New technologies like NFC, blockchain, and AI are transforming how we detect fake drugs. From tamper-proof packaging to smartphone verification, these innovations are stopping counterfeit medicine before it reaches patients.
Read moreLearn how to store medications properly to prevent early expiration, avoid wasted drugs, and ensure your pills stay safe and effective. Simple tips backed by science.
Read moreWhile generics save billions, some patients experience real side effects after switching. Learn why bioequivalence doesn't always mean identical results, especially for thyroid, seizure, and blood-thinner medications.
Read moreGenerics make up 90% of prescriptions but only 25% of drug spending - yet they drive 96% of pharmacy profits. Learn how PBMs, consolidation, and spread pricing are squeezing independent pharmacies - and what they're doing to survive.
Read moreThe FDA uses dissolution testing to ensure generic drugs release medicine at the same rate as brand-name versions, replacing human trials with reliable lab tests. This process guarantees safety, effectiveness, and affordability.
Read moreRifampin drastically reduces levels of anticoagulants and antivirals by activating liver enzymes that break them down. This can lead to dangerous treatment failures. Learn how to manage this life-threatening interaction.
Read moreCombination NTI drugs offer powerful treatment for complex conditions but face major barriers to generic availability. With no approved fixed-dose combinations in the U.S., patients face higher costs, increased monitoring, and greater risk of adverse events after generic switches.
Read moreHospital formularies make strategic decisions on generic drugs based on clinical safety, cost, and supply reliability-not just price. Learn how P&T committees choose generics to balance savings with patient outcomes.
Read moreStability testing ensures pharmaceuticals remain safe and effective over time. Learn the exact temperature and time conditions required by ICH Q1A(R2) for global drug approval, including long-term, accelerated, and refrigerated protocols.
Read moreREMS programs are FDA-mandated safety systems for high-risk medications. Learn how they work, which drugs require them, why they cause delays, and what’s being done to fix them in 2025.
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