Has anyone else here tried it?? Epi added this to my Tegretol XR in hopes it will stop my seizures completely since I still have a few after the last brain surgery. It's the lowest dose possible and so far nothing really bad to report other than the same side affects as any other anti-seizure med. I've had horrible headaches since my surgeries and now my mom who believes she's a doctor tells me that this medicine is what's causing my headaches and I should stop it. NO, I didn't listen to her just wondering if anyone else has any info to share about Vimpat?? Hope all of you are doing wonderful!

((((Tigerlilly))))

I've got no experience with that med but I am having dreadful headaches so I am sympathyzing with you. I'm ready to give up and just curl up in a ball and scream...

I hope you get the info you need,

Rhian

Hi Tiger Lilly,

I wish you the best on the Vimpat I know that some of the side effects are as follows:

dizzyness, faint feeling, slow or irregular heartbeat, very moody, poor balance, headaches, and sometimes a violent temper. If heart disease runs in your family I wouldn't take the drug because it puts you at a higher risk for heart attacks that's why I refused the drug when my epi wanted to put me on it. It also can cause suicidal thoughts like many AED's do. You have to watch your liver and kidneys while on this drug also. I hope the drug works well for you. Wishing you the best of luck and May God Bless You!

Sue

I am sorry to hear you are still having seizures after your surgery. I had surgery 12 years ago and still take one med. I also took Tegretol for many years, and it did not stop them. So after surgery. my Epileptologist changed me from Tegretol to Keppra and Lamical which kept me seizure free. I later on my own stopped one med because of cost and stayed with the Keppra. I still take it. The only seizure activity I ever had on Keppra after surgery was a rare aura. No one decreased my meds in the years after surgery, but my present doc suggested it. I am down to half my 2,000 of Keppra and have not even had an aura since I decreased it. I may try to go further. I feel happier too. If I did not have a mirror focus on the other side, I should be able to stop meds completely. My point is that because too much meds can also cause seizures, and because you have had surgery, the focus that was there is not there now. The med is acting on healthy tissue possibly and possibly producing seizures as a result. Are you still seeing your Epileptologist? See about getting off the Tegretol. If it did not help you before surgery, I cannot see why it would after, but I can see it possibly causing them now. Plus, it adds such a fogginess and a dulling cloudiness to daily life.
You are on Vimpat which seems to be a very good med and is made by the same company that makes Keppra. No seizures is your goal. I wrote a paper on Vimpat. The most effective dosage is 400mg. The literature said that they saw no more improvement with doses higher than 400. Good luck with the Vimpat and getting your life going again after surgery. I suggest that you get back in school soon to jump start the neurons that have been under in the influence of meds and seizures for a while. Tattoo

Sue and Tattoo, I did read about the side affects and so far I don't have a horrible temper. I was "moody" before taking this pill which is due to all my pills and my living situation. :-) I don't just have Epilepsy, I also have severe Asthma and Hypothyroidism.... yes fun! Tattoo, I have been taking a summer school class and it has kept me very busy! I have had horrible headaches since my third brain surgery but, I can tell my headaches are more frequent since I started Vimpat. Oh the joys of trying a new AED!! I just got blood work done to check how my kidneys are holding up.
Rhian, I know exactly how you feel with headaches. There have been many days when I've just cried because they just won't go away for me. Sending lots of *hugs* your way!

Are you still seeing the same group of docs who did three surgeries? Because you sill take lots of meds and still have seizures, a change is in order. Fast. Would scare me to be with the same ones. There are many talentes/experienced epileptologists out there who can offer a second opinion and might offer you a better quality of life that more pills and headaches. Consider a second opinion with your PCP doing the referraL. Surgery is supposed to stop the szeizures. I wish you the best.
P.S. My doc, after my switch to keppra, wanted to up me to 3,000mg a day. I wanted less and did not go for the higher dose. I was fine on that, and now down to half. More is not better in all cases, especially after surgey. Tattoo

I just wanted to say thanks for the info becaus i am currantly on topamax and vimpat. 125 mlg of topamax and 100mlg of vimpat. I am desperately trying to get off the topamax because i've been noticing alot of the symptoms in me. And lately i've been staying to myself crying hysterical, my teeth r decaying, i'm having complete outbursts, - i just cant deal with it.
My doc wants me on it still but i'm researching myself what would be a great combo with the vimpat- without alot of side effects- like the weight again- depression. I'm going nuts.

Hi amieet,

Welcome to the forum! I've been taking vimpat for almost a yr. now and I was taking topamax but the topamax increased my sz. like crazy and I felt really depressed just like you mentioned. Now I'm taking vimpat along with mysoline and diamox and my sz. have been cut back a lot. I have absence (petit mal) complex partial and aura (simple partial) sz. Since I've been on this combination I only have absence and once in a great while aura sz. The complex partial sz. have happened only a few times and they are nothing like they were before the vimpat. I take 200 mg. of vimpat a day 100 mg in the morning and 100 mg. in the evening.

Tell your Dr. to do a DNA test on you to find out what AED's (seizure meds) will work the best for you with the least side effect.
I wish you the best of luck and May God Bless You!

Sue

When I see my epileptologist I'm going to tell her to start me on vimpat. I have 3 friends that have started it, and they've been seizure free for over a year. the 3 of them haven't had any problems with the side affects. All I know about it is it's a med started in Europe, and then the USA decided to give it a try. I'm also on tegretolXR, and I hate that one. I ALWAYS get bad stomach cramps that say I'm about to poop, and I always have the runs for so many years I have the roids now.
Sincerely
Shawn

Sorry I forgot to tell you that a bunch of friends that I chat with on the epilepsy chat are starting to get migraines. I wonder if you are to, but I hope and pray you're not.
Shawn