Product image of Klaricid (Clarithromycin) supplied by GNH India

Klaricid

Active Ingredient:
Clarithromycin
Origin:
EU

Klaricid (Clarithromycin)

Clarithromycin, the active ingredient in Klaricid, is a macrolide presented as an intravenous solution for intravenous use. It treats a range of bacterial infections in adults and children when administered by infusion.

GNH India supplies Klaricid as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Viatris Healthcare Limited

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Indications & Clinical Uses

Clarithromycin is a macrolide antibiotic used to treat infections caused by susceptible bacteria.

  • Community‑acquired pneumonia: effective against typical and atypical pathogens, improving respiratory function.
  • Skin and soft‑tissue infections: eradicates susceptible Gram‑positive and some Gram‑negative organisms.
  • Upper respiratory tract infections: reduces bacterial load and alleviates symptoms.

How It Works

  • Clarithromycin binds to the 50S ribosomal subunit of susceptible bacteria, blocking the translocation step of protein synthesis. This inhibition prevents peptide chain elongation, halting bacterial growth and leading to a bacteriostatic effect against a broad spectrum of Gram‑positive, Gram‑negative, and atypical organisms.

Side Effects

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: loose stools, often transient.
  • Abdominal pain: cramping or discomfort.
  • Taste disturbance: altered or metallic taste.
  • Headache: mild to moderate intensity.
  • Vomiting: occasional episodes.

Serious or Rare Side Effects

  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • QT prolongation: risk of cardiac arrhythmias.
  • Severe allergic reactions: rash, angioedema, anaphylaxis.
  • Clostridioides difficile‑associated diarrhea: severe colitis.
  • Arrhythmias: ventricular tachycardia or fibrillation.
  • Stevens‑Johnson syndrome/toxic epidermal necrolysis: severe skin reactions.

Precautions & Warnings

Clarithromycin should be used with caution in specific clinical situations.

  • Renal impairment: monitor renal function and adjust therapy as needed.
  • Hepatic dysfunction: assess liver enzymes before and during treatment.
  • Cardiac risk: avoid in patients with known QT prolongation or electrolyte disturbances.
  • Drug interactions: review concomitant medications for potential CYP3A4 effects.
  • Pregnancy and lactation: evaluate risk‑benefit ratio before prescribing.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Clarithromycin interacts with several drugs; careful assessment is required.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, ritonavir): may increase clarithromycin levels.
  • QT‑prolonging agents (e.g., quinidine, sotalol): additive risk of arrhythmia.
  • Ergot alkaloids (e.g., ergotamine): risk of ergotism.

Moderate Interactions (Monitor Closely)

  • Warfarin: may increase INR and bleeding risk.
  • Theophylline: may raise plasma concentrations, causing toxicity.
  • Statins (especially simvastatin): increased risk of myopathy.

Frequently Asked Questions

Klaricid contains clarithromycin, a macrolide antibiotic administered intravenously to treat serious bacterial infections such as pneumonia, skin and soft‑tissue infections, and certain upper respiratory tract infections.

Clarithromycin binds to the bacterial 50S ribosomal subunit, inhibiting protein synthesis by blocking peptide chain elongation, which stops bacterial growth and helps clear the infection.

The dosage and infusion rate of Klaricid are determined by the prescribing clinician based on the infection type, severity, patient weight, renal and hepatic function, and local guidelines.

Clarithromycin is classified as a pregnancy‑category B drug in many regions, but its use should only be considered when the potential benefit justifies any potential risk to the fetus. Breastfeeding mothers should consult a healthcare professional before use.

Submit an enquiry on the Klaricid product page at gnhindia.com, specifying the required quantity. GNH India works with 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.

Klaricid (clarithromycin) offers a broader spectrum against atypical pathogens and better tissue penetration than some older macrolides like erythromycin, while sharing a similar safety profile. It is often preferred for severe infections requiring intravenous therapy.

Klaricid should be stored at 2‑8 °C, protected from light, and kept in its original container. Do not freeze or shake the solution. Once removed from refrigeration, use within the time frame specified by the manufacturer.

Klaricid is given as an intravenous infusion by a qualified healthcare professional. The infusion rate and duration are set by the prescriber, typically over 30‑60 minutes, and the solution should be administered using aseptic technique.

Serious risks include hepatic dysfunction, QT‑interval prolongation leading to arrhythmias, severe allergic reactions such as anaphylaxis, and Clostridioides difficile‑associated colitis. Patients should be monitored for these events during therapy.

Klaricid is contraindicated in patients with a known hypersensitivity to clarithromycin, other macrolides, or any component of the formulation. Caution is advised for individuals with significant hepatic impairment, prolonged QT interval, or those taking contraindicated interacting medications.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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