The idea is simple enough to fit on an index card: instead of manufacturer rebates flowing to pharmacy benefit managers...
Read moreA sixteen-year-old patient who has been taking puberty blockers for three years and gender-affirming hormones for one is, depending on...
Read moreThe compounding pharmacy that produces bioidentical hormone preparations for a clinic in Arizona may dispense thousands of monthly subscriptions to...
Read moreA drug priced at $400 in the United States and $80 in Germany is a shorthand the policy debate has...
Read moreIn 1992, when Congress created the 340B Drug Pricing Program as a quiet rider on a Veterans Affairs reauthorization, the...
Read moreOn January 1, 2026, the maximum fair prices Medicare negotiated for ten of its costliest drugs will take effect, and...
Read moreThe premise seemed elegant: require pharmaceutical manufacturers to disclose the data behind drug price increases, and the resulting transparency would...
Read moreEvery quarter, pharmaceutical manufacturers who want their drugs covered by Medicaid submit a number to CMS that determines how much...
Read moreThe word "negotiation" appears throughout the Inflation Reduction Act's drug pricing provisions, and it is doing considerable work. In ordinary...
Read moreThe modern American drug market was built on opacity, and then—suddenly—it was asked to explain itself. The Trump administration’s push...
Read moreTelemedicine was once described as the future of healthcare; today it resembles something more complicated—an infrastructure whose permanence remains politically...
Read morePolicy frameworks assume that therapies map cleanly to indications. Combination protocols blur that mapping. A GLP-1 agent prescribed for...
Read moreClinicians increasingly encounter patients using or requesting peptide-based therapies sourced through compounding pharmacies. The U.S. Food and Drug Administration has identified a subset of bulk drug substances, including certain peptides, that may present significant safety risks when used in compounded formulations. The clinical question is whether these regulatory signals reflect meaningful patient-level risk and how they should influence prescribing behavior. This matters because compounded peptides often sit outside traditional approval pathways, creating uncertainty around quality, dosing consistency, and safety. Understanding...
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© 2026 Daily Remedy