Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 2024 Nov 18;121(49):e2411919121. doi: 10.1073/pnas.2411919121

Global trends in antibiotic consumption during 2016–2023 and future projections through 2030

Eili Y Klein a,b, Isabella Impalli a, Suprena Poleon a, Philippe Denoel c, Mariateresa Cipriano d, Thomas P Van Boeckel a,e,f, Simone Pecetta d, David E Bloom g, Arindam Nandi a,h,1
PMCID: PMC11626136  PMID: 39556760

Significance

Antimicrobial resistance is a pressing global health challenge driven by human antibiotic consumption, among other factors. In this report, we investigate trends in human antibiotic consumption in 67 countries from 2016 to 2023, focusing on changes in consumption during the COVID-19 pandemic. We found that global antibiotic consumption declined during the COVID-19 pandemic, but rebounded thereafter, particularly in middle-income countries. While our estimate of 49.3 billion defined daily doses for total global use is lower than previous forecasts, reductions associated with the pandemic make it challenging to determine whether attempts to curb antibiotic use over the past decade have been effective. Moreover, postpandemic increases are worrying in their implications for the future trajectory of use.

Keywords: antibiotic resistance, AMR, global public health, antimicrobial resistance

Abstract

Antibiotic resistance is a global public health threat. Many factors contribute to this issue, with human antibiotic consumption being significant among them. Analyzing trends and patterns in consumption can aid in developing policies to mitigate the burden of antimicrobial resistance and global disparities in access to antibiotics. Using pharmaceutical sales data licensed from IQVIA, we estimate national-level trends in antibiotic consumption in 67 countries during 2016–2023 and analyze the effects of economic growth and the COVID-19 pandemic. Finally, we estimate global human consumption and project growth through 2030 assuming current trends. We find that estimated antibiotic consumption in reported countries increased 16.3% from 29.5 to 34.3 billion defined daily doses (DDDs) from 2016 to 2023, reflecting a 10.6% increase in the consumption rate from 13.7 to 15.2 DDDs per 1,000 inhabitants per day. Increases were most pronounced in upper-middle- and lower-middle-income countries. While the COVID-19 pandemic significantly reduced consumption globally, this was most pronounced in high-income countries, and in these countries, reductions in antibiotic use in 2020 were sharper, and lasted longer, than in other countries. By 2030, we project that, without reductions in rapidly developing nations, such as investments to improve infrastructure, particularly water and sanitation, along with improved access to vaccination, global antibiotic consumption will increase by 52.3% from an estimated 49.3 billion in 2023 to 75.1 billion DDDs.


Antibiotic resistance is a critical global health challenge. Estimates of the burden of resistance suggest that nearly 5 million deaths were associated with bacterial resistance to antibiotics in 2019 (1). Notably, low-income countries, particularly in sub-Saharan Africa, had the highest rates of mortality associated with bacterial resistance despite lower consumption rates. However, routine testing for resistance is relatively rare in Africa, which may underrepresent the true correlation between resistance and mortality. While resistance is driven by overuse and misuse of antibiotics in humans, animals, and agriculture, as well as poor infection prevention and control, human antibiotic use is a major driver (2, 3). Global human antibiotic consumption increased by 65% between 2000 and 2015, driven primarily by lower-middle-income countries (LMICs) and the rise in gross domestic product (GDP) in LMICs, though rates remained significantly higher in many high-income countries (HICs) (4, 5).

Since penicillin became widely available in the 1940s (6), antibiotics have played an indispensable role in reducing morbidity and mortality from both common ailments, such as streptococcal infections, and life-threatening conditions, like sepsis. However, while antibiotics have played a crucial role in reducing morbidity and mortality from bacterial infections (7, 8), the largest gains in life expectancy in HICs largely occurred prior to the introduction of antibiotics with the implementation of public health measures including improved sanitation and sewage management, public water treatment and food inspection, and surveillance and control of infectious diseases, including vaccination (9). In many LMICs, antibiotics are used to decrease the morbidity and mortality of illnesses that are directly attributable to lack of universal access to clean water and improved sanitation and hygiene (10). However, relying heavily on antibiotics in lieu of improving sanitation and other public health measures can exacerbate the problem of antibiotic resistance.

Surveillance of antibiotic consumption provides a foundation for improving antibiotic stewardship. Identifying trends in use can help to tailor educational and vaccination campaigns, policy recommendations, and clinical guidelines to the unique challenges of each region or country. This is especially important in LMICs, which are often forced to grapple with the juxtaposition of limited access to essential antibiotics and the indiscriminate or inappropriate use of these agents (4, 11). In HICs, which until now have had some of the highest per capita antibiotic consumption rates, inappropriate use of antibiotics, such as for influenza-like illnesses and other viral infections, continues to be a major challenge (4, 5). Monitoring consumption patterns can provide insights into these disparities, guiding equitable distribution and accessibility initiatives. Furthermore, as antibiotic resistance knows no borders, ensuring robust surveillance in LMICs, which might lack the resources or infrastructure for such efforts, is not only crucial for their local populations but also forms a linchpin in the global strategy to combat the escalating threat of antibiotic resistance.

