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 treats severe bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, hospital‑acquired and ventilator‑associated pneumonia, and is used in patients with severe sepsis or septic shock.

GNH India supplies Meropenem Fresenius Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Fresenius Kabi Nv/Sa

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Indications & Clinical Uses

Meropenem is a broad‑spectrum carbapenem antibiotic used to treat serious infections caused by susceptible bacteria.

  • Complicated intra‑abdominal infections: provides bacterial eradication and clinical cure in patients with intra‑abdominal sepsis.
  • Complicated urinary tract infections: eliminates uropathogens and resolves infection in the urinary system.
  • Hospital‑acquired pneumonia: achieves microbiological clearance and improves respiratory outcomes.
  • Ventilator‑associated pneumonia: targets resistant organisms and supports recovery in ventilated patients.
  • Severe sepsis and septic shock: offers rapid bactericidal activity to control systemic infection.

How It Works

  • Meropenem binds 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, cell lysis, and bacterial death. Its broad spectrum includes many Gram‑negative, Gram‑positive, and anaerobic organisms, and it is resistant to most β‑lactamases.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: may be watery and self‑limiting.
  • Vomiting: occasional post‑infusion emesis.
  • Headache: transient cranial discomfort.
  • Infusion site reactions: erythema or phlebitis at the injection site.
  • Rash: mild cutaneous eruption.

Serious or Rare Side Effects

  • Seizures: especially in patients with renal impairment or high doses.
  • Clostridioides difficile colitis: severe diarrhea due to gut flora disruption.
  • Anaphylaxis: acute hypersensitivity requiring immediate discontinuation.
  • Renal impairment: worsening kidney function in susceptible individuals.
  • Hepatic enzyme elevation: transient increase in liver transaminases.
  • Neutropenia: reduced white blood cell count, increasing infection risk.

Precautions & Warnings

Careful assessment and monitoring are required before and during therapy.

  • Renal function: adjust dose in patients with impaired clearance.
  • Hepatic function: monitor liver enzymes during prolonged treatment.
  • Allergic reactions: discontinue if signs of hypersensitivity appear.
  • Valproic acid co‑administration: increased risk of seizures; avoid combination.
  • Neonates and infants: higher seizure susceptibility; use with caution.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Meropenem may interact with other medicines, affecting efficacy or safety.

Major Interactions (Avoid)

  • Valproic acid: concurrent use can precipitate seizures.
  • Probenecid: may increase meropenem plasma concentrations, raising toxicity risk.
  • Carbapenem‑induced reduction of oral contraceptives: may decrease contraceptive effectiveness.

Moderate Interactions (Monitor Closely)

  • Loop diuretics: monitor renal function and electrolytes.
  • Aminoglycosides: watch for additive nephrotoxicity.
  • Anticoagulants (e.g., warfarin): observe coagulation parameters for potential changes.

Frequently Asked Questions

Meropenem Fresenius Kabi is indicated for serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, hospital‑acquired and ventilator‑associated pneumonia, as well as severe sepsis and septic shock caused by susceptible organisms.

Meropenem inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins, preventing the cross‑linking of peptidoglycan strands. This weakens the cell wall, leading to osmotic rupture and bacterial death, providing rapid bactericidal activity against a broad range of pathogens.

The specific dose of meropenem is determined by the prescribing clinician based on the type and severity of infection, patient weight, renal function, and local susceptibility patterns. Dosage regimens are individualized and should follow the prescriber’s instructions.

Safety data for meropenem in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made by a qualified healthcare professional.

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 if needed), and import documentation.

Meropenem shares a similar broad‑spectrum activity with other carbapenems such as imipenem and ertapenem, but it is often preferred for its stability against many β‑lactamases and its lower propensity to cause seizures compared with imipenem, making it suitable for a wide range of severe infections.

Meropenem Fresenius Kabi should be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen or shaken. Once reconstituted, use according to the manufacturer’s guidance and discard any remaining solution after the specified period.

Meropenem is supplied as an injectable solution for intravenous infusion. It is administered by slow IV infusion over 15‑30 minutes, following the dosing schedule prescribed by the treating physician, and should be given under aseptic conditions.

The most serious adverse events include seizures (especially in patients with renal impairment or high doses), severe Clostridioides difficile‑associated colitis, anaphylactic reactions, and significant renal or hepatic dysfunction. Prompt recognition and discontinuation are essential if these occur.

Patients with a known hypersensitivity to meropenem, other carbapenems, or any β‑lactam antibiotics should avoid the drug. Caution is also advised for individuals with a history of seizures, severe renal impairment, or those receiving valproic acid, unless the prescriber determines the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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