Topamax and medications

I was on 100mgs of Topamax a few years ago for migraines and lost about 15 pounds. It worked okay for the migraines, but I backed off on the dosage because of the side effects. But recently, the headaches returned so I increased back to my full dosage.

So now I feel exhausted all the time. I run a lot and have trouble getting energy to exercise. This morning at a meeting it took me about 30 seconds to remember my secretary's name. I feel like I have to push through this mental wall to concentrate, and on my job I need to concentrate. My mouth feels dry all the time. Some days good food just tastes like crap.

Now I'm remembering why I quit taking this drug in the first place. I don't have seizures, which is why they made it. I have migraines. There are other medications to fight headaches, and this drug just isn't worth the side effects.

As mentioned in a previous post, I started Topamax the end of October. Since then, I have lost 25lbs, I am 5'2 & weigh 90lbs.

I have been taking 50mg's, but as of last week, I have cut back to 25mg's. It has been really stressful for me because I am scared about getting my migraines again & possibly going thru the HORRIBLE side effects I went thru when I got on the pill.

In the last 8 days, my anxiety level has been really high. I have been taking more (sometimes 2x a day) of my .5mg of Xanax. I have felt myself gasping for breath from time to time. I think that my headaches come from tension/stress, my jaw tenses up. The headaches feel like brain freezes. I am also able to verbalize my thoughts better, so I don't feel so stupid.

My goal is to be more clear-headed, gain 15/18 lbs & hopefully my complexion will clear up. I will probably stay on 25mg's 2 more weeks before getting off. I will let ya'll know how it goes.

I am a 42 year old woman. I started taking Topamax in March of 2008 for severe migraines. The migraines often caused vomiting and for my body to jerk similar to having seizure. I have had migraines for the last 15 years, but prior to starting Topamax I was having migraines almost every day (for about 6 months). My life had come to a stop. I had been through all of the neurological tests, and CT scans, etc. with no results. Topamax has nearly halted my migraines. I have a severe "head-ache" about every 6 weeks now that last 3 days. A huge improvement! However, my doctor had said that I should not be on Topamax long term so I have tried going off of it twice in the last year, each time on the 5th day to be hit with an all consuming migraine. I had come to this website to find out why I should not be on Topamax long-term to discover that many of the other health problems that I have been complaining about in the last year are probably a result of Topamax and the doctor did not ever suggest that was the case. I have TINGLING IN MY HANDS AND LIPS...the doctor thought this might be my thyroid, but that test was normal. I have had REDUCED VISION, the doctor said it is due to age and working on a computer all day. I have had JOINT PAIN which they are treating with an anti-inflammatory and suggested it’s probably the onset of arthritis. I have had WEIGHT LOSS, SHORTNESS OF BREATH, and the PAIN IN THE BACK OF THE HEAD. These are all things that I see others describe as symptoms of Topamax! Wow! I wish my doctor would have told me this so I didn't think there was something else wrong. I WILL NOT STOP TAKING TOPAMAX. Even if taking Topamax meant that my life would be 2 years shorter or something like that, there is no living in that kind of daily pain. But I am grateful to know that the symptoms are normal. Topamax has giving me back my life.

I have had all 5 types of migraines for 30 years. It seems I have had them longer then husbands : ), my children thought it was normal to "go to the ER" or to be in a dark room. I became very good at overcoming the incredible pain and pressure, rising to the top in my profession and being a single parent. I applaud my neurologist & his compassionate assistant. I toughed it out, ultimately, until Topamax came available. I still have migraines. I still must manage all my triggers. And people still don't get that migraines are all consuming and to overcome a migraine to attend a function is huge. However, I am currently, as others, backing off of several medications in a safe manner. My vision is not consistent. I tend to not play games, or read out loud as I cannot see what I used to. When I get up in the morning, my feet are sore. I have a dry mouth when I am speaking. My hands tingle and my ears ring. My gums bleed from pressure. It feels like I have a sinus infection. I have a constant headache and muscle soreness and weakness along with joint pain and low back pain. Having been on 75 mg Topamax since it came out, I no longer have the benefit of weight loss and weight gain is suddenly upon me--suddenly!! I do not wish to influence anyone in his or her choice. Personally, I am considering titrating off Topamax to see if any or all of these health issues change for me. I, too, have memory issues that are not associated with menopause. The problem with the list of side effects is that they could be present with other drug therapies or conditions. Once I have isolated the problems to Topamax, I will then have to weigh the cost of migraines vs. fewer migraines. I must remember to manage all triggers, as I hope others will also. I hope to be migraine free, with the benefit of good vision and better rest. I desire this for the readers of my post as well. Blessings.

