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Total Results: 852 records

Showing results for "food".

161. FDASIA Health IT Report: Proposed Strategy and Recommendations for a Risk-Based Framework. | PSNet
     psnet.ahrq.gov/issue/fdasia-health-it-report-proposed-strategy-and-recommendations-risk-based-framework
     June 29, 2016 - Silver Spring, MD: Food and Drug Administration. April 2014. … Silver Spring, MD: Food and Drug Administration. April 2014. … Silver Spring, MD: Food and Drug Administration. April 2014.

162. Design of endoscopic retrograde cholangiopancreatography (ERCP) duodenoscopes may impede effective cleaning. | PSNet
     psnet.ahrq.gov/issue/design-endoscopic-retrograde-cholangiopancreatography-ercp-duodenoscopes-may-impede-effective
     March 11, 2015 - Silver Spring, MD: US Food and Drug Administration; February 23, 2015. … Silver Spring, MD: US Food and Drug Administration; February 23, 2015. … Silver Spring, MD: US Food and Drug Administration; February 23, 2015.

163. Computerized Prescriber Order Entry Medication Safety (CPOEMS): Uncovering and Learning From Issues and Errors. | PSNet
     psnet.ahrq.gov/issue/computerized-prescriber-order-entry-medication-safety-cpoems-uncovering-and-learning-issues
     February 05, 2014 - Silver Spring, MD: US Food and Drug Administration; December 15, 2015. … Silver Spring, MD: US Food and Drug Administration; December 15, 2015. … Silver Spring, MD: US Food and Drug Administration; December 15, 2015.

164. Infections associated with reprocessed flexible bronchoscopes. | PSNet
     psnet.ahrq.gov/issue/infections-associated-reprocessed-flexible-bronchoscopes
     March 11, 2015 - Silver Spring, MD: US Food and Drug Administration; September 17, 2015. … Silver Spring, MD: US Food and Drug Administration; September 17, 2015. … Silver Spring, MD: US Food and Drug Administration; September 17, 2015.

165. Apotex Corp. issues voluntary nationwide recall of Enoxaparin Sodium Injection, USP due to mislabeling of syringe barrel measurement markings. | PSNet
     psnet.ahrq.gov/issue/apotex-corp-issues-voluntary-nationwide-recall-enoxaparin-sodium-injection-usp-due
     March 22, 2010 - Silver Spring, MD: US Food and Drug Administration; February 3. 2021. … Silver Spring, MD: US Food and Drug Administration; February 3. 2021.    … Silver Spring, MD: US Food and Drug Administration; February 3. 2021.

166. FDA Safety Communication: use caution with implanted pumps for intrathecal administration of medicines for pain management. | PSNet
     psnet.ahrq.gov/issue/fda-safety-communication-use-caution-implanted-pumps-intrathecal-administration-medicines
     June 20, 2018 - Silver Spring, MD: US Food and Drug Administration; November 14, 2018. … Silver Spring, MD: US Food and Drug Administration; November 14, 2018. … Silver Spring, MD: US Food and Drug Administration; November 14, 2018.

167. Hospira issues a voluntary nationwide recall for one lot of 0.5% Bupivacaine Hydrochloride Injection, USP and one lot of 1% Lidocaine HCl Injection, USP due to mislabeling. | PSNet
     psnet.ahrq.gov/issue/hospira-issues-voluntary-nationwide-recall-one-lot-05-bupivacaine-hydrochloride-injection-usp
     June 20, 2018 - Silver Spring, MD: US Food and Drug Administration; May 4. 2021. … Silver Spring, MD: US Food and Drug Administration; May 4. 2021. … Silver Spring, MD: US Food and Drug Administration; May 4. 2021.

168. Roxane Laboratories initiates a nationwide voluntary recall of a single manufacturing lot of Azathioprine tablets in the U.S. and Puerto Rico. | PSNet
     psnet.ahrq.gov/issue/roxane-laboratories-initiates-nationwide-voluntary-recall-single-manufacturing-lot
     June 22, 2011 - Silver Spring, MD: US Food and Drug Administration; July 13, 2006. … Silver Spring, MD: US Food and Drug Administration; July 13, 2006. … Silver Spring, MD: US Food and Drug Administration; July 13, 2006.

169. FDA alerts health care professionals to the temporary absence of warning statement on the vial caps of two neuromuscular blocking agents. | PSNet
     psnet.ahrq.gov/issue/fda-alerts-health-care-professionals-temporary-absence-warning-statement-vial-caps-two
     June 22, 2011 - Silver Spring, MD: US Food and Drug Administration. June 2, 2020. … Silver Spring, MD: US Food and Drug Administration. June 2, 2020. … Silver Spring, MD: US Food and Drug Administration. June 2, 2020.

