Zopiclone - Side Effects
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I was prescribed Zopiclone about four years ago as a remedy for chronic insomnia - I have Fibromyalgia and the lack of sleep was absolutely killing me. At first I was just really, really happy to be getting 8 hours of solid sleep and woke up feeling like I could take on the world. However, one morning I woke up as usual and opened my bedside drawer to get my daily vitamins out and I discovered several chocolate wrappings! I couldn't remember eating any chocolate and so I asked Husband if he had put the wrappers in my drawer (even though I was pretty sure this wasn't something he would do). Husband then told me that about an hour after I had said goodnight and left him in the lounge watching telly, I'd come back into the lounge and asked if we had any chocolate. Seems that somewhere between getting into bed and actually falling asleep, a severe chocolate craving had overcome me! Even more odd was the fact that Husband told me this wasn't the first time it had happened and that I had regularly gotten up after going to bed and meandered around the house, eaten chocolates, drunk tea or coffee and had lucid conversations with him. Suffice to say I gave Husband strict instructions to hide the chocolates well and to send me back to bed should I ever get up after having said goodnight.
The second strange thing that occurred after starting with Zopiclone was that I could feel my teeth, and I mean really, FEEL. MY. TEETH. It was perhaps the most odd sensation I've ever had and together with the metallic taste (which I had been told to expect) it made eating, drinking, talking and smiling quite unbearable. I'm not sure why I never linked the feeling the teeth thing with Zopiclone and actually pursued other avenues like gum disease and receding gums in an attempt to 'cure' myself!
The third, and perhaps worst, side effect - also something I never linked to the use of Zopiclone until now, was recurrent urinary tract infections. We had just moved (in my defence) and I honestly thought there was just 'something in the water'! On average I would say I had a UTI every two to three weeks and they would vary in severity from mild irritation quickly remedied with Citrasoda to debilitating infections remedied only with a long course of anti-biotics.
Then about eight months ago now, I decided that I could no longer take Zopiclone, it had stopped working effectively and when my dosage was increased I was left feeling very foggy the next day and the metallic taste in my mouth was magnified and frankly, just unacceptable. If I had half an hour sleep a night for the first four weeks, I was lucky. To be honest I can't even tell you how I made it through but I was determined that I was not going backward and that this lack of sleep would have to kill me before I took another Zopiclone. The good news is that within weeks my teeth returned to normal, the metallic taste was almost non-existent and I hadn't had to see the doctor about a UTI in what seemed a lifetime.
I'm curious whether anyone else has had similar side effects (extra sensitive teeth and recurring urinary tract infections) - or is it just me?!
8 likes, 55 replies
mary_70540 NinaBallerina
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worrier mary_70540
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nigel24977 mary_70540
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I have been taking Zopiclone for over 7 years and often with alcohol. I have tried many times to stop this cycle as it has cost me many friends. In March this year I quit both for two months without any major side effects apart from depression during the day and nightmares that seemed to know exactly which insecurities to target. However I hung on in there and managed to lose over 2 stone in weight and I felt a lot better and proud of myself
I had a relapse in July and have just started what I see as my ‘recovery’ again. However this time I am finding it much harder mainly because of the nightmares which scare the life out of me. If I manage to get through the night though I can put them behind me and have a reasonable day although fighting the depression is a daily challenge. I am however taking 2 x 7.5 Zopiclone about every other night if the nightmares prove to be too much for me.
I feel very alone in this struggle as I buy the drugs off the internet and have not shared this struggle with anyone. I am hoping to share my struggle here and would appreciate any help or advice I could get
nicola99781 NinaBallerina
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worrier nicola99781
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nicola99781 worrier
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nigel24977 nicola99781
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henrybasset NinaBallerina
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Cant be a lot of help I am taking 3.75 dose which is the smallest I think I have only been taking them for a short period on a nightly basis however do not like side effects so over last week have cut in half & now take less than that. Strangely they still work in making me sleep however down side is that the side effects though not as bad are still there so hopefull to shortly come off them altogether.
Previously I found a low dose 10mg of amiltryptaline helped me sleep & took them for 15 years however although not addictive one of the longterm effects was that it dried up my voice box so that I virtually lost my voice.
A specialist diagnosed & within a few days of not taking voice was 90% better, but that took 15 years to happen.
one thing for sure long term Zopiclone is a no no, have you tried contacting a site called I think CITAP or similar
nicola99781 henrybasset
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jules1170 NinaBallerina
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Somnophage NinaBallerina
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By week five I decided out of curiosity to take a few crumbs of the last zopiclone in pack which was mouldering away in drugs cabinet. Symptoms were all gone within a few hours!..
As someone who has spent his life since childhood on opiates and opoids, I suspect that Zopiclone mimics morphine far more closely than the companies would have us believe..
Instead of the ridiculous, and dangerous, kneejerk policy by UK doctors; a more sympathetic approach through monitored withdrawal would be sensible.
SeaWhisper1 NinaBallerina
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I have also had a summer full of bladder infections and now none this year.
I have been on Zop (Imovane) for 19 years, and now after several months of horror stories I am in rehap to get off of this drug! Having a sleep study conducted this friday. I am so livid about this drug and what it had done to my life and sleep, I feel like writing a book. Imovaine was a blessing for the first 10 years (I have CFS and FM) and then I gradually built up a tolerance to the drug and now it has bitten me in the ass. I am so addicted and struggling to get off of this nightmare. Cathie
tessa17608 SeaWhisper1
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cindy78245 SeaWhisper1
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yvonney tessa17608
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