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 » How long to know if Levaquin is working

 - UBBFriend: Email this page to someone!    
Author Topic: How long to know if Levaquin is working
SickSam
LymeNet Contributor
Member # 45330

Icon 1 posted      Profile for SickSam     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi all,

I'm taking Levaquin to fight what my LLMD believes is Bart, but what I believe is Brucella.

I know, I advocate against fluoroquinolones usually, but my heart is inflamed and this is life or death I believe.

I'm two and a half weeks in, and still just getting sicker, as usual. How long does it usually take to know if Levaquin is going to work?

Thank you all so much,
Sam

Posts: 748 | From Texas | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
Jordana
Frequent Contributor (1K+ posts)
Member # 45305

Icon 1 posted      Profile for Jordana     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sam for both of those organisms you should have seen a response in 24 hours; if not then three days.

I don't think Levaquin hits any of the rickettsias. In other words if it's RMSF then you need a tetracycline.

ETA: If you really feel Levaquin is doing *nothing* then get off of it. Call the doc as soon as possible, ok?

Posts: 2057 | From Florida | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
SickSam
LymeNet Contributor
Member # 45330

Icon 1 posted      Profile for SickSam     Send New Private Message       Edit/Delete Post   Reply With Quote 
It doesn't feel like it's doing anything, but I guess I'm wondering if maybe either of those bugs could cause a long herx. I don't feel like I'm herxing, but maybe I am. A couple of days last week I did feel like maybe I was herxing.
Posts: 748 | From Texas | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
Jordana
Frequent Contributor (1K+ posts)
Member # 45305

Icon 1 posted      Profile for Jordana     Send New Private Message       Edit/Delete Post   Reply With Quote 
Or you could just feel so crappy you'd have no idea if anything was working at this point.

It sucks, I'd hate to see you on 30 days of Levaquin for no reason. You can recover from high dose Levaquin. The problem is that it is basically chemotherapy and you're already so sick.

You should be feeling...something, some easing of symptoms in some way. Easier breathing, less pain, more dependable heartbeat...something.

Posts: 2057 | From Florida | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
SickSam
LymeNet Contributor
Member # 45330

Icon 1 posted      Profile for SickSam     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yeah that's pretty much it. So crappy that I don't know if anything is working.

I'm definitely sicker than I was when I started though, but I was getting sicker daily even before I started taking it, so it's hard to tell if I'm herxing or not.

I did read an old thread where one person said they herxed for 6 weeks on Levaquin, but I haven't heard anyone else say that, so figured I'd ask what people's experiences have been.

Posts: 748 | From Texas | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
SickSam
LymeNet Contributor
Member # 45330

Icon 1 posted      Profile for SickSam     Send New Private Message       Edit/Delete Post   Reply With Quote 
I did take doxy with rifampin and Cefzil and had minimal improvement after a month. Not much, but noticeable.
Posts: 748 | From Texas | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
Jordana
Frequent Contributor (1K+ posts)
Member # 45305

Icon 1 posted      Profile for Jordana     Send New Private Message       Edit/Delete Post   Reply With Quote 
It might be the RMSF is the culprit right now.

With Levaquin it's also really hard to know whether it's a herx or just a toxic reaction. That stuff can mess you up; it happened to me.

Posts: 2057 | From Florida | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
SickSam
LymeNet Contributor
Member # 45330

Icon 1 posted      Profile for SickSam     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't know. I think RMSF and Brucella both would've responded better to doxy and rifampin the two months I was on those. It's so hard to know what's going on.

Levaquin did mess up my left knee 10 years ago. Still messed up to this day. I know they're bad drugs, but I had to make the tough call to take it after resisting my doctor for a year. We've tried so many other things that didn't work.

I don't know if this means anything, probably not, but I've had prostatitis for 10 years and right now it's burning more than it has in a long time. It burned bad like this on dexamethasone too. So maybe it's herxing, or maybe my immune system is so beat down that the bugs are growing in there like they did when I was on the steroid.

Posts: 748 | From Texas | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
Jordana
Frequent Contributor (1K+ posts)
Member # 45305

Icon 1 posted      Profile for Jordana     Send New Private Message       Edit/Delete Post   Reply With Quote 
You know, when the immune system gets dysregulated really weird things can happen, like mast cell disorders and other things just cause unexpected and hard to diagnose inflammation.