Like most of you all I am on Topamax 100mg. I am a 27 year old female that has suffered from severe migraines for over 20 years that would last up to 2-3 days and completely debilitated me. I would bleed from my tear ducts from the extreme pressure and I would need to be in a quiet, cold, closed off room to be left alone until the migraine was gone to continue on with my life. It was ruining my life and taking over my day to day routine. I could never really commit to anything without the constant worry in the back of my mind about a possible migraine until I found Topamax. Now on Topamax I went from 4-5 migraines weekly to 1-2 monthly, it is truly amazing, however there is a catch. Although the medication is wonderful and I will never get off of it at the rate of success that I am at, I do have side effects. I have extreme tingling in my extremities, (hands, feet) along with my face. It feels like they are constantly asleep. I also have noticed the poor tasting carbonating drinks along with my taste buds changing with certain foods that I use to be so fond of. I also have a very smokey haze where it almost feels euphoric if I wake up in the middle of the night. I have horrible nightmares of people that I have not seen in or thought of in years, memory loss and spelling issues-all goes away after 3-4 months of uses. I had shortness of breath, however that subsides as well with the use of the medications along with several other side effects. I have lost over 30lbs that is along with diet, so I can't say it is all Topamax. I have noticed little nodules that have been showing up on my hands since I stared taking the medication that I am in ? about I have a call in to my neurologist to see if he has heard of any such thing. Other than that I love the medication, because if not having migraines is one of the side effects-lol I can handle the side effects. I hope that this will help anyone that might have anything similar to what I am going through. If you can shed some light on my nodule situation please let me know. Thanks

First I want to say, after reading several posts, that it seems a lot of you are taking Topamax without food, which may be causing your "spaciness." My doctor suggested always taking it with food, even though it says with or without food, and I only experienced spaciness the few times I took it at bedtime without food. Once I started taking it with breakfast and dinner, that never happened again.

