Category: Medications - Page 2
Deprescribing Frameworks: How to Safely Reduce Medications and Cut Side Effects
Deprescribing frameworks help safely reduce unnecessary medications in older adults, cutting side effects, falls, and hospitalizations. Evidence shows it’s safe, effective, and urgently needed as polypharmacy rises.
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30-Month Stay: How Patent Litigation Delays Generic Drug Approval
The 30-month stay under the Hatch-Waxman Act delays generic drug approval when patent lawsuits are filed. Learn how this legal tool affects drug prices, innovation, and patient access to affordable medications.
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Polypharmacy in Older Adults: How Drug Interactions Risk Health and How to Safely Deprescribe
Polypharmacy in older adults increases the risk of dangerous drug interactions, falls, and hospitalizations. Learn how deprescribing can safely reduce medication burden and improve health outcomes.
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St. John’s Wort and Medication Interactions: What You Need to Know Before Taking It
St. John's Wort can dangerously reduce the effectiveness of warfarin, birth control, antidepressants, and transplant drugs. Learn which medications it interacts with, why it's risky even if you're healthy, and what to do instead.
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Questions to Ask Your Doctor About Medication Side Effects
Learn the essential questions to ask your doctor about medication side effects to avoid dangerous reactions, reduce ER visits, and take control of your health. Based on FDA, CDC, and clinical guidelines.
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Difference Between Medication Side Effects and Allergic Drug Reactions
Learn the key differences between medication side effects and true allergic reactions, why mixing them up is dangerous, and how to get tested to avoid unnecessary drug restrictions and healthcare costs.
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WHO Model Formulary: International Standards for Essential Generics
The WHO Model List of Essential Medicines sets global standards for affordable, life-saving generics. Used by over 150 countries, it ensures access to proven, cost-effective medicines-especially antibiotics, antivirals, and chronic disease treatments-while promoting quality-assured generics through strict bioequivalence and regulatory requirements.
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How to Report Adverse Drug Reactions to FDA MedWatch
Learn how to report adverse drug reactions to the FDA's MedWatch program. Understand what counts as reportable, who can file, and why your report matters for public safety.
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China and India Manufacturing: Risks and FDA Monitoring in Pharmaceuticals
China and India dominate global pharmaceutical manufacturing, but FDA monitoring reveals stark differences in quality control. India leads in compliance, while China supplies most APIs-but with higher risk. Here’s what you need to know.
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Common Manufacturing Defects in Generic Drugs and How They Impact Safety
Generic drugs save money but face higher rates of manufacturing defects like capping, contamination, and inconsistent dosing. Learn how these issues impact safety and what patients and providers can do.
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