VetSheet

Ceftriaxone

Ceftriaxone sodium

Antibiotic - 3rd Generation CephalosporinIVIMSCIntraosseousDogsCatsHorses

Also known as: Rocephin · ceftriaxonum natricum · Ro-139904 · Ro-13-9904/000

Reviewed by the VetSheet Veterinary TeamUpdated Apr 5, 2026Evidence-based veterinary reference

Audited v13 dosing evidence

Structured calculator evidence

Borreliosis | Lyme disease | Borrelia burgdorferi infection (extra-label)

25 mg/kgIVSC

Verified clinician required

  • q24h

NA

Governing clinical context (2)
  • NOTE: In humans, it is recommended that IV infusions be administered over 30 minutes (60 minutes in neonates) at concentrations between 10 – 40 mg/mL. 9
  • The sterile powder for reconstitution should be stored between 20°C to 25°C (68°F-77°F) and protected from light.
High riskVerified clinician requiredformularyProtocol 2023Audit dose-audit-plumb-v13

Doses are a clinical reference for licensed veterinary professionals. Always confirm against the current label and the individual patient.

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Overview

Ceftriaxone is a potent, injectable third-generation cephalosporin antibiotic.

  • Broad Spectrum: It retains the gram-positive activity of first- and second-generation agents but features significantly expanded gram-negative coverage (e.g., Enterobacteriaceae).
  • Clinical Utility: Often reserved for serious infections where less expensive agents are ineffective, or to avoid the nephrotoxicity associated with aminoglycosides.
  • Key Advantages: Exhibits excellent penetration into the central nervous system (CNS), making it highly effective for meningitis. Its long half-life and activity against Borrelia burgdorferi also make it a viable option for treating Lyme disease.

Mechanism of action

Like all beta-lactam antibiotics, ceftriaxone is bactericidal.

  • Mechanism: It binds to specific ​penicillin-binding proteins (PBPs)​ located inside the bacterial cell wall.
  • Pathway: Binding to PBPs → Inhibition of the third and final stage of bacterial cell wall synthesis → Disruption of peptidoglycan cross-linking → Autolysin-mediated bacterial cell lysis and death.

Safety & warnings

Contraindications

  • Prior allergic reaction to cephalosporins

Adverse effects

  • Pain on IM injection
  • Hypersensitivity reactions (rash)
  • Granulocytopenia / thrombocytopenia
  • Diarrhea
  • Mild azotemia
  • Biliary sludging (at very high doses)
  • Increased liver enzymes, BUN, and creatinine

Precautions

Important: Give IV injections slowly over at least 30 minutes to minimize adverse reactions.

  • Hypersensitivity: Contraindicated in patients with known cephalosporin allergies. Use with caution in penicillin-allergic patients due to potential cross-reactivity.
  • Hepatic/Coagulation Issues: Use cautiously in patients with severe hepatic disease or vitamin K synthesis abnormalities, as cephalosporins can rarely affect bleeding times.
  • Renal Impairment: Dosage adjustments may be necessary in severe uremia, especially if concomitant hepatic impairment exists.
  • Biliary Sludging: High doses may cause biliary sludging (pseudolithiasis), particularly noted in dogs at very high doses (100 mg/kg/day).

Drug interactions

Aminoglycosides / Nephrotoxic drugs

Potential additive nephrotoxicity; in vitro studies show synergistic or additive antibacterial activity.

Calcium

Concomitant use with calcium-containing solutions has caused fatal calcium-ceftriaxone precipitates in neonates. Do not mix with calcium or administer within 48 hours of ceftriaxone.

Monitoring

  • Clinical efficacy
  • CBC (with long-term therapy)
  • Renal function (BUN, Serum Creatinine, urinalysis)
  • Liver enzymes (AST, ALT)

Pharmacokinetics

Half-life

DogsIV: 0.88 hrs, IM: 1.17 hrs, SC: 1.73 hrs

Absorption

Not absorbed after oral administration; must be given parenterally. In dogs, IM and SC bioavailability equals IV. Peak levels occur faster after IM (~30 minutes) than SC (~80 minutes).

Distribution

Widely distributed throughout the body. CSF levels are higher when meninges are inflamed. Crosses the placenta and enters maternal milk in low concentrations.

Metabolism

Not extensively metabolized.

Elimination

Excreted by both renal and non-renal (biliary) mechanisms.

Overdose

Limited information is available regarding acute toxicity. Overdoses should be monitored and treated symptomatically and supportively if required.

Available products

Formulations

  • Injection powder for solution

Human-labeled

  • Ceftriaxone Injection Powder for Solution: 250 mg, 500 mg, 1 g, 2 g, & 10 g (as base) in vials, single-use duplex containers, and in bulk

Regulatory status

No regulatory data for: 🇺🇸 US · 🇪🇺 EU · 🇬🇧 UK · 🇭🇰 HK · 🇹🇼 TW · 🇯🇵 JP · 🇰🇷 KR · 🇦🇺 AU

Storage & stability

Store sterile powder at or below 25°C and protect from light. Reconstituted solutions (100 mg/mL) are stable for 3 days at room temperature and 10 days refrigerated. Solutions of 250 mg/mL are stable for 24 hours at room temperature and 3 days refrigerated. Frozen solutions (10-40 mg/mL) at -20°C are stable for 26 weeks.

Client information

Note: Ceftriaxone is an injectable medication typically administered in a hospital setting by veterinary professionals.

  • Injection Site Pain: Your pet may experience some pain or discomfort at the site of an intramuscular (IM) injection.
  • Gastrointestinal Upset: Watch for signs of diarrhea or loose stools, which can occur with many antibiotics.
  • Allergic Reactions: Contact your veterinarian immediately if you notice signs of an allergic reaction, such as facial swelling, hives, rash, or difficulty breathing.
  • Monitoring: If your pet is receiving this medication long-term, your veterinarian may recommend periodic blood tests to monitor liver and kidney function.

VetSheet drug reference is intended for licensed veterinary professionals as a clinical decision-support aid, not a substitute for professional judgement or the manufacturer’s current label.