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Dear Ruth,

As time passes Vioxx is getting more bad press for it's side effects. I

took it several years ago and my blood pressure went up and I retained fluid

like mad. I have since developed kidney disease and I (my own opinion only)

think that the Vioxx had something to do with it. The standard dose is 25

mg and 50 mg is a big dose and I certainly would not take more than that.

If you are having so much pain you may want to get some pain meds. If you

are only on the Vioxx for your arthritis you may want to consider a more

effective med, any of the ones you mentioned. Neurontin is for a different

kind of pain. Anne

[ ] VIOXX

Today the rheumy yelled at me for taking so much VIOXX. He wants me to

take it only when the pain is really bad. I take 50 mgs a day. He is

afraid that I will damage the liver or stomach. I get a blood test and it

is fine. I figure if it takes away the pain, why not use it? I try to back

off on the weekends but the pain/stiffness/ etc. comes right back. He wants

25 one day 50 the next. Does anyone else take 50 mgs daily or do you just

take it occasionally? I am also on Neurotin and will be up to the full dose

this week. Perhaps that will work better than the VIOXX. The doc said it

is like taking 16 Ibuprofen tablets a day and my daughter who was with me,

freaked out and said how can you take that much medicine and not listen to

the doctor? Think of all the damage you are doing? I didn't have the heart

to tell her that on some real bad days I have taken 100 mgs. How much more

damage can I do? At any rate, I didn't think that VIOXX is as potent as the

alternatives MTX, enbril, and probably the Neurotin?

relizabethb@...

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I have been on 50 mg Vioxx for almost a year. My GP had a fit and said no

one should be at that dose for more that a few days. I asked my rheumy, who

said he has had patients on it for years at that dose. I do have to take

Protonix for stomach. I'm sure that is related.

Ks Di

[ ] VIOXX

> Today the rheumy yelled at me for taking so much VIOXX. He wants me to

take it only when the pain is really bad. I take 50 mgs a day. He is

afraid that I will damage the liver or stomach. I get a blood test and it

is fine. I figure if it takes away the pain, why not use it? I try to back

off on the weekends but the pain/stiffness/ etc. comes right back. He wants

25 one day 50 the next. Does anyone else take 50 mgs daily or do you just

take it occasionally? I am also on Neurotin and will be up to the full dose

this week. Perhaps that will work better than the VIOXX. The doc said it

is like taking 16 Ibuprofen tablets a day and my daughter who was with me,

freaked out and said how can you take that much medicine and not listen to

the doctor? Think of all the damage you are doing? I didn't have the heart

to tell her that on some real bad days I have taken 100 mgs. How much more

damage can I do? At any rate, I didn't think that VIOXX is as potent as the

alternatives MTX, enbril, and probably the Neurotin?

> relizabethb@...

>

>

>

>

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Ruth, I don't know enough about meds to give any kind of opinion but if my

doctor yelled at me I'd find another doctor real fast. Good Luck! Cheri

[ ] VIOXX

Today the rheumy yelled at me for taking so much VIOXX. He wants me to take

it only when the pain is really bad. ...

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Hello

I have been taking 50mg of vioxx for about 1 and a 1/2 years.

Everything is fine. I had blood tests twice and they came back

excellent. My rhuemy said 50mg is the max but is ok to take daily.

Shane

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I have used all of the OTC anti-inflamatories. Although I don't think

Vioxx is more effective in reducing my symptoms, which include

stiffness and an occassional inflamed knuckle. I am using 25 mg of

Vioxx a day because it has less effect on my digestive system. I have

asked my doctor about going to a higher dose of vioxx and he said

that the company that produces Vioxx is or has done studies using

higher doses. He couldn't tell me the results of these studies, but

he suspects that there are reasons that higher doses are not

recommended because Merck (or whoever) would like to sell as much of

this product as possible, and would if the results of the studies

were good. Have you heard of any studies using higher doses?

