Category: Pharmaceutical Information

How to Ensure Accurate Dosing Devices with Liquid Prescriptions

By Lindsey Smith On 29 Dec, 2025 Comments (15)

Learn how to prevent dangerous dosing errors with liquid medications by using the right measuring devices, understanding label standards, and following proven techniques for accurate administration.

Immunosuppressants and Cancer History: What You Need to Know About Recurrence Risk

By Lindsey Smith On 28 Dec, 2025 Comments (15)

New research shows immunosuppressants do not increase cancer recurrence risk, even when started soon after cancer treatment. Learn how to make safe, evidence-based decisions about these medications.

Medicare Part D Formularies: How Generic Coverage Works

By Lindsey Smith On 26 Dec, 2025 Comments (14)

Learn how Medicare Part D covers generic drugs, how tiered formularies work, the $2,000 out-of-pocket cap, and how to save money on prescriptions in 2025 and beyond.

Medication Alternatives: What to Do During a Drug Shortage

By Lindsey Smith On 25 Dec, 2025 Comments (15)

When medications run out due to shortages, knowing your alternatives can protect your health. Learn how to find safe substitutes, work with your pharmacist, and avoid dangerous risks during drug shortages.

How to Recognize Changes in Color, Odor, or Texture in Expired Drugs

By Lindsey Smith On 18 Dec, 2025 Comments (8)

Learn how to spot dangerous changes in expired drugs-color shifts, odd smells, and texture problems-that signal degradation. A practical guide to keeping your medications safe.

FDA Foreign Facility Inspections: What Overseas Manufacturers Need to Know in 2025

By Lindsey Smith On 17 Dec, 2025 Comments (15)

The FDA now conducts unannounced inspections of overseas food and drug facilities to ensure U.S. safety standards. Learn how foreign manufacturers must adapt to avoid shipment refusals, fines, or criminal charges.

Quality by Design in Generic Drug Development: Modern Science-Based Approaches

By Lindsey Smith On 15 Dec, 2025 Comments (15)

Quality by Design (QbD) transforms generic drug development by building quality into the process from the start. Learn how modern science-based approaches improve approval rates, reduce costs, and ensure bioequivalence without relying on end-product testing.

Pharmacy Errors with Generics: Prevention and Correction Strategies

By Lindsey Smith On 15 Dec, 2025 Comments (9)

Generic medications are essential for affordable care, but they come with hidden risks. Learn how common pharmacy errors happen, why they occur, and what pharmacists and patients can do to prevent them.

Digoxin Interactions: What Heart Patients Need to Monitor

By Lindsey Smith On 15 Dec, 2025 Comments (15)

Digoxin helps manage heart failure and atrial fibrillation, but its narrow safety window makes interactions dangerous. Learn which drugs, foods, and supplements can raise toxicity risk - and how to stay safe.

How Government Controls Generic Drug Prices in the U.S. Today

By Lindsey Smith On 8 Dec, 2025 Comments (12)

The U.S. doesn't set generic drug prices directly, but Medicaid rebates, Medicare caps, and the 340B program help lower costs. Learn how government policies affect what you pay for generics today.

Biosimilar Cost Savings: How They Compare to Original Biologic Prices

By Lindsey Smith On 3 Dec, 2025 Comments (13)

Biosimilars offer real cost savings on expensive biologic drugs, with up to 85% lower list prices in some cases. Learn how they compare to originators, why savings vary, and why adoption remains low despite billions in potential savings.

How to Search FDA’s Drugs@FDA Database for Official Drug Information

By Lindsey Smith On 1 Dec, 2025 Comments (13)

Learn how to use FDA's Drugs@FDA database to find official drug approval information, labels, and regulatory documents. Free, no login required, updated daily.