P32 Sodium Phosphate description, usages, side effects, indications, overdosage, supplying and lots more!

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P32 Sodium Phosphate

AnazaoHealth Corporation

P32 Sodium Phosphate




FULL PRESCRIBING INFORMATION

Dear Medical Professional,

Per your order, we have compounded P32 Sodium Phosphate as a sterile intravenous solution dispensed in a 10 mL plastic vial with a total volume of 4 mL. The characteristics of this preparation are described below.

AnazaoHealth’s compounded P32 sodium phosphate vial is a sterile, non-pyrogenic radiopharmaceutical. The intravenous solution contains 0.25 N sodium acetate buffer, which is made of 0.9% sodium chloride and 0.09% sodium phosphate dibasic, and is compounded to a total volume of 4 mL. The pH of the solution is between 5 and 6.

P32 sodium phosphate is indicated for the treatment of polycythemia vera and is effective for the treatment of chronic myelocytic leukemia and chronic lymphocytic leukemia. It may also be used in the palliative treatment of selected patients with multiple areas of skeletal metastases

Radioactive phosphorous concentrates to a very high degree in rapidly proliferating tissues

P32 sodium phosphate should not be used as part of a sequential treatment with a chemotherapeutic agent. It should not be administered when the leukocyte count is below 5,000/cu mm or a platelet count that is below 150,000/cu mm.

In chronic myelocytic leukemia, it should not be administered when the leukocyte count is below 20,000/cu mm.

For the treatment of bone metastases, it is usually not administered when the leukocyte count is below 5,000/ cu mm and platelet count is below 100,000/cu mm

For polycythemia vera, intravenous dosages from 1 to 8 mCi are usually given depending upon the stage of disease and the size of the patient. Repeat doses must be adjusted to individual needs. For chronic leukemia, the individual dose is 6 to 15 mCi, usually administered with concomitant hormone manipulation

Figure 1

P32 Sodium Phosphate

P32 Sodium Phosphate

P32 Sodium Phosphate SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:51808-128
Route of Administration INTRAVENOUS DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PHOSPHORUS P-32 PHOSPHORUS P-32 10 mCi

Inactive Ingredients

Ingredient Name Strength
SODIUM ACETATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51808-128-01 4 in 1 VIAL

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2012-06-19


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