Here, we used antibiotic sales data from IQVIA MIDAS and conducted an analysis of trends in antibiotic consumption, focusing on the differences in consumption associated with World Bank income classification throughout the study period 2016–2023. Additionally, we quantify the impact of the COVID-19 pandemic on antibiotic use, where despite several studies finding low rates of bacterial coinfection, antibiotics were continually prescribed to COVID-19 patients at high rates (1216). Our study has important implications for the growing burden of multi-drug resistant (MDR) bacteria in many countries. The direct link between increased antibiotic consumption and prevalence of MDR bacteria (3, 17) is of significant concern globally.

Results

Total antibiotic consumption for countries with available data (n = 67) increased by 16.3% between 2016 and 2023, from 29.5 to 34.3 billion defined daily doses (DDDs), and the antibiotic consumption rate across these countries increased 10.6% from 13.7 to 15.2 DDDs per 1,000 inhabitants per day. The mean antibiotic consumption rate across those 67 countries increased by 5.5% from 19.5 DDDs per 1,000 inhabitants per day to 20.5, and the median antibiotic consumption rate increased by 1.7% from 18.5 to 18.8 DDDs per 1,000 inhabitants per day.

Increases in consumption varied across income groups. For this analysis, the income groups used as defined by the World Bank include middle-income countries (MICs), which are broken out into LMICs (n = 11) and upper-middle-income countries (UMICs, n = 17) where appropriate, and HICs (n = 39). Between 2016 and 2019, consumption rates increased in MICs (9.8%) while decreasing in HICs (−5.8%) (Fig. 1). The COVID-19 pandemic significantly reduced consumption across all income groups; this was most pronounced in HICs (−17.8%) in 2020. However, MICs saw rapid increases in 2021, and in that year, LMICs led HICs in consumption rate, at 17.7 and 17.3 DDDs per 1,000 inhabitants per day, respectively. For the entire study period 2016–2023, the consumption rate in MICs increased by 18.6% (23.4% in UMICs and 14.0% in LMICs), and the consumption rate in HICs decreased by 4.9%. Interrupted time series analysis (ITSA) results indicated that while consumption in HICs was decreasing at a rate of 0.34 (SE = 0.05) DDDs per 1,000 inhabitants per day before the onset of the pandemic, it fell by 5.73 DDDs per 1,000 inhabitants per day in 2020 and then increased at a rate of 1.39 DDDs per 1,000 inhabitants per day in the postpandemic period (SI Appendix, Fig. S1 and Table S1). In MICs, prepandemic trends were increasing (0.32 DDDs per 1,000 inhabitants per day, SE = 0.00) but decreased 1.50 DDDs per 1,000 inhabitants per day in 2020 and then increased at a faster rate after the pandemic (0.70 DDDs per 1,000 inhabitants per day annually) than before.

Fig. 1.

Fig. 1.

Change in global antibiotic consumption by country and country income classification, 2016–2023. (A) Yearly antibiotic consumption rate, measured in DDDs per 1,000 inhabitants per day, by country income classification. (B) Absolute change in antibiotic consumption rate between 2016 and 2023 by country in DDDs per 1,000 inhabitants per day. Countries in gray have no data in the database. Country income classifications noted as LMIC = lower-middle-income countries, MIC = middle-income countries, UMIC = upper-middle-income countries, HIC = high-income countries. Data Source: Based on IQVIA MIDAS® sales data for period 2016–2023. Copyright IQVIA. All rights reserved.

The top five largest percentage increases over the study period occurred in MICs (Fig. 2). The most significant consumption increases in LMICs were observed in Vietnam, where the consumption rate more than doubled from 25.6 to 54.0 DDDs per 1,000 inhabitants per day (111.2%), followed by West Africa (5.7 to 9.4, 64.8%). The most significant increases in UMICs were observed in Thailand, which increased from 12.7 to 28.3 DDDs per 1,000 inhabitants per day (122.8%) followed by Central America (4.0 to 6.8, 71.6%) and Malaysia (7.6 to 10.6, 39.6%). Three of the top ten countries with the highest consumption rates in 2023 were LMIC countries (Vietnam, Algeria, and Tunisia), compared with two in 2016 (Tunisia and Algeria) (SI Appendix, Fig. S2). Similarly, three of the top ten countries with the highest consumption rates in 2023 were UMICs (Ecuador, Türkiye, and Serbia) compared to only two in 2016 (Ecuador and Türkiye) (SI Appendix, Fig. S2).

Fig. 2.

Fig. 2.

Change in each antibiotic consumption rate, by country. Results are the percentage change between each country’s consumption rate in 2016–2023. Country income classifications noted as LMIC = lower-middle-income countries, UMIC = upper-middle-income countries, HIC = high-income countries. Data Source: Based on IQVIA MIDAS® sales data for period 2016–2023. Copyright IQVIA. All rights reserved.

During the COVID-19 pandemic, the countries with the greatest declines in antibiotic consumption were the Philippines (−41.8%), Malaysia (−28.4%), Uruguay (−27.5%), Ecuador (−27.2%), and Argentina (−26.8%). As a group, MICs had the largest rebounds in 2021, led by Indonesia (22.8%), Argentina (18.6%), and South Africa (15.4%) for UMICs, and India (16.5%) and West Africa (15.3%) for LMICs. UMICs and HICs experienced the largest percentage increases in antibiotic consumption rates from 2021 to 2023 (17.1% and 21.7%, respectively). The COVID-19 pandemic had a limited impact on which types of drugs were consumed (Fig. 3). Broad-spectrum penicillins (BSPs), cephalosporins, macrolides, fluoroquinolones, and tetracyclines remained the classes with the highest consumption rates by a large margin.