I am a 48 year old woman, prescribed Topamax in September of 08 for migraine associated vertigo without headaches, with facial numbness. The first thing I noticed was I immediately had headaches, which to me indicated it was dehydrating me as that is the only time I get a "normal" headache. So I knew I had to drink a lot of water. Soon after starting Topamax I developed a dry cough that lasted the entire time I was on the med. I did not relate it to the drug at the time, however. It never even occurred to me. After about two months on the drug I started having trouble breathing with extreme dryness in my airways. I was prescribed an albuterol inhaler which did not help. I was then prescribed a corticosteroid inhaler which also did not help. I thought the trouble breathing was from taking Nadolol which I was prescribed for occasional heart fluttering - the neurologist said this was a normal side effect of Topamax. I stopped taking the Nadolol but the trouble breathing continued. I also had more migraines with vertigo and facial numbness than before I started taking the drug. I hoped it would eventually stop and the drug would kick in to help the vertigo, so I stayed on the drug. I had very minor tingling in my feet, but it was tolerable. I became very stressed out, had trouble sleeping, depression, my face started breaking out in November (and still is), I lost interest in everything that I normally enjoy - reading, photography, following politics in the news (sort of an obsession of mine). In December I was so depressed that for the first time in my 11 year career I started canceling appointments and eventually took three weeks off from work to "re-group." In January the neurologist decided that we would increase the dose from 100 mg to 150 mg for one more month, and if it did not get rid of my migraines with vertigo, we would discontinue the drug. The first day on the increased dose I had a killer headache, and I drank 150 ounces of water before it went away. That night I did not have to go to the bathroom during the night, unheard of for me. That's a lot of water to drink and not have to pee. Within two days of increasing the dose, my cough became much worse, and within three days, the breathing became more difficult. Within five days, I was having trouble speaking because my airways felt so dry. I called the doctor the next morning and he said it was not the drug, but if I wanted to, stop taking it. So I went off it cold turkey, per his instructions. I had rebound migraines every day for a week or two and my heart was pounding, sometimes for three or four hours at a time. Eventually the cough and trouble breathing went away, however, I had to continue drinking lots of water or I would notice that I didn't have to urinate, sometimes not at all. Again, unheard of for me. I saw a cardiologist at the neurologist's urging and they said the heart pounding was just anxiety. I disagree, as did another doctor of mine. We both believe it was withdrawal. I have now found out (by getting copies of my medical records) that the neurologist is now attributing all of my side effects from the Topamax to "somatization." In other words, psychosomatic - not a side effect, but just a way of getting medical attention. I am seeing a few people on this board who have also experienced a dry cough and trouble breathing. Can I have the same side effects as other people and have them still be psychosomatic, even though I had no idea those side effects could occur? I don't think so.

I have a theory that Topamax interferes with hormones which causes a lot of the side effects like lack of concentration, memory loss, anxiety, depression, insomnia, acne, and hair loss - all symptoms of peri-menopause and menopause. Ask any woman in her 40's or 50's if she has these symptoms and most of them will say yes. My face has not been this broken out since high school! My hair is falling out at a rapid rate. I won't even bother mentioning these to the neurologist. He'll just say it's not the drug.

I'm very frustrated and not sure what to do at this point. The neurologist has me taking a supplement called Migrelief now, but I think it takes three months to kick in, so I have no relief at this point.

Has anyone else experienced the trouble breathing with dry cough? I don't believe for a moment that it was psychosomatic.

I am a 24 Female that was prescribed 50 mg twice a day for my mood swings, migraines, and being overweight. I have been on topamax for two days now. My family physician prescribed this to me knowing that I am sensitive on medications at first. Well I had no idea that these particular side effects were from this drug until I found this website. I have had 24/7 nausea for 2 days straight, throwing up, BAD tingling in my legs (needle sensations), irritability, inability to concentrate or spell. It's terrible because my job AND FUTURE require me to concentrate, SPELL, and REMEMBER which are three things that I have completely lost while being on topamax. I cannot even type. The greatest impairment I have is what I call ZONING OUT which is - I will being doing something such as watching a tv show or reading an article and I must have dozed off in my brain for a few minutes and then came back. It literally feels as if I left my body for several minutes and then came back! It's a very strange feeling! I would only recommend this medication for someone that has tried EVERY OTHER HEADACHE medication!

Ok so im 18 years old and I pass out frequently, I have been unsuccessfully diagnosed with several different theories over the past two years, Recently some doctors though that my passing out may be an aura to the headaches and migraines i receive after, my doctor just prescribed Topamax to me and Im really nervous about taking it after reading about these side effects, has anyone else been prescribed topamax who has similar symptoms?

I've only been taking this drug for two days - 25mg in the evening - and I've already got side effects. I get tingling in my fingertips, and all down along the bottom of my fingers. I've been feeling nausea as well, and writing this, my brain feels a little blocked and slow. I also think I'm losing my appetite, which could be a good thing, considering that I do need to lose weight. But I don't think it is worth it if I end up getting side effects like the ones that have been posted by other people.
I'm a writer, and I cannot afford to lose my memory, or suddenly not remember how to spell words, or to communicate effectively. Should I stop taking Topamax?

