Product image of Meropenem Acs Dobfar (Meropenem Anhydrous) supplied by GNH India

Meropenem Acs Dobfar

Active Ingredient:
Meropenem Anhydrous
Origin:
EU

Meropenem Acs Dobfar (Meropenem Anhydrous)

Meropenem, the active ingredient in Meropenem Acs Dobfar, is a carbapenem antibiotic presented as a sterile powder for intravenous infusion use. It treats a range of serious bacterial infections in hospitalized patients, including intra‑abdominal, urinary, respiratory, central nervous system and bloodstream infections.

GNH India supplies Meropenem Acs Dobfar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Acs Dobfar S.P.A.

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Indications & Clinical Uses

Meropenem is a broad‑spectrum carbapenem used for severe bacterial infections across several organ systems.

  • Complicated intra‑abdominal infections: provides rapid bacterial eradication in severe abdominal sepsis.
  • Complicated urinary tract infections: eliminates resistant uropathogens causing pyelonephritis and cystitis.
  • Nosocomial pneumonia: treats hospital‑acquired and ventilator‑associated lung infections.
  • Meningitis: penetrates the cerebrospinal fluid to clear central nervous system infections.
  • Sepsis: offers bactericidal activity in systemic bloodstream infections.
  • Skin and soft tissue infections: resolves deep tissue and necrotizing infections caused by Gram‑negative organisms.

How It Works

  • Meropenem binds to penicillin‑binding proteins (PBPs) on bacterial cell walls, 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 affinity for multiple PBPs underlies its activity against many Gram‑negative, Gram‑positive and anaerobic organisms, including many resistant strains.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Vomiting: occasional emesis during or after infusion.
  • Diarrhea: loose stools, sometimes watery.
  • Headache: transient cranial discomfort.
  • Rash: mild erythematous skin eruption.
  • Phlebitis at infusion site: local irritation or inflammation.

Serious or Rare Side Effects

  • Seizures: especially in patients with renal dysfunction or high doses.
  • Clostridioides difficile colitis: severe diarrhea due to gut flora disruption.
  • Anaphylaxis: acute hypersensitivity reaction with respiratory or cardiovascular compromise.
  • Renal toxicity: worsening kidney function in susceptible individuals.
  • Hepatic enzyme elevation: transient increase in liver transaminases.
  • Neutropenia: marked reduction in white blood cell count.

Precautions & Warnings

Careful assessment and monitoring are required before and during therapy.

  • Renal function: adjust dose in patients with impaired clearance.
  • Allergy: avoid in individuals with known carbapenem hypersensitivity.
  • Pregnancy: use only when the potential benefit justifies the risk to the fetus.
  • Concomitant valproic acid: monitor for reduced antiepileptic levels.
  • Drug interactions: review all concurrent medications for possible effects.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Meropenem may interact with several agents, requiring clinical vigilance.

Major Interactions (Avoid)

  • Valproic acid: carbapenems can markedly reduce serum valproate concentrations, risking seizure breakthrough.
  • Cytotoxic chemotherapy: increased risk of myelosuppression when combined.

Moderate Interactions (Monitor Closely)

  • Probenecid: may decrease renal excretion of meropenem, raising plasma levels.
  • Loop diuretics: potential for enhanced nephrotoxicity, especially in renal impairment.
  • Warfarin: occasional alteration of INR, requiring coagulation monitoring.

Frequently Asked Questions

Meropenem Acs Dobfar is indicated for serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, hospital‑acquired pneumonia, meningitis, sepsis, and severe skin and soft‑tissue infections. It is reserved for cases where broad‑spectrum coverage against resistant Gram‑negative and Gram‑positive organisms is required.

Meropenem inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins. This blocks the cross‑linking of peptidoglycan strands, weakening the wall and causing osmotic lysis of the bacterial cell. Its high affinity for multiple PBPs gives it activity against a wide range of resistant organisms.

The dosing regimen for Meropenem Acs Dobfar is determined by the prescribing clinician based on infection severity, site, and patient factors such as renal function. The product is supplied as a sterile powder for intravenous infusion, and the exact dose and infusion rate are individualized for each patient.

Meropenem should be used in pregnancy only when the potential benefit to the mother outweighs any possible risk to the fetus. Limited data are available, and it is excreted in breast milk, so caution is advised for nursing mothers. Clinicians should evaluate the risk‑benefit profile for each case.

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 any required import documentation.

Meropenem offers a broader spectrum against certain Gram‑negative organisms, including Pseudomonas aeruginosa, and has a lower risk of seizures compared with imipenem. Both are administered intravenously, but meropenem is often preferred when a higher safety margin for neurotoxicity is desired, especially in patients with renal impairment.

Meropenem Acs Dobfar should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen. Once reconstituted, the solution should be used promptly according to the manufacturer’s stability guidelines and kept at room temperature if administered within the specified time frame.

The product is supplied as a sterile powder for intravenous infusion. After reconstitution with the appropriate diluent, it is infused over a prescribed period, typically 15‑30 minutes, depending on the dose and clinical protocol. Administration is performed by qualified healthcare professionals in a hospital setting.

Serious adverse events include seizures, especially in patients with renal dysfunction or high doses, Clostridioides difficile‑associated colitis, severe allergic reactions such as anaphylaxis, and potential renal or hepatic toxicity. Prompt recognition and management of these events are essential during treatment.

Meropenem is contraindicated in individuals with a known hypersensitivity to carbapenems or other beta‑lactam antibiotics. Caution is also advised for patients with a history of seizures, severe renal impairment without dose adjustment, or those receiving valproic acid, as the drug can reduce antiepileptic levels.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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