Fig. 3.

Fig. 3.

Global antibiotic consumption by antibiotic class. (A) Yearly changes in DDDs per 1,000 inhabitants per day for the top five antibiotic classes by consumption amount. All other classes were combined into other. (B) Antibiotic consumption differences between 2016 and 2023 for the top five antibiotic classes by consumption amount, with all other classes combined into other. DDD = defined daily dose. Data Source: Based on IQVIA MIDAS® sales data for period 2016–2023. Copyright IQVIA. All rights reserved.

Differences in the consumption rates by class and income group were apparent as well. The use of BSPs increased in all income classes throughout the study period (Fig. 4A), though during the pandemic, the largest decline was seen in HICs (−23.8%). Cephalosporin consumption rates in HICs were greater than that in MICs in 2016, but by the end of the study period, MICs had higher consumption, though the rates were over twice as high in LMICs as UMICs throughout the study period (mean, 1.7 vs. 4.9 DDDs per 1,000 inhabitants per day) (Fig. 4B). Macrolide use decreased sharply in 2020 in HICs but rose in MICs, driven largely by LMICs, and in 2020, macrolide use in LMICs surpassed that in HICs (2.8 compared to 2.6 DDDs per 1,000 inhabitants per day) (Fig. 4C). Fluoroquinolone consumption rates similarly started the period higher in HICs but by the end of the period had switched. However, in this case, the switch was largely due to use in HICs decreasing significantly. While consumption of “last-resort” antibiotics (carbapenems, oxazolidinones, glycylcyclines, and monobactams) remained at low levels relative to other antibiotic classes, MICs saw substantial percentage increases between 2016 and 2023: Carbapenem use increased 74.0%, oxazolidinone use increased 285.8%, and glycylcyclines use increased 221.5%. Only monobactam use decreased 82.0% (SI Appendix, Fig. S3).

Fig. 4.

Fig. 4.

Global antibiotic consumption for the top five most consumed antibiotic classes by country income classification. Data are displayed as DDDs per 1,000 inhabitants per day. (A) BSP. (B) cephalosporins. (C) macrolides. (D) fluoroquinolones. (E) tetracyclines. Country income classifications noted as LMIC = lower-middle-income countries, MIC = middle-income countries, UMIC = upper-middle-income countries, HIC = high-income countries. Data Source: Based on IQVIA MIDAS® sales data for period 2016–2023. Copyright IQVIA. All rights reserved.

Rates of consumption of Access and Watch antibiotics differed by income group, as well. HICs consumed consistently more Access antibiotics relative to Watch, with the Access-to-Watch index growing from 1.70 in 2016 to 2.14 in 2023 (Fig. 5A). MICs, on the other hand, consumed more Watch antibiotics than Access, with the Access-to-Watch index falling from 0.96 in 2016 to 0.92 in 2023. UMICs had a higher Access-to-Watch index than LMICs in all years. HICs outpaced MICs in Access consumption rates, as well, despite HIC Access consumption falling by 17.2% in 2020 (Fig. 5B). UMICs had the lowest Access consumption of all income groups. Watch consumption varied substantially by income group. While HICs had higher rates of Watch consumption than MICs in 2016 (7.7 vs. 5.0 DDDs per 1,000 inhabitants per day), in 2021, the MIC rate of 5.9 DDDs per 1,000 inhabitants per day surpassed the HIC rate of 5.3 DDDs per 1,000 inhabitants per day (Fig. 5C). The decrease in HIC Watch consumption preceded the onset of the COVID-19 pandemic and fell 29.5% from 2016 to 2020. The increase in MIC Watch consumption was driven largely by LMICs, whose rate of Watch consumption outpaced HICs by 2018 (7.2 vs. 7.0 DDDs per 1,000 inhabitants per day). In 2023, LMICs led all groups in Watch consumption at 8.2 DDDs per 1,000 inhabitants per day.

Fig. 5.

Fig. 5.

Global access and watch antibiotic consumption by country income classification. We illustrate (A) the Access-to-Watch index, as well as (B) Access and (C) Watch consumption by income classification for the period 2016–2023. The Access-to-Watch index is the ratio of Access to Watch consumption each year. Consumption data are displayed as DDDs per 1,000 inhabitants per day. Country income classifications noted as LMIC = lower-middle-income countries, MIC = middle-income countries, UMIC = upper-middle-income countries, HIC = high-income countries. Data Source: Based on IQVIA MIDAS® sales data for period 2016–2023. Copyright IQVIA. All rights reserved.

In 2023, estimated global antibiotic consumption (including estimates for countries for which data were unavailable) was 49.3 billion DDDs, or 17.0 DDDs per 1,000 inhabitants per day. This was an increase of 20.9% in total use and of 13.1% in the consumption rate from 2016, when global antibiotic consumption was estimated to be 40.8 billion DDDs, or 15.1 DDDs per 1,000 inhabitants per day. Assuming that future consumption in countries falls within current ranges of the study period, and assuming no changes in policy, our projections suggest that global antibiotic consumption could increase by 52.3% (uncertainty range [UR]: 22.1 to 82.6%) to a total of 75.1 (UR: 60.2 to 90.1) billion DDDs by 2030, and the antibiotic consumption rate could increase by 43.8% (UR: 15.2 to 72.3%) to 24.5 (19.6 to 29.4) DDDs per 1,000 inhabitants per day (Fig. 6).

