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 » Ceftin Experiences

 - UBBFriend: Email this page to someone!    
Author Topic: Ceftin Experiences
pini
LymeNet Contributor
Member # 1405

Icon 1 posted      Profile for pini     Send New Private Message       Edit/Delete Post   Reply With Quote 
Good evening all. I was on Biaxin for a month, but had a lot of trouble getting my prescription filled due to Biaxin shortage.

My doctor gave me Ceftin instead. I got about 80% better on Biaxin, but I am not sure if Ceftin is doing anything. I started the Ceftin about a week ago.

My lingering symptoms are severe foot spasms and pain. Before abx is was constant pain, now the foot pain is about half the day. Please share about Ceftin and/or foot pain. Thanks.

Posts: 260 | From Long Island, New York | Registered: Jul 2001  |  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 
Biaxin was great for me. Don't remember much from Ceftin.

Back when I had foot and hand spasms, I was told it could be a mineral deficiency. So I started taking a mineral supplement. NO more spasms!!

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
cleo
LymeNet Contributor
Member # 6646

Icon 1 posted      Profile for cleo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ceftin did nothing for me. Slight herx but it caused me to really backtrack.
Posts: 433 | From new york | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
pini
LymeNet Contributor
Member # 1405

Icon 1 posted      Profile for pini     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for the responses.

What is the best mineral supplement for foot spasms?

Also is anyone else having trouble getting meds. because of drug shortages?

Posts: 260 | From Long Island, New York | Registered: Jul 2001  |  IP: Logged | Report this post to a Moderator
one4islands
LymeNet Contributor
Member # 28187

Icon 1 posted      Profile for one4islands     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am taking a low dose once a day and don't know if it's helping.

I've been on it for about 45 days.

I've tolerated it well, except I've been having some esophageal spasm chest pain I think may be related to it and all the other pills I am taking.

Posts: 412 | From Virginia | Registered: Sep 2010  |  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 
I'm taking NOW Full Spectrum Minerals Caps. I think you can get it at Swanson's.

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  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.