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Third-generation cephalosporin Pregnancy: Ceftriaxone crosses the placental barrier; limited data in pregnant women. Should only be administered during pregnancy, in particular the first trimester, if the benefit outweighs the risk. Excreted into human milk in low concentrations; at therapeutic doses no effects on breastfed infants anticipated (risk of diarrhoea and fungal mucosal infection cannot be excluded).

Ceftriaxone

Brand names: Rocephin

Used in: Sepsis Pneumonia Meningitis & Encephalitis

Ceftriaxone is a third-generation cephalosporin given intravenously or intramuscularly for serious infections, including bacterial meningitis, sepsis and gonorrhoea. Its long half-life permits once-daily dosing.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: 1-2 g
Route: Intravenous or intramuscular
Frequency: Once daily
Max: 4 g daily
Adults and children over 12 years (>=50 kg). Dose depends on severity, susceptibility, site and type of infection and on hepato-renal function. Per SPC table: 1-2 g once daily for community acquired pneumonia, acute exacerbations of COPD, intra-abdominal infections and complicated urinary tract infections (including pyelonephritis); 2 g once daily for hospital acquired pneumonia, complicated skin and soft tissue infections and infections of bones and joints; 2-4 g once daily for management of neutropenic patients with fever suspected bacterial, bacterial endocarditis and bacterial meningitis. In documented bacteraemia the higher end of the range should be considered. Twice daily (12 hourly) administration may be considered where doses greater than 2 g daily are administered. Specific schedules: acute otitis media 1-2 g as a single IM dose (may be 1-2 g daily IM for 3 days if severely ill or previous therapy failed); pre-operative prophylaxis of surgical site infections 2 g as a single pre-operative dose; gonorrhoea 500 mg as a single IM dose; syphilis 500 mg-1 g once daily increased to 2 g once daily for neurosyphilis for 10-14 days (limited data; follow national/local guidance); disseminated Lyme borreliosis 2 g once daily for 14-21 days. Duration: continue for 48-72 hours after the patient has become afebrile or bacterial eradication achieved. Paediatric (SPC): children with bodyweight 50 kg or more should receive the usual adult dosage; for children 15 days to 12 years (<50 kg) and neonates 0-14 days the SPC gives weight-based dosing (see paediatric formulary) — ceftriaxone is contraindicated in premature neonates up to a postmenstrual age of 41 weeks; verify all paediatric dosing against a children's formulary.

Dose adjustments

Renal

In impaired renal function there is no need to reduce the dosage provided hepatic function is not impaired. Only in preterminal renal failure (creatinine clearance <10 mL/min) should the ceftriaxone dosage not exceed 2 g daily. In mild or moderate hepatic impairment no dose adjustment needed provided renal function is not impaired.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

US labelling (FDA)

Reference — US labelling, may differ from UK

DOSAGE AND ADMINISTRATION Ceftriaxone may be administered intravenously or intramuscularly. Do not use diluents containing calcium, such as Ringer’s solution or Hartmann’s solution, to reconstitute ceftriaxone vials or to further dilute a reconstituted vial for IV administration because a precipitate can form. Precipitation of ceftriaxone-calcium can also occur when ceftriaxone is mixed with calcium-containing solutions in the same IV administration line. Ceftriaxone must not be administered simultaneously with calcium-containing IV solutions, including continuous calcium-containing infusions such as parenteral nutrition via a Y-site. However, in patients other than neonates, ceftriaxone …

Source: US FDA prescribing information (openFDA / DailyMed), label dated 2026-01-19. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.

Contraindications

  • Hypersensitivity to ceftriaxone, to any other cephalosporin, or to any of the excipients
  • History of severe hypersensitivity (e.g. anaphylactic reaction) to any other type of beta-lactam antibacterial agent (penicillins, monobactams and carbapenems)
  • Premature neonates up to a postmenstrual age of 41 weeks (gestational age + chronological age)
  • Full-term neonates (up to 28 days) with hyperbilirubinaemia, jaundice, or who are hypoalbuminaemic or acidotic
  • Full-term neonates (up to 28 days) if they require or are expected to require intravenous calcium treatment or calcium-containing infusions (risk of ceftriaxone-calcium precipitation)
  • Ceftriaxone solutions containing lidocaine must never be administered intravenously; contraindications to lidocaine must be excluded before IM injection when lidocaine is the solvent

Side effects

  • Eosinophilia, leucopenia, thrombocytopenia
  • Diarrhoea, loose stools, nausea, vomiting
  • Rash, pruritus, urticaria
  • Hepatic enzyme increased
  • Phlebitis, injection site pain, pyrexia

Clinical monograph

How it works

It is a beta-lactam that binds penicillin-binding proteins and inhibits bacterial cell-wall synthesis, producing a bactericidal effect with good central nervous system penetration.

Prescribing in practice

  • Never co-administer with calcium-containing intravenous fluids in neonates, as fatal ceftriaxone-calcium precipitates may form; avoid altogether in jaundiced neonates.
  • Use with caution in penicillin allergy because of the potential for cross-reactivity, and avoid where there is a history of severe (immediate) beta-lactam hypersensitivity.
  • It can cause biliary pseudolithiasis ('biliary sludge'), which is usually reversible on stopping treatment.

Monitoring

Monitor for hypersensitivity and clinical response; consider full blood count and liver and renal function during prolonged or high-dose therapy, and remain alert to antibiotic-associated diarrhoea. Use in line with local antimicrobial guidance and stewardship principles.

Counselling the patient

  • Report any rash, swelling, breathlessness or other signs of an allergic reaction promptly.
  • Tell staff about any previous reaction to penicillins or cephalosporins.
  • Seek advice if severe or persistent diarrhoea develops during or after treatment.

Evidence & guidelines

A standard agent in UK empirical regimens for meningitis, sepsis and gonorrhoea; use should follow local antimicrobial guidance.

Reference: NICE NG240 Bacterial Meningitis; PHE guidelines; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.

📚 MRCEM Revision

Featured in these MRCEM clinical pathways

Ceftriaxone is a core drug in the following exam-focused workups on our sister siteReviseMRCEM.

MRCEM Primary / Intermediate / OSCE candidates: each pathway includes exam-style questions, RCEM/NICE citations, and FAQ summaries.