Fig. 6.

Fig. 6.

Estimated total global antibiotic consumption in DDD (billions). Global consumption estimates include totals for all countries in the database and use country income classification to estimate per capita use for countries not included. Per capita estimates were multiplied by each country’s estimated or forecasted population to generate estimated total. Line from 2023–2030 is the average projected change in antibiotic consumption assuming countries future rate of change is between their compounded annual growth rate from 2016 to 2019 and the rate from 2020–2023. The shaded region is the uncertainty range of the projection (includes only variance from projected rate of change). Data Source: Based on IQVIA MIDAS® sales data for period 2016–2023. Copyright IQVIA. All rights reserved.

Discussion

Global antibiotic consumption in DDDs rose by 20.9% from 2016 to 2023, which was lower than the increase of 35.5% in the prior 7-y period (2008–2015) (4); however, a significant decrease occurred across all income groups in 2020 due to the COVID-19 pandemic, without which the total increase likely would have been higher. The relative impact of the pandemic on antibiotic use differed across countries, with the largest decreases taking place in HICs. In MICs, the largest declines were seen in those countries that had been increasing most rapidly prepandemic, reflecting the strong relationship between GDP growth and antibiotic use (4). During the pandemic, the vast majority of these countries maintained higher use than HICs and rebounded strongly in 2021, surpassing prior consumption rates. HICs experienced a “delayed rebound” in antibiotic consumption following the pandemic, with a very small (0.8%) increase in consumption in 2021 followed by larger increases in 2022 and 2023. While antibiotic consumption rates rose in 2023 in HICs, they had not quite returned to prepandemic levels by the end of 2023.

The delayed rebounds observed in HICs were likely due to longer adherence to policies and strategies to reduce transmission of SARS-CoV-2, such as mask wearing. As most antibiotic use in HIC occurs in the outpatient setting (18) and a significant fraction is driven by inappropriate use for respiratory infections (19), reductions in transmission of respiratory pathogens overall likely reduced antibiotic use. Another contributing factor to reduced transmission was likely an increase in individuals working from home. In higher-income economies, a larger fraction of jobs can be done at home (20), and though the pandemic officially ended in May 2023, working from home has remained at higher levels in HIC than prepandemic. What impact this may have on antibiotic use long term is worth further analysis.

Assessing antibiotic use at the national level is important because antimicrobial stewardship programs (ASPs) are often designed and implemented at that level. Several factors drive the rapid increase in antibiotic consumption in developing settings, including environmental, political, socioeconomic, and cultural factors (21, 22), though economic growth is likely the most important factor in lower-income settings. Recommendations to restrict antibiotic consumption must be context-specific as many policies intended to combat antimicrobial resistance (AMR) and avert antibiotic misuse/overuse have implications for sustainable development goals (SDGs). As countries grow economically and attempt to break out of the poverty cycle (SDG 1), they may be at risk for inappropriate antibiotic use, which could drive AMR and threaten progress toward healthcare goals (SDG 3) (23). Thus, increasing support for the development of national action plans and ASPs is necessary. However, equally important are the investments needed in measures to prevent infection (23, 24). Improvements in sanitation and hygiene measures, including the widespread implementation of water treatment facilities, sewer systems, and personal hygiene practices, played a pivotal role in significantly reducing the burden of infectious diseases and increasing life expectancies in HICs in the early 1900s. Many growing economies are facing rapid urbanization and population growth associated with higher population density and promotion of infectious disease spread (25, 26), which a focus on access to sanitation could alleviate.

In addition, increasing use of vaccines and point-of-care diagnostics could substantially decrease unnecessary antibiotic use, particularly in resource-limited environments. Such a reduction can occur directly, through vaccination against bacterial infections, such as pneumococcal conjugate vaccine, and indirectly, by diminishing the prevalence of viral illnesses that are frequently and inappropriately treated with antibiotics. Several recent studies have highlighted how vaccines (against bacterial pathogens and viruses) can help curb AMR and avert antibiotic prescriptions (2731) and highlight the potential and importance of robust immunization programs and proper diagnostics as an AMR mitigation strategy, particularly in resource-poor settings.

However, investments and a focus on prevention do not diminish the need to reduce the misuse and overuse of antibiotics globally. A particularly useful mechanism is the World Health Organization’s Access, Watch and Reserve (AWaRe) framework (32, 33). AWaRe categories delineate which drugs should be prioritized for widespread access and which should be more strictly deployed. Crafting national action plans and ASPs with AWaRe at the forefront has the potential to preserve the power of antibiotics as a common, global resource and aligns with the theme of sustainable development. Cooperation regarding antibiotic stewardship and access, which has been major a focus of the 2024 United Nations General Assembly (UNGA) High-level Meeting on AMR, is crucial for the success of a global framework (34, 35). As shown in this analysis, Watch group antibiotic consumption relative to Access group antibiotic consumption in MICs, particularly LMICs, has increased over the period 2016–2023. Further study on the extent of the impact of the framework on global antibiotic consumption since its release in 2017 is warranted. This is especially important considering that the 2024 UNGA AMR High-level meeting declaration has set a target of increasing Access group antibiotic consumption to at least 70% of human antibiotic consumption globally by 2030 (35).