> Today the rheumy yelled at me for taking so much VIOXX. He wants

me to take it only when the pain is really bad. I take 50 mgs a

day. He is afraid that I will damage the liver or stomach. I get a

blood test and it is fine. I figure if it takes away the pain, why

not use it? I try to back off on the weekends but the

pain/stiffness/ etc. comes right back. He wants 25 one day 50 the

next. Does anyone else take 50 mgs daily or do you just take it

occasionally? I am also on Neurotin and will be up to the full dose

this week. Perhaps that will work better than the VIOXX. The doc

said it is like taking 16 Ibuprofen tablets a day and my daughter who

was with me, freaked out and said how can you take that much medicine

and not listen to the doctor? Think of all the damage you are

doing? I didn't have the heart to tell her that on some real bad

days I have taken 100 mgs. How much more damage can I do? At any

rate, I didn't think that VIOXX is as potent as the alternatives MTX,

enbril, and probably the Neurotin?

> relizabethb@e...

>

>

>

>

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That frightens me as I use 50mg of vioxx a day, and my doc never mentioned any

of this, other than to go any higher than 50 mg would do serious digestive

damage..let me know what you find out =)

[ ] Re: VIOXX

I have used all of the OTC anti-inflamatories. Although I don't think

Vioxx is more effective in reducing my symptoms, which include

stiffness and an occassional inflamed knuckle. I am using 25 mg of

Vioxx a day because it has less effect on my digestive system. I have

asked my doctor about going to a higher dose of vioxx and he said

that the company that produces Vioxx is or has done studies using

higher doses. He couldn't tell me the results of these studies, but

he suspects that there are reasons that higher doses are not

recommended because Merck (or whoever) would like to sell as much of

this product as possible, and would if the results of the studies

were good. Have you heard of any studies using higher doses?

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No studies. I have been on 50 mg for over a year. My doctor says he has

had people on this dosage for years with good results. I do have to take

stomach medicine.

Ks Di

[ ] Re: VIOXX

> I have used all of the OTC anti-inflamatories. Although I don't think

> Vioxx is more effective in reducing my symptoms, which include

> stiffness and an occassional inflamed knuckle. I am using 25 mg of

> Vioxx a day because it has less effect on my digestive system. I have

> asked my doctor about going to a higher dose of vioxx and he said

> that the company that produces Vioxx is or has done studies using

> higher doses. He couldn't tell me the results of these studies, but

> he suspects that there are reasons that higher doses are not

> recommended because Merck (or whoever) would like to sell as much of

> this product as possible, and would if the results of the studies

> were good. Have you heard of any studies using higher doses?

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I was wondering if there'd be a point where stomach meds would come to play....

I've only been on 50 mg for a few months... so we'll see

[ ] Re: VIOXX

> I have used all of the OTC anti-inflamatories. Although I don't think

> Vioxx is more effective in reducing my symptoms, which include

> stiffness and an occassional inflamed knuckle. I am using 25 mg of

> Vioxx a day because it has less effect on my digestive system. I have

> asked my doctor about going to a higher dose of vioxx and he said

> that the company that produces Vioxx is or has done studies using

> higher doses. He couldn't tell me the results of these studies, but

> he suspects that there are reasons that higher doses are not

> recommended because Merck (or whoever) would like to sell as much of

> this product as possible, and would if the results of the studies

> were good. Have you heard of any studies using higher doses?

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I had reflux before Vioxx, so I am probably not a good example. The Vioxx

did make me leave OTC behind and stay on prescription for the stomach.

Ks Di

[ ] Re: VIOXX

> > I have used all of the OTC anti-inflamatories. Although I don't think

> > Vioxx is more effective in reducing my symptoms, which include

> > stiffness and an occassional inflamed knuckle. I am using 25 mg of

> > Vioxx a day because it has less effect on my digestive system. I have

> > asked my doctor about going to a higher dose of vioxx and he said

> > that the company that produces Vioxx is or has done studies using

> > higher doses. He couldn't tell me the results of these studies, but

> > he suspects that there are reasons that higher doses are not

> > recommended because Merck (or whoever) would like to sell as much of

> > this product as possible, and would if the results of the studies

> > were good. Have you heard of any studies using higher doses?

