Amoxycillin sodium injection

Product Details
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Name Of Product(Genric Name) :

Amoxycillin sodium injection

Dosage :

250MG/500MG/1GM

Product Description :

AMOXYCILLIN SODIUM INJECTION
250 mg / 500 mg / 1 g

Sterile Powder for Solution for Intravenous or Intramuscular Administration

  1. COMPOSITION

Each vial contains:

Amoxycillin Sodium equivalent to Amoxycillin ............... 250 mg

or

Amoxycillin Sodium equivalent to Amoxycillin ............... 500 mg

or

Amoxycillin Sodium equivalent to Amoxycillin ............... 1 g

Excipients: As applicable.

  1. PHARMACEUTICAL FORM

Sterile, white to off-white powder for solution for intravenous or intramuscular administration.

  1. THERAPEUTIC CLASS

Aminopenicillin Antibiotic

  1. INDICATIONS

Amoxycillin Sodium Injection is indicated for the treatment of bacterial infections caused by susceptible microorganisms.

It may be used in the treatment of:

• Respiratory tract infections
• Urinary tract infections
• Skin and soft-tissue infections
• Bone and joint infections
• Intra-abdominal infections
• Biliary tract infections
• Septicemia and bloodstream infections
• Meningitis caused by susceptible organisms
• Other infections caused by susceptible bacteria

Treatment should be guided by the susceptibility of the causative organism and applicable antimicrobial guidelines.

  1. CONTRAINDICATIONS

Amoxycillin Sodium is contraindicated in patients with known hypersensitivity to amoxycillin, penicillins, cephalosporins, or any component of the formulation.

  1. DRUG INTERACTIONS

Particular consideration may be required with concomitant use of:

• Probenecid
• Methotrexate
• Anticoagulants such as warfarin
• Other β-lactam antibiotics
• Other medicines requiring renal monitoring

The treating physician should review all concomitant medications before administration.

  1. ADMINISTRATION

Amoxycillin Sodium Injection may be administered by intravenous or intramuscular route according to the approved product information.

The contents of the vial should be reconstituted with a suitable compatible diluent under appropriate aseptic conditions.

For intravenous administration, the reconstituted solution should be further diluted as required and administered by a qualified healthcare professional according to the approved product information and institutional protocol.

For Intravenous or Intramuscular Use Only.

  1. STORAGE

Store according to the storage conditions stated on the approved product label.

Protect from excessive heat, moisture and light.

After reconstitution/dilution, use within the period specified in the approved product information.


Dry Powder Injection