Antimicrobial Atlas

Evidence-based antimicrobial
knowledge, organized.

A structured reference for antimicrobial agents, pathogens and stewardship — built for clinical pharmacists, physicians, microbiologists and students.

CeftriaxoneVancomycinMeropenemAzithromycin
Antimicrobial Stewardship

Using antimicrobials safely, effectively, and responsibly.

Antimicrobial stewardship (AMS) is an interprofessional effort focused on timely, appropriate antimicrobial use — improving outcomes for the individual patient while protecting the effectiveness of these drugs for everyone else.

Timely and optimal antimicrobial selection
Appropriate drug selection
Correct dose
Appropriate duration
Appropriate route of administration
Prevention of unnecessary antimicrobial exposure
Improving clinical outcomes
Minimizing antimicrobial resistance
Reducing ecological/adverse effects such as C. difficile infection
WHO

World Health Organization

Antimicrobial stewardship (AMS) is defined as a coherent set of actions that promote the responsible use of antimicrobials. This definition can be applied at the individual, national, and global levels, and across human health, animal health, and environmental health.

CDC

Centers for Disease Control and Prevention

Antimicrobial stewardship is defined as the use of the right antimicrobial, for the right patient, at the right time, at the right dose, and for the right duration, causing the least harm to the patient and future patients.

IDSA

Infectious Diseases Society of America

Antimicrobial stewardship refers to interventions designed to improve and measure the appropriate use of antimicrobials by promoting the selection of the optimal antimicrobial drug regimen, dose, duration of therapy, and route of administration.

The 8 Ds of Antimicrobial Stewardship

A practical framework for every antimicrobial decision. Tap a card to expand it.

Make the right clinical diagnosis.

Use the right antimicrobial drug according to the suspected or confirmed pathogen, infection site, allergies, resistance patterns, and patient-specific factors.

Use the right dose according to the infection, patient characteristics, renal/hepatic function, and other relevant factors.

Perform appropriate microbiological investigations to establish the etiologic agent whenever appropriate.

Narrow-spectrum therapy and/or adjust antimicrobial therapy when appropriate based on clinical response and microbiological results.

Administer antimicrobials only for the recommended duration.

Provide appropriate source control, including drainage of abscesses and removal of necrotic tissue or foreign material when required.

Implement infection-prevention and control measures to prevent transmission of infection.

AMS as a clinical decision framework

The same 8 Ds, arranged as the sequence a stewardship-minded clinician follows.

  1. 01

    Diagnosis

  2. 02

    Microbiological investigation

  3. 03

    Right drug

  4. 04

    Right dose

  5. 05

    Right route

  6. 06

    De-escalation

  7. 07

    Right duration

  8. 08

    Source control

  9. 09

    Infection prevention & control

Antimicrobial agents

Penicillins

Beta-lactams that block cell-wall synthesis; foundational and widely combined with inhibitors.

Beta-lactam ring, PBP binding1 in atlas

Cephalosporins

Generational beta-lactams with broadening gram-negative coverage across generations.

Generational spectrum shift1 in atlas

Carbapenems

Broadest-spectrum beta-lactams, often reserved for resistant gram-negative infections.

Ultra-broad spectrum1 in atlas

Macrolides

Protein-synthesis inhibitors valued for atypical pathogen coverage.

50S ribosomal binding1 in atlas

Fluoroquinolones

DNA gyrase/topoisomerase inhibitors with broad oral bioavailability.

DNA gyrase inhibition0 in atlas

Aminoglycosides

Concentration-dependent agents requiring careful renal and ototoxicity monitoring.

Concentration-dependent killing0 in atlas

Stewardship

Empirical antimicrobial therapy

Selecting a starting regimen before culture results return — through to de-escalation, IV-to-oral switch, dose and duration optimization.

Database

Antibiotic database

Cephalosporin

Ceftriaxone

Label lists activity in vitro and in clinical infections against most isolates of many Gram-negative organisms (e.g. E. coli, K. pneumoniae, H. influenzae, N. gonorrhoeae, N. meningitidis), Gram-positive organisms (e.g. S. aureus, S. pneumoniae, S. pyogenes) and some anaerobes. No activity against Chlamydia trachomatis; most C. difficile strains are resistant.

Lower respiratory tract infectionsAcute bacterial otitis media

Source-verified clinical information · Last reviewed: October 2026

References

Glycopeptide

Vancomycin

Label lists activity in vitro and in clinical infections against most isolates of Corynebacterium spp., Enterococcus spp. (including E. faecalis), Staphylococcus aureus (methicillin-resistant and -susceptible), coagulase-negative staphylococci, Streptococcus gallolyticus and viridans group streptococci. Not active in vitro against Gram-negative bacilli, mycobacteria or fungi.

SepticemiaInfective endocarditis

Source-verified clinical information · Last reviewed: October 2026

References

Carbapenem

Meropenem

Label lists activity in vitro and in clinical infections against most isolates of E. faecalis (vancomycin-susceptible), methicillin-susceptible S. aureus, streptococci (S. agalactiae, penicillin-susceptible S. pneumoniae, S. pyogenes, viridans group), E. coli, H. influenzae, K. pneumoniae, N. meningitidis, P. mirabilis, P. aeruginosa, and Bacteroides and Peptostreptococcus spp. No in vitro activity against MRSA or methicillin-resistant S. epidermidis.

Complicated skin and skin structure infections (adults and pediatric patients ≥3 months)Complicated intra-abdominal infections (complicated appendicitis and peritonitis; adult and pediatric patients)

Source-verified clinical information · Last reviewed: October 2026

References

Macrolide

Azithromycin

Label lists activity in vitro and in clinical infections against most isolates of S. aureus, S. agalactiae, S. pneumoniae, S. pyogenes, H. ducreyi, H. influenzae, M. catarrhalis, N. gonorrhoeae, Chlamydophila pneumoniae, Chlamydia trachomatis and Mycoplasma pneumoniae. Cross-resistance with erythromycin is demonstrated.

Adults: acute bacterial exacerbations of chronic bronchitis; acute bacterial sinusitisAdults and pediatric patients ≥6 months: community-acquired pneumonia in patients appropriate for oral therapy

Source-verified clinical information · Last reviewed: October 2026

References

Microbiology

Microbiology & pathogens

Gram-positive

Thick peptidoglycan cell wall retaining crystal violet stain; includes staphylococci, streptococci and enterococci (demo).

Gram-negative

Thin peptidoglycan layer with an outer membrane; includes Enterobacterales and non-fermenters like Pseudomonas (demo).

Anaerobes

Organisms that grow without oxygen, relevant in intra-abdominal and odontogenic infections (demo).

Culture

Growing organisms from a clinical specimen to identify the causative pathogen and guide targeted therapy (demo).

MIC

Minimum inhibitory concentration — the lowest antibiotic concentration that prevents visible growth (demo).

Susceptibility

Interpretation of MIC against breakpoints to classify an isolate as susceptible, intermediate or resistant (demo).

Clinical tools

Resistance Atlas

Browse resistance mechanisms — ESBL, AmpC, MRSA, VRE and carbapenem resistance.

Coming soon

Renal Dose Calculator

Future tool: adjust dosing regimens against renal function tiers.

Resources & references

WHO

World Health Organization — AMS guidance

Global antimicrobial stewardship policy and technical guidance.

CDC

CDC — Core Elements of Antibiotic Stewardship

Core elements for hospital, outpatient and nursing home stewardship programs.

IDSA

IDSA — Stewardship guidelines

Clinical practice guidelines for implementing an antimicrobial stewardship program.