I just want to make sure if there has been new research about this medicine and pregnancy, I will like my future children to be healthy. Is there also a big percentage for my children to have epilepsy? How can I prevent any birth defect from happening? What medicine will be better or safer to have children with and still treat my epilepsy? I do not know what type of epilepsy I have, the doctor never told me.
1 hour after I got home he had a Tonic Clonic seizure and turned blue. I called 911. They look him to Children Hospital in St. Paul. They put him the Epilepsy Unit and did an EEG. They found 5 other Myclonic seizures in his sleep. MRI looked fine and all blood tests came back fine. They diagnosed him with Generalized Infant Benign Epilepsy. They put him on Keppra. So far I have only witnessed 2 little jerks, I guess they are Myoclonic seizures.
I read something on rxlist about moodswings and irritibility related to Keppra. It's believed that Keppra makes your brain "dump" Vitamin B6 at times which lowers dopamine or seratonin levels and makes you feel horrible.
Does your daughter take vitamins? I'd try some Vitamin B6 if her multivitamin doesn't contain it. I started taking Trader Joe's High Potency vitamins and feel much, much better since starting.
Good luck.
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.
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 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?
Was on lamicatal er when shaking started on right side of body but had a allergic reaction to it..
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 chose not to because I knew it was from the Tramadol and am terrified of the Keppra side effects. Fast forward to a year and a half and I just had my 2nd seizure last Thursday night. My husband heard a strange noise when I was in our bedroom and called 911. So far I have had several tests done already and they are telling me that I need to for sure get started on Keppra now.
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..
I have no health insurance. I was finally got a really basic coverage, but it doesn't cover keppra. i've been taking keppra for a 2 months. I was switched to phenobarbitol for when I run out. since keppra is not on the charity's formulary.
I hope to God that I cant find some source of keppra before I run out. The phenobarb is scary.
So I'm excited about the links here:
http://brain.hastypastry.net/forums/index.php
http://www.needymeds.
I am pregnant with my second child. I'm 37 +2 and I have epilepsy. My 1st pregnancy was 11 yrs ago. I was actually on Depakote and high risk but I have a very health normal very active 10 yr old boy! I'm taking Keppra now and they still consider me high risk but the risk is much lower with Keppra then it was with Depakote. They have done several ultrasounds and baby is great!! They have me taking 1000mg of Folic acid in top of my prenatal vitamins.
Relative to your grandson's weight, Keppra (an anti-seizure medication) generally does not result in weight gain, but <1% of adult patients in clinical trials with Keppra did experience some weight gain. The weight gain is more likely the result of Risperdal, an anti-psychotic medication that often produces dramatic weight gain. That medication was likely prescribed to address the volatile behavior, not to address the seizure disorder.
As my DD is in Keppra, and has previously been on other seizure meds, the Keppra, by far has had the least amount of side-effects. You could ask if some of her mood changes, memory loss, etc. are from the stroke vs. the Keppra. Please do not wean her off the medication without a Dr's directive... that could cause withdrawal seizures.
My thoughts are with you that your mother gets well soon.
Hi. My dad is 63 years old, a survivor of 2 cardiac arrests, a stroke 5 years ago that was accompanied by a seizure. On Saturday he wasn't feeling well with a headache and then became unresponsive. He had a seizure in the ambulance and one in the ER. He was on life support for almost 2 days and thank goodness is is now awake and alert. His memory is very touch and go. He has come along way.
I started having seizures when I was 12 yrs. and they put me on dilantin and other meds. they never got under control so good until I went to a new doctor (because I moved) and at that time I was about 38, and the doctor did a MRI and other test. He then said to me the first thing we have to do is get you off of dilantin. He showed me that that pill was eating up half of my brain (it is called cerebellar atrophy). He slowly put me on different levels of Keppra and I haven't been better.
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