Mail-order pharmacies can save you hundreds a year on maintenance medications, but delivery delays and lack of immediate access are real drawbacks. Learn who benefits most and how to use it wisely.
Medication Therapy Management (MTM) is a free service for Medicare Part D patients taking multiple chronic meds. Get a pharmacist-led review to avoid dangerous interactions, save money, and understand your meds better.
Many medications cause brain fog and memory problems - especially sleep aids, painkillers, and antihistamines. Learn which drugs are most likely to blame and how to reverse the effects safely with your doctor.
Learn how to approach your doctor with confidence when you see a new drug safety alert. Get practical steps to discuss FDA warnings, ask the right questions, and ensure your medication is still safe for you.
In 2025, PBC treatment has shifted dramatically with the withdrawal of Ocaliva and the approval of seladelpar and elafibranor. Learn how UDCA remains first-line, why new drugs work better, and what patients should know now.
Green tea can affect warfarin's effectiveness by introducing vitamin K, which counteracts blood thinning. Moderate consumption (1-3 cups daily) is safe, but excessive intake or matcha can lower INR and increase clot risk. Consistency matters more than avoidance.
Learn how to check formularies and preferred drug lists before prescribing to avoid costly coverage surprises. Understand tiers, prior authorization, and tools to ensure patients get the meds they need.
The Beers Criteria identify medications that pose higher risks than benefits for adults over 65. Learn which drugs to avoid, why they're dangerous, and how to use this guide for safer prescribing and better health outcomes.
In 2025, drug shortages are worsening because 90% of active ingredients still come from just two countries. Dependence on foreign manufacturing makes supply chains fragile - and patients are paying the price.
Generic drugs are approved based on bioequivalence, not full safety trials. Post-market studies track real-world side effects, manufacturing flaws, and rare reactions that pre-approval studies miss. Here's how the FDA monitors safety after launch.