A few days ago, I got a Macmillan advice of a new forum entry about possible side effects to Prostap, Every time I click on it, it says "being reviewed!" or something like that - Why has it not appeared? - I am very interested in what replies may be forthcoming
Hi Cambrian, I’ve been waiting for this one as well to see what came up. I’m getting my 4th injection on Tuesday and I’d be interested to hear from others. Personally I feel a fair bit of joint stiffness, muscle weakness and fatigue at times. The hot flushes although maybe not so frequent are pretty intense at times , especially at night. This wakens me and then it’s time to go for a pee and if this occurs a few times there’s another night of disrupted sleep. My specialist did state at my meeting after my RT that because my PSA was undetectable I could speak to my GP and come off the 2 year course, but, as this was originally the timeline I have decided to stick with it. Hope this gives some others a bit of an insight on things whereby they are not alone on this treatment plan. Best wishes to all ️
Thanks Beefy. I have been on Prostap since 2021. No side effects for three years, then same as you, joint stiffness, muscle weakness and fatigue. The hot flushes do not bother me much, usually come in the night, but not often. I just fold the bedclothes back and wait for it to cool down, after which, I go to sleep quite easily. I have not had surgery or radiotherapy. I am now 81 and have never had any pain from it, but these side effects are really wearing me down, and I am fed up of "see your GP!" GP says "everything has side effects, even crossing the road !" I have been crossing the road on my own for more that 70 years, and never had any side effects from it! When lying down, or sitting down, I feel quite normal, but start moving about and "wham" side effects! I still hope to hear that something can be done about it! I generally sleep very well. Get up sometimes 2 or 3 times a night, sometimes not at all, but always back to sleep easily.
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