170. FDA identifies harm reported from sudden discontinuation of opioid pain medicines and requires label changes to guide prescribers on gradual, individualized tapering. | PSNet
     psnet.ahrq.gov/issue/fda-identifies-harm-reported-sudden-discontinuation-opioid-pain-medicines-and-requires-label
     March 12, 2010 - Silver Spring, MD: US Food and Drug Administration; April 9, 2019. … Twitter Linkedin Copy URL April 17, 2019 Silver Spring, MD: US Food … Silver Spring, MD: US Food and Drug Administration; April 9, 2019.

171. Electronic data collection using MedWatchPlus portal and rational questionnaire. | PSNet
     psnet.ahrq.gov/issue/electronic-data-collection-using-medwatchplus-portal-and-rational-questionnaire
     July 03, 2013 - This announcement invites field review of proposed information elements to be included in a Food and … Draft guidance for industry and Food and Drug Administration staff.

172. Medical gas containers and closures; current good manufacturing practice requirements. | PSNet
     psnet.ahrq.gov/issue/medical-gas-containers-and-closures-current-good-manufacturing-practice-requirements
     April 24, 2015 - Food and Drug Administration (FDA) guideline supports good manufacturing practices by suggesting several … Draft guidance for industry and Food and Drug Administration staff.

173. Implantable infusion pumps in the magnetic resonance (MR) environment: FDA safety communication—important safety precautions. | PSNet
     psnet.ahrq.gov/issue/implantable-infusion-pumps-magnetic-resonance-mr-environment-fda-safety-communication
     February 07, 2018 - Silver Spring, MD: US Food and Drug Administration; January 11, 2017. … Silver Spring, MD: US Food and Drug Administration; January 11, 2017. … Silver Spring, MD: US Food and Drug Administration; January 11, 2017.

174. Adverse drug event surveillance and drug withdrawals in the United States, 1969-2002. | PSNet
     psnet.ahrq.gov/issue/adverse-drug-event-surveillance-and-drug-withdrawals-united-states-1969-2002
     October 08, 2014 - Food and Drug Administration (FDA). … 2014 Quality assessment of spontaneous triggered adverse event reports received by the Food

175. Enteral Nutrition Safety Toolkit. | PSNet
     psnet.ahrq.gov/issue/enteral-nutrition-safety-toolkit
     February 01, 2023 - February 17, 2015 Use of recalled devices in new device authorizations under the US Food … 25, 2023 COVID-19 crisis, safe reopening of simulation centres and the new normal: food

176. Delayed Clozapine Prescription in an Elderly Man With Dementia | PSNet
     psnet.ahrq.gov/web-mm/delayed-clozapine-prescription-elderly-man-dementia
     August 06, 2014 - US Food and Drug Administration. [Available at] 2. Roles of Different Participants in REMS. … US Food and Drug Administration. [Available at] 3. … Silver Spring, MD: US Food and Drug Administration. [Available at] 4. What's in a REMS? … US Food and Drug Administration. [Available at] 5. Clozapine REMS. [Available at] 6. … US Food and Drug Administration. [Available at] 7. ASSESS-ERR Medication System Worksheet.

177. Comparative, cross-sectional study of the format, content and timing of medication safety letters issued in Canada, the USA and the UK. | PSNet
     psnet.ahrq.gov/issue/comparative-cross-sectional-study-format-content-and-timing-medication-safety-letters-issued
     March 21, 2012 - study, researchers evaluated medication safety letters issued by Health Canada, the United States Food … July 29, 2020 Completeness of serious adverse drug event reports received by the US Food

178. McNeil Consumer & Specialty Pharmaceuticals announces nationwide recall of Children's Tylenol Meltaways - 80 Mg, Children's Tylenol Softchews - 80 Mg and Jr. Tylenol Meltaways - 160 Mg [press release]. | PSNet
     psnet.ahrq.gov/issue/mcneil-consumer-specialty-pharmaceuticals-announces-nationwide-recall-childrens-tylenol
     August 19, 2020 - Same Author(s) COVID-19 crisis, safe reopening of simulation centres and the new normal: food … A proposed rule by the Food and Drug Administration.

179. Public comment period extended for strategies to improve patient safety: Draft Report to Congress for Public Comment and Review by the National Academy of Medicine. | PSNet
     psnet.ahrq.gov/issue/public-comment-period-extended-strategies-improve-patient-safety-draft-report-congress-public
     June 16, 2021 - A proposed rule by the Food and Drug Administration. … A proposed rule by the Food and Drug Administration.

180. Problems with medical devices may be severely under-reported. | PSNet
     psnet.ahrq.gov/issue/problems-medical-devices-may-be-severely-under-reported
     November 16, 2022 - May 3, 2023 Use of recalled devices in new device authorizations under the US Food and … August 20, 2021 Reporting of death in US Food and Drug Administration medical device