Gabapentin :: For Essential Tremors - How Long To Take It?
Nov 21, 2015
I have only been on Gabapentin for 6 wks. 100 mg. 1 x day. Do I need to taper off. From what I read, I don't want to continue or increase it. I have essential tremors and they have been a lot worse. Also, I have extreme fatigue.
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I was prescribe gabapentin and on day one I has blurred vision and felt like someone was sitting on my chest it was hard to breath I gelt winded and anxious now day three and its getting worse I had my pulse and oxygen level checked it was 97 pulse and 10 oxygen level this time I was feeling tremors, winded, heaviness to my chest, blurred vision, extremely dizzy (I actually feel), numbness and tingling in my hands and feet...
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i was on lyrica. Worked great but too costly. Switched to gabapentin 300 3x daily 4 days ago. Flu like symptoms... Body aches but legs and joints so achy and small stabbing pains all over. How long does this last?
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My wife has had migraines every day since January 2014. The last 9 months have been very difficult. We have tried many types of medication/treatments.
Currently she is trying Gabapentin (600mg per day).
Does anybody know how long it can take for Gabapentin to have an effect?
Is it possible for Gabapentin to make migraines worse?
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I have been on Gabapentin on and off for about 7 months (since approx January). I was taking it for chronic pelvic pain, and it worked well, but it made me very emotional and made higher cognitive functions difficult. After 4 months of semi-regular use, I got off it quickly, but kept it around in case of a severe pain flare up. As of now I have gone through 2 "100 capsule" bottles of 100mg pills, so not too much. Never took a higher dosage then 300 mg and never took more than 300 mg in one day.
I've used it a few times recently (in July, just a few weeks ago) when the pain really flared up, thinking it would only have minimal side effects, but it has resulted in continual severe depression and dark thoughts even though I haven't taken any in two weeks. I took it occasionally because I thought the depression was predominantly from the chronic pain, but now I realize the gabapentin was the root of it. I'm terrified because I know the drug has long since left my system but I can't shake the side effects. Doctors and psychologists won't listen to me. They say I'm just depressed and it isn't the medication, but I'm positive it is. The pain is finally improving, I'm going back to school, and things are looking up. But there is this unshakable aurora that is plaguing me. No matter how hard I distract myself and push through there's this cloud that impairs my ability to emotionally and physical function (feelings of detachment, separation, depression, and some suicidal thoughts). Words come slower, it's harder to focus, memory is very dull. I wasn't concerned within the first few days, but it's been a few weeks now and I'm alarmed that it doesn't seem to be improving.
Do the side effects ever go away... How long does it take and what can catalyze the healing process? Is it possible to incur permanent damage from a low dosage, or does it take months to heal. Can anyone explain the biomechanics behind how gabapentin can affect patients weeks after usage.
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My husband has been suffering with unbearable headaches for 15 years. Over the last few months they have become so much worse to the point that he is in a ball, crying in pain, he can't see, can't walk, he was ranting during one attack that he was going to take all of the tablets he could find. He has no memory of saying these things when the headache has eased. He tells me the headache is there constantly but gets worse really quickly. He usually wakes up with the headache although they sometimes come on during the day. They are usually at the sides of his head above his eyes but swaps sides and sometimes goes down his neck. He gets them everyday for a week then has a few days to a week then they start again. He has had a number of GPs all of which have said he doesn't need to be referred to a specialist it is migraines as if it was anything 'serious' we'd have known by now ie nOt a brain tumour. He has had many preventative medicines but none have helped. His latest GP has prescribed gabapentin which was prior to his last and worst attack so far. When we explained what happened she merely raised the dosage and gave imigran for pain relief. I just wondered if anyone has been prescribed gabapentin long term for migraines and if there are any long term side effects as I've heard there are a number namely vitamin B 12 deficiency, pulmonary problems, long and short term memory loss.
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I'm 19 Years old and I have Essential Tremor.
So, I've been taking Inderal for the last 3 months and it's not working on my tremors. Have you had any experience with Primidone and, if so, can you tell me if it worked on you?
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I'm 19 years old and I have ET and anxiety because of that.
