Veklury, which is the first COVID-19 treatment to gain FDA approval, was approved based on the ACTT-1 clinical trial in which the median time to recovery was fewer days for patients treated with remdesivir plus standard of care compared with those treated with placebo plus standard of care which was a significant difference. This also provides you with a guide on how to disable cookies, but please be aware that parts of the site will not function correctly if you disable them. In particular, health care facilities and providers have reported that care of ventilated patients can be complicated by the need to discard containers and unused portions before drugs are fully administered because of the in-use time specified on the FDA-approved label. Click on the grey "Download Mobile Apps" button in the middle of the homepage . For the full FDA press announcement, visit the following link: https://www.fda.gov/news-events/press-announcements/fda-approves-first-treatment-covid-19. Direct your browser to the Micromedex website. It contains summary drug information on over 4,500 terms. Evidence-based, fully referenced pediatric-specific drug information enables clinicians to make informed treatment decisions. Please enter it exactly as it appears on the mobile Micromedex page. Scroll down to the "IBM Micromedex Neofax" installation instructions. IBM Micromedex IV Comp. With Drug Interactions, clinicians can check a patient's entire medication list simultaneously for potentially harmful interactions and view severity ratings that range from contraindicated to minor. ; Click the Download Center link in the upper right. IBM Micromedex is a trusted source for neonatal drug dosing, based on the strict editorial policies and practices that have guided Micromedex for more than 30 years. All users should read each product's complete Warranty & Disclaimer for special terms and conditions prior to using a product. For a detailed analysis, please refer to this guide I did in the past. Our physician editors lead a team of physicians, allied health professionals, medical trainees, and mHealth analysts in providing reviews, research, and commentary of mobile medical technology. NOTE: Do not share the password. Click the Download Center link in the upper right. Clinical Knowledge Solutions: Micromedex® Medication, Disease and Toxicology Management - Evidence based clinical resources. All rights reserved. Baricitinib is not authorized or approved as a stand-alone treatment for COVID-19, For the full FDA press announcement, visit the following link: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-drug-combination-treatment-covid-19. Changes to Micromedex and Drugex 2020. Those on Android did not notice anything and this will probably be news to them. In addition, for those that have used Micromedex prior to … The app is part of the Micromedex Medication Management apps bundle, which includes Micromedex Drug Interactions and Micromedex IV Compatibility. Addendum to Step 4: Upon opening the app, tap Neofax Customer. At the Pumerantz Library home page, click on the E-Resources tab in the top menu header bar.. Complete the installation up to Step 4. Check back frequently for new updates to our COVID-19 vaccine content. (new Nov 19). We have included a how to guide below to help those new to Micromedex or wishing to transition over to their institutions provided free service. IBM Micromedex® is a trusted source for neonatal drug dosing, based on the strict editorial policies and practices that have guided Micromedex for more than 30 years. Select the app you want to access. Evidence-based, fully referenced neonatal-specific drug information enables clinicians to make informed treatment decisions. ; In step 4, retrieve the new password for your app and … The Drug Reference App is a subset of the full Micromedex site. For the full FDA press announcement, visit the following link: https://www.fda.gov/news-events/press-announcements/fda-issues-emergency-use-authorization-convalescent-plasma-potential-promising-covid-19-treatment. On November 21, 2020, the US FDA issued an Emergency Use Authorization (EUA) for casirivimab intravenous solution and imdevimab intravenous solution to be administered together for the treatment of mild to moderate COVID-19 in adults and pediatric patients who are 12 years of age and older weighing at least 40 kg (about 88 lbs) with positive results of direct SARS-CoV-2 viral testing and who are at high risk for progressing to severe COVID-19 and/or hospitalization. To retrieve the password for each of these apps, go to the Micromedex homepage and click "Download Mobile Apps" at the bottom. Since this is a public library guide, we have blanked out the password. The trio is an inexpensive solution to your on-the-go medication management needs. Click on the Download Mobile Apps button on the bottom right side of the page. DrugDex(R) Information can be found In the COVID-19 Investigational