Have you tried, like -- any of the histamine blockers, 1, 2, or 3?

Prostatitis is often candida or a fungal infection, which is not going to be helped at all by Levaquin, or dexamethasone. If you've done a lot of abx and you have a low functioning immune system, you could have invasive candida. Have you ever gotten a trial of diflucan?

Posts: 2057 | From Florida | Registered: Feb 2015  |  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 
When I was treating lyme and cos, I took Levaquin for 30 days for bart.

I never felt any different the entire time.

Then, I went on to treat babs. I guess the Levaquin worked because after babs treatment I was finished. That was nearly 11 years ago now. Never relapsed.

Posts: 9931 | From Maryland | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
bcb1200
Frequent Contributor (1K+ posts)
Member # 25745

Icon 1 posted      Profile for bcb1200     Send New Private Message       Edit/Delete Post   Reply With Quote 
When I started Levaquin I took it with doxy. I noticed zero difference at all. I felt the same.

I stopped levaquin after 3 weeks because my tendons got a bit tight.

2 days after stopping I had a huge flare / relapse.

Guess it was working!!

--------------------
Bite date ?
2/10 symptoms began
5/10 dx'd, after 3 months numerous test and doctors

IgM Igenex +/CDC +
+ 23/25, 30, 31, 34, 41, 83/93

Currently on:

Currently at around 95% +/- most days.

Posts: 3134 | From Massachusetts | Registered: May 2010  |  IP: Logged | Report this post to a Moderator
SickSam
LymeNet Contributor
Member # 45330

Icon 1 posted      Profile for SickSam     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks guys [Smile] I'm wondering if I'm in that same boat, maybe it's working but I just can't tell yet.

Jordana, yeah I've been on diflucan for a while now. I've tried histamine blockers too, but I probably didn't take them long enough to make a difference. I should probably try again.

Posts: 748 | From Texas | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
SacredHeart
LymeNet Contributor
Member # 44733

Icon 1 posted      Profile for SacredHeart     Send New Private Message       Edit/Delete Post   Reply With Quote 
For me I could tell the difference. I just went off lev a few weeks ago. The pain was much different. My knees felt like they were going to explode and my tendons in my foot felt like they would pop.

It took several weeks for things to get back to normal.

--------------------
Lyme flare June, July, August of 2013. Diagnosed September 2014 Lyme, Bartonella, Mycoplasma, Mono

Posts: 595 | From Texas Crossroads | Registered: Oct 2014  |  IP: Logged | Report this post to a Moderator
SickSam
LymeNet Contributor
Member # 45330

Icon 1 posted      Profile for SickSam     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yeah I'm definitely not floxed. I can tell that. I had a little tendon pain when I started Levaquin but it got better with magnesium.

Today makes one month of Levaquin. Nothing improved yet. I'm wondering how long I should stick with this...

My heart needs something to start working to get rid of the inflammation around it. I don't have extra time to waste if this isn't gonna do the trick...

Posts: 748 | From Texas | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
Judie
Frequent Contributor (1K+ posts)
Member # 38323

Icon 1 posted      Profile for Judie     Send New Private Message       Edit/Delete Post   Reply With Quote 
What's your goal with levaquin?

Levaquin can cause heart problems:

http://www.rxlist.com/levaquin-drug/medication-guide.htm

"LEVAQUIN may cause a rare heart problem known as prolongation of the QT interval."

If you're taking it to cure bart, it won't. It just makes it more resistant after the initial die off.

Bartonella Infection: Treatment and Drug Resistance
http://www.medscape.com/viewarticle/734138_1

http://lymemd.blogspot.com/2013/07/updates-antibiotics.html

Floxing happens when you stop the med. You're tendons can rupture 6 months or even a year after stopping it.

Floxing is complicated. It's a cascade of problems that happen when you stop the drug though problems can happen while on the drugs too.

Posts: 2839 | From California | Registered: Jul 2012  |  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 
Sam, I know you are very ill .. but this is one of the most dangerous drugs on the market. I will NEVER take it again.