I went to my second appointment with my neurologist and I told him about my tremors and my anxiety. And that the dose I was taking (10mg Inderal 3 times a day) was not working. I was feeling no side effects or improvements on my tremors and anxiety. So this time he raised the dose to 20mg 3 times a day and he said that If 60 mg per day doesn't improve my tremors It's not worth to give me a higher dose. So, I told him If he could give me some medicine to take in anxious situations. He gave me Alprazolam 0.25 mg to take only in anxious situations in a maximum of one per week, because taking it in long term can affect my mental ability.
So, let me ask you some questions:
If 60 mg of Inderal per day doesn't improve my tremors, it means that's not worth taking a higher dose?
There is something alternative to improve my tremors If Inderal can't?
There is any anti-anxiety medicine that's not too strong that could calm down my anxiety and I could take it long term? (I only need to take it in 6 months or less depending on how I'm adapting, because I'm going to work for the first time outside my country for 6 months and I will feel very anxious because of my tremors.)
Since my doctor prescribed me Alprazolam 0.25 mg in stressful situations to calm down my anxiety, can I take a higher dose, like 0.50 mg If I feel that 0.25 mg doesn't get me more relaxed?
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The doctor told me that I have a fatty liver & they told me that I shuold take 'Essential Forte' a vitamin tablet. I couldn't get the tablet.Is it worsen the situation if I do not take the medicine?
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wanting to contact others who have the same condition. Sometimes it is genetically related or not.
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I noticed tremors on my body since I was 12. But it was mild tremors that I didn't care about. But since November 2014 my tremors got worse and now I have tremors all over my body. For example, when I try to do abs my trunk starts to tremble, when I lift my legs against the gravity, they start to tremble a lot, when I try to smile my face trembles, when I'm with my friends and try to drink some tea from a tea cup my hand and my head starts to tremble, and I feel that my neck and my head will start to tremble if I move in a "No" movement, and sometimes when I am in a place with lots of people my legs starts to shake and I get very embarrassed about that and they start to shake even more. So I went to a neurologist and I showed to him the positions that I tremble and my situation, and he said that some people has more physiologic tremor than others (even though I think that I have essential tremor), and he had to give me something for the anxiety, but I tremble a lot, and when I'm cold my body trembles a lot (a lot more than normal people). He gave me Inderal 10 mg to take 3 times a day . But it's not working on controlling my anxiety. I also tried to take 20mg and it didn't work as well and I'm not having side effects too. But the problem is I get anxious because of my tremors and not the opposite . If I had no tremors, I wouldn't have a reason to be anxious. I already went to the only 2 neurologists that I have on my city and only the second one gave me some medication. I really want this tremors to stop. I know he gave me that dosage because the anxiety makes the tremors worse but not even for the anxiety it's working. And I'm going to work out of my country with people that I don't talk and I will get very embarrassed with this tremors... So what should I do?
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Has anyone had this happen? I had gone up from the 20mg dose to the 40mg dose and was doing better. Less depression and the goal was to ease my fibro pain (I currently take Gabapentin and Tramadol) and eventually stop taking Tramadol. I suddenly started shaking. I had muscle jumps (can't think of another way to describe it) in my legs and I literally shook so bad I couldn't turn pages on my Kindle without trying a few times. It was disturbing.
The doctor called me back said to go back to the 20mb dose. I continued to shake...but it lessened. I am now going off it by taking it every other day (20mb) and can't get the Dr. to return my call.
I have tried all the Fibro drugs. Lyrica didn't work. Savella caused bad rapid h/b. Effexor caused muscle jumps in my legs too (but not hand shaking).
If I continued to take it would the hand tremors go away? No one can answer that. Pain is worse since I have eased off so it was actually working. I want to continue if it will lesson, but I don't know if it will.
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I suffered severe depression and anxiety and began to get bad tremors around 6 months ago, this was a first for me. My psychiatrist and GP thought it was because I was taking Sodium Valproate which is a mood stabiliser, however I have now come off that (still taking antidepressants, 80mg Lovan daily) but I still have the tremors.
My GP suggested Parkinson's but that I shouldn't have the brain scan now because medicare are not covering them.
Could anyone give me their thoughts on what I should look for in Parkinson's other than the tremors?
