When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Pharmacovigilance - Wikipedia

    en.wikipedia.org/wiki/Pharmacovigilance

    Pharmacovigilance (PV, or PhV), also known as drug safety, is the pharmaceutical science relating to the "collection, detection, assessment, monitoring, and prevention" of adverse effects with pharmaceutical products. [1]: 7 The etymological roots for the word "pharmacovigilance" are: pharmakon (Greek for drug) and vigilare (Latin for to keep watch

  3. Medicines Act 1968 - Wikipedia

    en.wikipedia.org/wiki/Medicines_Act_1968

    The Medicines Act 1968 (c. 67) is an act of Parliament of the United Kingdom.Its official long title is "An Act to make new provision with respect to medicinal products and related matters, and for purposes connected therewith."

  4. Access to medicines - Wikipedia

    en.wikipedia.org/wiki/Access_to_medicines

    It is argued that competition is necessary to lower drug prices and improve access to affordable medications. [10] [11] Price gouging is defined as the excessive increase in prices by sellers of essential goods to a level deemed higher than reasonable or fair. This sharp increase in prices may leave the buyer vulnerable.

  5. Patient safety - Wikipedia

    en.wikipedia.org/wiki/Patient_safety

    The Patient Safety Reporting System (PSRS) is a program modeled upon the Aviation Safety Reporting System and developed by the Department of Veterans Affairs (VA) and the National Aeronautics and Space Administration (NASA) to monitor patient safety through voluntary, confidential reports. [79]

  6. Regulation of therapeutic goods - Wikipedia

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

    Drug legislation in both the EU and US were passed in order to assure drug safety and efficacy. Of note, increased regulations and standards for testing actually led to greater innovation in pharmaceutical research in the 1960s, despite greater preclinical and clinical standards. [ 6 ]

  7. Kefauver–Harris Amendment - Wikipedia

    en.wikipedia.org/wiki/Kefauver–Harris_Amendment

    The U.S. Kefauver–Harris Amendment or "Drug Efficacy Amendment" is a 1962 amendment to the Federal Food, Drug, and Cosmetic Act. It introduced a requirement for drug manufacturers to provide proof of the effectiveness and safety of their drugs before approval, [1] [2] required drug advertising to disclose accurate information about side effects, and stopped cheap generic drugs being marketed ...

  8. Mounjaro vs. Ozempic: Which One Is Best for Me to Try for ...

    www.aol.com/mounjaro-vs-ozempic-one-best...

    The medication can also reduce the risk of major adverse cardiovascular events (like heart attack) in those with type 2 diabetes and cardiovascular disease. Ozempic is often prescribed alongside ...

  9. Patients' rights - Wikipedia

    en.wikipedia.org/wiki/Patients'_rights

    The Charter of Patients' Rights lists seventeen rights that patients are entitled to: [6] Right to information: Every patient has the right to know what is the illness that they are suffering, its causes, the status of the diagnosis (provisional or confirmed), expected costs of treatment. Furthermore, service providers should communicate this ...