Evigrade

Meropenem

AEMPS

Carbapenem antibiotic for intravenous use

ATC code: J01DH02

Brand names: Merrem

Updated · Methodology

Indications

A

Acute bacterial meningitis

Second line

Acute bacterial meningitis stands among the indications in the AEMPS Archifar label, with its own higher dose: inflamed meninges let meropenem into the cerebrospinal fluid, but the concentration has to be kept high. Empirical first-line therapy in Europe usually differs – ceftriaxone with vancomycin, plus ampicillin where listeriosis is a risk. Meropenem comes in when a cephalosporin does not fit: severe allergy to it, hospital-acquired meningitis after neurosurgery, or cultured flora resistant to cephalosporins. Carbapenems carry a rare adverse effect that matters here: the label lists seizures among uncommon reactions, and in a patient with meningitis they are easy to read as the illness itself. Valproic acid in this combination is followed by drug levels.

ICD-10: G00

A

Complicated intra-abdominal infection

First line

Complicated intra-abdominal infection is listed outright among the indications in the AEMPS Archifar label. The reasoning sits in the spectrum: with perforation or an anastomotic leak the peritoneal cavity receives mixed flora, and meropenem covers enteric gram-negative rods together with anaerobes in a single drug, with no metronidazole added. This is not first-line for every appendicitis: the carbapenem is chosen for hospital-acquired infection, recent antibacterial therapy, severe illness or known carriage of resistant flora. The antibiotic does not replace source control – without surgery or drainage it does not rescue. Course length is counted from the day of adequate drainage, not from the first dose.

ICD-10: K65.0

A

Complicated urinary tract infection

Second line

Complicated urinary tract infections appear in the AEMPS Archifar label. Complicated means infection over a stone, a stent, a catheter, a neurogenic bladder, prostatic enlargement or after a urological procedure, and the flora there is more often resistant. Meropenem is picked after culture, when an extended-spectrum beta-lactamase producer grows or the patient has just failed a cephalosporin and a fluoroquinolone. Plain cystitis in a healthy woman needs no carbapenem: fosfomycin, nitrofurantoin and trimethoprim do the work. Once the patient improves and the isolate is susceptible, intravenous meropenem steps down to a narrow oral agent, which shortens the hospital stay and eases resistance pressure.

ICD-10: N10 · ICD-11: GB51

A

Gram-negative sepsis

First line

Meropenem is a hospital carbapenem, and in gram-negative sepsis it goes in where earlier beta-lactams no longer hold the flora: extended-spectrum beta-lactamase producers, Pseudomonas aeruginosa, Acinetobacter. The AEMPS Archifar label names bacteraemia associated with a severe infection as a separate entry and allows the drug from 3 months of age. Dosing follows creatinine clearance, and in renal failure the interval stretches. An extended 3-hour infusion keeps the concentration above the MIC longer than a bolus, and severe sepsis is dosed that way. Once cultures return, the regimen narrows: the carbapenem stays only for confirmed resistant flora. If the patient takes valproic acid, the treating neurologist hears about the meropenem start: the anticonvulsant level collapses within two days.

ICD-10: A41.5 · ICD-11: 1G40

Marketing claims without evidence base

The drug is promoted for these uses outside international guidelines. Each entry below is analyzed against AEMPS, FDA, EMA, Cochrane and major RCTs.

F

Acute viral bronchitis

Not recommended

Meropenem is an intravenous reserve antibiotic for inpatients, and in acute bronchitis it sometimes goes in for reassurance when the fever runs longer than expected. In bronchitis in an adult without chronic lung disease the cause is overwhelmingly viral, and a carbapenem does nothing to viruses. The Cochrane review of antibiotics for acute bronchitis (2017) found cough shortened by less than a day alongside a clear rate of adverse effects. The price of that reassurance is concrete: a line and a drip, the risk of Clostridioides difficile colitis, seizures as a rare labelled reaction, and selection of resistant flora that will make the carbapenem fail when it is genuinely needed. If meropenem has been offered for a cough without pneumonia, consider seeking a second opinion from another doctor.

ICD-10: J20 · ICD-11: CA42

How to read tiers A–F
  • AStrong evidence – first or second line in international guidelines
  • BRecommended in selected cases
  • CStudy data contradict each other
  • DBenefit not proven, no documented harm
  • FDocumented harm, or risk without benefit

Mechanism of action

Meropenem binds penicillin-binding proteins and cuts off peptidoglycan cross-linking, after which the bacterial wall tears under its own osmotic pressure. A methyl group at the second carbon shields the molecule from renal dehydropeptidase, so it needs no cilastatin. The spectrum runs wider than that of cephalosporins: the carbapenem withstands most beta-lactamases, AmpC and extended-spectrum enzymes included, and fails only against carbapenemases. Plasma protein binding sits near 2%, hepatic enzymes barely touch it, the kidneys clear it and the half-life is about an hour. That shapes its interactions: few in number, but one hits hard – valproic acid levels fall by 60–100% within two days.

Safety

Contraindications

  • Hypersensitivity to meropenem or to any excipient
  • History of severe immediate hypersensitivity to any beta-lactam antibiotic (anaphylaxis, severe skin reaction)

Serious adverse effects

  • Clostridioides difficile-associated colitis, up to the pseudomembranous form
  • Anaphylaxis and angioedema
  • Seizures (rare, carried as a separate warning in the label)
  • Drug-induced liver injury
  • Agranulocytosis, neutropenia, thrombocytopenia, haemolytic anaemia
  • Severe skin reactions: Stevens-Johnson syndrome, toxic epidermal necrolysis, DRESS

Common adverse effects

  • Diarrhoea, nausea, vomiting, abdominal pain
  • Headache
  • Raised transaminases, alkaline phosphatase and lactate dehydrogenase
  • Thrombocythaemia
  • Pain and inflammation at the injection site
  • Rash, itching

Pregnancy: can you take Meropenem?

