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Generic Drugs By: Brittany Smith
What is a generic drug? A generic drug is called by its basic chemical name instead of a registered brand-name chosen by the manufacturer. Generic drugs have the same active ingredients as brand-name drugs. One difference between them is the name; another, usually, is the price. If your pharmacist gives you a generic drug in place of a brand-name product, good standard practice and most state laws require that it be generically and therapeutically equivalent.
Ed. Drugs sold over the internet… are not approved by the United States Food and Drugs Administration (FDA)  are considered illegal to the United States Government and are subject to seizure  can contain unknown and possibly harsh, harmful chemicals  can be made in underdeveloped countries such as India, China, Mexico, Belize and are manufactured in unsanitary and unregulated factories  are not proven to be safe and effective
Potential Health Risks With Imported Drugs: Quality assurance concerns. Medications that have not been approved for sale in the United States may not have been manufactured under quality assurance procedures designed to produce a safe and effective product.  Counterfeit potential. Some imported medications--even those that bear the name of a U.S.-approved product--may, in fact, be counterfeit versions that are unsafe or even completely ineffective.  Presence of untested substances. Imported medications and their ingredients, although legal in foreign countries, may not have been evaluated for safety and effectiveness in the United States . These products may be addictive or contain other dangerous substances.  Risks of unsupervised use. Some medications, whether imported or not, are unsafe when taken without adequate medical supervision. You may need a medical evaluation to ensure that the medication is appropriate for you and your condition. Or, you may require medical checkups to make sure that you are taking the drug properly, it is working for you, and that you are not having unexpected or life-threatening side effects.  Labeling and language issues. The medication's label, including instructions for use and possible side effects, may be in a language you do not understand or may make medical claims and suggest specific uses that have not been adequately evaluated for safety and effectiveness.  Lack of information. An imported medication may lack information that would permit you to be promptly and correctly treated for a dangerous side effect caused by the drug.
Laws Broken by the Makers, Sellers and Buyers of Illegal Generic Medications: Copyright laws  Importation Laws  FDA Packaging and Labeling Laws  Public Health Laws  Federal and State Laws  Anti-Counterfeiting Laws

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Generic drugs

  • 1. Generic Drugs By: Brittany Smith
  • 2. What is a generic drug? A generic drug is called by its basic chemical name instead of a registered brand-name chosen by the manufacturer. Generic drugs have the same active ingredients as brand-name drugs. One difference between them is the name; another, usually, is the price. If your pharmacist gives you a generic drug in place of a brand-name product, good standard practice and most state laws require that it be generically and therapeutically equivalent.
  • 3. Ed. Drugs sold over the internet… are not approved by the United States Food and Drugs Administration (FDA) are considered illegal to the United States Government and are subject to seizure can contain unknown and possibly harsh, harmful chemicals can be made in underdeveloped countries such as India, China, Mexico, Belize and are manufactured in unsanitary and unregulated factories are not proven to be safe and effective
  • 4. Potential Health Risks With Imported Drugs: Quality assurance concerns. Medications that have not been approved for sale in the United States may not have been manufactured under quality assurance procedures designed to produce a safe and effective product. Counterfeit potential. Some imported medications--even those that bear the name of a U.S.-approved product--may, in fact, be counterfeit versions that are unsafe or even completely ineffective. Presence of untested substances. Imported medications and their ingredients, although legal in foreign countries, may not have been evaluated for safety and effectiveness in the United States . These products may be addictive or contain other dangerous substances. Risks of unsupervised use. Some medications, whether imported or not, are unsafe when taken without adequate medical supervision. You may need a medical evaluation to ensure that the medication is appropriate for you and your condition. Or, you may require medical checkups to make sure that you are taking the drug properly, it is working for you, and that you are not having unexpected or life-threatening side effects. Labeling and language issues. The medication's label, including instructions for use and possible side effects, may be in a language you do not understand or may make medical claims and suggest specific uses that have not been adequately evaluated for safety and effectiveness. Lack of information. An imported medication may lack information that would permit you to be promptly and correctly treated for a dangerous side effect caused by the drug.
  • 5. Laws Broken by the Makers, Sellers and Buyers of Illegal Generic Medications: Copyright laws Importation Laws FDA Packaging and Labeling Laws Public Health Laws Federal and State Laws Anti-Counterfeiting Laws