Product image of Klaritromicin Krka (Clarithromycin) supplied by GNH India

Klaritromicin Krka

Active Ingredient:
Clarithromycin
Origin:
EU

Klaritromicin Krka (Clarithromycin)

Clarithromycin, the active ingredient in Klaritromicin Krka, is a macrolide antibiotic presented as an oral tablet for systemic use. It treats a range of bacterial infections, including respiratory and skin infections, and is used in combination regimens for Helicobacter pylori eradication.

GNH India supplies Klaritromicin Krka as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Clarithromycin is employed to treat bacterial infections affecting the respiratory tract, sinuses, skin and gastrointestinal system.

  • Community‑acquired pneumonia: eradicates susceptible pathogens, improving breathing and preventing complications.
  • Acute bacterial sinusitis: relieves sinus inflammation by eliminating the causative bacteria.
  • Acute bacterial bronchitis: reduces cough and bacterial load in the lower airways.
  • Skin and soft‑tissue infections: clears susceptible skin pathogens and promotes healing.
  • Helicobacter pylori eradication: part of combination therapy to eliminate H. pylori and heal gastric ulcers.

How It Works

  • Clarithromycin binds to the 50S subunit of bacterial ribosomes, blocking the translocation step of protein synthesis. This inhibition prevents elongation of the peptide chain, exerting a bacteriostatic effect against susceptible Gram‑positive and some Gram‑negative organisms. By halting bacterial growth, the immune system can more effectively clear the infection.

Side Effects

Clarithromycin may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Nausea: transient upset stomach.
  • Diarrhea: loose stools, often mild.
  • Abdominal pain: cramping or discomfort.
  • Altered taste: metallic or bitter sensation.
  • Headache: mild to moderate.
  • Vomiting: occasional episodes.

Serious or Rare Side Effects

  • Severe allergic reactions (anaphylaxis): rash, swelling, difficulty breathing.
  • QT interval prolongation: risk of cardiac arrhythmias.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.
  • Clostridioides difficile‑associated diarrhea: severe colitis.
  • Stevens‑Johnson syndrome/toxic epidermal necrolysis: extensive skin blistering.
  • Cardiac arrhythmias: irregular heartbeats beyond QT prolongation.

Precautions & Warnings

When prescribing clarithromycin, clinicians should consider several safety measures.

  • Assess renal and hepatic function: dose adjustment may be required in impairment.
  • Avoid use in patients with known macrolide hypersensitivity: discontinue if reaction occurs.
  • Monitor ECG in patients with cardiac risk factors: risk of QT prolongation.
  • Use caution in pregnancy: limited data, weigh benefits against potential risks.
  • Avoid concomitant use with other QT‑prolonging agents: increased cardiac risk.
  • Store at ambient temperature below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Clarithromycin interacts with several medicines; some require avoidance, others close monitoring.

Major Interactions (Avoid)

  • Erythromycin or other macrolides: additive toxicity and increased risk of QT prolongation.
  • Cisapride or domperidone: heightened risk of serious cardiac events.
  • HIV protease inhibitors (e.g., ritonavir): markedly increased clarithromycin plasma levels.
  • Theophylline: elevated theophylline concentrations leading to toxicity.

Moderate Interactions (Monitor Closely)

  • Warfarin: enhanced anticoagulant effect, monitor INR.
  • Statins such as simvastatin or lovastatin: increased risk of myopathy.
  • Carbamazepine: reduced clarithromycin exposure, may diminish efficacy.
  • Digoxin: modest increase in serum levels, monitor for toxicity.

Frequently Asked Questions

Klaritromicin Krka, containing clarithromycin, is indicated for community‑acquired pneumonia, acute bacterial sinusitis, acute bacterial bronchitis, skin and soft‑tissue infections, and as part of combination therapy for Helicobacter pylori eradication. The drug targets susceptible bacterial strains in these conditions.

Clarithromycin binds to the 50S ribosomal subunit of bacteria, blocking the translocation step of protein synthesis. This inhibition stops the formation of new proteins, exerting a bacteriostatic effect that limits bacterial growth and allows the immune system to clear the infection.

The dosage of Klaritromicin Krka is determined by the prescribing clinician based on the specific infection, patient age, weight, renal and hepatic function, and other clinical factors. Patients should follow the exact regimen prescribed by their healthcare professional.

Safety data for clarithromycin in pregnancy are limited, and the drug is classified as pregnancy category unknown. It should only be used when the potential benefit justifies any potential risk to the fetus. Clarithromycin is excreted in breast milk; breastfeeding mothers should consult their physician before use.

To order Klaritromicin Krka, 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 (including any cold‑chain requirements) and necessary import documentation.

Clarithromycin, the active ingredient in Klaritromicin Krka, offers a broader spectrum against certain atypical pathogens compared with older macrolides like erythromycin. It also has a more favorable pharmacokinetic profile, allowing twice‑daily dosing, but shares class‑related risks such as QT prolongation and drug‑interaction potential.

Klaritromicin Krka should be stored at ambient temperature below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct sunlight, and ensure they are out of reach of children.

Klaritromicin Krka is administered orally, typically as whole tablets swallowed with a glass of water. The exact dosing schedule, including frequency and duration, is set by the prescriber based on the infection being treated.

Serious risks include severe allergic reactions (anaphylaxis), QT interval prolongation leading to potentially life‑threatening arrhythmias, hepatic dysfunction, Clostridioides difficile‑associated diarrhea, and rare skin reactions such as Stevens‑Johnson syndrome. Patients should seek immediate medical attention if they experience symptoms like rash, chest pain, or persistent vomiting.

Klaritromicin Krka should be avoided in individuals with known hypersensitivity to clarithromycin or other macrolides, patients with a history of significant QT prolongation, and those taking medications that strongly interact to increase cardiac risk. Clinicians must also assess renal or hepatic impairment before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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