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  1. Article ; Online: Summary of adverse drug events for hydroxychloroquine, azithromycin, and chloroquine during the COVID-19 pandemic.

    Dauner, Daniel G / Dauner, Kim Nichols

    Journal of the American Pharmacists Association : JAPhA

    2021  Volume 61, Issue 3, Page(s) 293–298

    Abstract: Objective: Given the increased use of hydroxychloroquine (HCQ), chloroquine (CQ), and azithromycin (AZM) during the early months of the coronavirus disease 2019 (COVID-19) pandemic, there is a need to evaluate the associated safety concerns. The ... ...

    Abstract Objective: Given the increased use of hydroxychloroquine (HCQ), chloroquine (CQ), and azithromycin (AZM) during the early months of the coronavirus disease 2019 (COVID-19) pandemic, there is a need to evaluate the associated safety concerns. The objective of this study was to summarize the adverse drug events (ADEs) associated with HCQ, CQ, and AZM use during the national COVID-19 emergency and compare the results with known adverse reactions listed in the drugs' package inserts.
    Methods: A cross-sectional study design was used. The publicly available Food and Drug Administration Adverse Event Reporting System quarterly data extract files from January 1, 2020 to June 30, 2020 were downloaded. A disproportionality analysis was conducted using the proportional reporting ratio to identify possible ADE signals. A Poisson regression was used to assess if the number of ADE reports for the 3 drugs increased over time.
    Results: There was a statistically significant increasing trend in the reported ADEs for both HCQ (P < 0.001) and AZM (P < 0.001). Before the declaration of the national emergency, there were 592 reported drug-ADE pairs for the 3 drugs compared with 2492 drug-ADE pairs reported after March 13, 2020. These 2492 drug-ADE pairs represented 848 ADEs across the 3 drugs, of which 114 (13.4%) were identified as potential signals including 55 (48.2%) that were not listed in the prescribing information.
    Conclusions: Our results showed that the reported ADEs for HCQ and AZM have increased during the COVID-19 pandemic. Differences were observed in both the type of and frequency of the highest reported ADEs for the 3 selected drugs before and after the national emergency declaration. Although causation cannot be determined from ADE reports, further investigation of some reports may be warranted. Our results highlight the need for pharmacovigilance and education of health care professionals on the safety of these drugs when being used for COVID-19 prophylaxis or treatment.
    MeSH term(s) Azithromycin/adverse effects ; Chloroquine/adverse effects ; Cross-Sectional Studies ; Drug-Related Side Effects and Adverse Reactions/epidemiology ; Humans ; Hydroxychloroquine/adverse effects ; Pandemics ; SARS-CoV-2 ; COVID-19 Drug Treatment
    Chemical Substances Hydroxychloroquine (4QWG6N8QKH) ; Azithromycin (83905-01-5) ; Chloroquine (886U3H6UFF)
    Language English
    Publishing date 2021-01-11
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2118585-2
    ISSN 1544-3450 ; 1544-3191 ; 1086-5802
    ISSN (online) 1544-3450
    ISSN 1544-3191 ; 1086-5802
    DOI 10.1016/j.japh.2021.01.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Comparing the use of individual and composite terms to evaluate adverse drug event disproportionality: a focus on glucagon-like peptide-1 receptor agonists and diabetic retinopathy.

    Dauner, Daniel G / Farley, Joel F

    Expert opinion on drug safety

    2021  Volume 20, Issue 4, Page(s) 475–480

    Abstract: ... ...

    Abstract Background
    MeSH term(s) Adverse Drug Reaction Reporting Systems ; Diabetic Retinopathy/epidemiology ; Diabetic Retinopathy/etiology ; Drug-Related Side Effects and Adverse Reactions/epidemiology ; Glucagon-Like Peptide-1 Receptor/agonists ; Glucagon-Like Peptides/administration & dosage ; Glucagon-Like Peptides/adverse effects ; Humans ; Hypoglycemic Agents/administration & dosage ; Hypoglycemic Agents/adverse effects ; United States ; United States Food and Drug Administration
    Chemical Substances Glucagon-Like Peptide-1 Receptor ; Hypoglycemic Agents ; semaglutide (53AXN4NNHX) ; Glucagon-Like Peptides (62340-29-8)
    Language English
    Publishing date 2021-03-26
    Publishing country England
    Document type Journal Article
    ZDB-ID 2088728-0
    ISSN 1744-764X ; 1474-0338
    ISSN (online) 1744-764X
    ISSN 1474-0338
    DOI 10.1080/14740338.2021.1887136
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Direct-acting antiviral retreatment patterns for hepatitis C.

