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 » FLAGYL AND PERIPHERAL NEUROPATHY

 - UBBFriend: Email this page to someone!    
Author Topic: FLAGYL AND PERIPHERAL NEUROPATHY
Deep in 'tis pear
LymeNet Contributor
Member # 10427

Icon 1 posted      Profile for Deep in 'tis pear     Send New Private Message       Edit/Delete Post   Reply With Quote 
I was on Biaxin and 500 mg of Flagyl twice a day for close to two months. Didn't have a problem till about a month and three weeks into it. I started getting pins and needles all over my hands and feet and various parts of my body. Stopped the Flagyl a week ago, but the pins and needles feeling has not subsided... Has anyone had the same problem, and has it gotten better with time? Thanks.
Posts: 123 | From Los Angeles | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Flagyl flared nerve pain for me. I still have it in my feet.

There are several drugs that flare nerve pain for me.. quinolones do too.

Mine comes and goes.

Try antioxidants and healthy eating!

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
TF
Frequent Contributor (5K+ posts)
Member # 14183

Icon 1 posted      Profile for TF     Send New Private Message       Edit/Delete Post   Reply With Quote 
From page 15 of Burrascano:

"Flagyl can be irritative to the nervous system- in the short term, it may cause irritability, "spacey" feelings, etc. Longer term, it can affect the peripheral nerves, causing tingles, numbness, etc. If mild, a change in dose may be required. Often, extra vitamin B can clear these symptoms. If the nerve symptoms persist or are strong, then metronidazole must be discontinued or these symptoms may become very long lasting."

http://www.ilads.org/lyme_disease/B_guidelines_12_17_08.pdf

I would try the extra vitamin B as he suggests. I would add sublingual (under the tongue) vitamin B12 also because that's what my lyme doc had me take for any symptoms like this and they cleared up right away.

Posts: 9931 | From Maryland | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
girl
LymeNet Contributor
Member # 18022

Icon 1 posted      Profile for girl     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had this with Flagyl and liquid B vitamins did wonders for me. Best not to take them at night as they may keep you awake.
Posts: 631 | From the south | Registered: Nov 2008  |  IP: Logged | Report this post to a Moderator
susank
Frequent Contributor (1K+ posts)
Member # 22150

Icon 1 posted      Profile for susank     Send New Private Message       Edit/Delete Post   Reply With Quote 
Does Tindamax do the same thing?

--------------------
Pos.Bb culture 2012
Labcorp - no bands ever
Igenex - Neg. 4 times
With overall bands:
IGM 18,28,41,66 IND: 23-25,34,39
IGG 41,58 IND: 39
Bart H IGG 40

Posts: 1613 | From Texas | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
TF
Frequent Contributor (5K+ posts)
Member # 14183

Icon 1 posted      Profile for TF     Send New Private Message       Edit/Delete Post   Reply With Quote 
It is in the same drug family so it can likely do the same thing as flagyl. But, Tindamax (tinidazole) has fewer side effects according to Burrascano.
Posts: 9931 | From Maryland | Registered: Dec 2007  |  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.