In addition, strengthening regulatory agencies and ministries of health in MICs is critical to improving antibiotic stewardship in these countries. The diverging trend in fluoroquinolone use between HICs and MICs highlights this issue as HICs steady decrease in use was due to regulatory agency warnings against fluoroquinolone use for risk of disabling and potentially permanent side effects (36, 37). The fact that use did not decline, but continued to increase in MICs, could lead to increased rates of adverse events potentially impacting public health and healthcare systems and exacerbating existing health disparities within these countries. Additionally, given the widespread unregulated use of antibiotics in many countries [e.g., without prescription (38)], educational campaigns in MICs advising against the use of this class of drugs for empiric therapy and respiratory infections need to target pharmacies and consumers as well as providers. The need for strengthening the capacity of regulatory agencies in MICs is also indicated by the rapid increases seen in the use of last-resort antibiotics (carbapenems, oxazolidinones, glycylcyclines, and monobactams). While rising resistance rates in many MIC countries suggest a need for access to more effective antibiotics, this must be balanced with increased regulation to prevent overuse and misuse.

Our analysis has some limitations. First, IQVIA MIDAS data were available for only 67 countries, most of which are HICs and UMICs. Thus, results may not be representative of all nations categorized by income levels, and not all countries had data categorized by sector, which may have impacted the total DDDs for drugs that have both an oral and intravenous formulations. Furthermore, data provided were estimated sales in kilograms, which may not accurately reflect consumption. Second, while identifying the burden of diseases requiring antibiotics provides a good baseline for measuring antibiotic overuse, the data utilized were aggregated sales data, which limits the ability to draw conclusions on overuse or misuse due to the absence of reasons for prescribing. Third, data only included human consumption; a more comprehensive One Health approach that includes surveillance of animal antibiotic consumption and agricultural use is needed to more effectively combat overuse and detect concerning AMR trends (39). Fourth, changes in countries’ economic categorization make it difficult to fully compare LMICs and UMICs to prior analyses—that is why we combined most analyses as MICs. An analysis of the data using income classifications from 2007 [2007 classifications were used in the previous analysis of data from 2000 to 2015 (4)] found that the major differences in the current paper were due largely to switches between class and not differences in consumption (SI Appendix, Fig. S4).

In conclusion, our findings show that while the COVID-19 pandemic had a major impact on antibiotic use across all income levels, the overarching trend of increasing global antibiotic consumption fueled by economic development in MICs remains. Our estimate of 49.3 billion DDDs for global use in 2023 was lower than our prior forecast for 2023 of 70.3 billion DDDs which assumed increasing annual growth rates. However, while the results were only slightly higher than our forecast assuming convergence toward a global median, because growth was interrupted by the pandemic, it is difficult to evaluate whether efforts to curb antibiotic use over the last decade have been effective. Furthermore, the rapid increases postpandemic suggest that the trajectory of growth may be continuing to increase. Thus, policies are urgently needed to promote increased antibiotic access and ensure that antibiotics are not misused or overused in the process. In addition, greater emphasis is needed globally on preventing transmission of infections to reduce the need for antibiotics, particularly the most effective drugs. Improving infrastructure and access to water, sanitation, and hygiene, particularly in rapidly developing nations, along with improved access to vaccination should be an important pillar in the fight against AMR.

Materials and Methods

Data were retrieved for 67 countries from the IQVIA MIDAS® database, which provides estimated sales data for pharmaceutical drugs. IQVIA MIDAS® data are collected on a monthly basis from a sample of pharmacies and other outlets through which antibiotics and pharmaceutical drugs are dispensed. Each country’s data are split by year and sector (hospital and retail). In total, we used data from 67 countries over the period 2016–2023. See Table 1 for included countries and their data availability.

Table 1.

Country data available by sector

Country Retail Hospital Country Retail Hospital
Algeria Yes No Malaysia Yes No
Argentina Yes No Mexico Yes No
Australia Yes Yes Morocco Yes No
Austria Yes Yes Netherlands Yes Yes
Belarus Yes Yes New Zealand Yes Yes
Belgium Yes Yes Norway Yes Yes
Brazil Yes Yes Pakistan Yes No
Bulgaria Yes Yes Peru Yes No
Canada Yes Yes Philippines Yes Yes
Central America* Yes No Poland Yes Yes
Chile Yes No Portugal Yes Yes
China No Yes Puerto Rico Yes Yes
Colombia Yes No Romania Yes Yes
Croatia Yes Yes Russia Yes Yes
Czech Republic Yes Yes Saudi Arabia Yes Yes
Denmark Yes Yes Serbia Yes No
Ecuador Yes No Slovakia Yes Yes
Egypt Yes Yes Slovenia Yes No
Finland Yes Yes South Africa Yes No
France Yes Yes South Korea Yes Yes
Germany Yes Yes Spain Yes Yes
Greece Yes No Sweden Yes Yes
Hong Kong Yes No Switzerland Yes Yes
Hungary Yes Yes Taiwan Yes Yes
India Yes No Thailand Yes Yes
Indonesia Yes No Tunisia Yes Yes
Ireland Yes No Türkiye Yes Yes
Italy Yes Yes United Arab Emirates Yes No
Japan Yes Yes United Kingdom Yes Yes
Jordan Yes No United States Yes Yes
Kuwait Yes No Uruguay Yes No
Latvia Yes No Vietnam Yes Yes
Lebanon Yes No West Africa Yes No
Luxembourg Yes No

Data Source: Based on IQVIA MIDAS® sales data for period 2016–2023. Copyright IQVIA. All rights reserved.

