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I have been thru several med changes. And Yes, DRs Usually introduce system to New med B4 titrating off the Old. As Long as he titrates off Dilantin, Slowly, he will do fine.
The Important thing to do while going off a med & going on a new med is Keeping Up w/ A Journal! More Info as to what to include under Tips.

Keep us Posted. And do your 'homework' about Keppra. Use the Drug Info Tab at top of page. And If he starts experiencing 'mood swings' it has been suggested that vitamin B6 & B Complex be added to his daily med regimen.

Keep us posted. Know I care. Hugs for you & yours!
Love Candi
Dilantin was my 1st? med. It didn't work for me, either. I continued to have seizures & the side effects were horrible. My Daughter was on Keppra. DRS determined it wasn't the med for her, either.
As w/ all our meds: What works for one may not work for another.
What medication are you on Now? Is it Working?

Love Candi
I see my neuro on August 29th and am going totell him toget rid of the lamictal and find something else. IT feels like I am getting immune to it and it can metablize its own self much in the same way Tegretol has autoinduction.
so he will find somethingand cross titrate it slowly and will tale at least a month to do if not more becuase I am at 600 mgs.
phoenix_sun
I went through this. My Neuro Doc had it so that within 6 weeks I would be totally off of dilantin and on the generic Keppra. He slowly takes away dilantin and increases the Keppra during this time. By the 6th week,I was no longer taking the dilantin and Taking the full 3,000 mg keppra per day, spaced out in 12 hour intervals. I also take phenobarbital 180 mgs per day. 60 mg in the morning and 120 at night.
During this time of transition I only expierienced 1 minor seizure(around week3) but have not had one since and it will be coming up that I have not had 1 for a year. Trust me on this,it's the best thing that has ever happened to me,getting off Dilantin and going over to generic Keppra. Keep us posted on this. And yes this is the only way to switch meds accordingly.
John
I have been through this many, many times. Again just trying a new med myself. It is the typical way of switching meds. You will never know what your body will tolerate well unless you try. Most doctors do not like to have you on more than 3 at a time. Most just like have you on 2 but if you are still having the seizures they will put you on a 3rd to see if you can handle the side effects. I myself have been through brain sx, have had the VNS implant and still have the seizures but not too often. Best wishes in finding the right drug for your husband.
Please visit epilepsytalk.com Phylis posted a form letter for Pharmacies that you can print up & give them. It will ensure they do Not switch brand name w/ generic or substitute w/ new manufacturer of the meds.
I do hope you stick around & share your story w/ others'. You are an amazing young lady & have been thru a lot for someone your age. Also, have you ever 'chatted' w/ others' your age w/ EP? Resources: epilepsyfoundation.org link, use search for teen EP forum/support group. Search will provide you w/ the nearest 'live' support group in your area, too.
Take care & please let us know how you are doing occasionally.

HUGS! Love Candi
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