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  2. MedWatch - Wikipedia

    en.wikipedia.org/wiki/MedWatch

    In 2013, MedWatch introduced Form 3500B, which is designed to facilitate reporting by healthcare consumers. [4] The MedWatch system is intended to detect safety hazard signals for medical products. If a signal is detected, the FDA can issue medical product safety alerts or order product recalls, withdrawals, or labeling changes to protect the ...

  3. Medical device reporting - Wikipedia

    en.wikipedia.org/wiki/Medical_device_reporting

    Medical device reporting (MDR) is the procedure for the Food and Drug Administration to get significant medical device adverse events information from manufacturers, importers and user facilities, so these issues can be detected and corrected quickly, and the same lot of that product may be recalled.

  4. FDA Adverse Event Reporting System - Wikipedia

    en.wikipedia.org/wiki/FDA_Adverse_Event...

    The FDA Adverse Event Reporting System (FAERS or AERS) is a computerized information database designed to support the U.S. Food and Drug Administration's (FDA) postmarketing safety surveillance program for all approved drug and therapeutic biologic products.

  5. Consumer Assessment of Healthcare Providers and Systems

    en.wikipedia.org/wiki/Consumer_Assessment_of...

    To receive the CAHPS trademark, patient experience surveys must meet specified standards established by AHRQ.In particular, AHRQ requires that developers of CAHPS surveys use both cognitive and psychometric testing methods to maximize the reliability and validity of the survey instruments.

  6. Cardiopulmonary bypass - Wikipedia

    en.wikipedia.org/wiki/Cardiopulmonary_bypass

    Cardiopulmonary bypass (CPB) or heart-lung machine, also called the pump or CPB pump, is a machine that temporarily takes over the function of the heart and lungs during open-heart surgery by maintaining the circulation of blood and oxygen throughout the body. [1]

  7. Belantamab mafodotin - Wikipedia

    en.wikipedia.org/wiki/Belantamab_mafodotin

    Belantamab mafodotin was evaluated in DREAMM-2 (NCT 03525678), an open-label, multicenter trial. [5] Participants received either belantamab mafodotin, 2.5 mg/kg or 3.4 mg/kg intravenously, once every three weeks until disease progression or unacceptable toxicity.

  8. Resuscitative endovascular balloon occlusion of the aorta

    en.wikipedia.org/wiki/Resuscitative_endovascular...

    Resuscitative endovascular balloon occlusion of the aorta (REBOA) is a minimally-invasive procedure performed during resuscitation of critically-injured trauma patients.. Originally developed as a less invasive alternative to emergency thoracotomy with aortic cross clamping, REBOA is performed to gain rapid control of non-compressible truncal or junctional hemorrh

  9. 35th century BC - Wikipedia

    en.wikipedia.org/wiki/35th_century_BC

    The 35th century BC in the Near East sees the gradual transition from the Chalcolithic to the Early Bronze Age. Proto-writing enters transitional stage, developing towards writing proper.