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(Approval lapsed) TAZOCIN EF 4g/500mg powder for injection vial (New Zealand)

Section 19A approved medicine
(Approval lapsed) TAZOCIN EF 4g/500mg powder for injection vial (New Zealand)
Section 19A approval holder
Pfizer Australia Pty Ltd ABN 50 008 422 348
Phone
1800 675 229
Approved until
Status
Expired
Medicines in short supply/unavailable
TAZOCIN EF 4g/500mg powder for injection vial - ARTG 132525
Indication(s)

TAZOCIN EF is indicated in the treatment of serious bacterial infections caused by susceptible strains of β-lactamase producing organisms in the conditions listed below:

  1. Lower respiratory tract infections
  2. Urinary tract infections (complicated and uncomplicated)
  3. Intra-abdominal infections
  4. Skin and skin structure infections
  5. Bacterial septicaemia
  6. Gynaecological infections
Children under the age of 12 years

In hospitalised children aged 2 to 12 years, TAZOCIN EF is indicated for the treatment of serious intra-abdominal infections. It has not been evaluated in this indication for paediatric patients below the age of 2 years.

TAZOCIN EF is indicated in the treatment of serious bacterial infections caused by susceptible strains of β-lactamase producing organisms in the conditions listed below:

  1. Lower respiratory tract infections
  2. Urinary tract infections (complicated and uncomplicated)
  3. Intra-abdominal infections
  4. Skin and skin structure infections
  5. Bacterial septicaemia
  6. Gynaecological infections
Children under the age of 12 years

In hospitalised children aged 2 to 12 years, TAZOCIN EF is indicated for the treatment of serious intra-abdominal infections. It has not been evaluated in this indication for paediatric patients below the age of 2 years.

While TAZOCIN EF is indicated only for the conditions listed above, it may be used as a single agent in the treatment of mixed infections caused by piperacillin susceptible and β-lactamase producing, piperacillin-resistant organisms. Appropriate culture and susceptibility tests should be performed before treatment in order to identify organisms causing infection to determine their susceptibilities to TAZOCIN EF. Therapy with TAZOCIN EF, however, may be initiated before results of such tests are known when there is reason to believe the infection may involve any of the β-lactamase producing organisms listed above; however, once these results become available, appropriate therapy should be continued.

In serious infections, presumptive therapy with TAZOCIN EF may be initiated before susceptibility test results are available.

Combination therapy with TAZOCIN EF and aminoglycosides may be used in the treatment of serious infections caused by Pseudomonas aeruginosa. Both drugs should be used in full therapeutic doses. As soon as results of culture and susceptibility tests become available, antimicrobial therapy should be adjusted.

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