# Fosfomycin Use in Treating Severe Difficult-to-Treat Gram-Negative Infections—A Comprehensive Review

**Authors:** Despoina Koulenti, Jean-François Timsit

PMC · DOI: 10.3390/antibiotics15030234 · Antibiotics · 2026-02-24

## TL;DR

Fosfomycin, an older antibiotic, is being reconsidered for treating severe infections caused by drug-resistant Gram-negative bacteria due to its unique properties and effectiveness in combination therapies.

## Contribution

This paper provides a comprehensive review of fosfomycin's use in severe infections caused by difficult-to-treat Gram-negative bacteria.

## Key findings

- Fosfomycin's IV formulation is increasingly used in critically ill patients with multidrug-resistant infections.
- It shows synergy with other antibiotics and has a favorable pharmacokinetic profile with good tissue penetration.
- Safety data for higher doses are limited, but it is generally well-tolerated with mostly non-serious side effects.

## Abstract

Background/Objectives: Fosfomycin is an old antimicrobial agent historically used in its oral formulation for uncomplicated urinary tract infections. In the current context of rising antimicrobial resistance and limited antimicrobial options, fosfomycin has attracted renewed interest. Methods: A comprehensive review on the IV fosfomycin use focusing on critically ill patients and/or severe infections due to difficult-to-treat (DTR) Gram-negative bacilli (GNB). Results: Fosfomycin’s IV formulation is now being used more widely, particularly in critically ill patients with multidrug-resistant (MDR) or DTR-GNB infections. It offers several attractive features: a unique mechanism of action that minimizes cross-resistance; a broad spectrum of activity, covering both Gram-negative and Gram-positive pathogens; and consistent synergy with multiple pivotal antimicrobials. Its pharmacokinetic/pharmacodynamic (PK/PD) profile is favorable, with extensive tissue penetration, including the central nervous system. The ratio of area under the concentration–time curve to the minimum inhibitory concentration of the pathogen (AUC/MIC) is considered the optimal PK/PD target for fosfomycin. The adverse events are mainly non-serious (most frequently, hypernatremia and hypokalemia), although safety data for higher dosing regimens remain limited. Growing clinical evidence supports IV fosfomycin as an effective and well-tolerated component of combination therapy for severe infections in critically ill patients, including those infections caused by extended-spectrum beta-lactamases-, carbapenemase-producing Enterobacterales, and DTR non-fermentative GNB. Nevertheless, as with many rediscovered antimicrobials, its expanded role requires confirmation through rigorously designed clinical trials to better define its efficacy, optimal use, and safety profile in the treatment of severe DTR-GNB infections.

## Linked entities

- **Chemicals:** fosfomycin (PubChem CID 441029)

