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  2. Prescription monitoring program - Wikipedia

    en.wikipedia.org/.../Prescription_monitoring_program

    v. t. e. In the United States, prescription monitoring programs ( PMPs) or prescription drug monitoring programs ( PDMPs) are state-run programs which collect and distribute data about the prescription and dispensation of federally controlled substances and, depending on state requirements, other potentially abusable prescription drugs.

  3. Therapeutic drug monitoring - Wikipedia

    en.wikipedia.org/wiki/Therapeutic_drug_monitoring

    Therapeutic drug monitoring (TDM) is a branch of clinical chemistry and clinical pharmacology that specializes in the measurement of medication levels in blood. Its main focus is on drugs with a narrow therapeutic range, i.e. drugs that can easily be under- or overdosed. [1] TDM aimed at improving patient care by individually adjusting the dose ...

  4. Pseudomyxoma peritonei - Wikipedia

    en.wikipedia.org/wiki/Pseudomyxoma_peritonei

    Pseudomyxoma peritonei ( PMP) is a clinical condition caused by cancerous cells (mucinous adenocarcinoma) that produce abundant mucin or gelatinous ascites. [1] The tumors cause fibrosis of tissues and impede digestion or organ function, and if left untreated, the tumors and mucin they produce will fill the abdominal cavity.

  5. Ohio Automated Rx Reporting System - Wikipedia

    en.wikipedia.org/wiki/Ohio_Automated_Rx...

    The Ohio Automated Rx Reporting System (OARRS) is Ohio's state Prescription Monitoring Program (PMP) and is controlled by the Ohio State Board of Pharmacy. [1] The law permitting the Board of Pharmacy to create the PMP was signed on March 18, 2005, and became effective January 1, 2006. The OARRS program began operation on October 2, 2006.

  6. Monitoring in clinical trials - Wikipedia

    en.wikipedia.org/wiki/Monitoring_in_clinical_trials

    Clinical monitoring is the oversight and administrative efforts that monitor a participant's health and efficacy of the treatment during a clinical trial.Both independent and government-run grant-funding agencies, such as the National Institutes of Health (NIH) and the World Health Organization (WHO), require data and safety monitoring protocols for Phase I and II clinical trials conforming to ...

  7. Monitoring (medicine) - Wikipedia

    en.wikipedia.org/wiki/Monitoring_(medicine)

    Monitoring (medicine) Display device of a medical monitor as used in anesthesia. A patient of an intensive care unit in a German hospital in 2015, with a monitoring screen displaying a graphical electrocardiogram, the heart rate and blood pressure all in real time. In medicine, monitoring is the observation of a disease, condition or one or ...

  8. Postmarketing surveillance - Wikipedia

    en.wikipedia.org/wiki/Postmarketing_surveillance

    Postmarketing surveillance ( PMS ), also known as post market surveillance, is the practice of monitoring the safety of a pharmaceutical drug or medical device after it has been released on the market and is an important part of the science of pharmacovigilance. Since drugs and medical devices are approved on the basis of clinical trials, which ...

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