Product image of Meropenem Fresenius Kabi (Meropenem Trihydrate) supplied by GNH India

Meropenem Fresenius Kabi

Active Ingredient:
Meropenem Trihydrate
Origin:
EU

Meropenem Fresenius Kabi (Meropenem Trihydrate)

Meropenem, the active ingredient in Meropenem Fresenius Kabi, is a carbapenem antibiotic presented as an injectable solution for intravenous use. It provides broad‑spectrum bactericidal activity against Gram‑negative and Gram‑positive organisms and is employed in the treatment of serious infections in hospitalized patients.

GNH India supplies Meropenem Fresenius Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and clinics worldwide, ensuring quality and regulatory compliance across all markets. Our distribution network adheres to stringent cold‑chain requirements for injectable products.

Manufacturer / TM Owner

Fresenius Kabi Norge As

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Indications & Clinical Uses

Meropenem is a carbapenem antibiotic used to treat severe bacterial infections across several organ systems.

  • Complicated intra‑abdominal infections: achieves rapid bacterial clearance in severe abdominal sepsis.
  • Complicated urinary tract infections: eradicates resistant uropathogens causing pyelonephritis and cystitis.
  • Nosocomial pneumonia: provides effective coverage against hospital‑acquired Gram‑negative pathogens in ventilated patients.
  • Bacterial meningitis: penetrates the cerebrospinal fluid to treat acute meningitis caused by susceptible organisms.
  • Septicemia: delivers systemic bactericidal activity to control bloodstream infections.
  • Skin and soft tissue infections: resolves deep tissue infections caused by multidrug‑resistant bacteria.

How It Works

  • Meropenem exerts its antibacterial effect by binding to penicillin‑binding proteins (PBPs) on the bacterial cell wall, inhibiting the final transpeptidation step of peptidoglycan synthesis. This disruption weakens the cell wall, leading to osmotic instability and cell lysis, resulting in rapid bactericidal activity against a broad range of Gram‑negative and Gram‑positive organisms, including many resistant strains. The drug’s stability against most β‑lactamases further enhances its spectrum.

Side Effects

Meropenem may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea or vomiting
  • Diarrhea, including possible Clostridioides difficile colitis
  • Headache
  • Injection site pain or phlebitis
  • Rash or other skin eruptions

Serious or Rare Side Effects

  • Severe allergic reactions such as anaphylaxis
  • Seizures, particularly in patients with renal impairment
  • Hepatotoxicity presenting as elevated liver enzymes
  • Thrombocytopenia or neutropenia
  • Renal dysfunction or acute kidney injury

Precautions & Warnings

When using Meropenem, clinicians should consider several precautionary measures to minimize risks.

  • Renal function: adjust dose in patients with impaired kidney function.
  • Hypersensitivity: avoid in individuals with known allergy to β‑lactam antibiotics.
  • Concomitant CNS disease: monitor for seizures in patients with pre‑existing neurological disorders.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk, as safety data are limited.
  • Antibiotic stewardship: limit duration to the shortest effective course to reduce resistance.
  • Store at 2‑8 °C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Meropenem can interact with other medicines, influencing efficacy or safety.

Major Interactions (Avoid)

  • Valproic acid: concomitant use may reduce serum valproate levels, risking seizure breakthrough.
  • Probenecid: may increase meropenem plasma concentrations, heightening toxicity risk.

Moderate Interactions (Monitor Closely)

  • Aminoglycosides: combined nephrotoxic potential requires renal function monitoring.
  • Loop diuretics: may enhance ototoxicity when used with other nephrotoxic agents.
  • Anticoagulants (e.g., warfarin): may alter INR, necessitating closer coagulation monitoring.
  • Oral contraceptives: possible reduction in efficacy, advise additional contraceptive measures.

Frequently Asked Questions

Meropenem Fresenius Kabi is an injectable carbapenem antibiotic indicated for the treatment of serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, hospital‑acquired pneumonia, bacterial meningitis, septicemia, and severe skin and soft‑tissue infections.

Meropenem binds to penicillin‑binding proteins on the bacterial cell wall, blocking the final step of peptidoglycan cross‑linking. This inhibition weakens the wall, causing osmotic lysis and rapid bacterial death, and it remains active against many β‑lactamase‑producing organisms.

The prescribed dose is set by the treating physician based on the type and severity of infection, the patient’s renal function, body weight, and local susceptibility patterns. Dosing adjustments are required for impaired kidney function.

Safety data for meropenem in pregnancy and lactation are limited, and the product carries an unknown pregnancy category. It should be used only when the potential benefit to the mother outweighs any possible risk to the fetus or infant.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and any necessary import documentation.

Meropenem offers a broad spectrum that includes many resistant Gram‑negative organisms and retains activity against most β‑lactamases, similar to imipenem and ertapenem. Compared with non‑carbapenem β‑lactams, it provides more reliable coverage for multidrug‑resistant infections, though choice depends on local resistance patterns and patient factors.

The product should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Once reconstituted, the solution should be used within the time frame specified in the product labeling and kept under the same temperature conditions.

Meropenem is supplied as a sterile injectable solution for intravenous infusion. It is reconstituted with the appropriate diluent, then administered over a short (typically 15‑30 minutes) or extended (up to 3 hours) infusion, according to the prescribing information and clinical judgment.

Serious adverse events include severe allergic reactions such as anaphylaxis, seizure activity—especially in patients with renal impairment or pre‑existing CNS disorders—and organ toxicity such as hepatotoxicity, thrombocytopenia, neutropenia, or acute kidney injury. Prompt medical evaluation is required if any of these occur.

Meropenem should be avoided in patients with a known hypersensitivity to meropenem, other carbapenems, or any β‑lactam antibiotics. Caution is also advised for individuals with severe renal impairment, a history of seizures, or those receiving valproic acid, unless the benefits clearly outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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