## Full-text entities

- **Genes:** MBL3P (mannose-binding lectin family member 3, pseudogene) [NCBI Gene 50639] {aka COLEC2, MBL}, SLC37A1 (solute carrier family 37 member 1) [NCBI Gene 54020] {aka G3PP, SPX1}
- **Diseases:** injury to (MESH:D014947), Septic shock (MESH:D012772), respiratory tract infections (MESH:D012141), Ambler class B MBL (MESH:D006509), CRAB infection (MESH:D007239), nausea (MESH:D009325), torsade de pointes (MESH:D016171), DTR (MESH:D019553), bacterial infections (MESH:D001424), KPC (MESH:C565455), Renal Disease (MESH:D007674), death (MESH:D003643), bone and joint infections (MESH:D001847), K. pneumoniae (MESH:D011014), heart disease (MESH:D006331), bacteremia (MESH:D016470), hypocalcemia (MESH:D006996), QT interval prolongation (MESH:D008133), neutropenia (MESH:D009503), CRPA (MESH:D011552), laboratory abnormalities (MESH:D007757), ESBLs (MESH:C579922), toxicity (MESH:D064420), skin and soft tissue infections (MESH:D018461), critical illness (MESH:D016638), Hypokalemia (MESH:D007008), hyperaldosteronism (MESH:D006929), TDM (MESH:D000081015), AMR (MESH:D060467), bacteremic (MESH:D016870), VAP (MESH:D053717), headache (MESH:D006261), gastrointestinal events (MESH:D005767), CNS infections (MESH:D002494), HAP (MESH:D000077299), acute kidney injury (MESH:D058186), cUTIs (MESH:D014552), BSIs (MESH:D018805), infective endocarditis (MESH:D004696), community-acquired pneumonia (MESH:D003147), ICU (MESH:C000657744), MRSA (MESH:D013203), cUTI (MESH:D000092182), diarrhea (MESH:D003967), Infectious Diseases (MESH:D003141), heart failure (MESH:D006333), electrolyte disorders (MESH:D014883), hypertension (MESH:D006973), vomiting (MESH:D014839), DTR-GNB (MESH:D016905), renal insufficiency (MESH:D051437), ventricular arrhythmias (MESH:D001145), inflammatory (MESH:D007249), pyelonephritis (MESH:D011704), intra-abdominal infections (MESH:D059413), head injury (MESH:D006259), MDR (MESH:D018088), rectal colonization (MESH:D003108), Hypernatremia (MESH:D006955), hypophosphatemia (MESH:D017674)
- **Chemicals:** methicillin (MESH:D008712), CZA (-), ampicillin/sulbactam (MESH:C035444), meropenem (MESH:D000077731), Glycerol 3-Phosphate (MESH:C029620), eravacycline (MESH:C571179), calcium (MESH:D002118), ceftriaxone (MESH:D002443), cefiderocol (MESH:C000612166), oxazolidinones (MESH:D023303), beta-lactam (MESH:D047090), Carbapenem (MESH:D015780), ceftazidime (MESH:D002442), AG (MESH:D012834), ceftolozane-tazobactam (MESH:C000594038), Fosfomycin (MESH:D005578), potassium (MESH:D011188), F (MESH:D005461), cephalosporin (MESH:D002511), reactive oxygen intermediate (MESH:D017382), creatinine (MESH:D003404), sulbactam-durlobactam (MESH:C000714947), sodium (MESH:D012964), piperacillin-tazobactam (MESH:D000077725), aminoglycosides (MESH:D000617), UDP-N-acetylglucosamine (MESH:D014537), fluoroquinolones (MESH:D024841), penicillin (MESH:D010406), vancomycin (MESH:D014640), ceftazidime avibactam (MESH:C000595613), tigecycline (MESH:D000078304), N-acetylmuramic acid (MESH:C031651), phosphonic acid (MESH:C570063), PEP (MESH:D010728), cotrimoxazole (MESH:D015662), Sulbactam (MESH:D013407)
- **Species:** Staphylococcus aureus (species) [taxon 1280], Proteus vulgaris (species) [taxon 585], Enterobacterales (order) [taxon 91347], Staphylococcus epidermidis (species) [taxon 1282], Streptococcus pyogenes (species) [taxon 1314], Homo sapiens (human, species) [taxon 9606], Bacteroides sp. (species) [taxon 29523], Enterobacter (genus) [taxon 547], Acinetobacter baumannii (species) [taxon 470], Legionella pneumophila (species) [taxon 446], Pseudomonas aeruginosa (species) [taxon 287], Stenotrophomonas maltophilia (species) [taxon 40324], Proteus mirabilis (species) [taxon 584], Morganella morganii (species) [taxon 582], Streptomyces (genus) [taxon 1883], Staphylococcus saprophyticus (species) [taxon 29385], Escherichia coli (E. coli, species) [taxon 562], Klebsiella pneumoniae (species) [taxon 573], Enterococcus (genus) [taxon 1350], Citrobacter (genus) [taxon 544]

## Full text

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## References

77 references — full list in the complete paper: https://tomesphere.com/paper/PMC13024457/full.md

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Source: https://tomesphere.com/paper/PMC13024457