Hi all,been put on Neurontin / Gabapentin for a vestibular problem.Just 300mg a day (Built up over three weeks from 100mg to 300mg a day) . Just wondered as i have a side effect i believe as it started around the same time i started the tablets . I have a low level headache along with a mild flu like feeling . Did anyone else have similar?
View 4 RepliesHi, I have been reading this forum for a very long time. I have been on Gabapentin since October 2011. I injured my neck January 2011. Lost the use of my left arm. Had C6-C7 acdf September 2012, fell 3 weeks later due to ataxia that came on after the surgery. X-ray showed everything in place, Cervical MRI showed C5 disk herniated minimally. For the last couple of months I've been losing sensation feeling in my hands sometimes up to my elbows. It goes to one side and the other or both at the same time. My doctor thinks it's a side effect of Gabapentin and my gut says it's not it. Has anyone heard of this side effect? I have not found this loss of sensation as a side effect in my research.
View 14 RepliesI have now been on Gabapentin for 2 1/2 months. I started slowly and am now on 1800 mg a day. I have not noticed any benefits from the tablets and my legs seem stiffer than they were before. I am thinking of slowly coming off them as I don't want to take a drug that seems to be doing nothing for me.
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?
For two years I have been suffering with a burning pain on the top of my head that has been pretty much relentless. I have had an MR I and a CT scan which haven't showed anything. I have also had an MRI of my neck which showed that I have a disc bulge at C5 to C6 but again this is apparently isn't causing the pain.
I eventually got referred to the headache clinic who told me this sounded like allodynia and recommended I start gabapentin. This was two months ago and I have worked my way up from 300 mg a day to 1800 mg a day. It has done absolutely nothing but since last week I have had a proper headache not just the burning that I cannot get rid of. I have had four days off work now because I just feel like I wouldn't be able to function. My consultant is away and the secretary recommended that I just go down to a lower dose of the gabapentin so I am now on 1200 mg but the headache is persisting. It varies between a burning pain and I squeezing pain and moves from the back, to the top and forehead.
I went to see my GP who didn't really seem interested and gave me naproxen which hasn't done anything.
First of all I would like to know if anyone has suffered with allodynia on their head and how they treated it secondly has anyone tried gabapentin and feels like I do and thirdly can anyone give me some advice because I am going crazy!
I have been on 100 mg once or twice a day for a long time, originally after a foot operation. Advised to keep on, to help arthritis pain and after effects of hip operations etc. The dose was raised to 300 mg at night and 100 mg twice a day. I always feel rather odd and have muscular convulsions over a long time, before the dose increased. Currently have shoulder aches and stiff neck with headache, put down as tension. Has anyone had similar problems, could it be the gabapentin, - so difficult to tell?
View 4 RepliesFor the past year I have experienced mild to severe head and neck pain only on right side. What would cause it and can I get rid of it completely? Some things help but it always comes back. I have not had any injury to my knowledge if so it was due to possible moving wrong or something. I can relieve the pain slightly by pushing my head down and to the left with my left hand. It's really bad if I cough or sneeze. If I massage the indentation on the right of spine on neck at base of skull it helps a little. A chiropractor has helped as well as using a water pillow but the pain eventually comes back.
View 1 RepliesI've started taking 25MG of nortriptyline for migraines- my dosage goes up to 50 MG at the end of the week. The first few days of taking it, I experienced physical exhaustion and grogginess, as well as numbness in my legs, feet, and hands, but nothing too bad that impaired me. I also have felt more mentally focused. Any thoughts?
View 2 RepliesI had a heart attack 5 weeks ago and since have been on various medicines one of which is 5mg Ramipril every night. I read the booklet which explained that a side effect is a cough but agree with other inputs here that the cough is very depressing. It constantly disrupts my sleep pattern and it's so dry ! Im off to the GPs Tomorrow and hopefully he can prescibe something else. Is there anyway else of stopping the cough ?
View 1 RepliesDoes anyone seem to sweat more on venlafaxine. I know it is a side effect but how common is it
View 55 RepliesCan someone tell me how to stop trembling on lithium as a side effect? My whole body shakes. I can stop
View 12 Repliesa have been on sertraline 50mg for 4 weeks now into my second week on 100mg a feel things are getting a lot better it is just the headaches at times are quite severe am having to take strong painkillers a know it is a side effect but are they meant to be so severe or should i go to the doctors ?
View 4 Repliesis that true that the tubal ligation can make her dry or without fluids if they made love? what the possible common side effect of the tubal ligation? please find me the answer. thanks.
View 1 RepliesI have been taking Ramipril 10mg for a few months now.
I have experienced the tickly cough, but not often so that's ok, the one problem I'm worried by is joint pain.
I went from 5mg to 7.5mg to 10mg it has been whilst I have been on this higher dose that my arm joint to my shoulder have started to hurt, with sometimes sharp pain, also a sharp pain in the base of my index finger but again very occasionally.
I worry that if I go and talk to my doctor he may try and treat the joint pain with yet another drug which itself might have side effects, and the spiral then goes on into old age.
I am only 51 and will continue to take the medication but will monitor my problems and eventually have a chat with my GP.
I have suffered with depression for some time. I used to take Citalopram but my Doctor recently changed my prescription to Fluoxetine. I had some very weird side effects at first - very strange thoughts - almost like hallucinations and felt quite 'spaced out'. However, after reading the leaflet, I saw that this can happen and will generally disappear with continued use. So I persevered.
I have been taking it now for about 8 weeks. I did stop for about a week when I was away on holiday. I hurt my back and had to take anti-inflammatory medicine. I was worried about the risk of stomach bleed that this can cause when interacting with fluoxetine so I stopped taking it. This was about 5 weeks ago. I became extremely low with thoughts of harming myself. I resumed the fluoxetine and these thoughts have subsided.
My problem is that I feel constantly tired with no motivation to do anything; I have difficulty concentrating and feel generally lethargic and lacklustre.
Does anyone else feel like this while taking Fluoxetine? I recently had a general health 'MOT' with blood tests for liver/kidney function, thyroid, blood sugar etc so it is unlikely there is a different underlying cause. Or is it just a symptom of my age/state of mind? I am 58, generally fit and active.
I had a heart attack in mid October due to a congenital enlarged artery. The stent was unsuccessful and I lost 10-15% of my heart. My EF is around 46/48 and the doctor has never mentioned heart failure, but I know I need to do all I can to try to prevent that from happening.
Anyway I am on metoprolol tartrate (beta) 12.5 twice a day, plavix, aspirin, lipitor, and in December the dr put me on a very low dose of lisinopril (Ace) 5 mg.
Lately my back has been aching as the day goes on and I feel like I can't take a deep breath. Let me clarify, when I sleep and when I first wake up I feel good and normal. But as the day goes on I start to get some muscle aches and my breathing seems weird. I don't feel like I'm about to suffocate and I can breath normally fine, but it's like I feel the need every few minutes to take a big deep breath and when I try I can't totally get a full really deep breath like I used to.
Could this be the lipitor or the lisinopril or maybe it's anxiety and it's all in my head because sometimes I don't even notice it. I take the lipitor and the lisinopril at bedtime and sleep well and wake up feeling well, this usually happens about mid-day or so.
I know dreams are a common side effect of fluoxetine, but do they ever settle down?
I seem to be having quite a few vivid and realistic dreams per night, usually about things that are worrying me which then makes me question myself as to whether it was a dream or not!
Has anyone experienced this and did it settle for you? Or is there anything we can do to ease it?
Can anyone tell me if dizzy spells are a side effect of coming off Citalopram. I have been reducing from 10mg to 5mg for the last 2 weeks and it has been going ok with a few moments of anxiety. But tonight I had to pull over on my way home after becoming dizzy at the wheel. Is this normal or might it be something else?
View 6 RepliesRECENT HISTORY
First, I am diabetic and have had a fairly normal healthy life except in the last two years where I gained 40 pounds, did not control my blood sugars well, and went off the rails. I have had a lot of issues this year, but to focus on my most recent issues, I had a A1c of 10.5 two month ago and went to 9.1 a month ago finally to 7.6 right before my single incision laparoscopic with robotic-assisted single-incision surgery to remove my infected gallbladder (Hida Scan 11% no gallstones). 6 month ago i started experiencing a lot of bloating, indigestion and took charcocaps that helped a lot after meals.
Two weeks ago I went out for a cup of iced coffee (huge coffee drinker 3-4 cups a day for a long time no problems for years), and something hit me, it felt like a sharp pain and instant feeling of bleh no appetite and sick feeling the rest of the day. This continued for a week before I knew something was wrong, I could not have anything acidic or felt like I could eat anything. I had just seen my doctor for a bike accident a month prior to get a referral to a PT and osteopathic doctor. I had a l3/l4 compressed nerve with a twisted sacral (this is much better now with some minor spasms in my right leg from time to time). With all of that pain (took hydrocodone and muscle relaxants to sleep, sleep was poor) and school, I figured I must have given myself an Ulcer. My doctor game me a ppi-omeprazole (i've never had reflux and didn't then) since I had symptoms of some burning sensations and this chronic dyspepsia so this would treat the possible Ulcer for two weeks while I was sent for an ultrasound to check out my gallbladder (family history - Mom, aunt, and uncle had their's out with gallstones). The ppi sort of helped but I just was fatigued, could not eat anything but a bland diet, I had chronic dyspepsia and general nausea that I could never shake. My daily caloric intake decreased with each new day and food just made me generally feel sick, however if I skipped meals it would still be bad, worse with food.
TEST RESULTS
After the Hida scan came back positive with an ejection rate of 11%, I scheduled my new a1c test, ekg (family history of heart disease), I was cleared and scheduled for surgery. I stopped taking the ppi as I believed this to be the cause of all my problems. btw, I was 254 the end of june and lost 25 pounds by the time of surgery (average daily caloric intake ~900-1200 prior to surgery
POST SURGERY
After the surgery 7/21-one week ago, I had my two days of pain and adjustment, and recovered decently with a soft food and liquid diet. I noticed the general sickness was gone! Hazzah!, except on Saturday I was feeling bloated, cramping, and I could not eat a solid one bite without feeling sick. I knew I was constipated. I stopped the pain meds the day before and I knew I had not eaten too much but it was over a week since i went. I took magnesium citrate and nothing after 7 hours, I drank another 1/2--then BOOM it was insane. I was sooo wiped out and tried to replace lost liquids but I believe I was dehydrated. I was sick that night and stomach was not happy.
Sunday was much better but I was wiped out still and felt generally just depleted of all my energy. I ate, walked a bit and then came back home. That night I started feeling very uncomfortable and the symptoms were somewhat similar to prior to surgery of the general dyspepsia and nausea chronically. I could not sleep because of my back problems (had to sleep upright on my back all week). I woke up in the middle of the night turned to my side and then all of a sudden I felt a warm rush of something just above my stomach and the constant burn in my stomach no reflux. I could not sleep until the morning.
NOW,
I have had really bad gas (low fat diet) for the past few days. I was getting and feeling better on day four but now this!
I felt extreme discomfort all day, felt like a low grade fever 98.6 (no fever) incision site is also slightly red, but the doctor said to call if I had a fever. I was worried about an SSI. The pain was like I threw up (I never have even starting out back in at the coffee shop) and that ache afterwards. The burning sensation let up later in the day after I took some antacids and saltines (I must have some acid issues, but I have read a lot of people suspecting many people may actually have low acid).
The thing is a lot of people have episodes after food, but mine is chronic with mild discomfort, burning sensations, upper abdomen and stomach discomfort (with some nausea), and food helps it initially and then it comes back. I feel week, slight low grade fever even though I don't have one. I keep thinking I have an infection of H. Pylori or something. Food takes a while to do much, I walk after I eat everything. I feel like I could eat but I get so much bloating and indigestion that it is uncomfortable. I drink plenty of water, but I wonder if I am low on essential things for the long ongoing low calorie daily diet. I can't eat more then 800 calories even with smaller meals-since Thursday.
Why was my gall bladder inflamed in the first place? I had no stones, and the surgeon said I had a very long a big gallbladder (ready to rupture!) that was really inflamed including a little on the liver. Pathology reports came back negative. I theorize my rapid change in weight and blood sugar levels inflamed the organ or an infection.
Possibilities:
diabetic Gastroparesis
H. Pylori
Peptic Ulcer (was never officially tested)
Gastritis
Anxiety
Low/High Stomach Acid
Low bile leak?
Sphincter of oddi dysfunction
What I feel could help:
HCL Betaine
Digestive Enzyme (Garden of life chewable vegetarian)
ppi (I would hate to take them unless I had to)
something to coat my stomach if I do have an ulcer to heal
ability to eat more so I can have more assimilated minerals, ect.
Anxiety med (first year i've had a lot of anxiety-mainly school related and upcoming wedding planning for next year
more tests!
My burning anxiety questions:
When will I get my appetite back?
(i really suspected my odds were decently good that I would get better after surgery, I had a great surgeon)
Did anyone have any of these chronic symptoms? Is it due to an infection or some issue with surgery?
Have some people eventually been able to eat what they wanted after a period of time?
How many had these excessive bloating, indigestion, nausea and general malaise through the day, worse a little while after food or between meals?
Is there anyone out there who is taking the anti-hypertensive Perindopril [ACE Inhibitor] and has developed Pulsatile Tinnitus as a side effect? I take this drug and do not have any side effects only that last February I was diagnosed with slight hearing loss for which I was given hearing aids and had Pulsatile Tinnitus which sent me rapidly to the G.P. from where I was referred to the ENT dept. at the hospital. I've had a MRI brain scan, Intercranial CT scan and Doppler scan on my neck in the Vascular Dept. where I saw a consultant. He told me there was nothing wrong in my brain or my ears but he couldn't help my problem as it is very rare and he hadn't seen a similar case for 17yrs. He said maybe my brain will eventually get fed up of listening to my heart beat swishing through my left ear. Has anyone experienced the same?
View 1 RepliesI take lithium carbonate for bipolar and think it's the best thing since sliced bread for the bipolar but there's a chance that the distended stomach I have is a side effect.Does anyone else have this side effect?
View 1 Replies