Product image of Meropenem Hikma Farmacêutica (Portugal) (Meropenem Anhydrous) supplied by GNH India

Meropenem Hikma Farmacêutica (Portugal)

Active Ingredient:
Meropenem Anhydrous
Origin:
EU

Meropenem Hikma Farmacêutica (Portugal) (Meropenem Anhydrous)

Meropenem, the active ingredient in Meropenem Hikma Farmacêutica, is a carbapenem antibiotic presented as an injection for intravenous use. It treats severe bacterial infections such as complicated intra‑abdominal infections, pneumonia, meningitis, and sepsis in hospitalized adults and children.

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

Manufacturer / TM Owner

Hikma Farmacêutica (Portugal), S.A.

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Indications & Clinical Uses

  • Meropenem is a broad‑spectrum carbapenem antibiotic used for serious bacterial infections.
  • Complicated intra‑abdominal infections: provides rapid bactericidal activity to resolve infection and reduce mortality.
  • Complicated urinary tract infections: eradicates resistant uropathogens and improves clinical cure rates.
  • Skin and soft tissue infections: eliminates mixed flora, aiding recovery of deep tissue infections.
  • Community‑acquired and hospital‑acquired pneumonia: achieves high lung concentrations to treat resistant pneumonia.
  • Meningitis: penetrates the cerebrospinal fluid to treat bacterial meningitis effectively.
  • Sepsis: offers broad coverage against Gram‑negative and Gram‑positive pathogens in systemic infection.

How It Works

  • Meropenem binds with high affinity to penicillin‑binding proteins (PBPs) on bacterial cell walls, inhibiting the final transpeptidation step of peptidoglycan synthesis. This disruption leads to loss of cell wall integrity and bacterial lysis, providing bactericidal activity against a wide range of Gram‑negative, Gram‑positive and anaerobic organisms, including many β‑lactamase‑producing strains.

Side Effects

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: may be watery and self‑limiting.
  • Headache: transient and usually resolves without intervention.
  • Rash: mild skin erythema or pruritus.
  • Infusion site phlebitis: localized pain or redness at the injection site.
  • Elevated liver enzymes: transient increase in transaminases.

Serious or Rare Side Effects

  • Seizures: especially in patients with renal impairment or CNS disorders.
  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Clostridioides difficile‑associated diarrhea: potentially life‑threatening colitis.
  • Neutropenia or thrombocytopenia: marked reduction in blood cell counts.
  • Renal toxicity: worsening kidney function in susceptible individuals.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

  • Meropenem should be used with caution in specific clinical situations.
  • Renal function: adjust dose in patients with impaired renal clearance.
  • CNS effects: monitor for seizures in patients with a history of epilepsy or high‑dose therapy.
  • Allergy: avoid in individuals with known hypersensitivity to carbapenems or β‑lactams.
  • Pregnancy: category B; use only when the potential benefit justifies the risk.
  • Valproic acid co‑administration: may reduce valproate levels, increasing seizure risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Meropenem may interact with other medicines, requiring attention to dosing and monitoring.

Major Interactions (Avoid)

  • Valproic acid: meropenem reduces serum valproate concentrations, risking breakthrough seizures.
  • High‑dose aminoglycosides: combined nephrotoxic potential may impair kidney function.
  • Loop diuretics: increased risk of renal impairment when used together.

Moderate Interactions (Monitor Closely)

  • Warfarin: may enhance anticoagulant effect, requiring INR monitoring.
  • Phenytoin: meropenem can lower phenytoin levels, potentially reducing seizure control.
  • Rifampin: may decrease meropenem exposure, necessitating dosage adjustment.

Frequently Asked Questions

Meropenem Hikma Farmacêutica is indicated for serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft‑tissue infections, community‑acquired and hospital‑acquired pneumonia, meningitis, and sepsis. It is administered intravenously in hospital settings to achieve rapid bacterial eradication.

Meropenem inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins, preventing the cross‑linking of peptidoglycan strands. This disruption weakens the cell wall, leading to osmotic instability and bacterial cell death, providing a bactericidal effect against a broad range of Gram‑negative, Gram‑positive, and anaerobic organisms.

The dosage of Meropenem Hikma Farmacêutica is determined by the prescribing clinician based on the type and severity of infection, patient weight, renal function, and other clinical factors. Healthcare professionals calculate the appropriate intravenous infusion rate and duration for each individual case.

Meropenem is classified as pregnancy category B, indicating that animal studies have not shown risk to the fetus and there are no adequate human studies. It may be used during pregnancy only if the potential benefit justifies any potential risk. Limited data are available for breastfeeding, so clinicians should weigh benefits against possible infant exposure.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams worldwide. After verification of trade or institutional credentials, the sales team will respond with pricing, availability, shipping details (including cold‑chain logistics if needed), and required import documentation.

Meropenem offers a broad spectrum of activity similar to other carbapenems like imipenem and ertapenem, but it has enhanced stability against many β‑lactamases and provides reliable coverage of Pseudomonas aeruginosa. Compared with non‑carbapenem broad‑spectrum agents, meropenet typically achieves higher tissue penetration and retains activity against multidrug‑resistant organisms.

Meropenem for injection must be stored at 2‑8 °C (refrigerated). Keep the vials in their original packaging, protect from light, and avoid freezing or shaking. Once reconstituted, use the solution within the time frame specified in the product labeling and discard any unused portion.

The product is supplied as a sterile powder for injection. It is reconstituted with the appropriate diluent and administered intravenously, typically as a short infusion over 15‑30 minutes. Administration is performed by qualified healthcare personnel in a clinical setting, with dosing adjusted for renal function and infection severity.

Serious adverse events include seizures, especially in patients with renal impairment or pre‑existing CNS disorders, severe allergic reactions such as anaphylaxis, Clostridioides difficile‑associated colitis, and significant hematologic abnormalities like neutropenia or thrombocytopenia. Prompt recognition and medical management are essential if these events occur.

Meropenem is contraindicated in individuals with a known hypersensitivity to carbapenems, other β‑lactam antibiotics, or any component of the formulation. Caution is also advised for patients with severe renal impairment, a history of seizures, or those receiving valproic acid, as the drug may lower valproate levels and increase seizure risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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