Therapies- Moderna Vaccine - Drug Consult by clicking on this link: https://ibm.biz/Bdq5JJ. Micromedex provides a wide range of databases tailored to meet the needs of healthcare professionals, including information related to drugs, acute care, toxicology, and patient education. Please login or register on iMedicalApps, the registration process is free. Scroll down to the "IBM Micromedex Pediatrics" installation instructions. Information regarding potential future products is intended to outline our general product direction and it should not be relied on in making a purchasing decision. IBM Micromedex® is a trusted source for pediatric drug dosing, based on the strict editorial policies and practices that have guided Micromedex for more than 30 years. ); Click the link Download Center. Non Vbv Bin List 2020. If a password is necessary, it will be included in the app download information (usually in step #4). End users must retrieve the new password from the Micromedex web site and reauthorize their app using the following instructions: Revisit the Micromedex web site (off-campus users will also be prompted for their TTUHSC eRaider. Need further assistance? End users must retrieve the new password from the Micromedex web site and reauthorize their app using the following instructions: Revisit the Micromedex web site (off-campus users will also be prompted for their TTUHSC eRaider. IBM® Micromedex® NeoFax® & Pediatrics Server Migration Client FAQ. IBM Micromedex solutions now combine the evidence-based clinical content of Micromedex with the industry-leading AI capabilities of IBM Watson. For a detailed analysis, please refer to this guide I did in the past. If your institution has Micromedex 2.0, then you are in luck! Further information regarding the FDA's guidance for extended "in-use time" can be found at the following link: https://www.fda.gov/drugs/coronavirus-covid-19-drugs/information-health-care-facilities-and-providers-use-time-covid-19. For the full FDA press announcement, visit the following link: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-monoclonal-antibody-treatment-covid-19. Evidence-based, fully referenced neonatal-specific drug information enables clinicians to make informed treatment decisions. https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/761171lbl.pdf, http://www.micromedexsolutions.com/micromedex2/librarian/deeplinkaccess?source=deepLink&SearchTerm=naxitamab-gqgk, http://www.micromedexsolutions.com/micromedex2/librarian/deeplinkaccess?source=deepLink&SearchTerm=remdesivir, http://www.micromedexsolutions.com/micromedex2/librarian/deeplinkaccess?source=deepLink&SearchTerm=propofol, http://www.micromedexsolutions.com/micromedex2/librarian/deeplinkaccess?source=deepLink&SearchTerm=favipiravir, https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-monoclonal-antibodies-treatment-covid-19, https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-drug-combination-treatment-covid-19, https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-monoclonal-antibody-treatment-covid-19, https://www.fda.gov/news-events/press-announcements/fda-approves-first-treatment-covid-19, https://www.fda.gov/news-events/press-announcements/fda-issues-emergency-use-authorization-convalescent-plasma-potential-promising-covid-19-treatment, https://www.fda.gov/drugs/coronavirus-covid-19-drugs/information-health-care-facilities-and-providers-use-time-covid-19, https://www.fda.gov/emergency-preparedness-and-response/mcm-issues/coronavirus-disease-2019-covid-19. The monograph for naxitamab-gqgk can be found at: http://www.micromedexsolutions.com/micromedex2/librarian/deeplinkaccess?source=deepLink&SearchTerm=naxitamab-gqgk. Micromedex periodically makes unannounced password rotations.TTUHSC users must retrieve the new password from the Micromedex web site to reauthorize their app as follows: Revisit the Micromedex web site (off-campus users will be prompted for their TTUHSC eRaider. Login on the left or click the register button below to proceed. FDA COVID-19 Update: EUA Issued for Convalescent Plasma. IBM Micromedex® customers simply follow these instructions to obtain a password: 1. Th ese instructions accompany each of the three IBM Micromedex apps (Drug Ref, Drug Int, and IV Comp). In clinical trials, patients treated with casirivimab and imdevimab were shown to have a larger viral load reduction (primary endpoint) compared with those treated with placebo. Back to top. Complete the installation up to Step 4. 5. Don't contact the Library for passwords. As such, the app was yanked from the store and will be updated again as soon as Apple gives it a go. Please view our cookie policy that explains what cookies are and how they are used on our website. 6. In any event, it appears that the issue of the app requesting a password is due to an error on Truven’s part. Click on Micromedex Native Mobile Apps. Patient education materials are included in the CareNotes module of Micromedex. Some facilities and providers are considering use of certain drugs, for which supplies may not be consistently available, beyond the labeled "in-use times." 