LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Can anyone offer any info on Flagyl / seizures and seizure med Topamax???

 - UBBFriend: Email this page to someone!    
Author Topic: Can anyone offer any info on Flagyl / seizures and seizure med Topamax???
Julz
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Just to fill you in, I have been on treatment for 2 1/2 years now. I am supposed to start Flagyl and zithromax. I am worried becuase when I read Flagyl can cause seizures, and not to take it with Tegretol, an anti seizure medication. I had been on treatment for over a year, and just as I was feeling better I had 2 "seizure-like" episodes, 3 weeks apart. I started taking anti- seizure medication Topamax, and have not had another episode for a year. I am worried about starting the Flagyl when it lists seizures as a side effect, and also lists drug interaction with another anti seizure med. Anyone have any experience or knowledge with any of this?? Please help!!!
IP: Logged | Report this post to a Moderator
valbeth
Member
Member # 12715

Icon 1 posted      Profile for valbeth     Send New Private Message       Edit/Delete Post   Reply With Quote 
Julz, this is a question for your doc, but I can say that I have taken Lamictal with both of these abx without a problem and I believe Lamictal is more similar to Tegretol than Topamax is. BTW, the Lamictal has been a HUGE help to my CNS lyme/babs/bart? symptoms especially pain and sleep cycle disturbance. If you have to take an anti-seizure medication anyway switching to Lamictal might be worth thinking about. Please note, I am NOT taking the Lamictal for seizures, so can't speak to that, and I AM NOT A DOCTOR! Good luck.

--------------------
Valerie
***********************************
"A woman is like a tea bag- you never know how strong she is until she gets in hot water." Eleanor Roosevelt

Posts: 63 | From Jim Thorpe, PA | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
Julz
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Thanks so much for the reply. Why are you taking tamictal??as a treatment for the lyme and co's??? I never heard of that!! I take so many things to help with pain and sleeping problems...maybe the tamictal could help everything. I have never taken Flagyl...how is it?
IP: Logged | Report this post to a Moderator
Julz
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
sorry for the miss up on the letters...I was thinking Lamictol...its just the lyme brain!!
IP: Logged | Report this post to a Moderator
lucy96734
LymeNet Contributor
Member # 8372

Icon 1 posted      Profile for lucy96734     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had been taking Topomax for years for nerve pain prior to knowing I had Lyme. I took it during my treatment with Tindamax, which I hear is similar to Flagyl.

I am sure that doesn't help you at all [Smile]

I would talk to your LLMD.

--------------------
Lucy

Posts: 342 | From Hawaii | Registered: Nov 2005  |  IP: Logged | Report this post to a Moderator
Julz
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
THanks for the reply. I am really sick with neuro lyme, we considered going back on Bicillin LA IM shots, but that's what I was on when I had the seizures, so he thought Flagyl was the best choice. I have never been on Tindamax either...I have no idea why Flagyl for neuro lyme.
IP: Logged | Report this post to a Moderator
Cobweb
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
I was diagnosed with a "seizure disorder"-just prior to starting treatment for lyme.

Anyway-the neurologist has me taking Keppra-500mg 2x daily.

I have pulsed through 3 cycles of Flagyl-without a problem.

I know this doesn't exactly answer your question-but it's as close as I can get.

Take Care,
Carol

IP: Logged | Report this post to a Moderator
Julz
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Thank you so much for your reply...it definitely
helps alot! Do you think your seizure disorder is from the Lyme? How long have you been taking treatments for Lyme? and how is it taking Keppra? any significant side effects? The topamax has many side effects...so we are not sure if some of my problems are actually from the Lyme and Co's or the topamax!!!

Thanks very much!!

Julz

IP: Logged | Report this post to a Moderator
Cobweb
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
I definitely think it was/is from lyme. In fact it was the last straw that made me say that's it-I'm going to an LLMD.

I was extremely hesitant at first to take the Keppra-as I am with most meds-finally worked up the nerve-and was quickly impressed by improvement.

No side effects from Keppra that I can tell. I was supposed to take 500 3x day, but find that 2 x day is fine-with neurologist's approval.

Brief history-first dignosed with lyme July 2004-treated inadequately with 3 weeks low dose ceftin.

Health continued to decline- made the rounds of specialists.

Diagnosed in Spring 2005 with seizures. Went to LLMD in May 2005-was retested for lyme-diagnosed with "persistent lyme" Have been on orals and IV since then.

Heading for bed,
Take Care,
Carol

IP: Logged | Report this post to a Moderator
valbeth
Member
Member # 12715

Icon 1 posted      Profile for valbeth     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by Julz:
Thanks so much for the reply. Why are you taking tamictal??as a treatment for the lyme and co's??? I never heard of that!! I take so many things to help with pain and sleeping problems...maybe the tamictal could help everything. I have never taken Flagyl...how is it?

My LLMD psychiatrist started me on the Lamictal for depression which it has also helped, certainly worth talking about. I am just finishing up a month of Levaquin for my brain problems. Also taking Samento and Arteminisin. Since the Levaquin has helped I suspect I'm dealing with Bartonella (what my LLMD was thinking it was too). As far as Flagyl, do remember too much except everything makes me herx! [Big Grin] If you also have neurogenic pain and/or problems with irregular sleep cycles I would definitely talk to your LLMD about the Lamictal. Good luck.

--------------------
Valerie
***********************************
"A woman is like a tea bag- you never know how strong she is until she gets in hot water." Eleanor Roosevelt

Posts: 63 | From Jim Thorpe, PA | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
Michelle M
Frequent Contributor (1K+ posts)
Member # 7200

Icon 1 posted      Profile for Michelle M   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I take Topamax for migraines.

I also did six weeks of Flagyl while on Topamax.

The Flagyl about did me in! But I saw a lot of improvement afterward.

I would go slow on the Flagyl, for sure. It's a "barn burner." However, I've never heard I couldn't do them at the same time.

Good luck to you.

Michelle

Posts: 3193 | From Northern California | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.