it is one month since I started taking Casodex and 17 days since first Lupron shot. Now I am having hot flashes regularly. Every day when I get up from bed I have an episode like clockwork. Somedays it is very intense and other days moderately strong. Throughout the day I get more episodes at random.
I never had any testosterone blood test before Firmagon and Lupron shots as part of cyberknife treatment for an extra capsular recurrence in 2016. In January 2018, when my PSA was undetectable I had T value of 44. Then when my PSA started rising I recovered T. But the recovered T value hovered around 300 between August and November.
One explanation of why I started having hot flashes a week after starting Casodex could be low normal T. Also the residual hot flashes after last Lupron shot in April 2017 did not go away completely.
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dac500
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Yep, I am on Lupron and zytiga.....get hot flashes as well...it stinks...for women, they advise use of black cohash tea for perimenopausal/menopausal women....some of the other people on this forum may have ideas.... Good luck and hang tough....keep fighting
Hi . It is said over and over in so many posts but I have to agree - exercise does wonders to reduce/minimize so many adverse side effects of so many treatments/drugs.
I’ve been on Lupron for almost 18 months ..... since I started walking (3 to 5 miles most days according to my phone ) hot flashes have been less frequent and more moderate when they do occur . Plus , weight gain is minimized .
So if you can , there are so many reasons to get moving .
Everyone reacts differently to these medications. Prior to my diagnosis at age 54, I had gained 15 pounds in the last 37 years. Following the start of treatment, I gain 15 pounds in six weeks. Exercise had a little to do with it. I just couldn’t stop eating. That remains the same today, eight years following my diagnosisRegardless of exercise
ALL DIFFERENT.... Venlafaxine raised my hot flashes at night compared to Megace. Also eye sight deteriorated the whole time I was on it.. 20/30 to 20/200. Eye sight changes listed in side effects, just didn't expect it to be me. Back on megace and hoping for eyes to improve.
Mine lasted for about 5 weeks and then they are gone . Till the next shot which I just got and they are back. But my testosterone is down and my PSA are only .21 that worth the hot flashes
Was given gabapentin for foot neuropathy. Doesn't seem to have made that much better (but is it keeping it from getting worse?). Only side effect I've had: almost took away all my hot flashes.
Interesting... I was taking gabapentin after my heart surgery. Hot flashes stopped after heart surgery, but then I stopped taking gabapentin as nerve pain had subsided. Sadly, hot flashes came back. Must have been the gabapentin stopping the damn hot flashes....
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