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  2. Drug resistance - Wikipedia

    en.wikipedia.org/wiki/Drug_resistance

    Drug resistance is the reduction in effectiveness of a medication such as an antimicrobial or an antineoplastic in treating a disease or condition. [1] The term is used in the context of resistance that pathogens or cancers have "acquired", that is, resistance has evolved.

  3. List of off-label promotion pharmaceutical settlements

    en.wikipedia.org/wiki/List_of_off-label...

    The following are settlements reached with US authorities against pharmaceutical companies to resolve allegations of "off-label" promotion of drugs. Under the Federal Food, Drug, and Cosmetic Act, it is illegal for pharmaceutical companies to promote their products for uses not approved by the Food and Drug Administration (FDA), and corporations that market drugs for off-label indications may ...

  4. Counterfeit medications - Wikipedia

    en.wikipedia.org/wiki/Counterfeit_medications

    A counterfeit drug may contain inappropriate quantities of active ingredients, or none, may be improperly processed within the body (e.g., absorption by the body), may contain ingredients that are not on the label (which may or may not be harmful), or may be supplied with inaccurate or fake packaging and labeling. Counterfeit drugs are related ...

  5. Drug Quality and Security Act - Wikipedia

    en.wikipedia.org/wiki/Drug_Quality_and_Security_Act

    Drug products compounded by or under the direct supervision of a licensed pharmacist at an outsourcing facility may be able to qualify for exemptions from the following three sections of the FD&C Act: (1) section 505 (concerning FDA approval of drugs); (2) section 502(f)(1) (concerning the labeling of drug products with adequate directions for ...

  6. Drug labelling - Wikipedia

    en.wikipedia.org/wiki/Drug_Labelling

    Drug labelling is also referred to as prescription labelling, is a written, printed or graphic matter upon any drugs or any of its container, or accompanying such a drug. Drug labels seek to identify drug contents and to state specific instructions or warnings for administration, storage and disposal.

  7. Off-label use - Wikipedia

    en.wikipedia.org/wiki/Off-label_use

    Off-label use is the use of pharmaceutical drugs for an unapproved indication or in an unapproved age group, dosage, or route of administration. [1] Both prescription drugs and over-the-counter drugs (OTCs) can be used in off-label ways, although most studies of off-label use focus on prescription drugs.

  8. Community Guidelines - AOL Legal

    legal.aol.com/legacy/community_guidelines/index.html

    We offer a diverse and robust community through a wide range of products, Services, and online areas (such as chat rooms and message boards). Some products, Services, or areas may carry additional standards. Please review and abide by the standards of the areas you frequent. The account holder is responsible for all activities on that account.

  9. Regulation of therapeutic goods - Wikipedia

    en.wikipedia.org/wiki/Regulation_of_therapeutic...

    In the United States, regulation of drugs was originally a state right, as opposed to federal right. But with the increase in fraudulent practices due to private incentives to maximize profits and poor enforcement of state laws, the need for stronger federal regulation increased. [7]