Cloxacillin is indicated for the treatment of infections caused by Gram-positive organisms. It is also indicated for infections caused by penicillinase-producing staphylococci. Such infections include:
500 mg four times daily, taken 30 minutes to 1 hour before meals.
250 mg every 4 to 6 hours.
500 mg every 4 to 6 hours. The dose may be doubled if clinically necessary.
500 mg once daily.
500 mg once daily.
Dissolve 250 mg in 1.5 mL, or 500 mg in 2 mL, of Water for Injections BP.
Alternatively, cloxacillin for injection may be added to a compatible infusion fluid or diluted appropriately and given via a drip tube over 3 to 4 minutes.
Dissolve 500 mg in 5–10 mL of Water for Injections BP before administration.
Dissolve 500 mg in not more than 5 mL of Water for Injections BP or 0.5% lignocaine hydrochloride solution before administration.
Administer 30 minutes to 1 hour before meals.
Cloxacillin is a semi-synthetic, penicillinase-resistant isoxazolyl penicillin. It exerts a bactericidal effect by inhibiting bacterial cell wall synthesis. Its resistance to hydrolysis by penicillinase (beta-lactamase) enzymes allows it to remain active against beta-lactamase-producing staphylococci that would otherwise inactivate standard penicillins.
Following oral administration, bioavailability ranges from approximately 37% to 60%; absorption is reduced when the drug is taken with food. Cloxacillin is widely distributed to the liver, kidneys, bone, bile, pleural fluid, synovial fluid, and ascitic fluid; only minimal amounts reach the cerebrospinal fluid. Approximately 90–95% of the drug is bound to plasma proteins. It is partially metabolised to active and inactive metabolites, and both the parent compound and metabolites are rapidly excreted in the urine by glomerular filtration and tubular secretion.
The side effects of cloxacillin are similar to those of other penicillins and are generally mild and transient. They include fever, diarrhoea, indigestion, and rash (urticarial or erythematous). If a rash of any type develops, cloxacillin should be discontinued immediately.
Cloxacillin is contraindicated in patients with a known hypersensitivity to penicillin.
Cloxacillin should be used with caution in patients with a history of allergy. It must not be administered as a subconjunctival injection or as eye drops.
Cloxacillin syrup and drops should be freshly prepared immediately before use and stored in a cool place (refrigerated if possible). Once reconstituted, syrup and drops must be used within 5 days if stored at room temperature, or within 7 days if refrigerated.
Solutions prepared for intramuscular or intravenous use should be administered within 30 minutes of preparation. However, aqueous solutions of cloxacillin remain stable at room temperature (25°C) for up to 24 hours.
Cloxacillin for injection may be mixed with most intravenous infusion fluids. It must never be mixed with protein-containing fluids such as protein hydrolysates.
Patients with significantly reduced renal function (creatinine clearance below 10 mL/min) are at increased risk of cloxacillin accumulation. Doses should be carefully monitored and reduced as appropriate in these patients.
Each 500 mg capsule of cloxacillin sodium contains a small amount of sodium. This should be taken into account in patients who require dietary sodium restriction, such as those with congestive heart failure, hypertension, or fluid retention.
Cloxacillin is classified as Pregnancy Category B. There are no adequate and well-controlled studies in humans, and no literature reports of congenital abnormalities associated with its use. Cloxacillin should be used during pregnancy only when clearly necessary.
Cloxacillin passes into breast milk in small amounts. After a single 500 mg intramuscular dose, milk concentrations of 0.1 to 0.3 mg/L have been measured at 1 to 6 hours post-dose. These levels are not expected to cause adverse effects in breastfed infants; however, as with other penicillins, occasional disruption of the infant's gastrointestinal flora resulting in diarrhoea may occur. Cloxacillin is generally considered acceptable for use in nursing mothers.
No specific overdose data for cloxacillin capsules are established. In cases of significant overdose, particularly in patients with severe renal impairment, high concentrations of cloxacillin may cause neurological effects. If overdose is suspected, discontinue the drug, provide symptomatic and supportive care, and seek immediate medical attention.
Warfarin: Cloxacillin may reduce the anticoagulant effect of warfarin. Patients receiving both drugs should have their coagulation status monitored closely.
Probenecid: Co-administration with probenecid may increase and prolong cloxacillin plasma concentrations by reducing renal tubular secretion of the antibiotic.
All dosage forms of cloxacillin should be stored in a cool, dry place. Cloxacillin injection vials should be stored at a temperature not exceeding 25°C.
A-Clox 500 mg price in Bangladesh is ৳5.98 per capsule (৳598 per strip). Prices may vary by pharmacy and are updated regularly on this page.
Cloxacillin is indicated for the treatment of infections caused by Gram-positive organisms. It is also indicated for infections caused by penicillinase-producing staphylococci. Such infections include: Skin and Soft…
Yes, A-Clox is an antibiotic. Antibiotics should only be taken on a doctor's advice and the full course should be completed even if symptoms improve early.
Always consult a registered physician before taking any medicine. Prices shown are MRP and may vary by pharmacy.
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