anyone get muscle pain from melatonin?

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The last time I tried melatonin, several years ago, I woke up with severe muscle pain. (Actually I usually have severe muscle pain, but this was much worse.) Any ideas why this could be, or what I could try instead?

Mike
 

rosie26

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How much were you taking ? I started on 1mg at night and am now taking only 1/2 tablet each night. I haven't noticed any increase in muscle pain while taking melatonin.
 
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It didn't help noticeably. At the time I had a number of other things interfering with my sleep which have since improved, so maybe it's worth trying again. The major improvement is that I take Neurontin which cures my restless legs syndrome.
 

rosie26

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Perhaps it's worth trying again, but start out on a lower dose of 1mg or 1/2mg.

I don't know anything about Neurontin, so you should check first about interactions before starting melatonin.
 

ukxmrv

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I changed to a different brand of relayed release 3mg tablets and the side effects I had before (grogginess, almost a depression like a constant lower mood, brainfog) disappeared straight away.
 

Purple

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The last time I tried melatonin, several years ago, I woke up with severe muscle pain. (Actually I usually have severe muscle pain, but this was much worse.) Any ideas why this could be, or what I could try instead?

Mike

Hi Mike,

My experience with melatonin has been mixed. For a while, it helped greatly with sleep but as my ME progressed, it was no longer helping with sleep and eventually it gave me not only a groggy feeling (without actually sleeping) but also within about an hour of taking it my bodywide pain would increase greatly and I would be breathless and brainfogged to the point of being zombified. My own theory (which could be completely wrong, so please bear this in mind) is that melatonin being a hormone with which other hormones interact meant that this was a reaction caused by many hormones being out of sync. I have not changed brands/dosages during this time period and am not particularly sensitive to chemicals or drugs (unless feeling very ill in general) so I think this was due to the fact that as the disease progressed, the hormonal and chemical imbalances have changed and adding melatonin to this mix was causing a havoc. As I said, this is my own lay-person theory and observation :)
 
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