I have been on Topamax for about a month now and going to give it a couple more to see if it is the med for me. I use it for migraines. I usually get at least 6 migraines a month - this month I got 4 and only one was really bad. I am very disappointed that beer no longer tastes good and am hoping that if this med does work to reduce or stop my migraines that my taste sense for at least beer will return. Also, I had an odd experience last night - I had 1 1/2 Mai Tai's last night - both of my arms went totally numb/tingly - not just my hands and not just a little tingly - totally scary numb/tingly to the point of considering an ER visit but I assumed the alcohol in the drink just exacerbated the side effect. I may become a non drinker if this med actually works. Guess you have to take the good with the bad! The cognitive stuff---that only lasted the first couple weeks thanks goodness for me. Not giving up yet!

I am almost 41, and have had migraine headaches most of my life which I could manage with 800mg of Naproxen Sodium, or a Norgesic Forte, and when Imitrex came out, I could just administer that. Six months ago, my headaches got so frequent that I had to start taking my Relpax (similar to Imitrex) and/or Fioricet more than 2X per week. According to my neurologist, this is a no no, as both of those meds can couse rebound headaches. He started me on Topamax, 50mg per day. It did nothing. He bumped it to a 100, nothing. Now I'm a 200 mgs, I am still have a migraine in left temple as I write this. I have the tingling, the daytime sleepiness, but my mind is fine, and my appetite is just swell (regretfully). What the hell am I going to do now? Ask him to bump me up to 400 mg? Now I have these headaches every "F"ing day, and I can't take anything. I just have to suffer.

Topamax is NOT working!!!!!

I am a 39 year old man with peripheral neuropathy and migraines. When I was diagnosed 3 years ago, the pain in my right leg was horrible and headaches daily. My Dr. put me on Topamax and I was so happy, it seemed to help but one night( about three weeks into it) I went to bed and awoke in the morning legally blind. Topamax was stopped that day but it took 4 months ( and changing the prescription in my glasses 3 times) for my vision to return to 20/20. The doctors tell me I was lucky as some people have perminate lens damage from the optical pressure change.
My doctor said I could not take any thing in that class of medications as it would probably have the same effect on me. So he decided to put me on Cymbalta for the neuropathy. He said it was being tested as a possible use for neuropathy but had not been proven. It works great for the pain and oddly my migraines have gone down to about two a month.

My 6 year old daughter is taking topamax. Since the time she been taking it she has forgotten who she was and everyone around her, she went for an excellent student to not be able to do simple things like reading writing and math. She does even seem like the same child. She is very emotional and I just want my little girl back.

2 yrs ago I was diagnosed with peripheral neuropathy. I have been on Topamax since, because of the severe pain it causes. I have never experienced weight loss and I was on up to 400mg a night. I am now on 200mg a night. My tastes are fine and my drinking sodas were never like metal. But for the fatigue of the disease I also take Provigil in the morning. I have noticed my eyes have changed. Never gave it a thought to be Topamax. Plus I just got new glasses again 3 months ago and am seeing a change in my sight again. Also there is a noise in my ears,not ringing,but sounds like crickets. Never had that before. I was on 2 other meds but I took myself off of them because I really don't like taking so many. The others had worse side effects. Until they find a cure for this disease it looks like I'm stuck with Topamax. This is one pain I will not and can not live with.

I am also experiencing hair loss and have been on Topamax about 2 months. I had no idea this was a side effect. I initially lost weight which was wonderful, but then my weight dipped so low my family and friends thought I was anorexic. I was finally wearing a size 3 pants. I normally am in size 8's. I am on it for bi-polar and to help with binge-eating. But I cannot deal with the hair loss. I don't think that being skinny is worth losing my hair for. No other meds have helped my depressive moods without making me gain weight and at this point I just don't want to take any drugs. I would rather try some therapy...that has become less common. The doctors just want to give you a pill now-a-days.

