Results

Total Results: 934 records

Showing results for "food".

181. 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.

182. 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.

183. 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.

184. 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.

185. 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.

186. 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.

187. 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.

188. 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.

189. 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.

190. System Approaches to Social Determinants of Health Screening and Intervention Innovation Summary | PSNet
     psnet.ahrq.gov/innovation/system-approaches-social-determinants-health-screening-and-intervention-innovation
     July 23, 2024 - UNC Health created an innovative screening program with a focus on four high priority SDOH domains: food … adult and 53% of pediatric primary care patients were screened for at least one of the SDOH domains: food … insecurity, housing stability, financial resource strain, and transportation. 3   Food insecurity was … the top domain, with 29% of all patients screened, with 4% of those screened indicating food insecurity … program pharmacy assistance. 3 There were 375 referrals for housing instability, 400 referrals for food

191. Prescription opioid analgesics commonly unused after surgery: a systematic review. | PSNet
     psnet.ahrq.gov/issue/prescription-opioid-analgesics-commonly-unused-after-surgery-systematic-review
     March 30, 2022 - often go unused, are not stored in a locked location, and are rarely disposed of in compliance with Food … extended-release/long-acting opioid prescribing Risk Evaluation and Mitigation Strategy Program by the US Food

192. 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.

193. 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.

194. Safety Information on Alaris SE Infusion Pumps. | PSNet
     psnet.ahrq.gov/issue/safety-information-alaris-se-infusion-pumps
     June 07, 2006 - Citation Text: Food and Drug Administration. 2006. … Share Facebook Twitter Linkedin Copy URL November 15, 2006 Food … Linkedin Copy URL Cite Citation Citation Text: Food … Draft guidance for industry and Food and Drug Administration staff. … August 25, 2021 Reporting of death in US Food and Drug Administration medical device

195. 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.

196. 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

197. 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

198. 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.

199. 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.

200. 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