GNH USA

Europe — EMA

Meropenem Actavis

GNH USA supplies Meropenem Actavis (Meropenem), a carbapenem antibiotic for severe intra‑abdominal, urinary tract, pneumonia, septicemia and meningitis

Meropenem

Request sourcing

1
Pack/s

What is Meropenem?

Meropenem, the active ingredient in Meropenem Actavis, is a carbapenem antibiotic presented as an injection for intravenous use. It treats severe bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, nosocomial pneumonia, septicemia and meningitis in hospitalized patients.

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

What is Meropenem used for?

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

Complicated intra‑abdominal infections: achieves clinical cure by eradicating mixed aerobic and anaerobic pathogens. Complicated urinary tract infections: eliminates resistant Gram‑negative organisms to resolve infection. Nosocomial pneumonia: provides rapid bacterial clearance in ventilated patients. Septicemia: controls bloodstream infection caused by susceptible bacteria. Meningitis: penetrates the cerebrospinal fluid to treat bacterial meningitis.

What are the side effects of Meropenem?

Adverse reactions may occur with any antimicrobial therapy and should be monitored.

Common Side Effects: - Nausea or vomiting - Diarrhea, including mild colitis - Headache - Rash or mild pruritus at the infusion site - Transient elevation of liver enzymes - Infusion‑related phlebitis

Serious or Rare Side Effects: - Seizures, especially in patients with renal impairment or CNS disease - Severe allergic reactions such as anaphylaxis or Stevens‑Johnson syndrome - Clostridioides difficile‑associated colitis - Acute renal failure or worsening of existing renal dysfunction - Hepatotoxicity with marked transaminase elevation - Hemolytic anemia or thrombocytopenia

What precautions apply to Meropenem?

Meropenem should be used with careful clinical assessment and monitoring.

Renal function: adjust dose in patients with impaired renal clearance. Allergy history: avoid in individuals with known hypersensitivity to carbapenems or other β‑lactams. Seizure risk: monitor neurologic status, especially in patients with CNS disorders. Concomitant antibiotics: evaluate for additive toxicity when combined with other nephrotoxic agents. Pregnancy and lactation: use only if potential benefit justifies potential risk. Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Meropenem interact with?

Meropenem may interact with several medicines; monitoring is advised.

Major Interactions (Avoid): - Valproic acid: meropenem can lower valproate concentrations, risking seizure breakthrough. - Cisplatin or other nephrotoxic agents: increased risk of renal toxicity. - Probenecid: may raise meropenem plasma levels, enhancing toxicity. - Live vaccines: concurrent use can reduce vaccine efficacy. - Other β‑lactam antibiotics: potential for antagonistic effects.

Moderate Interactions (Monitor Closely): - Loop diuretics: monitor electrolytes and renal function. - Aminoglycosides: watch for additive nephrotoxicity. - Warfarin: may affect INR, requiring coagulation monitoring.

Frequently asked questions

What is Meropenem Actavis used for?+
Meropenem Actavis is indicated for the treatment of severe bacterial infections in hospitalized patients, including complicated intra‑abdominal infections, complicated urinary tract infections, nosocomial (hospital‑acquired) pneumonia, septicemia (bloodstream infection), and bacterial meningitis. It is reserved for infections caused by organisms susceptible to carbapenems.
How does Meropenem work?+
Meropenem belongs to the carbapenem class of β‑lactam antibiotics. It binds to penicillin‑binding proteins on the bacterial cell wall, inhibiting the final transpeptidation step of peptidoglycan synthesis. This disruption weakens the cell wall, leading to osmotic lysis and bacterial death. Its stability against most β‑lactamases expands its spectrum of activity.
What is the usual dose of Meropenem Actavis?+
The dose of Meropenem Actavis is individualized by the prescribing clinician based on the type and severity of infection, the patient’s renal function, weight and age. Typical regimens range from 500 mg to 2 g administered intravenously every 8 hours, but exact dosing must be determined by a qualified healthcare professional.
Is Meropenem Actavis safe in pregnancy or breastfeeding?+
Safety data for Meropenem in pregnancy and lactation are limited. The drug should be used only when the potential benefit to the mother outweighs any possible risk to the fetus or infant. Breastfeeding mothers should consult their physician, as the medication may be excreted in breast milk.
How do I order Meropenem Actavis from GNH USA?+
To place an order, submit an enquiry on the Meropenem Actavis product page at gnh-usa.com, specifying the required quantity. GNH USA 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 handling if needed) and any required import documentation.
How does Meropenem compare with other carbapenems or alternative antibiotics?+
Meropenem offers a broad spectrum of activity against many Gram‑negative, Gram‑positive and anaerobic bacteria, and it is stable against most β‑lactamases. Compared with imipenem‑cilastatin, meropenem has a lower risk of seizures and does not require co‑administration of a renal dehydropeptidase inhibitor. It is often chosen when resistance to other β‑lactams is suspected.
What are the storage and handling requirements for Meropenem Actavis?+
Meropenem Actavis for injection must be stored refrigerated at 2 °C to 8 °C. The vial should be kept in its original packaging, 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 label and kept refrigerated if not administered immediately.
How is Meropenem Actavis administered?+
Meropenem Actavis is supplied as a sterile powder for injection. It is reconstituted with the appropriate diluent and administered intravenously, usually over 15–30 minutes. The infusion rate and duration are determined by the prescriber, taking into account the infection type and patient-specific factors such as renal function.
What are the most serious risks to watch for with Meropenem Actavis?+
Serious adverse events include seizures (particularly in patients with renal impairment or pre‑existing CNS disorders), severe allergic reactions such as anaphylaxis or Stevens‑Johnson syndrome, Clostridioides difficile‑associated colitis, and significant renal or hepatic dysfunction. Prompt medical attention is required if any of these events occur.
Who should not use Meropenem Actavis?+
Meropenem Actavis should not be used in individuals with a documented hypersensitivity to meropenem, other carbapenems, or any β‑lactam antibiotics. Caution is also advised for patients with a history of seizures, severe renal impairment, or known colonization with carbapenem‑resistant organisms, unless no alternative therapy is available.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Meropenem
Route
Intravenous Use
Manufacturer
Actavis Group Ptc Ehf.
Origin
EU

Related products