I'm a 26 year old female and I've been on Topamax since March 2007. It has completely gotten rid of the debilitating headaches I experienced 3-6 times a week. It also got rid of my anxiety. I got my life back, my antidepressant kicked in at the same time. I experienced all the usual side-effects, tingling hands and feet, forgetting words, memory problems, loss of appetite, but was COMPLETELY pain-free. I still am. However, I never remember anything now, forget whether or not I did something, paid my bills, etc, lose things constantly, and I have lost about 20 lbs. Not good. I look anorexic. I have bones sticking out. Eating is hard. I forget to eat and drink all day and food is just unappealing. I feel fuzzy and stupid and slow. Not sharp like I used to be. It has killed my confidence and self-esteem. But I was wondering if any women out there got yeast infections while they were on Topamax. I've had one monthly since I started it, and my doc said it's a rare side effect. Oh yeah, I've had mild hair loss and mild to moderate acne now. This drug, it is such a 50-50. Living with chronic pain, those headaches were awful. But doubting yourself is awful too. Anyone have similar experiences?

Hi all,
Unfortunately, I didn't read all of these comments before I started taking Topamax.
I have migraines for 25 years, and decided to try Topamax.
Week 1-25mg, Diet coke tasted strange. Tingling. Tiredness. Forgetfulness. Can't think clearly. Hard to spell. Or do any task.
Week 2-50mg...a zombie-all of the above and more. Couldn't remember how to get back to my house..and I was just 5 streets away.
I stopped taking Topamax 2 days ago.
I feel much better.
Plz beware.
Having migraines for so many years (i am 38 now) I learned how to control them and Imitrex does work for me.
If I need to choose between having migraines 3-4 times a week and the side affects of Topamax-I choose migraines.

I have been taking Topamax (25mg twice a day) for about 2 years now and it has greatly improved the frequency and intensity of my migraines. (I used to have a minimum of 4 migraines per week, and though medications such as Immitrex and Zomig often work, it's still hard to function properly when you have so many headaches. The Topamax has brought that number down to about 1 per week.) The side effects are not too bad, but I am freezing all the time and very tired - complete lack of energy. I almost feel like my head is in a cotton ball, like everything is just slightly fuzzy and I'm a bit disconnected. I wouldn't call it feeling stupid though... I am still able to do my job well; perhaps a slight lack of concentration. Some dizziness, but nothing serious. I have recently started experiencing weight gain, rather than weight loss (not sure if this is related to the Topamax). When I first started taking the medication, I also had that horrible numbness in the tips of my fingers, but that went away.
I wouldn't want to give up Topamax now, because I just can't go back to having that kind of pain and vomiting 4 to 5 times per week.
Good luck to everyone!

I have been on Topamax for two years had most of the side effects I am used to them. The only thing is I am freezing all the time . Anyone have this?? I am cold all the time!!! I also experiance, in the summer, the no sweating thing, that makes me dizzy in the sun, I have to stay under an umbrella at the beach etc. I never had to do this , I was always a sun worshiper and could take it.

I have been taking Topomax for quite some time.Tried it several years ago, the mgs were not high enough (only 25mg/day).My doctor didn't really know the prpoer dosage.It didn't help the migraines.My new doctor has me on it again.50 mgs/day.Here's the good - NO MIGRAINES! Here's the bad: Acne at 45 years old, tingling doesn't even describe my legs or face, ringing in the ears, remembering names and places just doesn't happen, I'm eating less but gaining weight quickly,& one last thing- Itchy spots that I would describe as "hot spots" if I were speaking of my dog. Still sticking with it because I don't have the migraines.I tried to slowly take myself off and the headaches came back.What choice is there?

