Klarix 250 mg is a macrolide antibiotic formulated with Clarithromycin, widely used for the treatment of a variety of bacterial infections affecting the respiratory tract, skin, and soft tissues. It is also an important component of combination therapy for the eradication of Helicobacter pylori in patients with duodenal ulcers. Klarix 250 mg offers improved acid stability and better gastrointestinal tolerability compared to erythromycin, making it a reliable option in both adult and pediatric populations.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Macrolides
Klarix 250 mg is indicated for the treatment of infections caused by susceptible organisms, including:
Upper Respiratory Tract Infections
Streptococcal pharyngitis
Acute sinusitis
Lower Respiratory Tract Infections
Infective exacerbations of chronic bronchitis
Community-acquired pneumonia
Atypical pneumonia
Skin and Soft Tissue Infections
Mild to moderate infections of the skin and underlying soft tissues
Gastrointestinal Infections
Adjunct therapy in the eradication of Helicobacter pylori in patients with duodenal ulcers
Clarithromycin acts by inhibiting bacterial protein synthesis. It binds to the 50S subunit of the bacterial ribosome, blocking translocation and thereby preventing the growth of susceptible organisms. Klarix 250 mg is active against most Gram-positive bacteria, Chlamydia, Mycoplasma, and selected Gram-negative organisms. It demonstrates greater in vitro activity than erythromycin against many Gram-positive bacteria and has approximately twice the activity against Haemophilus influenzae. Due to limited penetration, most Gram-negative bacteria remain resistant.
Adults:
Pharyngitis/Tonsillitis: 250 mg every 12 hours for 10 days
Acute maxillary sinusitis: 500 mg every 12 hours for 14 days
Chronic bronchitis: 250–500 mg every 12 hours for 7–14 days
Pneumonia: 250 mg every 12 hours for 7–14 days
Uncomplicated skin and soft tissue infections: 250 mg every 12 hours for 7–14 days
Community-acquired upper and lower respiratory tract infections: 250–500 mg every 12 hours for 5–14 days
Children:
Bodyweight under 8 kg: 7.5 mg/kg twice daily
8–11 kg (1–2 years): 2.5 ml twice daily
12–19 kg (3–6 years): 5 ml twice daily
20–29 kg (7–9 years): 7.5 ml twice daily
30–40 kg (10–12 years): 10 ml twice daily
Klarix 250 mg may be administered with or without meals.
Theophylline: Concomitant use may increase serum theophylline levels.
Terfenadine: Clarithromycin may interfere with terfenadine metabolism, increasing the risk of cardiac adverse effects.
Known hypersensitivity to clarithromycin, erythromycin, or other macrolide antibiotics
Patients receiving terfenadine with pre-existing cardiac abnormalities or electrolyte disturbances
Klarix 250 mg is generally well tolerated. Reported side effects include:
Nausea, vomiting, diarrhoea, and abdominal pain
Stomatitis and glossitis
Headache and taste perversion
Allergic reactions ranging from mild skin rashes to anaphylaxis
Rare transient central nervous system effects such as dizziness, anxiety, insomnia, and hallucinations
Klarix 250 mg is not recommended during pregnancy due to limited clinical data. Breastfeeding should be avoided during treatment, as clarithromycin is excreted in breast milk.
Use with caution in patients with hepatic or renal impairment
Prolonged or repeated use may lead to overgrowth of non-susceptible organisms, including fungi
Discontinue treatment and initiate appropriate therapy if superinfection occurs
Overdose may result in gastrointestinal symptoms. Rare cases have reported altered mental status and electrolyte imbalance following large ingestions. Management includes supportive care and elimination of unabsorbed drug. Haemodialysis and peritoneal dialysis are not effective in significantly reducing serum clarithromycin levels.
Klarix 250 mg may be used in neonates and children at appropriate dose levels.
Adults and children over 12 years: Typically 6–14 days
H. pylori eradication in duodenal ulcers: Usually 6–14 days as part of combination therapy
Store in a cool, dry place, protected from light and moisture.
Reconstituted suspension should be used within 7 days at room temperature or within 14 days if refrigerated. Keep out of reach of children.
Add 45 ml of water to the granules in the bottle and shake well to prepare 70 ml of suspension.
Each 5 ml of the reconstituted suspension contains clarithromycin 125 mg.
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