Ceftriaxone
Brand names: Rocephin
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.
Adult dose
Dose adjustments
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 UKDOSAGE 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.
- Difficult Airway Algorithm (DAS) · DAS 2015; Royal College of Anaesthetists
- Major Haemorrhage Protocol · NICE NG24; UK MHP guidelines
- New-Onset Atrial Fibrillation · ESC 2020 AF Guidelines; NICE NG196
- Hypertensive Emergency · ESC/ESH 2018 Hypertension Guidelines; NICE NG136
- Bradycardia Management · Resuscitation Council UK ABCDE; ESC 2021 Pacing Guidelines
- Ventricular Tachycardia / Fibrillation · Resuscitation Council UK ACLS; ESC 2022 Ventricular Arrhythmia Guidelines
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.