    Hasan, Shaquib Al / Dauner, Daniel G / Rajpurohit, Abhijeet / Farley, Joel F

    Journal of managed care & specialty pharmacy

    2022  Volume 28, Issue 10, Page(s) 1100–1110

    Abstract: BACKGROUND: ...

    Abstract BACKGROUND:
    MeSH term(s) Antiviral Agents/therapeutic use ; Hepacivirus ; Hepatitis C/drug therapy ; Hepatitis C, Chronic/drug therapy ; Humans ; Liver Neoplasms/drug therapy ; Liver Neoplasms/epidemiology ; Retreatment ; Retrospective Studies
    Chemical Substances Antiviral Agents
    Language English
    Publishing date 2022-09-19
    Publishing country United States
    Document type Journal Article
    ISSN 2376-1032
    ISSN (online) 2376-1032
    DOI 10.18553/jmcp.2022.28.10.1100
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: FDA's Unimproved Enforcement of Postmarketing Requirements and Commitments: Implications for Providers and Patients.

    Dauner, Daniel G / Dauner, Kim Nichols / Peterson, Annalisa L H

    Research in social & administrative pharmacy : RSAP

    2019  Volume 16, Issue 6, Page(s) 844–847

    Abstract: Background: The 2007 reauthorization of the Prescription Drug User Fee Act empowered the Food and Drug Administration (FDA) to require and enforce postmarketing studies to monitor the safety of prescription drugs, an increasing number of which are ... ...

    Abstract Background: The 2007 reauthorization of the Prescription Drug User Fee Act empowered the Food and Drug Administration (FDA) to require and enforce postmarketing studies to monitor the safety of prescription drugs, an increasing number of which are approved under expedited development or review programs. However, compliance rates for postmarketing requirements are low, and the FDA has not exercised its enforcement authority, allowing the very safety concerns that prompted the expansion of its power to continue. Prior evaluations have found that the FDA lacks reliable, timely, and readily accessible data for tracking postmarket safety issues, and that it has failed to enforce the postmarket surveillance measures it requires of the pharmaceutical industry.
    Objective: This study provides an updated evaluation of FDA oversight of postmarketing requirements and commitments and assesses whether there have been improvements since 2010.
    Methods: This study utilized data from the FDA's annual Report on the Performance of Drug and Biologics Firms in Conducting Postmarketing Requirements and Commitments. It evaluated studies opened in FY 2011-2014 and tracked their status through the FDA's FY 2018 report (data as of September 30, 2018), thereby allowing the pharmaceutical industry 4-7 years to complete a given PMR/PMC. Descriptive statistics were calculated, and differences in the status of postmarketing requirements and postmarketing commitments between FYs 2011-2014 and FY 2009-2010 were evaluated.
    Results: During fiscal years 2011-2014, there was little difference in the FDA's oversight of postmarketing studies compared to fiscal years 2009-2010. While there were some year-to-year significant differences, the overall trend indicated no change.
    Conclusions: The FDA's oversight of postmarketing studies has not improved since 2010. This paper discusses implications for providers and patients who unduly assume the responsibility of postmarketing surveillance due to the lack of FDA oversight.
    MeSH term(s) Drug Approval ; Drug Industry ; Humans ; Pharmaceutical Preparations ; Product Surveillance, Postmarketing ; United States ; United States Food and Drug Administration
    Chemical Substances Pharmaceutical Preparations
    Language English
    Publishing date 2019-11-07
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2192059-X
    ISSN 1934-8150 ; 1551-7411
    ISSN (online) 1934-8150
    ISSN 1551-7411
    DOI 10.1016/j.sapharm.2019.11.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Performance of subgrouped proportional reporting ratios in the US Food and Drug Administration (FDA) adverse event reporting system.

    Dauner, Daniel G / Zhang, Rui / Adam, Terrence J / Leal, Eleazar / Heitlage, Viviene / Farley, Joel F

    Expert opinion on drug safety

    2023  Volume 22, Issue 7, Page(s) 589–597

    Abstract: Background: Many signal detection algorithms give the same weight to information from all products and patients, which may result in signals being masked or false positives being flagged as potential signals. Subgrouped analysis can be used to help ... ...

