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3rd 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.

Ceftriaxone

Brand names: Rocephin

Ceftriaxone is a third-generation cephalosporin with a long half-life allowing once-daily dosing, used for serious infections including bacterial meningitis, pneumonia, gonorrhoea, sepsis and surgical prophylaxis.

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. SPC table: 1-2 g once daily for community acquired pneumonia, acute exacerbations of COPD, intra-abdominal infections, complicated UTI/pyelonephritis; 2 g once daily for hospital acquired pneumonia, complicated skin and soft tissue infections, bone and joint infections; 2-4 g once daily for neutropenic patients with fever suspected to be bacterial, bacterial endocarditis and bacterial meningitis. In documented bacteraemia use the higher end of the range. Twice daily (12 hourly) may be considered where doses greater than 2 g daily are given. Specific ID indications: 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 (early Stage II and late Stage III) 2 g once daily for 14-21 days; acute otitis media 1-2 g single IM dose (or 1-2 g daily IM for 3 days if severely ill or previous therapy failed); pre-operative surgical prophylaxis 2 g single dose. Duration of therapy varies; continue for 48-72 hours after the patient is afebrile or bacterial eradication achieved. Paediatric weight-based schedules (children 15 days-12 years <50 kg and neonates 0-14 days) are given in the SPC — contraindicated in premature neonates up to postmenstrual age 41 weeks; verify all paediatric dosing against a children's formulary.

Dose adjustments

Renal

No dose reduction needed in impaired renal function provided hepatic function is not impaired. Only in preterminal renal failure (creatinine clearance <10 mL/min) should the dosage not exceed 2 g daily. No adjustment needed in mild/moderate hepatic impairment 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.

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
  • Ceftriaxone solutions containing lidocaine must never be administered intravenously

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 inhibits bacterial cell-wall synthesis by binding penicillin-binding proteins, with broad Gram-negative and useful Gram-positive activity and good penetration into cerebrospinal fluid.

Prescribing in practice

  • It must not be co-administered with calcium-containing intravenous fluids in neonates because of the risk of fatal calcium-ceftriaxone precipitates, and is contraindicated in such neonates.
  • Contraindicated in cephalosporin hypersensitivity and used cautiously with significant penicillin allergy.
  • It can cause biliary pseudolithiasis or sludging, so consider this in patients with right upper quadrant symptoms during treatment.

Monitoring

Monitor clinical response, and consider full blood count, liver and renal function and biliary symptoms during prolonged or high-dose therapy.

Counselling the patient

  • This injectable antibiotic is given once daily for many serious infections.
  • Report severe diarrhoea, rash, or yellowing of the skin or eyes.
  • Tell staff about previous penicillin or cephalosporin reactions.

Evidence & guidelines

Ceftriaxone is recommended in UK and international guidance as first-line therapy for bacterial meningitis and as part of treatment for gonorrhoea.

Reference: NICE Bacterial Meningitis Guidelines; BASHH STI 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.