Related topic: Prostate cancer, Urine albumin/creatinine ratio increased
Review: could Prostate cancer cause Urine albumin/creatinine ratio increased?
Summary: Urine albumin/creatinine ratio increased could be caused by Prostate cancer, especially for people who are male, 60+ old, also have Cerebrovascular disorder, and take Casodex.
We study 14,127 people who have Prostate cancer from FDA and social media. Among them, 4 have Urine albumin/creatinine ratio increased. Find out below who they are, other conditions they have and drugs they take.
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Prostate cancer (latest reports from 53,417 patients) is typically treated by Flomax, Casodex, Avodart, Zoladex, Lupron, Lupron Depot.
Urine albumin/creatinine ratio increased
Urine albumin/creatinine ratio increased (latest reports from 509 patients) has been reported by people with high blood pressure, diabetes, type 2 diabetes, hyperlipidaemia, prostate cancer.
On Apr, 11, 2014: 14,124 people who have prostate cancer are studied. Among them, 4 (0.03%) have Urine Albumin/creatinine Ratio Increased. They amount to 0.79% of all the 508 people who have Urine Albumin/creatinine Ratio Increased on eHealthMe.
Age of people who have prostate cancer and experienced Urine albumin/creatinine ratio increased * :
|Urine albumin/creatinine ratio increased||0.00%||0.00%||0.00%||0.00%||0.00%||0.00%||0.00%||133.33% |
Severity of the symptom * :
Top co-existing conditions for these people * :
- Cerebrovascular disorder (2 people, 50.00%)
- Deep vein thrombosis (2 people, 50.00%)
Most common drugs used by these people * :
- Casodex (4 people, 100.00%)
- Diovan (2 people, 50.00%)
* Approximation only. Some reports may have incomplete information.
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I had prostate surgery at Alexian Bros Hospital in Hoffman Estates in June, 2005. Radiation treatment began Northwestern Hospital in October and a Zoladex injection in early November.
Taste loss occurred about 3 to 4 weeks after injection. Taste came back within 1 month.
one night,about 3 weeks after the zoladex was injected, I felt as if I had bugs crawling under my skin from the knees down. It felt as if my nerve were misfiring. It was not painful.However, I lost all muscular control of my feet from my ankle down which gradually improved over the 12 to 18 months. Since then, I have regained complete muscular control of my feet, but I do not have 100% feeling in my feet. Also, my legs feel heavy and it is sometimes difficult to walk. My brain says go, but my legs wont fully respond.
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