Fosfomycin
ANTIINFECTIVES FOR SYSTEMIC USE
Also known as: fosfomycin trometamol, fosfomycin tromethamine
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Fosfomycin is an ofp drug catalogued in DrugCentral. It was first approved by the FDA in 1996. DrugCentral lists 4 molecular targets, including murA, murA and murA1. Recorded indications include Enterococcus Urinary Tract Infection, Escherichia coli urinary tract infection and Urinary tract infectious disease.
- Approval status: ofp (first approved 1996 by the FDA).
- Molecular targets: murA, murA, murA1 and murA2 (4 listed in DrugCentral).
- Indications: Enterococcus Urinary Tract Infection, Escherichia coli urinary tract infection and Urinary tract infectious disease.
- ATC code: J01XX01 (Other antibacterials).
- Molecular formula: C3H7O4P; molecular weight 138.06 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (3)
- Enterococcus Urinary Tract Infection
- Escherichia coli urinary tract infection
- Urinary tract infectious disease
Contraindications (2)
- Kidney disease
- Pseudomembranous enterocolitis
Mechanism & targets
Molecular targets (4)
| Target | Gene | Action | Activity |
|---|---|---|---|
| UDP-N-acetylglucosamine 1-carboxyvinyltransferase | murA | inhibitor | IC50 7.00 |
| UDP-N-acetylglucosamine 1-carboxyvinyltransferase | murA | unknown | IC50 4.98 |
| UDP-N-acetylglucosamine 1-carboxyvinyltransferase 1 | murA1 | unknown | — |
| UDP-N-acetylglucosamine 1-carboxyvinyltransferase 2 | murA2 | unknown | — |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1996-12-19 | FDA | — | ZAMBON SPA |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
J01XX01 | ANTIINFECTIVES FOR SYSTEMIC USE › ANTIBACTERIALS FOR SYSTEMIC USE › OTHER ANTIBACTERIALS › Other antibacterials |
S02AA17 | SENSORY ORGANS › OTOLOGICALS › ANTIINFECTIVES › Antiinfectives |
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Cardiospasm | 793.1 |
| Palmoplantar keratoderma | 769.2 |
| Pruritus genital | 729.5 |
| Sleep terror | 723.2 |
| Atrial tachycardia | 685.7 |
| Carotid artery occlusion | 670.2 |
| Tension headache | 654.9 |
| Anosmia | 609.9 |
| Facial pain | 587.0 |
| Immunisation | 549.1 |
| Pain of skin | 522.1 |
| Subarachnoid haemorrhage | 476.1 |
Chemical structure
| Molecular formula | C3H7O4P |
|---|---|
| Molecular weight | 138.06 g/mol |
| CAS number | — |
| InChIKey | YMDXZJFXQJVXBF-STHAYSLISA-N |
| PubChem CID | 446987 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Fosfomycin used for?
DrugCentral lists the following indications for Fosfomycin: Enterococcus Urinary Tract Infection, Escherichia coli urinary tract infection and Urinary tract infectious disease.
How does Fosfomycin work?
Its molecular targets in DrugCentral include murA (inhibitor), murA, murA1 and murA2.
When was Fosfomycin first approved?
Fosfomycin was first approved by the FDA in 1996.
What is the chemical formula of Fosfomycin?
Fosfomycin has the molecular formula C3H7O4P and a molecular weight of 138.06 g/mol.
Browse: all drugs starting with F · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 1243 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1200331 — compound record and bioactivity
- PubChem CID 446987 — chemical identifiers
- DrugBank DB00828 — drug record
- FDA UNII 2N81MY12TE — substance identity
- DailyMed: FDA labels for Fosfomycin — current prescribing information (label search)
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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