    Abstract Background: Many signal detection algorithms give the same weight to information from all products and patients, which may result in signals being masked or false positives being flagged as potential signals. Subgrouped analysis can be used to help correct for this.
    Research design and methods: The publicly available US Food and Drug Administration Adverse Event Reporting System quarterly data extract files from 1 January 2015 through 30 September 2017 were utilized. A proportional reporting ratio (PRR) analysis subgrouped by either age, sex, ADE report type, seriousness of ADE, or reporter was compared to the crude PRR analysis using sensitivity, specificity, precision, and c-statistic.
    Results: Subgrouping by age (n = 78, 34.5% increase), sex (n = 67, 15.5% increase), and reporter (n = 64, 10.3% increase) identified more signals than the crude analysis. Subgrouping by either age or sex increased both the sensitivity and precision. Subgrouping by report type or seriousness resulted in fewer signals (n = 50, -13.8% for both). Subgrouped analyses had higher c-statistic values, with age having the highest (0.468).
    Conclusions: Subgrouping by either age or sex produced more signals with higher sensitivity and precision than the crude PRR analysis. Subgrouping by these variables can unmask potentially important associations.
    MeSH term(s) United States ; Humans ; Adverse Drug Reaction Reporting Systems ; United States Food and Drug Administration ; Software ; Algorithms ; Drug-Related Side Effects and Adverse Reactions/epidemiology ; Pharmacovigilance
    Language English
    Publishing date 2023-03-07
    Publishing country England
    Document type Journal Article
    ZDB-ID 2088728-0
    ISSN 1744-764X ; 1474-0338
    ISSN (online) 1744-764X
    ISSN 1474-0338
    DOI 10.1080/14740338.2023.2182289
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Evaluation of four machine learning models for signal detection.

    Dauner, Daniel G / Leal, Eleazar / Adam, Terrence J / Zhang, Rui / Farley, Joel F

    Therapeutic advances in drug safety

    2023  Volume 14, Page(s) 20420986231219472

    Abstract: Background: Logistic regression-based signal detection algorithms have benefits over disproportionality analysis due to their ability to handle potential confounders and masking factors. Feature exploration and developing alternative machine learning ... ...

    Abstract Background: Logistic regression-based signal detection algorithms have benefits over disproportionality analysis due to their ability to handle potential confounders and masking factors. Feature exploration and developing alternative machine learning algorithms can further strengthen signal detection.
    Objectives: Our objective was to compare the signal detection performance of logistic regression, gradient-boosted trees, random forest and support vector machine models utilizing Food and Drug Administration adverse event reporting system data.
    Design: Cross-sectional study.
    Methods: The quarterly data extract files from 1 October 2017 through 31 December 2020 were downloaded. Due to an imbalanced outcome, two training sets were used: one stratified on the outcome variable and another using Synthetic Minority Oversampling Technique (SMOTE). A crude model and a model with tuned hyperparameters were developed for each algorithm. Model performance was compared against a reference set using accuracy, precision, F1 score, recall, the receiver operating characteristic area under the curve (ROCAUC), and the precision-recall curve area under the curve (PRCAUC).
    Results: Models trained on the balanced training set had higher accuracy, F1 score and recall compared to models trained on the SMOTE training set. When using the balanced training set, logistic regression, gradient-boosted trees, random forest and support vector machine models obtained similar performance evaluation metrics. The gradient-boosted trees hyperparameter tuned model had the highest ROCAUC (0.646) and the random forest crude model had the highest PRCAUC (0.839) when using the balanced training set.
    Conclusion: All models trained on the balanced training set performed similarly. Logistic regression models had higher accuracy, precision and recall. Logistic regression, random forest and gradient-boosted trees hyperparameter tuned models had a PRCAUC ⩾ 0.8. All models had an ROCAUC ⩾ 0.5. Including both disproportionality analysis results and additional case report information in models resulted in higher performance evaluation metrics than disproportionality analysis alone.
    Language English
    Publishing date 2023-12-25
    Publishing country England
    Document type Journal Article
    ZDB-ID 2583589-0
    ISSN 2042-0994 ; 2042-0986
    ISSN (online) 2042-0994
    ISSN 2042-0986
    DOI 10.1177/20420986231219472
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Ceftobiprole: A novel, broad-spectrum cephalosporin with activity against methicillin-resistant Staphylococcus aureus.

    Dauner, Daniel G / Nelson, Robert E / Taketa, Donna C

    American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists

    2010  Volume 67, Issue 12, Page(s) 983–993

    Abstract: Purpose: The pharmacology, antimicrobial activity, pharmacokinetics, pharmacodynamics, clinical efficacy, safety, and place in therapy of ceftobiprole are reviewed.: Summary: Ceftobiprole, a novel, broad-spectrum, parenteral cephalosporin, inhibits ... ...