7. IBM Micromedex solutions now combine the evidence-based clinical content of Micromedex with the industry-leading AI capabilities of IBM Watson. Please search in iTunes … With Drug Interactions, clinicians can check a patient's entire medication list simultaneously for potentially harmful interactions and view severity ratings that range from contraindicated to minor. The US FDA has granted Emergency Use Authorization (EUA) for the following: The following is a selected investigational drug monograph for a drug that is being researched for COVID-19: FDA COVID-19 Update: EUA Issued for Monoclonal Antibody Cocktail. The only caveat is that the password expires every few weeks and needs to be updated frequently, which can be a problem when you need to use the app and then find the password had expired. Password ; Remember Password: 24 x 7 Technical Support and Call Center Access are available from Micromedex Support. The current Micromedex apps available are: IBM Micromedex Drug Reference; IBM Micromedex Drug Interactions; IBM Micromedex IV Compatibility IBM Micromedex® NeoFax is available free to online subscribers of Micromedex Standard NeoFax. On November 9, 2020, the US FDA issued an Emergency Use Authorization (EUA) for the investigational monoclonal antibody therapy bamlanivimab for the treatment of mild-to-moderate COVID-19 in adult and pediatric patients who are 12 years of age and older weighing at least 40 kg (about 88 lbs). To get mobile app passwords, follow these steps: Access the Micromedex database … Click on the Download Mobile Apps button on the bottom right side of the page. Download IBM Micromedex Drug Ref apk 2.5 for Android. v2.5 (Subscribed) 2.5 Application, Medical Mobile Micromedex 3.4 | 1978 Ratings | 94029 Views. Scroll down to the "IBM Micromedex Neofax" installation instructions. Open the app on your device. Micromedex with Watson uses cognitive computing in the IBM cloud to gather search intent through conversation, provide specific clinical answers, and guide clinicians to relevant evidence. Watson … Now you can access the same evidence-based Micromedex content you rely on, anytime, anywhere, via your iPhone and iPad. On November 25, 2020, the US FDA approved Danyelza(R) (naxitamab-gqgk) IV injection indicated, in combination with granulocyte-macrophage colony-stimulating factor (GM-CSF), for the treatment of pediatric patients 1 year of age and older and adult patients with relapsed or refractory high-risk neuroblastoma in the bone or bone marrow who have demonstrated a partial response, minor response, or stable disease to prior therapy. Patient education materials are included in the CareNotes module of Micromedex. Watson … Ask questions in a natural way, the way clinicians ask clinicians. FDA COVID-19 Update: First COVID-19 Treatment. If the facility you work at subscribes to Micromedex via the internet, follow these instructions to obtain a password: 1.Login to IBM Micromedex through your subscribing facility IBM Watson Health provides its products AS IS. IBM Micromedex(R) has the following selected resources to provide assistance during the COVID-19 crisis: Per the Centers for Disease Control and Prevention (CDC), IBM Micromedex(R) has been granted permission to publish SARS-Cov-2 (COVID-19) vaccine information ahead of FDA Emergency Use Authorization (EUA) approval to enable healthcare providers and public stakeholders to order, manage inventory, administer, monitor, and support reporting of vaccine use. Micromedex is constantly tweaking apps as well as updating clinical content. Biedt on-the-go toegang tot de industrie de meest betrouwbare informatie over drugs U.S. and Canada Phone: (877) 843-6796 Speak product name, then pick Option 3 - Customer Resource Center. This app provides insight into: - why the drugs in question interact. Hopefully this will help some out there trying to access their Micromedex Drug Information app on their iPhone or iPad, and if we come across any further information we will be sure to add onto this article. Intrathecal administration of tranexamic acid injection may result in serious life-threatening injuries (ie, seizures, cardiac arrhythmias, paraplegia, permanent neurological injury, death). Micromedex can now be accessed anywhere, anytime! IBM Micromedex is a trusted source for neonatal drug dosing, based on the strict editorial policies and practices that have guided Micromedex for more than 30 years. Evidence-based, fully referenced neonatal-specific drug information enables clinicians to make informed treatment decisions. The more specific the question, the more specific the answer. Evidence-based, fully referenced pediatric-specific drug information enables clinicians to make informed treatment decisions. 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