2 years. In this latest alert regarding tofacitinib, the FDA warned providers of an increased risk for serious heart-related issues and cancer among older patients, compared with TNF inhibitors.This has left many experts anxious to dig into the full
Source: www.healio.comCategories: Latest Headlines, RheumatologyTweet
Patients with active #PsoriaticArthritis who received @pfizer 's #Xeljanz experienced a shorter timeline to initial clinical response vs. placebo #RheumTwitter https://t.co/mtjf2Gz4f1