    Abstract Purpose: The pharmacology, antimicrobial activity, pharmacokinetics, pharmacodynamics, clinical efficacy, safety, and place in therapy of ceftobiprole are reviewed.
    Summary: Ceftobiprole, a novel, broad-spectrum, parenteral cephalosporin, inhibits the cell-wall synthesis of penicillin-binding proteins (PBPs) PBP2a and PBP2x, responsible for the resistance in staphylococci and pneumococci, respectively. Ceftobiprole has good activity against gram-positive aerobes and anaerobes, and its activity against gram-negative aerobes and anaerobes is species dependent. Ceftobiprole is relatively inactive against Acinetobacter species. Its ability to bind relevant PBPs of resistant gram-positive and gram-negative bacteria indicates its potential use in the treatment of hospital-acquired pneumonia and complicated skin and skin-structure infections (cSSSIs). Ceftobiprole is primarily excreted unchanged by the kidneys and exhibits linear pharmacokinetics. The half-life of the drug is approximately 3-4 hours. It exhibits minimal plasma protein binding (16%). Ceftobiprole does not inhibit the cytochrome P-450 isoenzyme system, so the possibility of drug-drug interactions is low. The drug has not been approved for use in the United States but has been approved in Canada and elsewhere. Ceftobiprole is currently undergoing Phase III clinical trials and has demonstrated activity against methicillin-resistant Staphylococcus aureus, penicillin-resistant Streptococcus pneumoniae, and Pseudomonas aeruginosa. Completed Phase III trials used i.v. dosages of 500 mg every 8-12 hours. The most commonly observed adverse effects of ceftobiprole included headache and gastrointestinal upset.
    Conclusion: Ceftobiprole is a novel, broad-spectrum, parenteral cephalosporin undergoing Phase III clinical trials. Its broad spectrum of activity makes it a candidate for monotherapy of cSSSIs and pneumonias that have required combination therapy in the past.
    MeSH term(s) Animals ; Anti-Bacterial Agents/adverse effects ; Anti-Bacterial Agents/chemistry ; Anti-Bacterial Agents/pharmacokinetics ; Anti-Bacterial Agents/pharmacology ; Anti-Bacterial Agents/therapeutic use ; Bacteria/drug effects ; Bone Diseases, Infectious/drug therapy ; Cephalosporins/adverse effects ; Cephalosporins/chemistry ; Cephalosporins/pharmacokinetics ; Cephalosporins/pharmacology ; Cephalosporins/therapeutic use ; Drug Resistance, Bacterial ; Endocarditis, Bacterial/drug therapy ; Humans ; Infusions, Intravenous ; Methicillin-Resistant Staphylococcus aureus/drug effects
    Chemical Substances Anti-Bacterial Agents ; Cephalosporins ; ceftobiprole (5T97333YZK)
    Language English
    Publishing date 2010-05-27
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1224627-x
    ISSN 1535-2900 ; 1079-2082
    ISSN (online) 1535-2900
    ISSN 1079-2082
    DOI 10.2146/ajhp090285
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Clozapine-induced pericardial effusion.

    Dauner, Daniel G / Deremer, Christina E / Haburchak, David

    Journal of clinical psychopharmacology

    2008  Volume 28, Issue 4, Page(s) 455–456

    MeSH term(s) Adult ; Antipsychotic Agents/adverse effects ; Antipsychotic Agents/therapeutic use ; Clozapine/adverse effects ; Clozapine/therapeutic use ; Echocardiography ; Female ; Humans ; Pericardial Effusion/chemically induced ; Pericardial Effusion/etiology ; Schizophrenia/drug therapy
    Chemical Substances Antipsychotic Agents ; Clozapine (J60AR2IKIC)
    Language English
    Publishing date 2008-08
    Publishing country United States
    Document type Case Reports ; Letter
    ZDB-ID 604631-9
    ISSN 1533-712X ; 0271-0749
    ISSN (online) 1533-712X
    ISSN 0271-0749
    DOI 10.1097/JCP.0b013e31817d86f0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Statewide sentinel surveillance for antibiotic nonsusceptibility among streptococcus pneumoniae isolates in South Carolina, 2003-2004.

    Dauner, Daniel G / Roberts, Dixie F / Kotchmar, George S

    Southern medical journal

    2006  Volume 100, Issue 1, Page(s) 14–19

    Abstract: Background: In 2003, the South Carolina Department of Health and Environmental Control established the Carolina Antibiotic Resistance Surveillance System (CARSS), an active sentinel surveillance system for antibiotic-resistant Streptococcus pneumoniae.!# ...

