Category: Medications
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Vybrique Now FDA Approved: A New, Discreet Oral Film for Erectile Dysfunction
Erectile dysfunction (ED) affects millions of men and can be stressful to manage. A new option just cleared by the U.S. Food and Drug Administration (FDA) may make treatment easier and more discreet: Vybrique™, the first FDA‑approved sildenafil oral film that dissolves on the tongue. What is Vybrique and why does it matter? Vybrique is
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FDA Approves Darzalex Faspro as Part of a New First‑Line Quadruplet Regimen for Multiple Myeloma
Multiple myeloma is a type of blood cancer that affects plasma cells – specialized white blood cells that help the body fight infections. For years, treatment options have steadily improved, but the newest development marks one of the most meaningful steps forward yet. The U.S. Food and Drug Administration (FDA) has approved a new four‑drug
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Levalbuterol Tartrate Uses, Safety, and Alternatives
Levalbuterol tartrate is an effective short‑acting bronchodilator for acute bronchospasm and is an alternative to albuterol. For most patients, clinical outcomes are similar between levalbuterol and albuterol; cost, individual tolerance, and device preference usually determine which product is best. Always use rescue inhalers as directed, maintain controller therapy when prescribed, and seek medical care for
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FDA Approves Exdensur: A Twice‑Yearly Shot That Could Change Life for People with Severe Asthma
Severe asthma can be frightening: sudden attacks, emergency visits, and daily limits on what you can do. On December 16, 2025, the U.S. Food and Drug Administration (FDA) approved Exdensur (depemokimab‑ulaa) as an add‑on maintenance treatment for people aged 12 and older with severe asthma characterized by an eosinophilic phenotype – a type of asthma
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FDA Approves Breyanzi for Relapsed or Refractory Marginal Zone Lymphoma
The U.S. Food and Drug Administration approved Breyanzi for adults with relapsed or refractory marginal zone lymphoma who have already tried at least two prior systemic therapies. This approval expands the list of cancers for which Breyanzi is authorized and gives patients a new option when other treatments have failed. In plain language: what is
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FDA Approves Armlupeg – New Pegfilgrastim Biosimilar
The U.S. Food and Drug Administration has approved Armlupeg™ (pegfilgrastim‑unne) as a biosimilar to Neulasta® (pegfilgrastim) for decreasing the incidence of infection manifested by febrile neutropenia in patients with non‑myeloid malignancies receiving myelosuppressive chemotherapy, and for increasing survival after acute exposure to myelosuppressive radiation. This approval adds another pegfilgrastim biosimilar to the U.S. market and
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FDA Approves Reformulated Ranitidine Following Comprehensive Safety Review
The U.S. Food and Drug Administration (FDA) has approved a reformulated ranitidine tablet after a comprehensive safety review addressing prior concerns about N‑nitrosodimethylamine (NDMA) impurity formation; the approval includes updated storage and handling requirements to mitigate impurity risk and preserve product stability. Background and regulatory context Ranitidine, an H2‑receptor antagonist widely used for gastroesophageal reflux
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The Price Paradox: Why Your Prescription Costs 278% More Than the Same Pill Abroad
The United States leads the world in pharmaceutical innovation, developing life-saving therapies that benefit global health. Yet, a striking paradox exists: Americans pay significantly more for prescription drugs than consumers in virtually every other high-income country. This disparity isn’t a minor difference; it’s a chasm, rooted in fundamental differences in how the U.S. and its