Hello, everyone. I didn't know there was a page like this, but I'm glad there is. I've been on Topamax for 3 weeks because the medicine I was on for 2 years didn't do anything and the headaches weren't going away at all anymore; they were continuous. The first week at 25 mg I had the tingling for a day or two, the involuntary muscle twitches, the terrible mouth taste, and the chest pain. All but the terrible taste went away by the second week at 50 mg but I started getting wobbly legs and dropsy. I read an article somewhere where a person on Tomamax called the drug Stupamax or Dopamax and said anyone on it turned into a box of rocks. The box hit me at 3 weeks and 75 mg. I'm not wobbly anymore, I'm still irritatingly dropsy, and I am doing things that only a person with half a brain would do. Plus, my ears have been ringing for two days, and today I feel like I'm in a tunnel and everything is far away. I'm getting ready to call my doctor. On the OTHER hand, I haven't had a headache that lasted for more than a half hour in 3 weeks. So what's best? Going back to headaches or continue to evolve into a box of rocks?

I took Topamax about 6 years ago for migraines, and experienced no side effects. Just started it up again 3 days ago, and I feel like I am totally drugged and my head is spinning, can not drive, can barely hold a conversation, only started with 25mg, and can say that each day I feel a little better, but the only difference this time is that I am on Lexapro and my Dr. said the side effects could be worse till I get used to it..anyone else take this combination? And how long till I can function again?

I have been a migraine sufferer for over 13 years and have run the gammut of medications to prevent and deal with them. My mother took Topamax a couple of years ago with disastrous results. I didn't realize, but I guess she was so loopy and forgetful that it was enough to cause my grandmother and stepfather to perfom an "intervention" to get her off of it. So, here I am a couple years later starting it myself, wondering if the side effects are worth the trade off. I'll be honest and say that I love Coke. I mean, loved. Carbonated drinks of all ethnicities taste like slimy metal now. How disappointing. And considering that if I went a day without drinking a Coke, I would get a wicked migraine, I've resorted to putting Crystal Light Energy (Wild Strawberry) in my water to give me the needed caffeine.

I've also noted tingling in my face, kinda like numbness. Nothing that is earth-shattering, but noticeable. I get dizzy a lot. I've also lost about 5 lbs since starting the medicine. And today, I could not find the word "prescription" in my mental warehouse. Not a difficult word on a normal day. I've only been on Topamax for a week though. I'm going to give it a good month to see if the side effects dissipate. But if I get any stupider, I'm going to have to go another route.

I have been on topamax for almost a year now. I had been having a nearly constant migraine cycle for three months which had to be broken with migranol nasal spray. I then started on escalating dosages of topamax. By 100mg I realized that life was wonderful but that I couldn't retain much information which was a problem as I had just gone back to school for an advanced degree. Upon consultation with my doctor, we reduced my dosage to 50mg and things improved dramatically.

I have experienced some fingertip and toe tingling which have been completely tolerable. I take the medication right before bed so that I don't have problems with fatigue during the day. I do get out of breath easily when I exert myself and carbonated beverages taste horrible. But my migraines are under control.

I have a Ph.D. in molecular biology and a few years of neuroscience research under my belt. I would like to say that it is EXTREMELY important for people to understand that no medication is going to work identically for any two people. What works for one person, may not work for everyone. I know people who swear by imitrex but this medication does absolutely nothing for me. You have to be your own advocate when it comes to medications and treatments. Your genetics will also determine how well, if at all, you respond to any medication. For some topamax is a life saver, for others it will be the bane of their existence. This will always be the case for any medication. Be tolerant of others' experiences and understanding of each others' pain and progress will be made.

I started topamax on Tuesday for bipolar disorder. My pdoc started me on 50 mg and I took one in the am and got really sleepy so I cut back to 25 mg at night and went back to 50 mg on the weekend. I was surprised to feel the effects the first day. I thought I had gotten a flat pepsi at lunch and then realized that my tastes had already been effected. I got the tingly hands and have noticed that my leg muscles have been twitching some. The very first day I felt like I was in a fog and I definitely don't want to feel dumb. I'm hoping that cutting back and titrating up more slowly, as well as taking the medicine at night will help. The side effects I can stand as I withstood 6 months on Accutane for acne which was waaayyy worse.

hello everyone ;) I'm Ana from Portugal, I just want you to know that I read all your comments, and i understand everything!
I would like to guive my contrubute about migraines too, but i don't know to write english, just 10%!
I have migraines for about 15 years, i already took so many medications to migraines and they never help me ( I have 1 or 2 crises for week ) 20 days ago i sarted to take topamax and i have benn free of migrains and I don't feel second efects, I feel just great!
I have 37 years old!
Hope eveyone understand my english :9
Thank you

Best regards for everyone

Ana

Hello.