    Abstract Background: In 2003, the South Carolina Department of Health and Environmental Control established the Carolina Antibiotic Resistance Surveillance System (CARSS), an active sentinel surveillance system for antibiotic-resistant Streptococcus pneumoniae.
    Methods: CARSS includes twelve hospitals. Each hospital was assigned a weighted sample size. Minimum inhibitory concentrations were determined using the E-test method.
    Results: A total of 452 isolates were collected. The prevalence of penicillin nonsusceptibility in the study was 44.9%. Penicillin intermediate resistance (PCN-I) was 33.2%, and penicillin high-level resistance (PCN-R) was 11.7%. One hundred six (23.5%) isolates were nonsusceptible to one antibiotic. One hundred twenty-four (27.4%) isolates were nonsusceptible to three or more antibiotics.
    Conclusions: CARSS confirmed the prevalences of antibiotic nonsusceptibility previously reported for South Carolina. However, CARSS suggests resistance is shifting from PCN-R to PCN-I in South Carolina. There is a high prevalence of multidrug nonsusceptibility in South Carolina. CARSS will continue to monitor these trends.
    MeSH term(s) Adolescent ; Adult ; Aged ; Anti-Infective Agents/therapeutic use ; Child ; Child, Preschool ; Community-Acquired Infections/drug therapy ; Community-Acquired Infections/epidemiology ; Community-Acquired Infections/microbiology ; Drug Resistance, Multiple, Bacterial ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Microbial Sensitivity Tests ; Middle Aged ; Pneumococcal Infections/drug therapy ; Pneumococcal Infections/epidemiology ; Pneumococcal Infections/microbiology ; Prevalence ; Sentinel Surveillance ; South Carolina/epidemiology ; Streptococcus pneumoniae/isolation & purification
    Chemical Substances Anti-Infective Agents
    Language English
    Publishing date 2006-12-01
    Publishing country United States
    Document type Journal Article ; Multicenter Study
    ZDB-ID 185329-6
    ISSN 1541-8243 ; 0038-4348
    ISSN (online) 1541-8243
    ISSN 0038-4348
    DOI 10.1097/01.smj.0000232968.56740.e1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Laboratory survey of antibiotic nonsusceptibility among Streptococcus pneumoniae isolates in South Carolina, 1998 versus 2000.

    Dauner, Daniel G / Gibson, James J / Roberts, Dixie F / Kotchmar, George S

    Southern medical journal

    2003  Volume 96, Issue 10, Page(s) 960–967

    Abstract: Background: In 1998, the South Carolina Department of Health and Environmental Control surveyed clinical microbiology laboratories statewide to determine the prevalence of antibiotic nonsusceptibility among isolates of Streptococcus pneumoniae. A follow- ...

    Abstract Background: In 1998, the South Carolina Department of Health and Environmental Control surveyed clinical microbiology laboratories statewide to determine the prevalence of antibiotic nonsusceptibility among isolates of Streptococcus pneumoniae. A follow-up study was conducted in 2001.
    Methods: A cross-sectional study was conducted to estimate the prevalence of penicillin nonsusceptibility (PCN-N), extended-spectrum cephalosporin nonsusceptibility (ESC-N), and levofloxacin nonsusceptibility (LEV-N) in South Carolina. A standardized questionnaire was mailed to 89 laboratories.
    Results: The prevalence of penicillin intermediate resistance increased from 1998 (17.6%) to 2000 (20.9%, chi2 P = 0.008). Furthermore, the prevalence of PCN-N increased from 1998 (34.5%) to 2000 (38.4%, chi2 P = 0.01). The prevalence of ECN-N decreased from 1998 (19.1%) to 2000 (17.7%), but the difference was not significant (chi2 P = 0.25).
    Conclusion: The laboratory survey was a low-cost method of estimating the change in prevalence of antibiotic nonsusceptibility, and it emphasizes regional surveillance because the prevalence of antibiotic nonsusceptibility varied geographically.
    MeSH term(s) Cross-Sectional Studies ; Drug Resistance, Bacterial ; Follow-Up Studies ; Humans ; In Vitro Techniques ; Laboratories ; Microbial Sensitivity Tests ; Microbiology ; Prevalence ; Rural Population ; South Carolina ; Streptococcus pneumoniae/drug effects ; Streptococcus pneumoniae/isolation & purification ; Time Factors ; Urban Population
    Language English
    Publishing date 2003-10
    Publishing country United States
    Document type Comparative Study ; Journal Article
    ZDB-ID 185329-6
    ISSN 1541-8243 ; 0038-4348
    ISSN (online) 1541-8243
    ISSN 0038-4348
    DOI 10.1097/01.SMJ.0000085768.21312.63
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