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      Quality and Characteristics of 4241 Case Reports of Lactic Acidosis in Metformin Users Reported to a Large Pharmacovigilance Database

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          Abstract

          Objective

          Metformin-associated lactic acidosis (MaLA) occurs rarely and is thus difficult to study. We analysed 4241 individual case safety reports of lactic acidosis (LA) that implicated metformin as a suspected drug reported to the pharmacovigilance database of Merck KGaA, Darmstadt, Germany. The primary objective was to review reports for quality and completeness of data to support diagnoses of MaLA. We also explored the correlations between reported biomarkers, and associations between biomarkers and outcomes.

          Research Design and Methods

          Records were analysed for completeness in supporting diagnoses of LA or metformin-associated LA (MaLA), against commonly used diagnostic criteria. Correlations between indices of exposure to metformin and biomarkers of LA and mortality were investigated.

          Results

          Missing data was common, especially for plasma metformin. Clinical/biomarker evidence supported a diagnosis of LA in only 33% of cases (LA subpopulation) and of MaLA in only 9% (MaLA subpopulation). The metformin plasma level correlated weakly with plasma lactate (positive) and pH (negative). About one-fifth (21.9%) of cases reported a fatal outcome. Metformin exposure (plasma level or dose) was not associated with increased mortality risk (there was a suggestion of decreased risk at higher levels of exposure to metformin). Plasma lactate was the only variable associated with increased risk of mortality. Examination of concomitant risk factors for MaLA identified renal dysfunction (including of iatrogenic origin) as a potential driver of mortality in this population.

          Conclusion

          Despite the high frequency of missing data, this is the largest analysis of cases of MaLA supported by measurements of circulating metformin, and lactate, and pH, to date. Plasma lactate, and not metformin dose or plasma level, appeared to be the main driver of mortality in the setting of LA or MaLA. Further research with more complete case reports is required.

          Most cited references38

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          Lactic acidosis.

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            Metformin in patients with type 2 diabetes and kidney disease: a systematic review.

            Metformin is widely viewed as the best initial pharmacological option to lower glucose concentrations in patients with type 2 diabetes mellitus. However, the drug is contraindicated in many individuals with impaired kidney function because of concerns of lactic acidosis.
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              Accumulation of metformin by tissues of the normal and diabetic mouse.

              1. Tissue accumulation of the antihyperglycaemic agent metformin (dimethylbiguanide) was examined after oral administration to the normal and streptozotocin (STZ) diabetic mouse. 2. Metformin (50 mg/kg body weight containing 14C-metformin 25 microCi/kg body weight), which is stable and not metabolized, resulted in maximum plasma concentrations at 0.5 h which declined to 1000 mumol/kg wet weight at 0.5-2 h, but declined to < 2% of maximum by 24 h. 4. Stomach, colon, salivary gland, kidney and liver accumulated metformin more than two-fold, and concentrations of the drug in heart and skeletal (gastrocnemius) muscle were greater than plasma concentrations on some occasions up to 8 h. 5. In a separate study, i.v.-administered metformin was selectively accumulated by tissues of the small intestine. Thus, retention of metformin by tissues of the small intestine may represent a deep compartment for the drug.
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                Author and article information

                Journal
                Ther Clin Risk Manag
                Ther Clin Risk Manag
                tcrm
                Therapeutics and Clinical Risk Management
                Dove
                1176-6336
                1178-203X
                04 November 2022
                2022
                : 18
                : 1037-1047
                Affiliations
                [1 ]Global Medical Affairs, Merck Healthcare KGaA , Darmstadt, Germany
                [2 ]Global Patient Safety, Merck Healthcare KGaA , Darmstadt, Germany
                [3 ]Global Epidemiology, Merck Healthcare KGaA , Darmstadt, Germany
                [4 ]Global Biostatistics, Merck Healthcare KGaA , Darmstadt, Germany
                Author notes
                Correspondence: Kerstin MG Brand, Global Medical Affairs, Merck Healthcare KGaA , F135/00_N1, Frankfurter Str. 250, Darmstadt, 64293, Germany, Tel +49 6151 72 2301, Email kerstin.brand@merckgroup.com
                Author information
                http://orcid.org/0000-0002-0430-4189
                http://orcid.org/0000-0001-9657-9376
                Article
                372430
                10.2147/TCRM.S372430
                9642855
                f2f58787-9f2c-42d9-a20f-2c26a588334a
                © 2022 Brand et al.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 04 May 2022
                : 11 July 2022
                Page count
                Figures: 1, Tables: 3, References: 39, Pages: 11
                Funding
                Funded by: Merck healthcare KGaA, Darmstadt, Germany. Dr. Mike Gwilt (GT Communications);
                Funded by: provided editorial assistance in the development of the manuscript;
                Funded by: funded by Merck Healthcare KGaA Darmstadt;
                Funded by: Germany;
                The study was funded by Merck healthcare KGaA, Darmstadt, Germany. Dr. Mike Gwilt (GT Communications), provided editorial assistance in the development of the manuscript, funded by Merck Healthcare KGaA Darmstadt, Germany.
                Categories
                Original Research

                Medicine
                lactic acidosis,metformin,type 2 diabetes,pharmacovigilance
                Medicine
                lactic acidosis, metformin, type 2 diabetes, pharmacovigilance

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