Contamination controls in generic drug manufacturing prevent harmful adulteration through cleanroom standards, human process discipline, and real-time monitoring. Learn how facilities avoid recalls, comply with FDA rules, and protect patient safety.
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GERD and acid reflux can be managed with lifestyle changes and smart use of PPIs. Learn how weight loss, food choices, and timing of meals reduce symptoms - and why long-term PPI use needs caution.
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Learn how to spot hidden allergens and inactive ingredients on prescription labels. Many pills contain milk, soy, or peanuts without clear labeling-here's how to stay safe.
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Pharmacy reimbursement laws determine how much pharmacies get paid for generic drugs. From MAC pricing to PBM spreads and Medicare’s new $2 list, these rules shape what you pay at the counter-and whether your local pharmacy can stay open.
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H2 blockers like famotidine and cimetidine can reduce the effectiveness of antivirals and antifungals by changing stomach acidity or blocking liver enzymes. Learn which combinations are dangerous and how to avoid treatment failure.
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Most medications remain effective years after their expiration date, but not all. Learn which pills are still safe to use, which ones you should never take, and why expiration dates are more about business than science.
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The first generic drug company to file a patent challenge gets 180 days of exclusive sales rights. This rule, from the Hatch-Waxman Act, was meant to speed up affordable drugs-but loopholes let some companies block competition without selling anything.
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Learn how to measure children's liquid medication accurately at home using oral syringes and milliliters only. Avoid dangerous dosing errors with proven steps, tools, and expert tips.
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Many common medications - from antidepressants to blood pressure pills - can cause sexual side effects like low desire, erectile dysfunction, or orgasm problems. Learn which drugs are most likely to cause these issues and what you can do about them.
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Regulatory exclusivity gives drugmakers exclusive market rights for 5 to 12 years after FDA approval, blocking generics even after patents expire. It's a key driver of drug pricing and innovation incentives.
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