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Oct 6: People with a range of rheumatic diseases have a new treatment delivery option after the FDA approved an intravenous formulation of Novartis IL-17A antagonist Cosentyx (secukinumab)

The two peptides have separate FDA concerns: FDA flagged CJC-1295 for limited clinical data and serious adverse events including increased heart rate and systemic vasodilatory reaction

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The use of Mounjaro can lead to a range of common side effects, which may include: These side effects can be bothersome but are not typically dangerous

Pancreatitis risk exists with both drugs, though actual cases remain rare