*Central America includes Guatemala, Honduras, El Salvador, Nicaragua, Costa Rica, and Panama.

Egypt did not have hospital-level data for Q1 2016–Q2 2018, so data were interpolated based on the ratio for 2023.

West Africa includes Benin, Burkina Faso, Cameroon, Chad, Republic of the Congo, Gabon, Guinea, Ivory Coast, Mali, Niger, Senegal, and Togo.

Antibiotic sales data were obtained in estimated kilograms per active ingredient and converted to DDDs utilizing the Anatomical Therapeutic Chemical Classification System (ATC/DDD) published by the WHO Collaborating Centre for Drug Statistics Methodology following protocols from prior study (4, 40). We accounted for the different sectors in our data by assuming that hospital antibiotics were administered parenterally (intravenously) and retail antibiotics were administered orally similar to ref. 4. DDD unit values by route of administration were obtained from the ATC/DDD index for all molecules (39). Combination drugs were broken into their individual molecules, and one main molecule was determined. For molecules in the IQVIA MIDAS data without defined DDDs, we estimated them from other sources. See SI Appendix, Tables S2–S4 and Supplementary Text for all included DDD unit values and sources which were not in the ATC/DDD database. See Dataset S1 for consumption data in DDDs for each country.

Antibiotic consumption rates were measured in DDDs per 1,000 inhabitants per day, utilizing population estimates retrieved from World Bank and country government data (41, 42). Consumption rates among groups of countries based on their World Bank income classification in 2023 were subsequently compared. The World Bank income classifications used in this study are LMIC (n = 11), UMIC (n = 17), and HIC (n = 39) for 2023 (43). West Africa was designated LMIC as that was the most reflective of the aggregate; Central America was designated UMIC as that was most reflective of the aggregate. See SI Appendix, Table S5 for the list of countries and their income classifications used in the analysis, as well as their 2007 income classifications which were used in the previous analysis (4).

Antibiotics and combinations were classified as either “Access” or “Watch” drugs per the most recent (2023) WHO AWaRe framework for further analysis (44). The Access-to-Watch index for a given year was calculated by dividing Access consumption by Watch consumption for that year. To evaluate the impact of the COVID-19 pandemic on antibiotic consumption, we conducted an ITSA. ITSAs are a type of study design often used in public health to evaluate the impact of an intervention (here, the onset of the COVID-19 pandemic) on an outcome of interest (here, antibiotic consumption rates) (45, 46). We conducted a separate ITSA for each income group on its annual antibiotic consumption rate from 2016 to 2023. The “intervention” point was set to the beginning of 2020 such that 2020 data were included in the “postintervention” period. Regressions were calculated using a generalized least squares model by maximum likelihood; we confirmed series stationarity and accounted for autocorrelation for each income group through autoregressive and moving average adjustments. See SI Appendix, Supplemental Text for extended methodology for the ITSAs.

Global antibiotic consumption was calculated by extrapolating antibiotic use for countries not included in the IQVIA data. Extrapolations were based on the average per capita antibiotic use for countries with data in the same income group. Low-income countries were grouped with LMICs in our analysis. To project global antibiotic use through 2030, we conducted a sensitivity analysis assuming that countries’ growth rates ranged between each countries’ compounded annual growth rate from 2016 to 2019 and their compounded annual growth rate from 2020 to 2023. For extrapolated countries, we used the income group’s growth rates. We used a triangular distribution with the peak midway between the two growth rates on the assumption that prior growth was a predictor for future growth. The mean and variance were calculated by calculating the projected change in antibiotic use in total DDDs for the entire distribution stratified into 1,000 segments. The uncertainty range was calculated as the SD of the variance. Stata 16.1, R version 4.3.2, and Microsoft Excel were used for cleaning, analyses, and data visualizations.

The statements, findings, conclusions, views, and opinions contained and expressed in this article are based in part on data obtained under license from the following: IQVIA MIDAS® sales data for the period 2016–2023: quarterly-country level sales of antibiotic sales (ATC3: J01). Geography: Global (Algeria, Argentina, Australia, Austria, Belarus, Belgium, Bulgaria, Canada, Chile, China, Colombia, Costa Rica, Croatia, Czech, Denmark, Ecuador, Egypt, El Salvador, Finland, France, Germany, Greece, Guatemala, Honduras, Hong Kong, Hungary, India, Indonesia, Ireland, Italy, Japan, Jordan, Kuwait, Latvia, Lebanon, Luxembourg, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Nicaragua, Norway, Pakistan, Panama, Peru, Philippines, Poland, Portugal, Puerto Rico, Romania, Russia, Saudi Arabia, Serbia, Slovakia, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Türkiye, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam, West Africa); Measures: DDDs, calculated by GSK using IQVIA MIDAS Volume Data, reflecting estimates of real world activity. Copyright IQVIA. All rights reserved. The statements, findings, conclusions, views, and opinions contained and expressed herein are not necessarily those of IQVIA.

