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Showing results for "food".

1. Misdiagnosed food allergy resulting in severe malnutrition in an infant. | PSNet
   psnet.ahrq.gov/issue/misdiagnosed-food-allergy-resulting-severe-malnutrition-infant
   April 24, 2018 - Commentary Misdiagnosed food allergy resulting in severe malnutrition in an infant … Misdiagnosed food allergy resulting in severe malnutrition in an infant. … This commentary illustrates how misdiagnosis of food allergies can delay correct diagnosis and treatment … Misdiagnosed food allergy resulting in severe malnutrition in an infant.

2. Clinical Decision Support Software: Guidance for Industry and Food and Drug Administration Staff. | PSNet
   psnet.ahrq.gov/issue/clinical-decision-support-software-guidance-industry-and-food-and-drug-administration-staff
   May 25, 2022 - Policy/Guidelines Clinical Decision Support Software: Guidance for Industry and Food … Citation Text: Clinical Decision Support Software: Guidance for Industry and Food and Drug Administration … Rockville, MD; US Food and Drug Administration: September 28, 2022. … CDS scope and software functions used to define their qualification as a device regulated by the US Food … Rockville, MD; US Food and Drug Administration: September 28, 2022.

3. Critical Issues in Food Allergy: A National Academies Consensus Report. | PSNet
   psnet.ahrq.gov/issue/critical-issues-food-allergy-national-academies-consensus-report
   November 16, 2022 - Commentary Critical Issues in Food Allergy: A National Academies Consensus Report … Critical Issues in Food Allergy: A National Academies Consensus Report. … findings of a consensus report and highlights challenges associated with diagnosing and treating food … Critical Issues in Food Allergy: A National Academies Consensus Report.

4. Quality assessment of spontaneous triggered adverse event reports received by the Food and Drug Administration. | PSNet
   psnet.ahrq.gov/issue/quality-assessment-spontaneous-triggered-adverse-event-reports-received-food-and-drug
   August 07, 2024 - Quality assessment of spontaneous triggered adverse event reports received by the Food … Quality assessment of spontaneous triggered adverse event reports received by the Food and Drug Administration … The Food and Drug Administration is piloting a new system that allows triggered reporting of suspected … Quality assessment of spontaneous triggered adverse event reports received by the Food and Drug Administration

5. The Food and Drug Administration's National Drug Code Directory. | PSNet
   psnet.ahrq.gov/issue/food-and-drug-administrations-national-drug-code-directory
   February 15, 2017 - Government Resource The Food and Drug Administration's National Drug Code Directory … Citation Text: The Food and Drug Administration's National Drug Code Directory. Levinson DR. … Linkedin Copy URL Cite Citation Citation Text: The Food

6. Medication guides: patient medication information. A proposed rule by the Food and Drug Administration. | PSNet
   psnet.ahrq.gov/issue/medication-guides-patient-medication-information-proposed-rule-food-and-drug-administration
   September 15, 2021 - A proposed rule by the Food and Drug Administration. … A proposed rule by the Food and Drug Administration. … The Food and Drug Administration (FDA) is proposing a rule which, if approved, would require an easily … A proposed rule by the Food and Drug Administration.

7. Over Not So Easy | PSNet
   psnet.ahrq.gov/web-mm/over-not-so-easy
   April 01, 2005 - been estimated at 2.6% ( 3 ) and true anaphylaxis to peanuts at 0.5%.( 4 ) Tolerance to allergenic foods … the patient was known to be allergic by 56%.( 8 ) Technological approaches to prevent delivery of foods … reduce the risk of patient exposure to non-medication allergens in the hospital, such as allergenic foods … Prospective appraisal of complaints of adverse reactions to foods in children during the first 3 years … Fatalities due to anaphylactic reactions to foods. J Allergy Clin Immunol. 2001;107:191-193.

8. Use of recalled devices in new device authorizations under the US Food and Drug Administration's 510(k) pathway and risk of subsequent recalls. | PSNet
   psnet.ahrq.gov/issue/use-recalled-devices-new-device-authorizations-under-us-food-and-drug-administrations-510k
   April 13, 2022 - Study Use of recalled devices in new device authorizations under the US Food and … Use of recalled devices in new device authorizations under the US Food and Drug Administration's 510( … The Food and Drug Administration (FDA) plays an important role in ensuring the safety of medical … Use of recalled devices in new device authorizations under the US Food and Drug Administration's 510( … February 15, 2023 Reporting of death in US Food and Drug Administration medical device

9. Completeness of serious adverse drug event reports received by the US Food and Drug Administration in 2014. | PSNet
   psnet.ahrq.gov/issue/completeness-serious-adverse-drug-event-reports-received-us-food-and-drug-administration-2014
   September 25, 2008 - Study Completeness of serious adverse drug event reports received by the US Food … Completeness of serious adverse drug event reports received by the US Food and Drug Administration in … According to this study, many adverse drug event reports submitted by drug manufacturers to the Food … Completeness of serious adverse drug event reports received by the US Food and Drug Administration in … Related Resources From the Same Author(s) Serious adverse drug events reported to the Food

10. Descriptive analysis on disproportionate medication errors and associated patient characteristics in the Food and Drug Administration's adverse event reporting system. | PSNet
    psnet.ahrq.gov/issue/descriptive-analysis-disproportionate-medication-errors-and-associated-patient
    February 14, 2024 - Descriptive analysis on disproportionate medication errors and associated patient characteristics in the Food … Descriptive analysis on disproportionate medication errors and associated patient characteristics in the Food … Using data from the Netherlands’ Food and Drug Administration’s Adverse Event Reporting System (FAERS … Descriptive analysis on disproportionate medication errors and associated patient characteristics in the Food

11. Bar code label requirement for human drug products and biological products. | PSNet
    psnet.ahrq.gov/issue/bar-code-label-requirement-human-drug-products-and-biological-products
    October 21, 2015 - Food and Drug Administration. Fed Register. February 26, 2004;69 9119-9171. … The US Food and Drug Administration (FDA) requires certain human drug and biological product labels to … Food and Drug Administration. Fed Register. February 26, 2004;69 9119-9171. … Draft guidance for industry and Food and Drug Administration staff. … Draft guidance for industry and Food and Drug Administration staff.

