Topamax And Eye Twitching (Page 6)
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Hi, I have been using Topamax for depression for 12 months and must admit that it has been very sucessful. The one major draw back is that I have developed a very annoying eye twitch. It only affects one eye, but is very noticeable. I was taking 100 mg twice a day, but have decreased it to 100 mg daily. The twitch has decreased somewhat, and I realize that I now have to come off this drug completely to get rid of the twitch entirely.
Has anyone else experienced this problem. I read 1 other reader, but are there more?

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14

I have been on this pill for close to 10 years now for epilepsy. It has its good parts but I definitly feel a lot of the side effects many people feel as well. Eye twitching has just recently started for me in the past few months. I find that every few months some new and weird side effect is felt in me.But then I tell myself I'm just being paranoid and never ask the doctor because they dont seem to care much here anyhow.

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13

i am on 300 mg a day and i have started to notice that my lips are twitching (yes i know that this sounds weird) but its starting to annoy and freak me out so much that im about to just throw the towl in.

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12

I would definitely let your doctor know about the eye twitching. Topamax has worked wonders for my migraines. My doctor had never heard of eye twitching as a side effect, but did not dismiss it. He lowered my daily dose and it has helped. I only get twitches once in awhile now and the headaches are still in good control. Talk to your doctor.c

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11

I started taking Topimax a few days ago and my right eye has been twitching ever since the first night I started taking it. I have to take the pill once a day for the first week then twice a day after that.... I'm afraid the twitching will get worse but I'm taking this for migraines. So far its not helping them but I'm willing to give it a shot just to see if this medicine works. Should I tell my dr about the twitching? Either way I'm miserable! Help!

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10

I too have the "twitchy eye" it's driving me nuts! I do not want to stop taking the Topamax because it has been a godsend for my migraines. Has anyone had labwork to have their potassium levels checked since the eye twitch started? I am supposed to have mine checked next month but I may have completely lost my mind from the twitching by then......

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9

The generic toprimate is NOT the same. when I use the generic I break out in a terrible rash! So I have to use the brand name topamax! And yes I get eye twitches , only in my left eye! drives me insane! I am like everyone.. i want it to go away .. but nee the meds! the doctors don't believe its the meds either!!! why don't they believe us??

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8

I've taken Topamax on and off for several years. I can't take the generic because it creates an eye twitch that could become permanent. (So says the doctor) I've never heard of it being the coating, but it is different from the brand name (yellow, not white). Since I don't have insurance I tried to get it via a Canadian pharmacy, only their "brand name" Topamax is simply the US version of a generic. I was told by the Canadian pharmacy that because it was manufactured outside the US it had to be coated differently, and the ingredients may be slightly different (as in, what you would find with a generic) Bottom line being, brand name US = no side effects, but "brand name" Canadian = eye twitch.
I called every reputable (yes, EVERY) Canadian pharmacy that sells to the US and they sell the "same" Topamax. (Manufactured by Janssen-Cilag, not Ortho-McNeil Neurologics)
I do get numbness from the generic, as well as foggy brained. Not so much from the US brand name. I'm not sure what the solution is for anyone, just thought I would put what I've found out there.
Despite being told the generic is EXACTLY the same and works EXACTLY the same way ..... not exactly. I don't know if it's the delivery system, the coating, or whatever. All I know is my body chemistry knows the generic when I take it. It is what it is.
Hope this helps.

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7

I was been on 400mg for about 8-9 years for migraines (the most I've ever heard), another doctor reduced my dosage last year to 350 because my memory is pretty shot and I'm concerned. About 6 months ago, my left eye started twitching. I received Botox in my lid, it lasted 3 months and the twitch is back. I'm just now realizing it's the meds. I need to cut back more...or maybe all the way. I read last night that many people have gone blind from this drug. I'm getting nervous the more I learn.

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6

I have recently come off of Topamax and the twitch has gone away completely!! What a relief. My GP also wanted to send me for a CAT scan, which I did not do because I KNEW it was the meds!...So there you go! Thanks to everyone who has responded!

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5

When I was taking Topmax for my Bi-Polar and PTSD I begain at 300MG and I too had the 1 eye Twitch from Beyond! Nobody would acknowledge it was the MED! SO after a BRAIN SCAN etc. I had to Force my Mental Health Dr. to LOWER my Meds to 100mg. Since then I Rarely get the Twitches or Muscle Spasms any more..

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4

Since my last post I switched to taking the 100 mg at night, which has helped me 2 folds. One with the annoying twitch and 2 with the lapse in recall (not sure if that has affected anyone). My pharmacist dispensed my last script in 25mg dosage, as they do not dispense it in 50 mg (here in Canada or only at my pharmacist I'm not sure). I still have the twitch so I guess they coat the tablets the same for 100 as they do 25s....... Not sure what to do now as I do not want to come off this medication. It is working too well.
thanks for the reply.

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3

Yes, the coatins on pills and the inactive ingredients can have an effect on your body and how it reacts to taking it, just as much as the drug itself can.

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2

I've developed an eye twitch recently, yes! I've been on 200 mg for about 6 weeks, but just in the last couple have switched to the 200 mg pill instead of 2 100 mg pills. Wonder if the coating could be an issue for me, too? That's certainly odd...

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1

Sorry it took so long to reply. I had the same problem with Topamax which I use for epilepsy. It is the coating of the 100 mg for me. The 50 mg does not cause this on me, so I take 2/50 mg tablets instead. Ever heard of Topamax causing gout?

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