Data on meropenem in pregnancy are limited. Animal studies showed no fetal harm. The label allows use when the expected benefit to the mother outweighs the possible risk, which in practice means severe infections where the carbapenem is the only option left.

Breastfeeding: can you take Meropenem?

Meropenem passes into breast milk in very small amounts. The infant receives a dose that produces no systemic effect, though loose stools and mucosal candidiasis are possible. Feeding usually continues with the baby watched.

Reference information, not a clinical decision. Discuss feeding pauses or changes with your physician or an IBCLC.

Drug–drug interactions

1 pair found. Sorted from critical to minor.

CriticalValproic acidAntiepileptics. Fatty acid derivatives

Mechanism

Carbapenems collapse valproic acid levels. The AEMPS meropenem label gives the figure: on concomitant use the blood level of valproate falls by 60–100% within about two days, and the same label states that because of the rapid onset and the depth of the fall the combination is not considered manageable and is therefore avoided. The valproate label repeats this from its own side. The mechanism has two parts: the carbapenem inhibits acylpeptide hydrolase, which converts valproate glucuronide back into the active drug, and speeds distribution of valproate into red cells. Raising the valproate dose does not rescue it: in published cases the level did not return to the therapeutic range while the carbapenem stayed in the regimen.

Symptoms

Loss of seizure control 1–3 days after the first meropenem dose: fits return after months without any, up to clusters and status epilepticus. In a patient taking valproate as a mood stabiliser, mania or an abrupt mood swing appears instead of seizures. The blood valproate level drops below the therapeutic range, sometimes to undetectable, with the dose unchanged and adherence intact. Fever and the infection itself lower the seizure threshold further, so the picture is easily written off as the underlying illness.

Management

The combination is taken apart. If meropenem is needed for a life-threatening infection, the anticonvulsant regimen is rebuilt in advance: a drug with a different mechanism is added (levetiracetam, lacosamide, a benzodiazepine for a short course) and kept through the antibiotic course and for several days after. Where the severity of the infection allows, the antibiotic is switched to a non-carbapenem: a cephalosporin with metronidazole, piperacillin-tazobactam, or a fluoroquinolone by susceptibility. Valproate levels are checked before meropenem starts, at 24–48 hours and after the antibiotic stops: recovery is not instant either, and by then the regimen needs revisiting again. Raising the valproate dose as the only measure does not work and adds toxicity risk once the antibiotic ends.

Pair details →Valproic acid →

Label mentions5 mentions

Verbatim lines from the interaction sections, in the language of the label

From this drug’s label

  • «Se han notificado descensos en los niveles sanguíneos del ácido valproico cuando se ha co-administrado con agentes carbapenemes, dando lugar en unos dos días a una disminución de un 60-100% en los…»

    AEMPS, section 4.5 · Open on CIMA

  • Moderateanticoagulantesclass named in the label
    «Anticoagulantes orales: La administración simultánea de antibióticos con warfarina puede aumentar sus efectos anticoagulantes. Ha habido muchas notificaciones de aumentos de los efectos…»

    AEMPS, section 4.5 · Open on CIMA

  • ModerateWarfarin
    «Anticoagulantes orales: La administración simultánea de antibióticos con warfarina puede aumentar sus efectos anticoagulantes. Ha habido muchas notificaciones de aumentos de los efectos…»

    AEMPS, section 4.5 · Open on CIMA

From other drugs’ labels

  • «Carbapenemes (panipenem, meropenem, imipenem): La administración de ácido valproico junto con antibióticos del grupo de los carbapenemes ha mostrado niveles disminuidos de ácido valproico, resultando…»

    AEMPS, section 4.5 · Open on CIMA

  • «Effects of Co-Administered Drugs on Valproate Clearance: A clinically significant reduction in serum valproic acid concentration has been reported in patients receiving carbapenem antibiotics (for…»

    FDA, section 7 · Open on DailyMed

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Frequently asked

What is Meropenem used for?

Meropenem is evaluated for the following indications with varying evidence strength: Gram-negative sepsis (evidence tier A), Complicated intra-abdominal infection (evidence tier A), Acute bacterial meningitis (evidence tier A). See the full indication matrix with dosing and citations above on this page.

What are the side effects of Meropenem?

Common side effects of Meropenem (≥ 1 in 100): Diarrhoea, nausea, vomiting, abdominal pain, Headache, Raised transaminases, alkaline phosphatase and lactate dehydrogenase, Thrombocythaemia, Pain and inflammation at the injection site, Rash, itching. See the Safety section for uncommon and serious reactions.

Is Meropenem safe during pregnancy?

Data on meropenem in pregnancy are limited. Animal studies showed no fetal harm. The label allows use when the expected benefit to the mother outweighs the possible risk, which in practice means severe infections where the carbapenem is the only option left.

Is Meropenem compatible with breastfeeding?

Meropenem passes into breast milk in very small amounts. The infant receives a dose that produces no systemic effect, though loose stools and mucosal candidiasis are possible. Feeding usually continues with the baby watched.

Who should not take Meropenem?

Meropenem is contraindicated in: Hypersensitivity to meropenem or to any excipient; History of severe immediate hypersensitivity to any beta-lactam antibiotic (anaphylaxis, severe skin reaction). Full list in the Safety section.

Official sources

Direct links to regulator labels. Open in a new tab.

Other drugs in this group

Metronidazole, Moxifloxacin, Norfloxacin, Trimethoprim, Amoxicillin + Clavulanic Acid, Ceftriaxone, Clindamycin, Flucloxacillin