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Ertapenem

Carbapenem beta-lactam antibiotic (group 1) · Antibiotic

Also known as Ertapenem sodium, Invanz

START
1 g IV once daily (IM with lidocaine diluent if IV not feasible)
TYPICAL MAX
1 g/day (500 mg/day if CrCl ≤30)
STOP IF
Anaphylaxis, seizures, severe CDI/skin reaction
WATCH
Renal function (dose-adjust), seizure risk factors, hypersensitivity/diarrhoea; not for Pseudomonas
CDSCO approvedSchedule HATC J01DH03
Dose laddermg/d
500start1kstandard/day
Renal dose adjustmenteGFR mL/min/1.73m²
FULL1 g once daily31REDUCE500 mg once daily (HD: +150 mg post-d…90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
30minONSET30minPEAK4h1dDURATION
ONSET
30min · IV onset
PEAK
30min · end of infusion
4h · plasma t½
DURATION
1d · once-daily
EXCRETION
~80% renal (≈38% unchanged) + metabolite
route + CYP
INTERACTIONS
7 major
SEVERE in our sources
PREGNANCY
Use only if clearly needed — limited human data
FDA category + note
Top interactionssee all 11
  • BupropionSevereDatabaseDDInter
  • DivalproexSevereDatabase
  • IohexolSevereDatabaseDDInter
  • IopamidolSevereDatabaseDDInter

Mechanism

Binds penicillin-binding proteins (esp. PBP2/PBP3) inhibiting cell-wall synthesis → bactericidal; broad Gram-positive/Gram-negative/anaerobe cover but NOT active against Pseudomonas aeruginosa or Acinetobacter; long half-life allows once-daily dosing.

Indications

Complicated intra-abdominal, skin/soft-tissue, urinary, and pelvic infectionsCommunity-acquired pneumoniaSurgical prophylaxis (colorectal)ESBL-producing Enterobacterales infections (non-pseudomonal)

Dosing

Adult
1 g IV (or IM) once daily.
Pediatric
3 months–12 years: 15 mg/kg IV BID (max 1 g/day); ≥13 years 1 g once daily.
Renal adjustment
CrCl ≤30 mL/min: 500 mg once daily. Haemodialysis: 500 mg/day; if dose within 6 h before HD give 150 mg supplement after.
Hepatic adjustment
No adjustment.
Geriatric
Adjust per renal function.
Max dose
1 g/day

Pharmacokinetics

Onset
IV immediate
Peak effect
End of 30-min infusion
Duration
Once-daily (long t½)
Half-life
~4 h
Bioavailability
IV 100%; IM ~90%
Protein binding
~85–95% (concentration-dependent)
Metabolism
Hydrolysis (dehydropeptidase-I) to inactive ring-opened metabolite
Excretion
Renal (~80%, ~38% unchanged + metabolite)

Contraindications

  • Anaphylaxis to ertapenem/carbapenems or beta-lactams
  • Hypersensitivity to amide local anaesthetics (IM diluent is lidocaine — for IM route)

Side effects

Common
Diarrhoea/nauseaHeadacheInfusion-site reactions/phlebitisRaised hepatic enzymes
Serious
  • Anaphylaxis/severe hypersensitivity (carbapenem cross-reactivity)
  • Seizures (esp. CNS disease, renal impairment, elderly)
  • Clostridioides difficile colitis
  • Severe skin reactions (DRESS/SJS rare)

Pregnancy & lactation

Pregnancy

Use only if clearly needed — limited human data

Lactation

Excreted in milk in small amounts; monitor infant — caution

Drug interactions

Bupropion
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Divalproex
Severe
Database

Rapid and significant decrease in valproate levels, leading to loss of seizure control.

Avoid co-administration. If ertapenem is essential, consider alternative anticonvulsants or closely monitor valproate levels and increase valproate dose significantly. Monitor for seizure recurrence.

Iohexol
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Iopamidol
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Sodium Valproate
Severe
Database

Rapid and significant decrease in valproate plasma concentrations, leading to loss of seizure control and increased risk of breakthrough seizures.

Avoid concomitant use if possible. If ertapenem is essential, consider alternative antiepileptic drugs. If co-administration is unavoidable, monitor valproate levels closely and consider increasing valproate dose significantly or switching to an alternative antiepileptic drug. Monitor for seizure recurrence.

Tramadol
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Valproic Acid
Severe
Database

Carbapenems markedly reduce valproate levels → breakthrough seizures

Avoid combination; alternative anticonvulsant + monitor levels

Source: Kimi deep-research + Cla

Amide Local Anaesthetics
Moderate
Database

IM formulation contains lidocaine — hypersensitivity/contraindication

Avoid IM route if amide-anaesthetic allergy

Source: Kimi deep-research + Cla

Live Oral Typhoid Vaccine
Moderate
Database

Antibacterial inactivation

Separate timing

Source: Kimi deep-research + Cla

Probenecid
Moderate
Database

Reduced renal clearance → raised ertapenem levels

Avoid co-administration

Source: Kimi deep-research + Cla

Warfarin
Moderate
Database

Possible altered INR (gut flora)

Monitor INR

Source: Kimi deep-research + Cla

1 additional low-confidence interaction hidden — those rows lack a documented mechanism or management plan in our sources.

Related guidelines

Ask House about Ertapenem

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: Goodman & Gilman 14e, Harrison 22e, Katzung, BNF·Verified: 2026-05-19 · House clinical team·Cockpit curated: 2026-05-19