>

>

>

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Well I've had previous tummy issues too.... colitis, and ulcers... but it's been

a really long time.. I had reflux really bad during pregnancy, but havnn't had a

real issue after birth.

Re: [ ] Re: VIOXX

I had reflux before Vioxx, so I am probably not a good example. The Vioxx

did make me leave OTC behind and stay on prescription for the stomach.

Ks Di

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It has worked for me for a couple of years and I've had no bad side

effects....but now 25mg is not always enough and I'm moving on to MTX.

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I have been on 50mg of Vioxx for about a year. It is really good. It is

hard on the stomach. I have to take protonix daily to tolerate the

medication.

Ks Di

[ ] Vioxx

> Hi all,

> Has anyone had any experience with Vioxx for PA? Right now I'm on

> Arava with no relief. I keep seeing ads for Vioxx and was wondering

> if it is even helpful to PA

> Thanks,

>

>

> [Ed. Note: Yes , I would say that most of us probably have experience

with Vioxx. Why don't you search the archives for past messages about Vioxx?

Just go to / and put Vioxx

into the " Search Archive " box. Ron]

>

>

> Please visit our Psoriatic Arthritis Group's informational web page at:

> http://www.wpunj.edu/pa/ -- created and edited by list member

aka(raharris@...).

>

> In August 2001 list member Jack aka(Cornishpro@...) began to

conduct extensive research which he publishes as the Psoriatic Arthritic

Research Newsletter monthly in our emails and digest format. Many thanks to

Jack. Back issues of the newsletter are stored on our PA webpage.

>

> Also remember that the list archives comprise a tremendous amount of

information (Over two years of messages and answers).Feel free to browse

them at your convenience.

>

> Let's hear from some of you lurkers out there! If you have a comment or

question chances are there is a person who has been around a while who can

help you out with an educated guess for an answer. If not we can at least

steer you in the right direction with a good website to go to for the

answers.

>

> Blessings and Peace,

>

> Atwood-Stack, Founder

> Alan , Web & List Editor

> Jack , Newsletter Editor

> Pat Bias, List Editor

> Ron Dotson, List Editor

> and many others who help moderate (thank you!)

>

>

>

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, I'm on Bextra, which is in the same family but is easier on the

stomach and is a sulfa based drug so is less likely to be harmful over the

long term unless you are allergic to sulfa drugs. Keeps the swelling down

and some of the pain in check. I have chosen to not do Enbrel or Metho or

any of the other drugs, so when the Bextra isn't enough for the pain, I use

paraffin wax on my hands and feet (insurance paid for a commercial paraffin

unit) and I spend a lot of time in the pool, which helps.

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,

How long have you been diagnosed? Bextra did nothing for me, but Celebrex

does... same kind of med. I have been trying to stay off of things too, but I

do have Enbrel waiting in my fridge whenever I get the nerve up to start the

injections. I am just SO nervous about going on more severe meds. Will you

tell me what problems your arthritis has caused you? Do you have any joints

starting to deform? I have a finger with a small hump on it, and my left

ankle is getting a little whaky. I am trying to be smart about taking meds,

but I always have said that when I start to see/feel joint changes I would do

something. Well, I am there now... and I still can't bring myself to take

anything more severe! So, there is my delimma. Since we see this drug issue

the same way I am asking you what you would do if you started to see joint

changes? I have had this disease for over 6 years now, but I was diagnosed in

1999. Thanks for any advice.

In a message dated 1/22/03 7:44:09 PM Eastern Standard Time,

rachelviognier@... writes:

> , I'm on Bextra, which is in the same family but is easier on the

> stomach and is a sulfa based drug so is less likely to be harmful over the

> long term unless you are allergic to sulfa drugs. Keeps the swelling down

> and some of the pain in check. I have chosen to not do Enbrel or Metho or

> any of the other drugs, so when the Bextra isn't enough for the pain, I use

>

> paraffin wax on my hands and feet (insurance paid for a commercial paraffin

>

> unit) and I spend a lot of time in the pool, which helps.

