Tag: FDA equivalence
Pharmaceutical Equivalence for Generics: What It Really Means When You Pick a Generic Drug
Pharmaceutical equivalence ensures generic drugs contain the same active ingredient, strength, and dosage form as brand-name versions. It's the first step to safe substitution-but not the only one. Learn what it really means for your prescriptions.
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Stigma around mental health medications stops many from getting care. Learn practical steps to address it, including how to talk about meds, respond to misconceptions, and find support. Evidence-based strategies from SAMHSA and NAMI can help reduce shame and improve treatment outcomes.
Published ON: 4 FebElectrolyte imbalances in potassium, phosphate, and magnesium can cause life-threatening heart and breathing problems. Learn how to recognize the signs, follow life-saving treatment protocols, and prevent complications-especially in kidney disease and critical care.
Published ON: 8 FebSerious adverse events from generic drugs are underreported, creating dangerous gaps in safety data. Learn how reporting works, why it fails, and what’s being done to fix it.
Published ON: 7 FebSSRIs are the most common antidepressants used today. Learn how they work in the brain, what side effects to expect, why they take weeks to work, and what to do if they don’t help.
Published ON: 7 FebThe FDA now conducts unannounced inspections at foreign food facilities to ensure imported products meet U.S. safety standards. This shift closes a long-standing gap in oversight and forces overseas plants to maintain compliance 24/7.
Published ON: 3 Feb