I have been taking topamax for bipolar II disorder. The first week or so, I experienced some very unpleasant side effects. I would become very disoriented while driving and get lost in locations that had previously been very familiar to me. I would also lose track of my thought process mid-sentence. An avid runner, I was unable to exercise for about a week. However, these side-effects have since subsided. I do experience a decrease in appetite, which is fine for now, but I'll have to see how that pans out in the future.

One thing I'd like to point out is that I would imagine topamax to be very unpleasant for somebody who does not have a mood disorder. I feel that it truely restrains my impulses (I suffer from impulse control disorder), and it has worked wonders for me in terms of my mental illness. I believe that topamax is a great alternative to some of the other medications for bipolar disorder in terms of weight gain. On the other hand, I think that those who do not require psychiatric attention would be better off with a drug that does not serve as a mood stabilizer.

That's just my opinion. Good luck!

I have suffered migraines for five years now, there horrible. I took topamax for the first four years as the doctors experimented with several drugs. After five months into the med I had my first kidney stone and two or three for the next 3 1/2 years. I went to so many doctors and none of them new what was wrong with me. I began searching online on all the medications and found out that topamax causes stones. I can see one here and there but I was having them every other week, and all of them were painful and caused a lot of bleeding. I would like to beat all the doctors and who invented this with a bat over and over again.

My daughter has been on Topamax for 5 weeks due chronic head pain from a fall she had a few years back. This had made her break out, she is already slender, and it has caused her to lose weight. Nightmares have flooded her sleep and causing her to wake up multipul times a night. She experiences rapid heart beat, plapatations if you will, and dizziness. We haven't even come close to what the doctor wants her to be on for her full dose, and quite frankly, I think this medications side effects are worse than the chronic pain she still suffers on top of the side effects.

I am a 62 yr old lady that was started on Topamax a little more than 2 yrs ago for migraines that were getting worse as I was aging. After the first "weaning on" period I have been taking 100mg a day at bedtime for the entire time. Initially, I had a lot of tingling in my hands and feet, but it subsided somewhat and never seemed like a big deal. The Topamax brought my migraines to a grinding halt. However, more recently I've noticed quite a number of new increasing symptoms that are bothersome and scary. Difficulty concentrating, a certain amount of confusion, and some eye pain that sometimes feels like pressure and my vision is blurry. My balance does not seem quite normal. I'm not really dizzy, but I have "missed" a step too many times lately. My mind functions do not seem all together "there". Normal functions like spelling, counting change, answering questions, like my address and phone number, aren't always easy especially if I'm under pressure or get upset. Backaches and joint pains are present, but since I have Degenerative Disc Disease it is hard to distinguish the source of the pain. The problem is I cannot determine if this is from the medication or if I am experiencing another kind problem. ? Most medications have side effects; however, if the benefits out weigh the (negative) side effects, it is worth it.

I have been on 100 mg of topamax twice a day now for over three years. Most of the early side effects have worn off like soda tasting bad and the memory loss. I never had any hair loss. Also the weight loss has stopped and I did gain it back which really stinks. Anyway, the reason I was looking, was that in the last several weeks, I have been suffering horrible body aches and joint pain. My hands and knees hurt very badly. I am 39 years old and hate to think that arthritis has set in so quickly. And I know that I can't have the flu with no other symptoms and so often. Does anyone else have these symptoms? Also I wonder why these could have started after so many years of taking it.I have tried to wean myself off in the past and the migrains came back full force.

