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Gdclar 250

Gdclar 250 Tablet is an antibiotic manufactured by G.D. Laboratories Pvt. Ltd. in Nepal. Its active ingredient is Clarithromycin 250mg. You might also find it available as a 500mg tablet.

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Description

Gdclar 250 is prescribed to treat a variety of bacterial infections. These include:

  • Respiratory tract infections: Such as pharyngitis, tonsillitis, acute maxillary sinusitis, acute bacterial exacerbation of chronic bronchitis, and pneumonia (including community-acquired pneumonia and legionellosis).
  • Skin and soft tissue infections.
  • Leprosy.
  • Peptic ulcer disease: Especially when caused by Helicobacter pylori. It’s often used as part of a multi-drug treatment plan.
  • Lyme disease.
  • Acne.

 

How Do You Take It?

 

The exact dosage depends on the specific infection and the patient’s age. Always follow your doctor’s instructions carefully.

 

Adult Dosing (Oral)

 

  • Acute Exacerbation of Chronic Bronchitis: Typically 250-500 mg by mouth every 12 hours for 7-14 days. An extended-release form might be 1000 mg once daily for 7 days.
  • Mycobacterial Infection (Prophylaxis and Treatment): Usually 500 mg by mouth every 12 hours for 7-14 days, often in combination with other anti-mycobacterial drugs like rifampin and ethambutol.
  • Peptic Ulcer Disease: 500 mg by mouth every 8-12 hours for 10-14 days. This is given as part of a 2- or 3-drug combination regimen (e.g., with bismuth subsalicylate, amoxicillin, an H2 receptor antagonist, or a proton pump inhibitor).
  • Pharyngitis, Tonsillitis: 250 mg by mouth every 12 hours for 10 days.
  • Community-Acquired Pneumonia, Skin/Skin Structure Infection: 250 mg by mouth every 12 hours for 7-14 days. The extended-release form might be 1000 mg once daily for 7 days.
  • Endocarditis Prophylaxis: 500 mg by mouth 30-60 minutes before a surgical procedure.

 

Adult Dosing (Intravenous)

 

  • Respiratory Tract Infections; Skin and Soft Tissue Infections; Susceptible Infections: 500 mg twice a day for 2-5 days, infused over 60 minutes using a 0.2% solution. Your doctor will switch you to oral therapy as soon as possible.

 

Adult Dosing (Topical)

 

  • Apply a thin layer to the affected area once daily.

 

Child Dosing (Oral)

 

  • 15 mg/kg per day, with a maximum of 1 gram per day, given every 12 hours.

 

Renal Impairment

 

  • If your creatinine clearance (CrCl) is less than 30 ml/min, your dosage may need to be halved or the dosing interval doubled.

 

Administration

 

  • Standard release tablets and oral suspension: You can take these with or without food.
  • Extended-release (XL) and modified-release (MR) tablets: These must be taken with food. Swallow them whole; do not chew or crush them.

 

Important Considerations

 

 

Contraindications (When NOT to take it)

 

  • If you have a known hypersensitivity to clarithromycin or other macrolide antibiotics.
  • If you are currently taking medications like terfenadine, astemizole, pimozide, cisapride, or ergot derivatives (e.g., ergotamine).
  • During pregnancy.
  • If you have a history of acute porphyria.

 

Precautions

 

  • Use with caution if you have kidney or liver impairment.
  • Be aware of the potential for macrolide cross-resistance (meaning resistance to clarithromycin might imply resistance to other macrolides).
  • Lactation: Clarithromycin is excreted in breast milk, so use with caution if you are breastfeeding.
  • Children: Use with caution as directed by a physician.

 

Drug Interactions

 

Clarithromycin can interact with many other medications, potentially altering their effects or increasing the risk of side effects. Some important interactions include:

  • Reduced efficacy of clarithromycin: This can occur with CYP3A inducers (e.g., phenytoin, carbamazepine, efavirenz, rifampicin).
  • Increased levels/toxicity of other drugs: This can happen with ritonavir, quinidine, disopyramide, sildenafil, tadalafil, vardenafil, digoxin, verapamil, HMG-CoA reductase inhibitors (statins), oral hypoglycemic drugs (e.g., pioglitazone), insulin, oral anticoagulants, aminoglycosides, and triabenzodiazepines (e.g., midazolam).
  • Bi-directional drug interactions: These can occur with atazanavir, itraconazole, or saquinavir.
  • Potentially Fatal Interactions:
    • Concurrent use with ergot alkaloids (e.g., ergotamine or dihydroergotamine): This can lead to acute ergot toxicity, characterized by vasospasm and ischemia of the extremities.
    • Concomitant use with astemizole, cisapride, pimozide, and terfenadine: This may result in QT prolongation or serious ventricular cardiac arrhythmias.

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