Supplementary Material

Appendix 01 (PDF)

Dataset S01 (XLSX)

pnas.2411919121.sd01.xlsx (137.4KB, xlsx)

Acknowledgments

Author contributions

E.Y.K., D.E.B., and A.N. designed research; E.Y.K., I.I., P.D., M.C., T.P.V.B., S. Pecetta, D.E.B., and A.N. performed research; E.Y.K., I.I., and S. Peleon analyzed data; and E.Y.K., I.I., S. Poleon, T.P.V.B., and A.N. wrote the paper.

Competing interests

P.D. and M.C. are employees of GSK group of companies. S. Pecetta was a GSK employee when the project started and he is currently an employee of Moderna Inc. D.E.B. has previously received research support or personal fees from GlaxoSmithKline plc, Merck, Pfizer, and Sanofi-Pasteur related to value-of-vaccination research, but not for this study. All other authors declare no competing interests.

Footnotes

This article is a PNAS Direct Submission C.M. is a guest editor invited by the Editorial Board.

Although PNAS asks authors to adhere to United Nations naming conventions for maps (https://www.un.org/geospatial/mapsgeo), our policy is to publish maps as provided by the authors.

Data, Materials, and Software Availability

All study data are included in the article and/or supporting information.

Supporting Information

References

  • 1.Murray C. J., et al. , Global burden of bacterial antimicrobial resistance in 2019: A systematic analysis. Lancet 399, 629–655 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Bell B. G., Schellevis F., Stobberingh E., Goossens H., Pringle M., A systematic review and meta-analysis of the effects of antibiotic consumption on antibiotic resistance. BMC Infect. Dis. 14, 1–25 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Sulis G., et al. , Exposure to World Health Organization’s AWaRe antibiotics and isolation of multidrug resistant bacteria: A systematic review and meta-analysis. Clin. Microbiol. Infect. 28, 1193–1202 (2022). [DOI] [PubMed] [Google Scholar]
  • 4.Klein E. Y., et al. , Global increase and geographic convergence in antibiotic consumption between 2000 and 2015. Proc. Natl. Acad. Sci. U.S.A. 115, E3463–E3470 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Van Boeckel T. P., et al. , Global antibiotic consumption 2000 to 2010: An analysis of national pharmaceutical sales data. Lancet Infect Dis. 14, 742–750 (2014). [DOI] [PubMed] [Google Scholar]
  • 6.Gaynes R., The discovery of Penicillin—New insights after more than 75 years of clinical use. Emerg. Infect. Dis. 23, 849–853 (2017). [Google Scholar]
  • 7.Hutchings M. I., Truman A. W., Wilkinson B., Antibiotics: Past, present and future. Curr. Opin. Microbiol. 51, 72–80 (2019). [DOI] [PubMed] [Google Scholar]
  • 8.Aminov R. I., A brief history of the antibiotic era: Lessons learned and challenges for the future. Front. Microbiol. 1, 134 (2010). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Centers for Disease Control and Prevention (CDC), Achievements in Public Health, 1900–1999: Control of Infectious Diseases. MMWR Morb Mortal Wkly Rep 48, 621–629 (1999). [PubMed] [Google Scholar]
  • 10.World Health Organization, "Antimicrobial resistance: Global report on surveillance" (World Health Organization, Geneva, 2014). [Google Scholar]
  • 11.Klein E. Y., et al. , Assessment of WHO antibiotic consumption and access targets in 76 countries, 2000–15: An analysis of pharmaceutical sales data. Lancet Infect. Dis. 21, 107–115 (2021). [DOI] [PubMed] [Google Scholar]
  • 12.Alshaikh F. S., Godman B., Sindi O. N., Seaton R. A., Kurdi A., Prevalence of bacterial coinfection and patterns of antibiotics prescribing in patients with COVID-19: A systematic review and meta-analysis. PLoS One 17, e0272375 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Karami Z., et al. , Few bacterial co-infections but frequent empiric antibiotic use in the early phase of hospitalized patients with COVID-19: Results from a multicentre retrospective cohort study in The Netherlands. Infect. Dis. 53, 102–110 (2021). [DOI] [PubMed] [Google Scholar]
  • 14.Calderon M., et al. , Bacterial co-infection and antibiotic stewardship in patients with COVID-19: A systematic review and meta-analysis. BMC Infect. Dis. 23, 14 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Chen N., et al. , Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: A descriptive study. Lancet 395, 507–513 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Nandi A., Pecetta S., Bloom D. E., Global antibiotic use during the COVID-19 pandemic: Analysis of pharmaceutical sales data from 71 countries, 2020–2022. EClinicalMedicine 57, 101848 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Jeon K., et al. , Impact of COVID-19 on antimicrobial consumption and spread of multidrug-resistance in bacterial infections. Antibiotics 11, 535 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Centers for Disease Control and Prevention, Centers for Disease Control and Prevention, National Center for Emerging and Zoonotic Infectious Diseases (NCEZID), Division of Healthcare Quality Promotion (DHQP), Outpatient Antibiotic Prescriptions—United States, 2022. (2023). https://www.cdc.gov/antibiotic-use/data/report-2022.html. Accessed 16 February 2024.
  • 19.Fleming-Dutra K. E., et al. , Prevalence of inappropriate antibiotic prescriptions among us ambulatory care visits, 2010–2011. JAMA 315, 1864 (2016). [DOI] [PubMed] [Google Scholar]
