Product image of Klaricid Iv (Clarithromycin) supplied by GNH India

Klaricid Iv

Active Ingredient:
Clarithromycin
Origin:
EU

Klaricid Iv (Clarithromycin)

Clarithromycin, the active ingredient in Klaricid Iv, is a macrolide antibiotic presented as an intravenous solution for intravenous use. It is indicated for the treatment of bacterial infections such as community‑acquired pneumonia, acute bacterial sinusitis, skin and soft tissue infections, bronchitis, and otitis media in adult patients. It is manufactured under EU GMP standards.

GNH India supplies Klaricid Iv as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with distribution across EU and other markets, ensuring quality and regulatory compliance.

Manufacturer / TM Owner

Mylan Products Limited

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Indications & Clinical Uses

Clarithromycin is a macrolide antibiotic used to treat bacterial infections of the respiratory and skin pathways.

  • Community‑acquired pneumonia: Reduces bacterial load and improves clinical outcomes in adult patients.
  • Acute bacterial sinusitis: Clears infection and relieves sinus inflammation.
  • Skin and soft tissue infections: Controls bacterial growth and promotes healing of cellulitis and abscesses.
  • Bronchitis: Alleviates bacterial bronchial infection and improves cough symptoms.
  • Otitis media: Eradicates middle‑ear pathogens and restores hearing function.

How It Works

  • Clarithromycin binds to the 50S ribosomal subunit of susceptible bacteria, inhibiting the translocation step of protein synthesis. This blocks peptide chain elongation, resulting in a bacteriostatic effect against Gram‑positive, Gram‑negative, and atypical organisms. It also interferes with bacterial adherence and may modulate host immune responses, contributing to its clinical efficacy in respiratory and soft‑tissue infections. The drug achieves high intracellular concentrations, enhancing activity against intracellular pathogens such as Mycoplasma and Chlamydia.

Side Effects

Clarithromycin may cause adverse reactions ranging from mild to serious.

Common Side Effects

  • Nausea: Mild stomach upset occurring shortly after infusion.
  • Diarrhea: Loose stools that may be self‑limiting.
  • Taste disturbance: Altered or metallic taste during treatment.

Serious or Rare Side Effects

  • Hepatotoxicity: Elevated liver enzymes or jaundice requiring monitoring.
  • QT prolongation: Potential cardiac rhythm disturbances in susceptible patients.
  • Severe allergic reactions: Anaphylaxis or skin rash demanding immediate medical attention.

Precautions & Warnings

Clarithromycin requires careful consideration of patient‑specific factors before use.

  • Renal impairment: Adjust therapy based on clinical response and monitor renal function.
  • Hepatic dysfunction: Monitor liver enzymes regularly during treatment.
  • QT prolongation risk: Avoid in patients with known cardiac arrhythmias or electrolyte disturbances.
  • Drug interactions: Review concomitant medications for CYP3A4 inhibitors and adjust as needed.
  • Pregnancy and lactation: Use only if benefits outweigh potential risks.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Clarithromycin interacts with several drugs that may alter its safety or efficacy.

Major Interactions (Avoid)

  • Erythromycin, ketoconazole, ritonavir: May increase clarithromycin levels leading to toxicity.
  • Cisapride, pimozide: Heightened risk of severe QT prolongation.
  • Statins metabolized by CYP3A4 (e.g., simvastatin): Increased risk of myopathy.

Moderate Interactions (Monitor Closely)

  • Warfarin: May enhance anticoagulant effect; monitor INR closely.
  • Theophylline: May raise serum concentrations; monitor for toxicity.

Frequently Asked Questions

Klaricid Iv contains clarithromycin, a macrolide antibiotic administered intravenously. It is used to treat serious bacterial infections such as community‑acquired pneumonia, acute bacterial sinusitis, skin and soft‑tissue infections, bronchitis, and otitis media in adult patients.

Clarithromycin binds to the bacterial 50S ribosomal subunit, blocking the translocation step of protein synthesis. This inhibition stops peptide chain elongation, producing a bacteriostatic effect against a broad range of Gram‑positive, Gram‑negative, and atypical organisms.

The dosing regimen for Klaricid Iv is determined by the prescribing clinician based on the infection type, severity, patient weight, renal and hepatic function, and local guidelines. Healthcare professionals should follow the approved prescribing information for exact dosing.

The pregnancy category for clarithromycin is listed as unknown. Use during pregnancy or lactation only if the potential benefits justify the potential risks to the fetus or infant. Clinicians should assess each case individually and consider alternative therapies when appropriate.

To order Klaricid Iv, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies 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.

Compared with other macrolides, clarithromycin offers a broader spectrum against atypical pathogens and achieves high intracellular concentrations. It is often preferred over erythromycin for its better tolerability and pharmacokinetic profile, but clinicians must consider local resistance patterns and patient‑specific factors when selecting therapy.

Klaricid Iv should be stored at 2‑8 °C in a refrigerator. Keep the solution in its original container, protect it from light, and avoid freezing or shaking. Do not use the product if it has been exposed to temperatures outside the recommended range.

Klaricid Iv is administered by intravenous infusion. The infusion rate and duration are determined by the prescribing physician, typically over 30‑60 minutes, and should be performed by qualified healthcare personnel in a clinical setting.

Serious risks include hepatotoxicity, QT‑interval prolongation leading to arrhythmias, and severe allergic reactions such as anaphylaxis. Patients should be monitored for liver function abnormalities, cardiac rhythm changes, and any signs of hypersensitivity during therapy.

Klaricid Iv is contraindicated in patients with known hypersensitivity to clarithromycin or other macrolide antibiotics. Caution is advised for individuals with pre‑existing QT prolongation, severe hepatic impairment, or those taking medications that strongly inhibit CYP3A4, unless benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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