I have just discovered this site and was amazed to find out that Topamax caused hair loss. I have been on Topamax 100 mg. for about 1 1/2 yrs. now and started to lose my hair, and didn't know why. Also I just recently in Nov. started to get ringing in my ears called Tinitis and contacted the Tinitis Assoc. and they sent me a list of medications that can cause ringing in the ear. Yes Topamax is one of the drugs listed that can cause ringing in the ears. I'm definitely going to stop taking Topamax and try the B vitamins that have been recommended. Thanks.

I've been on it for 5 weeks now, and I'm taking myself off it today. It was intended to help with a recurring headache/migraine issue. My migraine issue has improved, but the side effects are not worth it. I will instead go back to using Imitrex or similar medications as needed instead of a maintenance med like Topamax. I am frequently dizzy, and at times expreience the spins and bump into objects. My tongue feels and tastes like I smoked a fifty cent cigar, and any type of carbonated beverage tastes completely different and awful. I have been experiencing more frequent sinus pain and sore throats and thought that it was unrelated, but after reading some of the possible side effects I now realize that it may also be part of it. I also have frequent heartburn as well. Don't let this keep you from trying it out - it works well for some. Just don't be afraid to tell your doctor if it isn't worth the side effects. I just decided that it isn't worth it to me.

I am extremely sensitive to all medications, so I start at the very lowest doses; I have very bad migraines and am trying 25mg. of topamax. I can only take 1/2 of the 25 mg. pill at bedtime, and sleep well, but awaken with swelling around my lower eyes, and a feeling of "mucous" in the eyes that makes me want to blink all the time

I HAVE BEEN ON TOPAMAX FOR 3 YEARS. I AM NOW UP TO 3OOMG A DAY. I HAVE COMPLEX MIGRAINES THAT ARE LIKE SEIZURES. SINCE BEING ON THE MEDICATION I HAVE NOT HAD AN ATTACK. YES I HAVE SIDE AFFECTS, I AM VERY FORGETFUL, I CAN'T READ A BOOK, I START TALKING AND FORGET WHAT I AM GOING TO SAY. I HAVE ACHES AND PAINS AND MY EYE SIGHT IS WORSE.
BUT I REMEMBER 3 YEARS AGO THE WOMAN LAYING IN THE HOSPITAL BED WHO DIDN'T KNOW HER NAME OR HER FAMILY. MY LEFT SIDE OF MY BODY LOOKED LIKE I HAD A STROKE. i DON'T WANT TO GO THROUGH THAT AGAIN SO I WILL PUT UP WITH THE SYMPTOMS .
I ALSO TAKE EFFEXOR AND HAVE TAKEN THIS MEDICATION FOR 7 YEARS. I DID ASK THE DR. IN THE BEGINNING IF IT WAS OK TO TAKE THESE TWO MEDICATIONS TOGETHER AND WAS TOLD YES BY THE DR. AND THE DRUGGIST.

I CAN'T UNDERSTAND WHY ANYONE WOULD FEEL SUICIDAL TAKING THIS MEDICATION. I BELIEVE YOU SHOULD CALL YOUR DR. RIGHT AWAY.

Does anyone here have positive side effects on topomax??? All I have read are negative ones!

As for me it's been a blessing. I have noticed some side effects annoying, but not to the extent that I don't want to quit it.

If you are experiencing side effects to the point that you want to kill yourself, first of all call your doctor IMMEDIATELY! Check with your doctor to see if other medications you're taking could be causing your feelings.
I've noticed that many of you who are feeling suicidal are also taking Effexor or something else that could be interacting with Topomax. Check into it, and don't stop EVERYTHING at once!!! Doing THAT just might kill you!

Always wean off the drugs with the help of your doctor. If you don't agree with your doctor then go to another one or at least go to the ER and they will help you. Don't take matters into your own hands. Doing it yourself puts your life in risk.

If you think you are suicidal then remember you are not thinking objectively. YOU NEED HELP. If you make a foolish decision you will not only destroy your life, but the lives of many people who love you. GET HELP NOW. Please.