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November 18, 2024
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CDC: 1 dead in multistate outbreak of E. coli linked to organic carrots

Psoriatic Arthritis News

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January 18, 2022
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More than 60% of patients with RA, PsA report side effects in days after methotrexate dose

More than 60% of patients with RA, PsA report side effects in days after methotrexate dose

Approximately 61% of patients with rheumatoid arthritis or psoriatic arthritis who use methotrexate report side effects following weekly dosing, including fatigue and nausea, according to data published in Rheumatology and Therapy.

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January 12, 2022
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Flares, breakthroughs rare after COVID-19 vaccination in inflammatory rheumatic disease

Flares, breakthroughs rare after COVID-19 vaccination in inflammatory rheumatic disease

Just 0.7% of fully vaccinated patients with inflammatory rheumatic and musculoskeletal disease experience a breakthrough COVID-19 infection, while only 4.4% demonstrate disease flare reactions, according to data.

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AdobeStock_Carrots_1200x630
November 18, 2024
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CDC: 1 dead in multistate outbreak of E. coli linked to organic carrots

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January 12, 2022
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Quantifiable measures make treat-to-target viable for PsA

Quantifiable measures make treat-to-target viable for PsA

Though sometimes complex, treat-to-target strategies for psoriatic arthritis can lead to lower symptom states, better physical functionality and less structural damage to joints, according to Philip Mease, MD, a clinical professor at the University of Washington School of Medicine and Director of rheumatology research at the Swedish Medical Center in Seattle.

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January 10, 2022
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Risk for 'more severe, critical' COVID-19 higher in RA vs. PsA, ulcerative colitis

Risk for 'more severe, critical' COVID-19 higher in RA vs. PsA, ulcerative colitis

Patients with rheumatoid arthritis, but not psoriatic arthritis or ulcerative colitis, are at a greater risk for severe or critical COVID-19 versus those with COVID-19 alone, according to data published in The Journal of Rheumatology.

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January 07, 2022
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Cyltezo 'paid the price' for interchangeable biosimilar approval: Will it be worth it?

Cyltezo 'paid the price' for interchangeable biosimilar approval: Will it be worth it?

In October, Boehringer Ingelheim’s adalimumab-adbm secured a landmark FDA approval as the first interchangeable biosimilar to AbbVie’s blockbuster drug, Humira — but, as rivals scramble for second place, will the designation be worth the price?

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January 06, 2022
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Dactylitis signals greater disease burden in early psoriatic arthritis

Dactylitis signals greater disease burden in early psoriatic arthritis

Dactylitis indicates a more severe disease phenotype independently linked to increased disease burden, with greater bone erosion, in early DMARD-naïve psoriatic arthritis, according to data published in the Annals of the Rheumatic Diseases.

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December 30, 2021
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DMARD interruptions rose 80% in early 2021 among autoimmune rheumatic patients

DMARD interruptions rose 80% in early 2021 among autoimmune rheumatic patients

DMARD interruptions in patients with autoimmune rheumatic diseases increased more than 80% between December 2020 and May 2021, leading to higher rates of self-reported flares, according to data published in Arthritis Care & Research.

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December 23, 2021
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FDA approves Cosentyx for children with juvenile PsA, enthesitis-related arthritis

FDA approves Cosentyx for children with juvenile PsA, enthesitis-related arthritis

The FDA has approved secukinumab for the treatment of active psoriatic arthritis in patients aged 2 years and older, and for active enthesitis-related arthritis in those aged 4 years and older.

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December 21, 2021
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Upadacitinib effective as monotherapy, in combination with non-biologics for PsA

Upadacitinib effective as monotherapy, in combination with non-biologics for PsA

Upadacitinib demonstrates comparable efficacy and safety as monotherapy or in combination with non-biologic disease-modifying antirheumatic drugs in patients with psoriatic arthritis, according to data published in Rheumatology.

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December 20, 2021
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Coherus’ Yusimry nabs FDA approval as seventh Humira biosimilar in cramped market

Coherus’ Yusimry nabs FDA approval as seventh Humira biosimilar in cramped market

The FDA has approved the seventh biosimilar to adalimumab, adalimumab-aqvh, for all eligible indications of the biologic product, the latest in an increasingly crowded biosimilar logjam set to release in 2023.

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