The 30-month stay under the Hatch-Waxman Act delays generic drug approvals by tying FDA approval to patent litigation. This mechanism, meant to balance innovation and access, often extends brand monopolies, raising drug costs by billions annually.
High-potassium foods like bananas and spinach can help lower blood pressure - but they may be dangerous if you're taking certain medications. Learn what to eat, what to avoid, and how to stay safe.
NSAIDs and acetaminophen are the two most common pain relievers, but they work differently and carry unique risks. Learn which one to choose for headaches, arthritis, back pain, and more-and how to use them safely.
Counterfeit generics are fake medications that look real but contain dangerous or inactive ingredients. Learn how to spot them, where they come from, and how to protect yourself from deadly fakes like fake Ozempic.
Akathisia and restless legs syndrome both cause intense restlessness, but only one is caused by medication-and mistaking them can lead to dangerous treatment errors. Learn how to tell them apart and what to do next.
Pharmacy substitution laws vary by state, affecting whether you get generic or brand-name drugs. Learn how to check your state’s rules, understand biosimilar swaps, and protect your health when medications change.
Pharmacists play a critical role in medication therapy management by optimizing generic drug use to improve adherence, reduce costs, and prevent adverse effects. Learn how MTM works and why it's changing patient outcomes.
Some medications can trigger sudden suicidal thoughts - even in people who’ve never had them before. Learn the key warning signs, who’s most at risk, and what to do if you or someone you care about starts feeling this way.
When drug shortages hit, hospitals must make painful choices about who gets life-saving medication. This article explains the ethical frameworks guiding those decisions, how they're failing in practice, and what’s being done to fix them.
Registries and claims data are the backbone of modern drug safety monitoring. These real-world evidence sources help regulators detect rare side effects, track long-term outcomes, and make informed decisions after drugs hit the market.