Master Formula

Instructions on how to compound a sterile IV product in a hood while gowned and garbed appropriately:

Inpatient Pharmacy

IInfusion Pharmacy

  1. Assemble appropriate drug(s) and diluent; complete documentation of lot numbers, expiration dates & manufacturer name if not completed already. Affix auxillary labels as appropriate.

  2. Take the drug(s) & diluent to the appropriate hood to compound based on the information on the label.

  3. Hazardous drugs will be prepped within a class II, Type B2 Biological Safety Cabinet, in the ISO Class 7 negative pressure room.
  4. Non-hazadous drugs will be prepped in a laminar air flow hood in the ISO Class 7 positive pressure room.

  5. Assemble approriate syringe(s), needle(s), and alcohol swabs as required.

  6. For hazardous drugs requiring safe handling precaution, use the closed system transfer device (CSTD) on the vial and the syringe tip.
    • Use P14 (blue cap) for vial size of < 20 mL
    • Use P50 (green cap) for vial size of < 50 mL

  7. Inspect vials for particles and discoloration before removing vial caps; wipe rubber tops with alcohol swab.

  8. If drug requires reconstitution, obtain pharmacist precheck of the volume of diluent to be reconstituted with the drug.

  9. Draw up the amount of drug as directed according to the preparation label; eliminate air bubbles from the syringe.

  10. If the volume added to the bag is ≥ 10% of the volume of the diluent, then remove the same volume of diluent as the drug volume prior to adding the drug volume (e.g., if adding 30mL to a 250mL bag, then remove 30mL of diluent first).
    • Overfill volume average per manufacturer:
      • 50 mL = 5 mL
      • 100 mL = 10 mL
      • 250 mL = 30 mL
      • 500 mL = 50 mL
      • 1000 mL = 50 mL

  11. Place all items for checking in the pass through chamber.

  12. Pharmacist to perform quality review by verifying: all calculations are correct; ingredients are drawn up with correct volume and are free of particulates, cores, and discoloration; the selection of tubings, filter needle (if needed), base solution IV bags and auxillary labels are correct; and the expiration date is correct.

  13. After mixing, compounding technician will sign the bag product label indicating they compounded it.

  14. Place in amber bag if light protection required

  15. Dispose of waste in the appropriate waste container