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 » Any experiences with Factive?New/old?

 - UBBFriend: Email this page to someone!    
Author Topic: Any experiences with Factive?New/old?
mojo
Frequent Contributor (1K+ posts)
Member # 9309

Icon 1 posted      Profile for mojo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've been considering this drug for Bart since the ILADs conference last fall.

I would love any input as to how it has worked (or not).

thank you!

Posts: 1761 | From USA | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
BoxerMom
Frequent Contributor (1K+ posts)
Member # 25251

Icon 1 posted      Profile for BoxerMom     Send New Private Message       Edit/Delete Post   Reply With Quote 
It is a fluoroquinolone, like Levaquin and Cipro. I took it for 5 days last November and ruptured my Achilles tendon. (Side effect of the drug.) I had previously taken Cipro with no problems. I know two Lymies who developed tendonitis, one on Factive, the other on Levaquin.

I did herx, so it was working, but not worth the rehab I'm doing for my tendon.

--------------------
 - Must...find...BRAIN!!!

Posts: 2867 | From Pacific NW | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091

Icon 1 posted      Profile for Rumigirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
I used it for two 5 day cycles in Nov/Dec. It helped my neuro sxs miraculously. HOWEVER, I began seeing double on my fourth day on it!! And that continued on and off ever since. I've read that that effect may be from the effect on the tendons/ligaments of the eyes.

Plus, I got bad tendon/ligament problems on my thumbs, which hasn't gone away. I know someone else who also got tendon problems from it.

So, a double-edged sword to say the least. Supposedly, it doesn't have the same tendon problems as the other quinolones, but that info was from the company (and therefore unreliable).

Posts: 3771 | From around | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
mojo
Frequent Contributor (1K+ posts)
Member # 9309

Icon 1 posted      Profile for mojo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Wow, so more tendon issues than originally though.
Bummer!
I can't do Rifampin because it spiked my liver enzymes through the roof and I need to hit it hard.

Right now I'm rifing and "cleaning up" a bit - trying to figure out my next "attack"

Posts: 1761 | From USA | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
Ivy
Member
Member # 18365

Icon 1 posted      Profile for Ivy     Send New Private Message       Edit/Delete Post   Reply With Quote 
Unable to take Rifampin, Bactrim and Levaquin for Bart - I have been on Factive since January. I started with 1/2 per day for 2 months. Now I am on a full pill daily.

I am having good luck with it so far.

I read on the package insert that steroid use increases tendon problems.

Posts: 74 | From Maryland | Registered: Dec 2008  |  IP: Logged | Report this post to a Moderator
mojo
Frequent Contributor (1K+ posts)
Member # 9309

Icon 1 posted      Profile for mojo     Send New Private Message       Edit/Delete Post   Reply With Quote 
So you aren't pulsing it? Interesting.

Thanks so much for the input. Glad it is working for you.

Posts: 1761 | From USA | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
BoxerMom
Frequent Contributor (1K+ posts)
Member # 25251

Icon 1 posted      Profile for BoxerMom     Send New Private Message       Edit/Delete Post   Reply With Quote 
I should add that all of the Lymies I mentioned who developed tendon issues are chronic cases, 15+ years undiagnosed. I think we are more compromised that the acute cases.

I've never been on steroids.

I have read speculation that it's a combination of poor circulation to tendons and Mg deficiency that contribute to the tendon problems. That would make sense for us. Of course, it's only speculation.

--------------------
 - Must...find...BRAIN!!!

Posts: 2867 | From Pacific NW | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
mojo
Frequent Contributor (1K+ posts)
Member # 9309

Icon 1 posted      Profile for mojo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am definately chronic 15 + years.

My arms and hands fall asleep easily - so i may have poor circulation but I've been doing light weight work and I think my circulation is improving.

I take Mg so that may help make the decision.
Thanks again.

Posts: 1761 | From USA | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
merrygirl
Frequent Contributor (1K+ posts)
Member # 12041

Icon 1 posted      Profile for merrygirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
pulsed 5 days a month. noticed nothing. no side effects nothing positive
Posts: 3905 | From USA | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
mojo
Frequent Contributor (1K+ posts)
Member # 9309

Icon 1 posted      Profile for mojo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks, Merry. Sorry it didn't work for you.
Posts: 1761 | From USA | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
merrygirl
Frequent Contributor (1K+ posts)
Member # 12041

Icon 1 posted      Profile for merrygirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
thats ok thanks. I hope it works for you!!
Posts: 3905 | From USA | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
mojo
Frequent Contributor (1K+ posts)
Member # 9309

Icon 1 posted      Profile for mojo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank you! I hope I can get my Dr. to give it to me!
Posts: 1761 | From USA | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
Starch
Member
Member # 16205

Icon 1 posted      Profile for Starch     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've had chronic lyme for 2 years and just went on Factive for the first time. 1 pill once a day for five days and had to stop because both ankles felt really tight and burning.

My Doc took me off and has instructed me to wait for my ankles to get better (they started feeling better as soon as I stopped the drug but still bother me a week later). From there he wants me to get on low doses of Cipro and ramp up over a month or so.

Other than my ankles I felt great of Factive. Fog went away as did most other symptoms. Total bummer that it brought on some scary side effects.

So something to think about when weighing Factive against other alternatives.

Posts: 48 | From Baltimore, md | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
sammy
Frequent Contributor (5K+ posts)
Member # 13952

Icon 1 posted      Profile for sammy     Send New Private Message       Edit/Delete Post   Reply With Quote 
It helps, I take Factive daily. When I stop taking it my neurological symptoms increase and my GI symptoms flare.

I tried Avelox but didn't tolerate it well. It made me feel sicker all the time and irritated my stomach. I've taken Cipro in the past and tolerated it well though.

I'm just telling you this so that you can know that even if you don't tolerate Factive well, don't be afraid to try another drug in the same class (Cipro, Levaquin, Avelox).

Posts: 5237 | From here | Registered: Nov 2007  |  IP: Logged | Report this post to a Moderator
joysie
LymeNet Contributor
Member # 11063

Icon 1 posted      Profile for joysie     Send New Private Message       Edit/Delete Post   Reply With Quote 
I took Factive for three months daily. No side effects and it was helpful with neuro symptoms.
Kris

Posts: 520 | From Maryland | Registered: Jan 2007  |  IP: Logged | Report this post to a Moderator
Wonko
LymeNet Contributor
Member # 18318

Icon 1 posted      Profile for Wonko     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've posted before on threads about Factive.

For me, it was my "turn the corner" medication. I finally made real, lasting improvement with Factive. Shortly after my experience taking Factive, I was able to resume full time work.

At first I took it one week on, one week off. After I reported to my LLMD how well it was going, with no tendon issues, I then did a month straight on it.

I'm no longer taking it, my LLMD has moved me on to other medications. But I was very happy with this Rx and am glad it was able to help me improve.

Posts: 455 | From Was in PA, then MD, now in the Midwest | Registered: Nov 2008  |  IP: Logged | Report this post to a Moderator
blinkie
Frequent Contributor (1K+ posts)
Member # 14470

Icon 1 posted      Profile for blinkie     Send New Private Message       Edit/Delete Post   Reply With Quote 
wonko-that is great news. Did you test positive for bart?
Posts: 1104 | From N.California | Registered: Jan 2008  |  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.