Product image of Klacid I.V. (Clarithromycin) supplied by GNH India

Klacid I.V.

Active Ingredient:
Clarithromycin
Origin:
EU

Klacid I.V. (Clarithromycin)

Clarithromycin, the active ingredient in Klacid I.V., is a macrolide antibiotic presented as an intravenous solution for intravenous use. It treats a range of bacterial infections, including pneumonia, sinusitis, skin infections, certain mycobacterial diseases, and is part of combination regimens for Helicobacter pylori eradication, in both adult and pediatric patients when oral therapy is unsuitable.

GNH India supplies Klacid I.V. as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and oncology centres worldwide, with validated quality systems and reliable logistics.

Manufacturer / TM Owner

Viatris Sia

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Indications & Clinical Uses

Klacid I.V. (clarithromycin) is employed to treat bacterial infections that are susceptible to macrolide therapy.

  • Community‑acquired pneumonia: achieves clinical cure and bacterial eradication.
  • Acute bacterial sinusitis: reduces symptoms and clears infection.
  • Skin and soft‑tissue infections: resolves cellulitis, abscesses and related conditions.
  • Mycobacterial infections (e.g., Mycobacterium avium complex): used in combination regimens to suppress disease progression.
  • Helicobacter pylori eradication (in combination therapy): contributes to successful eradication when paired with other agents.

How It Works

  • Clarithromycin binds to the 50S subunit of bacterial ribosomes, inhibiting the translocation step of protein synthesis. This action blocks the elongation of the peptide chain, resulting in a bacteriostatic effect against susceptible organisms. By preventing the production of essential proteins, the drug curtails bacterial growth and facilitates clearance by the immune system.

Side Effects

Clarithromycin administered intravenously may be associated with a range of adverse reactions.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: frequent loose stools.
  • Abdominal pain: cramping or discomfort.
  • Taste disturbance: altered taste perception.

Serious or Rare Side Effects

  • Hepatotoxicity: elevated liver enzymes or jaundice.
  • QT prolongation: cardiac rhythm changes that may lead to arrhythmia.
  • Severe allergic reactions: anaphylaxis, angioedema, or Stevens‑Johnson syndrome.
  • Clostridioides difficile infection: risk of severe colitis.

Precautions & Warnings

When prescribing Klacid I.V., clinicians should consider several safety factors.

  • Renal impairment: dose adjustment may be required in patients with reduced kidney function.
  • Hepatic disease: monitor liver function tests during therapy.
  • Cardiac risk: avoid in patients with known QT prolongation or who are taking other QT‑prolonging drugs.
  • Pregnancy and lactation: safety not established; use only if benefits outweigh risks.
  • Drug interactions: review concomitant medications for potential macrolide interactions.
  • Store at below 25°C: keep in original container, protect from light and moisture.

Avoid Interactions

Clarithromycin can affect the plasma levels of several co‑administered drugs.

Major Interactions (Avoid)

  • Concomitant use with cisapride or pimozide: may cause serious cardiac arrhythmias.
  • Co‑administration with ergot alkaloids: risk of ergotism due to increased plasma levels.
  • Simultaneous use with colchicine in renal impairment: heightened risk of toxicity.

Moderate Interactions (Monitor Closely)

  • Statins (e.g., simvastatin, lovastatin): increased risk of myopathy; consider dose reduction.
  • Warfarin: may enhance anticoagulant effect; monitor INR closely.
  • Carbamazepine or phenytoin: may reduce clarithromycin levels; monitor therapeutic response.

Frequently Asked Questions

Klacid I.V. contains clarithromycin and is indicated for the treatment of bacterial infections such as community‑acquired pneumonia, acute bacterial sinusitis, skin and soft‑tissue infections, certain mycobacterial diseases, and as part of combination therapy for Helicobacter pylori eradication.

Clarithromycin inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit, blocking the translocation step of peptide chain elongation. This bacteriostatic action prevents growth of susceptible organisms and assists the immune system in clearing the infection.

The appropriate dose of Klacid I.V. is determined by the prescribing clinician based on the infection being treated, patient age, weight, renal and hepatic function, and local guidelines. Dosage regimens are not standardized in this summary.

Safety data for clarithromycin during pregnancy and lactation are limited, and the product is classified as pregnancy category unknown. It should only be used when the potential benefit justifies any potential risk to the fetus or infant.

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, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Clarithromycin offers a broader spectrum against certain Gram‑positive and atypical organisms compared with azithromycin, and it has a higher oral bioavailability, though the intravenous formulation is useful when oral intake is not possible. Both belong to the macrolide class, but clarithromycin may have more drug‑interaction potential due to CYP3A4 inhibition.

Klacid I.V. should be stored below 25 °C, protected from light and moisture, and kept in its original packaging until use. Once reconstituted, the solution should be used within the time frame specified in the product labeling and discarded if any discoloration or particulate matter is observed.

The product is given by intravenous infusion. It is typically diluted in a compatible IV fluid and infused over a period recommended by the prescriber, often 30 minutes to 1 hour, depending on the clinical situation and patient tolerance.

Serious risks include QT interval prolongation, which can precipitate life‑threatening arrhythmias, hepatotoxicity presenting as elevated liver enzymes or jaundice, and severe hypersensitivity reactions such as anaphylaxis or Stevens‑Johnson syndrome. Prompt monitoring and discontinuation are advised if these events occur.

Patients with a known hypersensitivity to clarithromycin or other macrolides, those with a history of significant QT prolongation, and individuals with severe hepatic impairment should avoid Klacid I.V. unless a clear clinical benefit outweighs the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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