BACKGROUND One of the greatest threats to global public health in the twenty first century is AMR (1-3) . AMR occurs when microorganisms such as bacteria, fungi, parasites, and viruses undergo evolutionary processes that make them resistant to antimicrobial drugs, such antibiotics which were previously used to treat them (1, 4, 5).This growing issue is mostly linked to the consequences of un-judicious use of antibiotics in a variety of settings, primarily in clinical treatment, farming, veterinary medicine, times of war, and the food chain (6-9). AMR, sometimes referred to as the "Silent Pandemic" demands prompt, total and effective action rather than being put off until a later time (10). According to the WHO, AMR in bacteria, viruses, and parasites is "one of the greatest challenges in public health" and may result into "a post-antimicrobial era" where prevalent illnesses could recur (11). Resistant pathogens have the potential to spread rapidly among patients, nations, and regions (12). Since AMR can spread over the borders, it is no longer a local concern but rather an international issue (13). According to 2019 statistics, the number of deaths attributed to AMR on a global scale exceeded 1.2 million. If effective strategies are not taken to counteract this menace, the number is expected to rise to almost 10 million deaths annually by 2050 (14) . The World Bank also estimates that drug-resistant diseases could cost the global economy up to 3.8% of its annual gross domestic product (GDP) by 2050 (15). AMR is a notable barrier to attaining the Sustainable Development Goals (SDG) framework's health-related objectives such as Universal Health Coverage (UHC). AMR is imperative to a number of other SDGs in addition to Goal 3, for example SDG 1 (no poverty), SDG 2 (zero hunger), and SDG 8 (decent work and economic growth) (16). It has disastrous effects on people's health and well-being, but also significantly affects financial prosperity. According to a World Bank evaluation, AMR will cause animal production to decline by 7.5% annually and world exports to drop up to 3.8%. By 2050, it will also lead to a $1 trillion increase in healthcare-related expenses (17). OBJECTIVE In this review, I highlighted a synopsis of the procedures used in the development of AMR, its global burden and factors that contribute to it, the information gaps that exist currently, monitoring parameters, and global mitigation strategies for AMR. METHODS A systematic literature search was conducted across multiple databases including PubMed, EMBASE, Science Daily, the Cochrane Database, AMR Journals, and Google Scholar for English-language articles published between January 1, 2013, and January 31, 2014 (102). The initial search yielded 41 references, of which 19 were selected after screening, while 22 were excluded due to irrelevance. Additionally, four older articles were included based on expert recommendation, resulting in a total of 23 articles for final analysis. The data were reviewed for inconsistencies and presented in both descriptive and tabular formats. Keywords included “Antimicrobial Resistance,” “AMR Mechanism,” “AMR on Public Health,” and “AMR Drivers” (102). RESULTS AMR as an Emerging Global Public Health Concern According to a recent estimate, AMR was linked to 3.57 million of the 4.95 million fatalities that occurred globally in 2019 (14), which is more than many other well-known causes of death, such as HIV/AIDS and malaria. The research indicates that the global burden of AMR surpasses the 700,000 annual deaths estimated by the WHO and the United Nations (25). AMR was once predicted to kill 10 million people annually by 2050 (26), however it has since been shown that the actual number is closer than previously believed. Globally, AMR developments varies greatly between different nations and frequently confront distinct main obstacles. AMR is a global issue affecting all countries, regardless of income. Although the development of new antibiotic classes once helped reduce infectious diseases, bacteria quickly developed resistance. For example, resistance to streptomycin in tuberculosis patients was reported just a year after its approval by the US FDA (19). When treating infections brought on by bacteria that produce a broad range of β-lactamases or are multidrug-resistant, antibiotics such as carbapenems and colistin are often reserved for last resort (27). One of the WHO's priority infections, Enterobacteriaceae, has become more resistant to carbapenems and colistin worldwide (28-30). Concerningly high resistance rates of about 83.35% were found in research for extensively drug-resistant (XDR) Klebsiella pneumoniae in newborn sepsis (31). Furthermore, multidrug resistance (MDR) was present in almost 500,000 new cases of rifampicin-resistant tuberculosis (RR-TB) that were detected globally in 2018 (32). The persistence of antibiotic tolerance can exacerbate medical conditions linked to diseases like HIV, cancers, and malaria (33). As the standard antibiotic treatment regimen becomes antiquated, the risks of AMR are expected to escalate sharply. This could potentially result in situations where patients who are terminally ill require palliative care, but the medications are no longer clinically effective (34). Additionally, hospital intensive care units (ICUs) could become breeding grounds for nosocomial MDR pathogens. Finally, it has been estimated by several studies that AMR-related diseases could cost USD 60–100 trillion by 2050, resulting in a 2% to 3.5% drop in the world total GDP (35-37). The ability of the human immune system to combat infectious infections is weakened by antibiotic resistance, which also increases the risk of many problems in susceptible individuals undergoing dialysis, surgery, chemotherapy, and joint replacement (38). Furthermore, antibiotic resistance will have a significant effect on individuals who have...