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 » Side effects of Flagyl, experiences with C diff, anyone?

 - UBBFriend: Email this page to someone!    
Author Topic: Side effects of Flagyl, experiences with C diff, anyone?
BenRoss
Member
Member # 20227

Icon 1 posted      Profile for BenRoss     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi to the thoughtful caring people reading this!

I got a lab back today saying I've got an overgrowth of C diff bacteria. I've been prescribed Flagyl and am a little concerned by hearing about side effects for people with neuropathy. I'm also wondering how my gut will tolerate it. Has anyone had experiences with this, and have people had their C diff subside without Flagyl? Thank you so much for your thoughts!!!

Ben

Posts: 11 | From Florence, MA | Registered: May 2009  |  IP: Logged | Report this post to a Moderator
cactus
Frequent Contributor (1K+ posts)
Member # 7347

Icon 1 posted      Profile for cactus     Send New Private Message       Edit/Delete Post   Reply With Quote 
You can do a search here for C Diff and probably find some good info.

Fortunately, not too many here have had it - but some have.

If you have trouble tolerating flagyl, you can ask your doc about oral vancomycin or xifaxin - both of which stay in the GI system only.

I do not tolerate flagyl well (because of neuropathy), but am currently on oral vanco for C. Diff.

Be sure to sterilize everything in your bathroom, as C. Diff is contagious. Use bleach.

You might also check out the C. Diff support forum - Google C Diff support and it should come up.

--------------------
�Did you ever stop to think, and forget to start again?� - A.A. Milne

Posts: 1987 | From No. VA | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
pryorka
LymeNet Contributor
Member # 13649

Icon 1 posted      Profile for pryorka     Send New Private Message       Edit/Delete Post   Reply With Quote 
Alinia is suppose to work on C Diff too. I think it's in clinical trials to be approved as an authorized treatment for C diff.
Posts: 499 | From Indiana | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
randibear
Honored Contributor (10K+ posts)
Member # 11290

Icon 1 posted      Profile for randibear     Send New Private Message       Edit/Delete Post   Reply With Quote 
be very careful with flagy. it gave me the worst case of thrush and yeast i've ever had!!

take tons of probiotics and if necessary, ask that doc for diflucan...

--------------------
do not look back when the only course is forward

Posts: 12262 | From texas | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
BenRoss
Member
Member # 20227

Icon 1 posted      Profile for BenRoss     Send New Private Message       Edit/Delete Post   Reply With Quote 
I really appreciate people's responses! I'm wondering when one takes the probiotics if Flagyl is a four-time-a-day med? Won't the med just kill the probiotics? I also wonder, cactus, what neuropathic side effects you experienced. I have intense neuropathic pain myself, and am very much not wanting to flare it up.

Thank you so much for your help!

Posts: 11 | From Florence, MA | Registered: May 2009  |  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.