Dec 6, 2025
Medication Errors vs Drug Side Effects: How to Tell Them Apart and Why It Matters
The FDA now enforces strict, unannounced inspections on foreign generic drug factories to ensure safety. Learn how CGMP standards, inspection gaps, and new policies are reshaping global drug manufacturing for American patients.
Levothyroxine is effective for hypothyroidism, but safety depends on proper dosing and regular TSH monitoring. Brand switches, missed tests, and poor timing can cause serious side effects. Know how to protect yourself.
Survivorship care plans guide cancer survivors through post-treatment follow-up, screening for late effects, and healthy living. Learn what’s included, why it matters, and how to get one-even if your hospital doesn’t offer it.
Generic drug exclusivity periods vary widely across countries, affecting drug prices and access. Learn how the U.S., EU, Canada, and others regulate generic entry and why these rules matter for patients and healthcare systems.
The FDA's 2025 update to biosimilar approval rules removes outdated clinical trial requirements, speeding up access to lower-cost biologic alternatives for cancer, arthritis, and other chronic conditions.
Stability testing ensures generic drugs remain safe and effective over time. The FDA requires rigorous testing of three batches under real and accelerated conditions to prove shelf life, potency, and purity match brand-name drugs.
Chronic pain and insomnia feed each other in a vicious cycle. Learn how CBT-I breaks this loop, why sleep aids fail, and what actually works to reduce pain by improving sleep-backed by science and patient results.
Sildenafil citrate may improve skin health by boosting blood flow, helping with rosacea, sun damage, and psoriasis. Learn what science says about its real benefits beyond erectile dysfunction.