  • 20.Dingel J. I., Neiman B., How many jobs can be done at home? J. Public Econ. 189, 104235 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Otaigbe I. I., Elikwu C. J., Drivers of inappropriate antibiotic use in middle-income countries. JAC Antimicrob. Resist. 5, dlad062 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Schmiege D., Evers M., Kistemann T., Falkenberg T., What drives antibiotic use in the community? A systematic review of determinants in the human outpatient sector Int. J. Hygiene Environ. Health 226, 113497 (2020). [DOI] [PubMed] [Google Scholar]
  • 23.Department of Economic and Social Affairs Sustainable Development, United Nations, The 17 goals. https://sdgs.un.org/goals. Accessed 28 November 2023.
  • 24.Ayukekbong J. A., Ntemgwa M., Atabe A. N., The threat of antimicrobial resistance in developing countries: Causes and control strategies. Antimicrob. Resist. Infect. Control 6, 47 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Ikhimiukor O. O., Odih E. E., Donado-Godoy P., Okeke I. N., A bottom-up view of antimicrobial resistance transmission in developing countries. Nat. Microbiol. 7, 757–765 (2022). [DOI] [PubMed] [Google Scholar]
  • 26.Allcock S., et al. , Antimicrobial resistance in human populations: Challenges and opportunities. Global Health Epidemiol. Genom. 2, e4 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Lewnard J. A., Fries L. F., Cho I., Chen J., Laxminarayan R., Prevention of antimicrobial prescribing among infants following maternal vaccination against respiratory syncytial virus. Proc. Natl. Acad. Sci. U.S.A. 119, e2112410119 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Lewnard J. A., Lo N. C., Arinaminpathy N., Frost I., Laxminarayan R., Childhood vaccines and antibiotic use in low-and middle-income countries. Nature 581, 94–99 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Fu H., Lewnard J. A., Frost I., Laxminarayan R., Arinaminpathy N., Modelling the global burden of drug-resistant tuberculosis avertable by a post-exposure vaccine. Nat. Commun. 12, 424 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Kumar C. K., et al. , Global, regional, and national estimates of the impact of a maternal Klebsiella pneumoniae vaccine: A Bayesian modeling analysis. PLoS Med. 20, e1004239 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Klein E. Y., et al. , The impact of influenza vaccination on antibiotic use in the United States, 2010–2017. Open Forum Infect. Dis. 7, ofaa223 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Simmons B., et al. , Progress towards antibiotic use targets in eight high-income countries. Bull. World Health Organ. 99, 550–561 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Charani E., et al. , An analysis of existing national action plans for antimicrobial resistance—gaps and opportunities in strategies optimising antibiotic use in human populations. Lancet Global Health 11, e466–e474 (2023). [DOI] [PubMed] [Google Scholar]
  • 34.Walsh T. R., Gales A. C., Laxminarayan R., Dodd P. C., Antimicrobial resistance: Addressing a global threat to humanity. PLoS Med. 20, e1004264 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.United Nations General Assembly, Political declaration of the high-level meeting on antimicrobial resistance. (2024). https://www.un.org/pga/wp-content/uploads/sites/108/2024/09/FINAL-Text-AMR-to-PGA.pdf. Accessed 15 October 2024.
  • 36.Food and Drug Administration, FDA Drug Safety Communication: FDA advises restricting fluoroquinolone antibiotic use for certain uncomplicated infections; warns about disabling side effects that can occur together. (2016). https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-fda-advises-restricting-fluoroquinolone-antibiotic-use-certain. Accessed 7 May 2024.
  • 37.European Medicines Agency, Quinolone- and fluoroquinolone-containing medicinal products—Referral. (2018). https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products. Accessed 29 May 2024.
  • 38.Nguyen T. T. P., et al. , A national survey of dispensing practice and customer knowledge on antibiotic use in Vietnam and the implications. Antibiotics 11, 1091 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Mulchandani R., Wang Y., Gilbert M., Van Boeckel T. P., Global trends in antimicrobial use in food-producing animals: 2020 to 2030. PLoS Glob. Public Health 3, e0001305 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.World Health Organization, ATC/DDD Index 2023 (2023). https://www.whocc.no/atc_ddd_index/. Accessed 26 April 2023.
  • 41.World Bank, DataBank|Population estimates and projections (2023). https://databank.worldbank.org/source/population-estimates-and-projections. Accessed 21 September 2023.
  • 42.United Nations Department of Economic and Social Affairs, World Population Prospects 2022 (2022). https://population.un.org/wpp/. Accessed 22 February 2024.
  • 43.World Bank, World Bank country and lending groups. https://datahelpdesk.worldbank.org/knowledgebase/articles/906519. Accessed 4 April 2024.
  • 44.World Health Organization, “WHO Access, Watch, Reserve (AWaRe) classification of antibiotics for evaluation and monitoring of use, 2023” (World Health Organization, Geneva, Switzerland, 2023).
  • 45.Bernal J. L., Cummins S., Gasparrini A., Interrupted time series regression for the evaluation of public health interventions: A tutorial. Int. J. Epidemiol. 46, 348–355 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Turner S. L., et al. , Comparison of six statistical methods for interrupted time series studies: Empirical evaluation of 190 published series. BMC Med. Res. Methodol. 21, 134 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Appendix 01 (PDF)

Dataset S01 (XLSX)

pnas.2411919121.sd01.xlsx (137.4KB, xlsx)

Data Availability Statement

All study data are included in the article and/or supporting information.


Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES