I just got back from my dr, they want to wean me from dilantin to Keppra, b/c of "chest pain side effects" and continued problems with balance issues after last sz.
Crabby'ness? oh just great! now i got that to ""look forward to""?
I had been taking it for 6 months. Not for chest pain but for Raynaud syndrome. I have been off for 12 days. I am a little light headed. The Dr says its sick sinus syndrome and I am scheduled for a pacemaker tomorrow. I am last minute looking for anything else this can be maybe causing a temporary slow heat rate. It was only detected 4 weeks ago.
In hiatal hernia a part of the stomach sticks upward into the chest and causes chest pain, heartburn, and swallowing difficulty. Since you have been operated for hiatal hernia it seems to be unlikely.Gastroesophageal reflux disease is another possibility. The common causes of chest pain are muscle strain, sprain, pleurisy, asthma, costochondritis.A bruised or broken rib, and panic attack all can lead to pain in chest.GERD can cause heartburn and chest discomfort.
My daughter is now experiencing several side effects to keppra. She is extremely drowsy, very short tempered, depressed, and is reporting to me that her memory is 'foggy'. She's on a very low dose of keppra, only 250 mg at night and 125 mg in the morning. She's been on it a total of 3 weeks now. I've been with her and she seems to be very melancholy and also short fused over the many situations. She weighs 100 pounds and is 20 years old.
I have muscle spazms along with the in my arms and legs. Chest pain occasionally. Ive had acid reflux and IBS since i was 16. Taking nexium, and whatever else they can prescribe to help, but mine is cronic so theres not much they can do. I have only had one seizure so far.. But im wondering what i can tell myself with all these symtoms im having. Iv heard people talk about Raynauds syndrom? But i dont seam to have cold feet or hands alot of the time, occasionally. And no discoloration.
i am confused now because this is rather sudden and my son is used to the valparin now and has no side effects as such. the doctor says that this is for better seizure control since eeg is abnormal but the eeg has been abnormal for the past 8 years then why now? i am all confused and when i told the doctor i will change medication only during vacation time so that i can moniter him.
They are like a partial complex seizure. I saw a neurologist and was started on Keppra. I was up to 2,500mg a day and they were not stopping. I began to track them carefully and I believe I saw a pattern of only during the 2nd half of my monthly cycle, days 15 - 28 (and usually between 18 and 21) My neurologist decided to put me in the hospital to do a video EEG monitoring and I told him the dates it needed to be. We hit it right and it was determined that my seizures are NES.
Anyone else on Keppra to prevent myoclonic jerks (JME diagnosed)? I am, and have been on Keppra for almost 5 years. Started at age 23 and I am now 28. At the beginning they made me very sluggish, but after about 2 months I felt wonderful (since it was the first time in my life I wasn't having seizures!!
after about a year the b6 injections were stopped as my b6 levels where back to normal
the vitamin injections had no effect on the muscle pain and pins and needles/numbnes in my hands and forearms . i have had many tests over the years to check my nervous system is ok and everything comes back fine
over the last 4 years i had had a few muscle injures in my arms and wrists which i think are connected to me taking kepra .then 2 months ago i injured my middle finger on my left hand.
After a very frightening last 2 weeks of my boyfriend on Keppra my doctor did say to ween him off which I've done. Today is the first day off it and he still seems to have the dillusional aggressive side effects that I am hopeful after reading your post.....I pray to god that the old person before this drug comes back. How was those last few weeks for your son?
Just recently I had a new diagnosis of Juvenile Myoclonic Epilepsy and was put on Folic Acid and Keppra. So now I'm taking three medications. I have only had one grand mal seizure, but every day my mind does this thing where it kind of blanks out when I'm talking and I stare for a couple of seconds, that's when I took an EEG and it determined I had JME. But since I have been on Keppra my mind hasn't spaced out, but I have been in a lot of pain.
TL;DR: I think Keppra makes me dehydrated because alcohol makes me feel super-dehydrated even if I follow the 2:1 water:alcohol ratio, and because I seem to have a hard time staying hydrated in general. But I'm seeing little if any literature to support dehydration as a Keppra side effect. Does anyone else have any ideas?
TL;DR: I think Keppra makes me dehydrated because alcohol makes me feel super-dehydrated even if I follow the 2:1 water:alcohol ratio, and because I seem to have a hard time staying hydrated in general. But I'm seeing little if any literature to support dehydration as a Keppra side effect. Does anyone else have any ideas?
Was on lamicatal er when shaking started on right side of body but had a allergic reaction to it..
Isn't this the gommunity due to neuropathy pain from keppra?
I to have been taking Keppra and told can't drive for six months, yesterday my Oncologist informed me that only a Neurologist can authorize driving and I will need to probably get off keppra to get permission to drive. Was also informed that you can not just stop this drug.
i take 3000 mg of keppra and 600 mg of tegratol a day,)not a typo) still not fully seizure free and am having alot of dizzy spells.which i was told by my neuro that it was vertigo due to the pollen in the air. can all this med make me gain weight. not a little person , but have gain about 20 pounds in the last month or so. wating or exercise habbits have not changed. could it be the meds.
But last month I started seeing a new neurologist, who said that this is neither a Keppra thing nor an epilepsy thing, and in fact, he has no idea what it's about. And that Keppra is processed through the kidneys, not the liver. So I'm back to the drawing board.
And two neurologists now have told me it's okay to drink, provided that I never get drunk (because that does lower your seizure threshold). And as previously stated, alcohol doesn't get me drunk anymore anyway.
So after staying overnight and at the vet the next day he came home and has been on Keppra and phenobarbital. 500mg 2x a day Keppra and 60mg 2x a day pheno. He has the side effects which are lessening but hasn't been as bad as I read could be. He is very responsive and is pretty much himself besides the side effects(weak legs, tired). It's been 6 days and no seizures so far. Will be going to vet in a week for check up and blood test again. I am so on edge..
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