Archive: 2025/12

Understanding Adverse Event Rates: Percentages and Relative Risk in Clinical Trials

Learn how adverse event rates in clinical trials are calculated, why simple percentages can mislead, and how exposure-adjusted methods like EAIR are changing FDA safety reporting standards.

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Batch Variability and Bioequivalence: What Acceptable Limits Really Mean for Generic Drugs

Batch variability can make or break bioequivalence for generic drugs. Learn why the 80-125% rule isn't enough, how new methods are fixing the system, and what it means for your health.

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Drug-Related Headaches: How to Spot Them and Find Real Relief

Medication overuse headache is a hidden cause of chronic pain. Learn how common painkillers can trigger daily headaches-and how to break the cycle safely with proven methods.

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How to Ensure Accurate Dosing Devices with Liquid Prescriptions

Use oral syringes and milliliter-only labels to prevent dangerous dosing errors with liquid medications. Learn why household spoons and dosing cups cause mistakes-and how to get the right tool every time.

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Antiseizure Medications and Generic Substitution: Risks and Best Practices

Generic antiseizure medications can save money, but for people with epilepsy, even small changes in drug absorption can trigger seizures. Learn the risks, real patient stories, and best practices to stay safe.

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