BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 34309624)

  • 1. Reporting of Death in US Food and Drug Administration Medical Device Adverse Event Reports in Categories Other Than Death.
    Lalani C; Kunwar EM; Kinard M; Dhruva SS; Redberg RF
    JAMA Intern Med; 2021 Sep; 181(9):1217-1223. PubMed ID: 34309624
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The nature, magnitude, and reporting compliance of device-related events for intravenous patient-controlled analgesia in the FDA Manufacturer and User Facility Device Experience (MAUDE) database.
    Lawal OD; Mohanty M; Elder H; Skeer M; Erpelding N; Lanier R; Katz N
    Expert Opin Drug Saf; 2018 Apr; 17(4):347-357. PubMed ID: 29463158
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Adverse Events Involving Radiation Oncology Medical Devices: Comprehensive Analysis of US Food and Drug Administration Data, 1991 to 2015.
    Connor MJ; Marshall DC; Moiseenko V; Moore K; Cervino L; Atwood T; Sanghvi P; Mundt AJ; Pawlicki T; Recht A; Hattangadi-Gluth JA
    Int J Radiat Oncol Biol Phys; 2017 Jan; 97(1):18-26. PubMed ID: 27979446
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An Analysis of the FDA MAUDE Database and the Search for Cobalt Toxicity in Class 3 Johnson & Johnson/DePuy Metal-on-Metal Hip Implants.
    Kavanagh KT; Kraman SS; Kavanagh SP
    J Patient Saf; 2018 Dec; 14(4):e89-e96. PubMed ID: 30308590
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detecting software failures in the MAUDE database: a preliminary analysis.
    Pecoraro F; Luzi D
    Stud Health Technol Inform; 2013; 192():1098. PubMed ID: 23920872
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Adverse Events and Device Failures Associated with Pancreatic Stents: A Comprehensive Analysis Using the FDA's MAUDE Database.
    Jaber F; Alsakarneh S; Alsharaeh T; Salahat AJ; Jaber M; Abboud Y; Aldiabat M; Ahmed K; Abdallah M; Abdel-Jalil A; Bilal M; Barakat M; Adler DG
    Dig Dis Sci; 2024 Jun; 69(6):2018-2025. PubMed ID: 38580887
    [TBL] [Abstract][Full Text] [Related]  

  • 7. FDA MAUDE data on complications with lasers, light sources, and energy-based devices.
    Tremaine AM; Avram MM
    Lasers Surg Med; 2015 Feb; 47(2):133-40. PubMed ID: 25655709
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of the Food and Drug Administration Manufacturer and User Facility Device Experience Database for Patient- and Circuit-Related Adverse Events Involving Extracorporeal Membrane Oxygenation.
    Khalid N; Javed H; Ahmad SA; Edelman JJ; Shlofmitz E; Chen Y; Musallam A; Rogers T; Hashim H; Bernardo NL; Waksman R
    Cardiovasc Revasc Med; 2020 Feb; 21(2):230-234. PubMed ID: 31767523
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Revealing the scope of surgical device malfunctions: Analysis of the "hidden" Food and Drug Administration device database.
    Benham DA; Calvo RY; Carr MJ; Diaz JA; Sise CB; Sise MJ; Bansal V; Martin MJ
    Am J Surg; 2021 Jun; 221(6):1121-1126. PubMed ID: 33745689
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An evaluation of the Manufacturer And User Facility Device Experience database that inspired the United States Food and Drug Administration's Reclassification of transvaginal mesh.
    Sandberg JM; Gray I; Pearlman A; Terlecki RP
    Investig Clin Urol; 2018 Mar; 59(2):126-132. PubMed ID: 29520389
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ultrasonic Device Complications in Endodontics: An Analysis of Adverse Events From the Food and Drug Administration Manufacturer and User Facility Device Experience.
    Rhodes SC
    J Patient Saf; 2022 Jun; 18(4):269-275. PubMed ID: 34508038
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Adverse Events Associated With the Use of Sipuleucel-T Reported to the US Food and Drug Administration's Adverse Event Reporting System, 2010-2017.
    Dores GM; Bryant-Genevier M; Perez-Vilar S
    JAMA Netw Open; 2019 Aug; 2(8):e199249. PubMed ID: 31411714
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Adverse Events Associated With Tracheostomy: A MAUDE Database Analysis.
    Narwani V; Dacey S; Lerner MZ
    Otolaryngol Head Neck Surg; 2024 Feb; 170(2):391-395. PubMed ID: 37622490
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Patient safety problems associated with heathcare information technology: an analysis of adverse events reported to the US Food and Drug Administration.
    Magrabi F; Ong MS; Runciman W; Coiera E
    AMIA Annu Symp Proc; 2011; 2011():853-7. PubMed ID: 22195143
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The First 4 Years of Postmarketing Safety Surveillance Related to the MitraClip Device: A United States Food and Drug Administration MAUDE Experience.
    Mahabir CA; DeFilippis EM; Aggarwal S; Bath A; Qamar A; Patel NK; Goldsweig AM; Vaduganathan M
    J Invasive Cardiol; 2020 May; 32(5):E130-E132. PubMed ID: 32269176
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deaths and cardiovascular injuries due to device-assisted implantable cardioverter-defibrillator and pacemaker lead extraction.
    Hauser RG; Katsiyiannis WT; Gornick CC; Almquist AK; Kallinen LM
    Europace; 2010 Mar; 12(3):395-401. PubMed ID: 19946113
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Device-related complications during renal cryoablation: insights from the Manufacturer and User Facility Device Experience (MAUDE) database.
    Kotamarti S; Michael Z; Silver D; Teper E; Aminsharifi A; Polascik TJ; Schulman A
    Urol Oncol; 2022 May; 40(5):199.e9-199.e14. PubMed ID: 35379535
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dental device-associated problems: an analysis of FDA postmarket surveillance data.
    Fuller J; Parmentier C
    J Am Dent Assoc; 2001 Nov; 132(11):1540-8. PubMed ID: 11806067
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of Device-Related Malfunction, Injury, and Death Associated with Using Elastomeric Pumps for Delivery of Local Anesthetics in the US Food and Drug Administration MAUDE Database.
    Teames R; Joyce A; Scranton R; Vick C; Nagaraj N
    Drug Healthc Patient Saf; 2020; 12():293-299. PubMed ID: 33380842
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Reporter's occupation and source of adverse device event reports contained in the FDA's MAUDE database.
    Kavanagh KT; Brown RE; Kraman SS; Calderon LE; Kavanagh SP
    Patient Relat Outcome Meas; 2019; 10():205-208. PubMed ID: 31308772
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.