Author: Dorian Wellings

Traveling With Medications: Security, Storage, and Refills Guide for 2025

Learn how to travel safely with medications in 2025-avoid confiscations, understand international rules, store insulin properly, and get refills abroad without stress.

Methadone and QT Prolongation: Essential ECG Monitoring Guidelines

Methadone can prolong the QT interval on an ECG, raising the risk of life-threatening arrhythmias. Learn who’s at risk, when to monitor, and how to stay safe while in treatment.

Antacids and Kidney Disease: What You Need to Know About Phosphate Binders and Risks

Antacids like Tums and Milk of Magnesia can be dangerous for people with kidney disease. Learn how calcium, aluminum, and magnesium in these meds affect phosphate levels, heart health, and kidney function - and what safer options exist.

Post-Market Surveillance: How Side Effects Are Discovered After Approval

Post-market surveillance uncovers hidden side effects of drugs and medical devices after approval, using real-world data from millions of users. Learn how systems like MedWatch and AI-powered analytics catch dangers clinical trials miss.

Blood Thinner Overdose and Internal Bleeding: What to Do Immediately

Learn the signs of blood thinner overdose and internal bleeding, what to do immediately, and how to prevent life-threatening complications. Critical info for warfarin and DOAC users.

International Pharmacovigilance: How Global Safety Monitoring Is Being Harmonized

Global pharmacovigilance harmonization is improving drug safety by aligning reporting standards across countries. Learn how ICH guidelines, AI, and real-world data are reducing delays and saving lives - and where the system still falls short.

What Are Drug Interactions and Why They Matter for Medication Safety

Drug interactions occur when medications, foods, or health conditions change how a drug works in your body-potentially causing serious harm or reducing effectiveness. Learn what causes them, who's at risk, and how to prevent dangerous combinations.

Replicate Study Designs for Bioequivalence Assessment: Advanced Methods for Highly Variable Drugs

Replicate study designs are essential for assessing bioequivalence of highly variable drugs. Learn how full and partial replicate methods reduce sample sizes, meet regulatory standards, and improve generic drug approval rates.

Lithium Carbonate Generics: What You Need to Know About Serum Levels

Lithium carbonate generics require careful serum level monitoring due to their narrow therapeutic window. Switching between brands can alter blood levels, risking toxicity or relapse. Learn safe targets, testing schedules, and how to avoid dangerous interactions.

Documentation Requirements for Recording Generic Substitution Decisions in Pharmacy Practice

Learn the essential documentation requirements for recording generic drug substitutions in pharmacy practice. Understand state laws, what to log, common mistakes, and how to avoid errors that impact patient safety.