Product image of Meropenem Inresa (Meropenem Trihydrate) supplied by GNH India

Meropenem Inresa

Active Ingredient:
Meropenem Trihydrate
Origin:
EU

Meropenem Inresa (Meropenem Trihydrate)

Meropenem, the active ingredient in Meropenem Inresa, is a carbapenem antibiotic presented as a sterile powder for intravenous use. It treats severe bacterial infections such as intra‑abdominal infections, urinary tract infections, pneumonia, septicemia and meningitis in hospitalized patients.
GNH India supplies Meropenem Inresa as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Inresa Arzneimittel Gmbh

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Indications & Clinical Uses

Meropenem is a broad‑spectrum carbapenem used for serious bacterial infections in the hospital setting.

  • Complicated intra‑abdominal infections: provides bacterial eradication in severe abdominal sepsis.
  • Complicated urinary tract infections: eliminates resistant uropathogens causing kidney and bladder infections.
  • Nosocomial pneumonia: treats hospital‑acquired lung infections resistant to other antibiotics.
  • Septicemia: rapidly clears bloodstream infections caused by Gram‑negative and Gram‑positive bacteria.
  • Meningitis: penetrates the cerebrospinal fluid to treat bacterial meningitis.

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 and bacterial cell death. Its high affinity for a broad range of PBPs gives it activity against many Gram‑negative, Gram‑positive and anaerobic organisms, including those resistant to other beta‑lactams.

Side Effects

Adverse reactions may occur with meropenem therapy.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhea: may be watery and self‑limiting.
  • Rash: skin redness or itching.
  • Headache: transient headache during treatment.
  • Elevated liver enzymes: mild, reversible increase in transaminases.
  • Injection site pain: discomfort at the IV site.

Serious or Rare Side Effects

  • Seizures: especially in patients with renal impairment or CNS disorders.
  • Clostridioides difficile‑associated diarrhea: severe colitis requiring medical attention.
  • Anaphylaxis: acute allergic reaction with respiratory and circulatory compromise.
  • Stevens‑Johnson syndrome/toxic epidermal necrolysis: severe skin reactions.
  • Neutropenia: marked reduction in white blood cells.
  • Acute renal failure: worsening kidney function in susceptible individuals.

Precautions & Warnings

Use meropenem with careful clinical monitoring and consider patient‑specific factors.

  • Renal function: adjust dose in patients with impaired renal clearance.
  • Allergy: avoid in individuals with known hypersensitivity to carbapenems or other beta‑lactams.
  • Pregnancy: prescribe only if the potential benefit justifies the potential risk to the fetus.
  • Valproic acid co‑administration: monitor for reduced valproate levels and possible seizure breakthrough.
  • Seizure risk: observe patients with a history of CNS disorders for neurologic signs.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Meropenem may interact with other medicines; some require avoidance while others need monitoring.

Major Interactions (Avoid)

  • Valproic acid: meropenem reduces plasma valproate concentrations, increasing seizure risk.
  • Probenecid: may decrease renal clearance of meropenem, leading to higher systemic exposure.

Moderate Interactions (Monitor Closely)

  • Loop diuretics: combined use may heighten nephrotoxicity.
  • Aminoglycosides: additive risk of kidney injury when given together.
  • Warfarin: monitor INR as meropenem can alter anticoagulant effect.
  • CNS stimulants (e.g., caffeine, theophylline): may lower seizure threshold.

Frequently Asked Questions

Meropenem Inresa is indicated for severe bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, hospital‑acquired (nosocomial) pneumonia, septicemia, and bacterial meningitis. It is typically reserved for patients in hospital settings where resistant organisms are a concern.

Meropenem inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins, which blocks the cross‑linking of peptidoglycan strands. This weakens the cell wall, causing osmotic lysis and bacterial death. Its broad affinity for many PBPs gives it activity against a wide range of Gram‑negative, Gram‑positive, and anaerobic bacteria.

The dosage of Meropenem Inresa is determined by the prescribing clinician based on the type and severity of infection, patient weight, renal function, and local antimicrobial guidelines. Healthcare professionals calculate the appropriate infusion rate and duration for each individual case.

Safety data for meropenem in pregnancy are limited, and the drug is classified as pregnancy category unknown. It should be used only when the potential benefit to the mother outweighs any possible risk to the fetus. Breastfeeding mothers should consult their physician, as the drug may be excreted in breast milk.

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, and will request trade or institutional credentials. The sales team then provides pricing, availability, shipping details (including cold‑chain if needed), and assists with import documentation.

Meropenem shares the carbapenem class’s broad‑spectrum activity and resistance to many beta‑lactamases, similar to imipenem and ertapenem. Compared with imipenem, meropenem has a lower risk of seizures and does not require co‑administration with cilastatin. It is often preferred for infections caused by multidrug‑resistant Gram‑negative organisms.

Meropenem Inresa should be stored at 2‑8 °C in a refrigerator, protected from light. The product must not be frozen or shaken. Once reconstituted for intravenous infusion, it should be used within the time frame specified in the product labeling and kept under the same temperature conditions.

Meropenem Inresa is supplied as a sterile powder for intravenous injection. It is reconstituted with a suitable diluent and administered as an IV infusion over a period defined by the prescriber, usually 15‑30 minutes, depending on the infection severity and patient factors.

The most 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 rare skin reactions like Stevens‑Johnson syndrome. Prompt medical attention is required if any of these occur.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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