Hi Aussie99, - Here in the U.S., the Manufacturer's printed Prescribing Instructions that is legally required to accompany the drug's prescript
ion fulfillment include the following statements (at least some, if not all, required by our Federal Drug Administration) due to acknowledged Study results.
WARNINGS AND PRECAUTIONS ----------------
•
AVODART reduces serum prostate-specific antigen (PSA) concentration by approximately 50%. However, any confirmed increase in PSA while on AVODART may signal the presence of prostate cancer and should be evaluated, even if those values are still within the normal range for untreated men. (5.1)
•
AVODART may increase the risk of high-grade prostate cancer. (5.2, 6.1)
•
Assess patients to rule out other urological diseases, including prostate cancer, prior to prescribing AVODART. (5.3)
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Women who are pregnant or could become pregnant should not handle AVODART Capsules due to potential risk to a male fetus. (5.4, 8.1)
•
Patients should not donate blood until 6 months after their last dose of AVODART. (5.5)
I am not sure that anyone completely understands the reasons for Avodarts reduction effect on PSA, EXCEPT that it is well established that the reduction in PSA that takes place with its use, is NOT proportionately due to reduction in Prostate size or ANY reduction in PCa tumor size. In fact the following statement is included as part of the required printed admonisions: "Limitations of Use: AVODART is not approved for the prevention of prostate cancer."
What IS clear, is that the doubling of PSA readings while on Avodart (after 3 to 6 months) is necessary, to provide accurate comparisons with readings when not on the drug and any increase while on the Avodart regimen, should specifically be assessed for a potential relationship to Prostate Cancer (PCa). Hope this helps and good luck in your continued AS. Remain vigilant! -
[email protected] (aka) az4peaks