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
SickSam
LymeNet Contributor
Member # 45330

Icon 1 posted      Profile for SickSam     Send New Private Message       Edit/Delete Post   Reply With Quote 
Trust me, I know they're super-dangerous. I hate taking them. I have friends whose floxing didn't appear until months after taking a quinolone. I have educated all of my doctors that didn't already know about the dangers of quinolones. Before I knew I had Lyme I was convinced I was floxed. I'm a member of floxie support groups. Turns out I'm not floxed yet though. I cringed when my grandma was given IV Levaquin and prednisone together (I couldn't stop it).

Judie, the goal is to first and foremost knock back the infection that is inflaming my heart. I know Levaquin won't cure it, I know levaquin can cause QT prolongation (so can Bactrim, Diflucan, Zithromax, Flagyl, even Plaquenil), but this infection has gotten so dangerous and I've tried my other oral options.

IV wasn't an option until Levaquin was tried first. So it was either try Levaquin and risk getting floxed or risk dying. I had to risk being floxed. I do monitor my QT interval daily. I have so much medical equipment at home...

I'm deathly ill. I had to do it. After telling my doctor "no" for a year, I had to try it. A devastating drug, I warn my family to not take the quinolones, but I didn't have another choice. After a lot of prayer I started taking it.

So even if it won't cure Bart, I can't let Bart continue to ravish my body (if it even is Bart). At this point, the goal is to save my life. [Frown] I am bedridden, non-functional. And I know the quinolones have killed people too. I actually posted the fda memo that reported the man dying from Levaquin in the quinolones warning thread several months ago.

Sorry to write so much. I really appreciate you all looking out for me. Very very much. I tell other people the exact same thing about quinolones. Levaquin injured my knee 10 years ago actually. I just didn't have another choice, and my body couldn't afford to wait anymore.

I hate every time I take it, which is why I'm trying to figure out how long I should keep putting this mess in my body before deciding that it didn't work. [Frown]

Posts: 748 | From Texas | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
dbpei
Frequent Contributor (1K+ posts)
Member # 33574

Icon 1 posted      Profile for dbpei     Send New Private Message       Edit/Delete Post   Reply With Quote 
So sorry, SickSam. You mentioned that you have had prostatitis for the last 10 years and it had recently worsened since taking the levaquin. (this is another clue that it might be brucellosis)

I think I remember reading in a previous thread how bactrim helped you at one point. Have you ever tried together the trio of doxy, rifampin and bactrim? These are used together for brucellosis and may be as effective, if not more effective, than levaquin.

If you end up stopping the levaquin, I wonder if you could discuss giving this trio a try with your doc.

Posts: 2386 | From New England | Registered: Aug 2011  |  IP: Logged | Report this post to a Moderator
SickSam
LymeNet Contributor
Member # 45330

Icon 1 posted      Profile for SickSam     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've tried doxy with rifampin, and bactrim with rifampin, but never all three of them together. I did try mino with bactrim and rifampin, but I didn't stick with it near long enough to tell if it would work or not.

Funny thing is I think my prostatitis might be a tiny bit better now for the first time in 10 years. Could just be my imagination, I can't say for sure yet. All my other symptoms are definitely worse.

I've also had bad lumbar spine pain (I've read Brucella likes that area), palpitations, and infrequent mild chest pain for 10 years too (much different from the chest inflammation I have now). And I've also had the mild sore throat when I'm tired for years also, which I've read is Bart??? But Cefzil gave me the biggest herx?

I've kinda concluded that you just have to try treating everything until something works I guess. You never really know what you're killing...

[ 01-19-2016, 02:46 PM: Message edited by: SickSam ]

Posts: 748 | From Texas | Registered: Feb 2015  |  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 
Sam .. keep writing. We care!!

[group hug]

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
dbpei
Frequent Contributor (1K+ posts)
Member # 33574

Icon 1 posted      Profile for dbpei     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, Sam. You are so right. That is what we all need to do with this. Please keep us posted.

I am going to ask my doc today to treat me with the big guns for brucellosis and we will see what happens. I hope I will be able to report some good news here in a few weeks. God bless.

Posts: 2386 | From New England | Registered: Aug 2011  |  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.