Pancuronium Bromide (AstraZeneca) is a medicine containing the active ingredient(s) pancuronium. On this page you will find out more about Pancuronium Bromide (AstraZeneca), including side effects, age restrictions, food interactions and whether the medicine is subsidised by the government on the pharmaceutical benefits scheme (PBS)
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Active ingredient in this medicine: pancuronium
Information for medicine and pack size:
Pancuronium Bromide (AstraZeneca) 4 mg/2 mL injection solution, 50 x 2 mL ampoules
Consumer Medicine Information leaflet:
This leaflet may also be found inside the medicine package. It contains information on side effects, age restrictions and other useful data.
What this medicine is for
INDIACTIONS AS AT 1 JANUARY 1991: 1. As an adjunct to surgical anaesthesia to induce skeletal muscle relaxation to facilitate operative manipulations. The necessary conditions for intubation can be achieved with pancuronium bromide alone or following suxamethonium. 2. Pancuronium bromide is also indicated to promote mechanical ventilation by reducing or eliminating spontaneous breathing effort in intensive care patients.
Table of characteristics
|Visual appearance||Clear colourless solution|
|Dosage Form||Injection, solution|
|Route of administration||Intravenous|
2mL x 50: Prescription Only Medicine, or Prescription Animal Remedy
There is one type of pack available.
Pack type 1
|Storage temperature||Store at 2 to 8 degrees Celsius|
|Storage conditions||Do not Freeze,Refrigerate|
|Life time||2 Years|
We were unable to verify that this medicine is available on the PBS (Pharmaceutical Benefits Scheme). Please consult your pharmacist if you need further information
The PBS provides a list of government subsidised medicines available to be dispensed to patients. Further information can be found on the Pharmaceutical Benefits Scheme website.
Is this medication banned in sport?
Check if you can use your medicine whilst playing sport. Search the Australian Sports Anti-Doping Authority (ASADA) database that provides information about the prohibited status of specific medications and/or the active ingredient based on the current World Anti-Doping Agency (WADA) Prohibited List.