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The only way to get through this "transition" in the best possible way is to stay informed as to what is going on with our bodies. Being as though every woman is different, what may work for one may not work for the other. But knowledge is key to being able to live our lives the best and healthiest way possible.
With that being said, I came across some information on the internal shaking and jitters. Now this info may not apply to you, but if if does, by all means take it and do more research on your own to help yourself. Some of the first symptoms that I experienced that started to really ramp up anxiety for me is the racing heart and the internal shaking. I felt the the shaking in my chest and stomach mainly, but I could feel it all over. At times I would get the racing heart with it.
The shakiness and jitters first. We already know that the decline in estradiol can affect blood sugars, and digestive issues. For some the shakiness and jitters can be due to the blood sugars and dietary changes can help to stable that during peri/meno if you are not a true diabetic. It can also be due to anxiety and adrenaline surges. The other possibility can be digestive related. Since the digestive system is affected by declining hormones we digest food slower and have more gas than we usually do as well as an excess of stomach acid. I since have been diagnosed with GERD as many women do in peri/meno and I do have excessive gas and stomach acid which causes that burning feeling. For me what has been causing that internal shaky feeling in my chest and stomach is stomach acid putting pressure behind the breast bone which irritates the vagus nerve that can cause the anxiety type symptoms. If I chew a tums or take an acid reflux tablet the internal shakiness and jitters stop. Drinking chamomile tea, ginger capsules or tea, tums, rolaids, omeprazole, zantac, cal/mags or whatever you choose to use calms the stomach acid, calms the vagus nerve and neutralizes excess gas. Also when the vagus nerve is irritated it can cause heart palps and that is why when your reflux is acting up the excess acid pushing the vagus nerve can start palps. Now again this may not be the case for all, but it may be for some. So I thought that I would share the info just in case it may help you.
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Does anyone that suffers from Benign Essential Tremor suffer from muscle twitching involuntary jumps and cramp in hands and fingers?
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I'm seeing a neurologist next week because of the above symptoms. I'm a 68 year old woman and my GP said it's the way my body is aging! I'm not so much worried (about for example Parkinson's) as intrigued. I know lots of people suffer hand and finger tremors but I am a bit unnerved by my hands and fingers moving very, very slowly on their own. As I stop typing for a moment my right little finger has raised itself from the keyboard as if it were being pulled but very very slowly. My whole hand will slowly curl and even my arms will move on their own if I am "at rest". It's probably something with no explanation but I wonder if anybody else who has been diagnosed with a neurological/muscular condition has experienced this symptom. I do feel as if I am trembling right through my body and my feet will also move independently if I keep still long enough. I don't seem to have any other Parkinson's symptoms.
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I was prescribed cyclizine tablets for vomiting and nausea. I was admitted into hospital for a week in 2014 suffering side effects from taking Cyclizine. I am still suffering side effects.
Below are some of my side-effects:
Chorea, tremors, affecting the head, hands, feet and face
neurological disorder characterized by jerky involuntary movements
disorientation, speech problem, blurred vision, hearing problem,
breathing problem and loss of balance.
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I have been on 1200 mil a day for 3 mos. my pain has gotten better and I an thinking about getting off of gabapentin . I am not going to stop a once. I will gradually get off. Is it any side effects I can expect from stopping the drug?
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I am now on my third rheumatologist who now tells me that the painkillers I take - oxycontin, co-codamol and oxynorm all of which are opiate painkillers are obviously not working -give the man a star - he has said that gabapentin may work has anyone used this for arthritis before.
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Dr. Just started me on Gabapentin. I'm taking it for anxiety. I'm very sensitive to meds so he started me on 100 mg 3x day. Depending on how I feel, he will up dosage in 2 wks. Will I feel anything on this low dose?
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Was on Gabapentin for a year and worked up to 3200 mgs a day. Was taking it for Osteo Arthritis in feet and knees. Didn't do much for pain so decided to get off of it. My Dr said to take 1600 mgs for 5 days the drop to 800 mgs for 5 days! This was 3 weeks ago still fighting withdrawal. It's eased up some but still have some anxiety and like pressure in my chest. Almost makes me feel short winded at times. Has anyone else had this and how long will the withdrawal last? Have heard the longer you was on it the longer it takes. Tired of it just want to feel normal again.
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