Updated: January 19, 2026
Fosfomycin Shortage: What Providers and Prescribers Need to Know in 2026
Author
Peter Daggett

Summarize with AI
- Current Supply Status: National vs. Local Availability
- The IV Formulation: Contepo (Fosfomycin for Injection)
- When to Prescribe Fosfomycin: Clinical Indications and Stewardship
- Evidence-Based Alternatives When Fosfomycin Is Unavailable
- Practical Steps for Providers: Reducing Patient Burden
- Drug Interactions and Prescribing Alerts
A clinical update for providers on fosfomycin availability in 2026: current supply status, alternatives, stewardship guidance, and how to help patients find it.
Fosfomycin (Monurol; fosfomycin tromethamine) continues to be a widely recommended first-line agent for uncomplicated urinary tract infections (UTIs) per IDSA guidelines. However, prescribers are increasingly hearing from patients who cannot fill the prescription at their preferred pharmacy. This guide summarizes the current supply situation, provides evidence-based alternatives, and offers practical tools to help your patients access treatment.
Current Supply Status: National vs. Local Availability
As of 2026, oral fosfomycin tromethamine is NOT listed in the FDA Drug Shortage Database as a national shortage. At the manufacturer and distributor levels, overall supply is considered adequate. Generic fosfomycin tromethamine is now FDA-approved and commercially available, complementing the brand Monurol.
However, individual retail pharmacies frequently carry low stock quantities — often fewer than 10 packets on hand — due to fosfomycin's single-dose nature and the resulting slow per-unit inventory turnover. A handful of prescriptions can deplete a pharmacy's entire supply within days. These are localized gaps, not a systemic shortage, but they generate significant patient friction.
The IV Formulation: Contepo (Fosfomycin for Injection)
In November 2025, the FDA approved intravenous fosfomycin (Contepo; Meitheal Pharmaceuticals) for adults with complicated UTIs (cUTIs) including acute pyelonephritis caused by susceptible E. coli and Klebsiella pneumoniae. This approval was supported by the phase 2/3 ZEUS trial, which demonstrated non-inferiority to piperacillin-tazobactam with an overall success rate of 63.5% versus 55.6%. This hospital-administered IV product is separate from the retail oral supply chain and does not affect outpatient availability.
Contepo is relevant for inpatient infectious disease and hospitalist providers managing resistant cUTIs, but does not alter the ambulatory prescribing landscape for oral fosfomycin.
When to Prescribe Fosfomycin: Clinical Indications and Stewardship
Oral fosfomycin (3g single dose) is FDA-approved for uncomplicated UTI (acute cystitis) in women caused by susceptible E. coli and E. faecalis. Key prescribing considerations include:
First-line preference: Particularly valuable in patients with known sulfa allergy (ruling out TMP-SMX), penicillin allergy, renal impairment that contraindicates nitrofurantoin, or documented resistance to other first-line agents.
MDR organisms: Fosfomycin retains activity against many ESBL-producing E. coli and other multidrug-resistant pathogens. Susceptibility testing should be specifically requested, as many laboratory panels do not include fosfomycin as a default.
Pregnancy: IDSA guidelines list fosfomycin as an acceptable option for UTIs during pregnancy. The oral bioavailability is 37%, concentrating in the urine.
NOT for pyelonephritis: Oral fosfomycin does not achieve adequate serum concentrations for upper tract infections. Reserve pyelonephritis treatment for fluoroquinolones (where susceptible) or IV agents.
Evidence-Based Alternatives When Fosfomycin Is Unavailable
IDSA 2011 guidelines (the most recent comprehensive UTI guidelines) designate three first-line agents for uncomplicated cystitis in women:
Nitrofurantoin macrocrystals/monohydrate (Macrobid): 100 mg BID × 5 days. Bacterial eradication rates consistently above 90% for E. coli. Avoid if CrCl < 30 mL/min.
TMP-SMX (Bactrim DS): 160/800 mg BID × 3 days. Appropriate when local resistance rates <20%. Not for sulfa allergy or near delivery in pregnancy.
Fosfomycin: 3g oral single dose. The drug in question; see alternatives above when unavailable.
Second-line alternatives include cephalexin 500 mg BID × 7 days. Fluoroquinolones should be reserved for complicated UTIs or culture-directed therapy due to resistance concerns and FDA safety warnings.
Practical Steps for Providers: Reducing Patient Burden
Specify generic substitution acceptable: Write "fosfomycin tromethamine 3g" and indicate generic substitution is acceptable, since some pharmacies stock only generic and not brand Monurol.
Send an alternate Rx concurrently: Consider sending a nitrofurantoin or TMP-SMX prescription alongside fosfomycin with instructions to fill only one, so the patient doesn't need to call back if fosfomycin is unavailable.
Direct patients to medfinder: medfinder for Providers (medfinder.com/providers) is a tool that contacts pharmacies near your patient to identify which ones have the medication in stock, eliminating the need for patients to make multiple calls.
Drug Interactions and Prescribing Alerts
Metoclopramide: Reduces fosfomycin absorption by increasing GI motility. Separate dosing or use an alternative antibiotic if metoclopramide is being used.
Live bacterial vaccines: Contraindicated concurrently with fosfomycin (BCG, cholera, typhoid). Complete antibiotic therapy before vaccine administration.
QTc prolongation (IV Contepo only): The IV formulation has interactions with QTc-prolonging agents (amiodarone, azithromycin, etc.). This is not a concern for the standard oral dose.
For a full provider guide on helping your patients locate fosfomycin, see our resource: How to Help Your Patients Find Fosfomycin In Stock. You can also enroll your practice at medfinder.com/providers
Frequently Asked Questions
Yes, in appropriate clinical situations. Fosfomycin remains a IDSA first-line agent for uncomplicated cystitis. Pharmacy-level gaps are real but usually resolve within 24-48 hours. Consider also noting on the prescription that generic fosfomycin tromethamine is acceptable, as it expands pharmacy options.
Fosfomycin retains activity against many ESBL-producing E. coli isolates. However, susceptibility must be confirmed by culture, as fosfomycin is not routinely included in standard susceptibility panels. Specifically requesting fosfomycin testing is advisable when managing documented ESBL UTIs.
Yes, multidose oral fosfomycin (3g every 48-72 hours for 6-21 days, typically 3 doses) is used off-label for complicated UTIs excluding pyelonephritis or bacteremia. This is distinct from the FDA-approved single-dose indication. Evidence is largely observational but supports use in appropriately selected patients.
Oral fosfomycin (Category B) is included in IDSA recommendations for UTI treatment during pregnancy. It is particularly useful when other first-line agents are contraindicated. Counsel patients on the limited controlled data in pregnancy and use clinical judgment.
medfinder (medfinder.com/providers) is a pharmacy-finding service that contacts pharmacies near the patient to identify which ones have the prescription in stock. You can recommend it directly to patients or integrate it into your after-visit patient instructions.
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