12. Psn-Pdf (pdf file)
    psnet.ahrq.gov/node/843083/psn-pdf
    January 25, 2023 - Use of recalled devices in new device authorizations under the US Food and Drug Administration's 510 … Use of recalled devices in new device authorizations under the US Food and Drug Administration's 510 … https://psnet.ahrq.gov/issue/use-recalled-devices-new-device-authorizations-under-us-food-and-drug- … administrations-510k The Food and Drug Administration (FDA) plays an important role in ensuring the … https://psnet.ahrq.gov/issue/use-recalled-devices-new-device-authorizations-under-us-food-and-drug-administrations

13. Best Practices in Developing Proprietary Names for Human Prescription Drug Products Guidance for Industry. | PSNet
    psnet.ahrq.gov/issue/best-practices-developing-proprietary-names-human-prescription-drug-products-guidance
    January 13, 2021 - Rockville, MD: US Department of Health and Human Services, Food and Drug Administration, Center for Drug … URL December 23, 2020 Rockville, MD: US Department of Health and Human Services, Food … provides a structure for industry to reduce instances of drug name similarities and describes the US Food … Rockville, MD: US Department of Health and Human Services, Food and Drug Administration, Center for Drug … November 18, 2009 The Food and Drug Administration's National Drug Code Directory.

14. Best Practices in Developing Proprietary Names for Human Nonprescription Drug Products. | PSNet
    psnet.ahrq.gov/issue/best-practices-developing-proprietary-names-human-nonprescription-drug-products
    December 23, 2020 - Rockville, MD: US Department of Health and Human Services, Food and Drug Administration, Center for Drug … URL January 13, 2021 Rockville, MD: US Department of Health and Human Services, Food … It describes the US Food and Drug Administration (FDA) vetting process for drug names to improve naming … Rockville, MD: US Department of Health and Human Services, Food and Drug Administration, Center for Drug … January 5, 2009 The Food and Drug Administration's National Drug Code Directory.

15. Quick Tips for Buying Medicines Over the Internet. | PSNet
    psnet.ahrq.gov/issue/buying-medicines-over-internet
    April 08, 2020 - Food and Drug Administration. … Share Facebook Twitter Linkedin Copy URL October 3, 2012 Food … medical products online, including a link for consumers to report suspected illegal sites to the US Food … Food and Drug Administration.

16. Psn-Pdf (pdf file)
    psnet.ahrq.gov/node/851066/psn-pdf
    June 28, 2023 - A proposed rule by the Food and Drug Administration. … https://psnet.ahrq.gov/issue/medication-guides-patient-medication-information-proposed-rule-food-and- … The Food and Drug Administration (FDA) is proposing a rule which, if approved, would require an easily … https://psnet.ahrq.gov/issue/medication-guides-patient-medication-information-proposed-rule-food-and-drug-administration … https://psnet.ahrq.gov/issue/medication-guides-patient-medication-information-proposed-rule-food-and-drug-administration

17. FDA public health notification: MRI-caused injuries in patients with implanted neurological stimulators. | PSNet
    psnet.ahrq.gov/issue/fda-public-health-notification-mri-caused-injuries-patients-implanted-neurological
    August 24, 2005 - Citation Text: Schultz DG; Center for Devices and Radiological Health, Food and Drug Administration … Copy URL May 25, 2005 Schultz DG; Center for Devices and Radiological Health, Food … patients with implanted neurological stimulators who underwent magnetic resonance imaging procedures, the Food … Citation Citation Text: Schultz DG; Center for Devices and Radiological Health, Food

18. Psn-Pdf (pdf file)
    psnet.ahrq.gov/node/60818/psn-pdf
    August 19, 2020 - COVID-19 crisis, safe reopening of simulation centres and the new normal: food for thought. … COVID-19 crisis, safe reopening of simulation centres and the new normal: food for thought. … https://psnet.ahrq.gov/issue/covid-19-crisis-safe-reopening-simulation-centres-and-new-normal-food- … https://psnet.ahrq.gov/issue/covid-19-crisis-safe-reopening-simulation-centres-and-new-normal-food-thought … https://psnet.ahrq.gov/issue/covid-19-crisis-safe-reopening-simulation-centres-and-new-normal-food-thought

19. MedWatch: The FDA Safety Information and Adverse Event Reporting Program. | PSNet
    psnet.ahrq.gov/issue/medwatch
    April 08, 2020 - US Food and Drug Administration Copy Citation Save Save to your library … Share Facebook Twitter Linkedin Copy URL October 10, 2016 US Food … The site shares safety information about medications and medical products that are regulated by the Food … US Food and Drug Administration Copy Citation Related Resources From the Same Author

20. Psn-Pdf (pdf file)
    psnet.ahrq.gov/node/49515/psn-pdf
    July 01, 2006 - has been estimated at 2.6% (3) and true anaphylaxis to peanuts at 0.5%.(4) Tolerance to allergenic foods … medications, which have few ingredients and are readily barcoded at the unit-dose level, prepared foods … reduce the risk of patient exposure to non-medication allergens in the hospital, such as allergenic foods … Prospective appraisal of complaints of adverse reactions to foods in children during the first 3 years … Fatalities due to anaphylactic reactions to foods. J Allergy Clin Immunol. 2001;107:191-193.