Cloxacillin Sodium for Injection

This product is a semi-synthetic penicillin with the characteristics of acid resistance and penicillinase resistance. It has antibacterial activity against Gram-positive cocci and Neisseria. Its antibacterial activity against enzyme-producing strains of Staphylococcus (including Staphylococcus aureus and coagulase-negative Staphylococci) is stronger than that of oxacillin, but its antibacterial effect on penicillin-sensitive Staphylococci and various streptococci is weaker than that of penicillin, and it is ineffective against methicillin-resistant Staphylococci.

The main component of this product is cloxacillin sodium, and its chemical name is (2S,5R,6R)-3,3-dimethyl-6-[5-methyl-3-(2-chlorophenyl)-4-isoxazolecarboxamido)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid sodium salt. Molecular formula: C19H17ClN3NaO5S Molecular weight: 457.87

This product is white powder or crystalline powder.

This product is only suitable for the treatment of penicillinase-producing staphylococcal infections, including sepsis, endocarditis, pneumonia, and skin and soft tissue infections, etc. It can also be used for mixed infections caused by pyogenic Streptococcus or pneumococcus and penicillin-resistant staphylococci.

1. Intramuscular injection: 2g per day for adults, divided into 4 times; 25-50mg/kg per day for children, divided into 4 times. 0.5% lidocaine can be added during intramuscular injection to reduce local pain. 2. Intravenous drip: 4-6g per day for adults, divided into 2-4 times; 50-100mg/kg per day for children, divided into 2-4 times. 3. For newborns weighing less than 2kg, 25mg/kg per day is given according to body weight every 12 hours from 1 to 14 days old, and 25mg/kg per day is given according to body weight every 8 hours from 15 to 30 days old; for those weighing more than 2kg, 25mg/kg per day is given according to body weight every 8 hours from 1 to 14 days old, and 25mg/kg per day is given according to body weight every 6 hours from 15 to 30 days old. Patients with mild and moderate renal impairment do not need to adjust the dose, and patients with severe renal impairment should avoid using large doses to prevent central nervous system toxicity.

1. Allergic reactions: Urticaria and other types of rashes are common, leukopenia, interstitial nephritis, asthma attacks and serum sickness reactions may also occur. Severe cases such as anaphylactic shock are occasionally seen; once anaphylactic shock occurs, it is necessary to rescue on the spot, keep the airway open, inhale oxygen, and give treatment measures such as epinephrine and glucocorticoids. 2. Intravenous injection of this product may occasionally cause nausea, vomiting and elevated serum aminotransferase. 3. Large doses of this product may cause convulsions and other central nervous system toxic reactions. 4. There are reports of hematuria, proteinuria and uremia in infants after taking large doses of this product. 5. Agranulocytosis or cholestatic jaundice occurs in some cases.

It is contraindicated in patients with a history of allergy to penicillins or a positive penicillin skin test.

1. This product is incompatible with aminoglycosides, norepinephrine, metaraminol, phenobarbital, vitamin B group, vitamin C and other drugs, and should not be dripped in the same bottle. 2. Probenecid can reduce the renal tubular secretion of cloxacillin and prolong the serum half-life of this product. 3. Aspirin and sulfonamides inhibit the binding of this product to serum proteins and increase the free blood concentration of this product.

Keep tightly closed in a dry place.

3.0g (calculated as C19H18ClN3O5S)

North China Pharmaceutical Company.Ltd

• Founded in:

  1992-12-20

• Address:

  No. 388, Heping East Road, Shijiazhuang City

• Tax NO.:

  91130100104397700P

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  1,715,730,370 yuan

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