>

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,

I so applaud you courage to do this drug free. I only wish that was an

option to me. You sound to be a very active and full of life. You see to

always be up beat and the words you use to encourage others is eloquent. I

do hope, for you sake that you can maintain your PA at this point with the

way you choose to manage your meds. The patient leaflets they give with

prescriptions are terrifying, but remember to look further...in FACTS, in the

PDR and look to your doctor for percentages that the side effects occur.

Because if some terrible side effect occurs in one-tenth of one percent of

patients they have to publish that information and many times what the

consumer gets is just the type of side effect that occurred and not how often

it was seen in patients. Keep up the smiles that you pass on to us here in

the group. I hope some of this information is useful to you!

PS - Hope you are staying warm today! We got 10 inches (maybe 12) of that

cold white stuff and it is hanging around 10 degrees outside right now! " )

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Hi ,

We have 8 inches here, and it is COLD! I had to close my office today

because of the snow.

Yes, I do always read up on percentages, and I guess I just let fear get the

best of me when it comes to stronger meds... which is really funny, since I

am normally not a paranoid kind of person. I am sure many here can relate

when I say I never thought at 23 I would get PA, so now I think hey if the

odds went that way, whose to say I want be one of the small percent that has

bad side effects.

I just try to base my decisions on how I feel, what I can take, and are my

joints being damaged. The damage is starting to happen... which is why I do

have Enbrel sitting in my fridge, waiting for me to get some courage.

Have fun in the snow, and thanks for the great comments you made.

P.S. You won't believe how many Rheums have told me that MTX has no side

effects in the amount I would be taking it in. That's how I gage if I am

going to stick with a Dr. or not.... when someone tells me that, I know they

are just trying to get rid of me so they can get to their next patient.

In a message dated 1/23/03 2:13:56 PM Eastern Standard Time,

CND110370@... writes:

> ,

>

> I so applaud you courage to do this drug free. I only wish that was an

> option to me. You sound to be a very active and full of life. You see to

> always be up beat and the words you use to encourage others is eloquent. I

>

> do hope, for you sake that you can maintain your PA at this point with the

> way you choose to manage your meds. The patient leaflets they give with

> prescriptions are terrifying, but remember to look further...in FACTS, in

> the

> PDR and look to your doctor for percentages that the side effects occur.

> Because if some terrible side effect occurs in one-tenth of one percent of

> patients they have to publish that information and many times what the

> consumer gets is just the type of side effect that occurred and not how

> often

> it was seen in patients. Keep up the smiles that you pass on to us here in

>

> the group. I hope some of this information is useful to you!

>

>

>

> PS - Hope you are staying warm today! We got 10 inches (maybe 12) of that

> cold white stuff and it is hanging around 10 degrees outside right now! " )

>

>

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Viox seems to work for me only if I take 50mg. The recommendation is 50mg

for only several days and then a daily dose of 25mg. Unfortunately that was

not strong enough. I am now taking Lodine and this helps somewhat. Does

anyone have experience with this drug?

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My GP has doubled Zocor to try to get my cholesterol down. My blood

pressure is up. It runs in my family, but I wonder if Vioxx has anything to

do with it. It seems I have heard other members blame Vioxx for HP.

Ks Di

Re: [ ] Vioxx

> ,

>

> How long have you been diagnosed? Bextra did nothing for me, but Celebrex

> does... same kind of med. I have been trying to stay off of things too,

but I

> do have Enbrel waiting in my fridge whenever I get the nerve up to start

the

> injections. I am just SO nervous about going on more severe meds. Will you

> tell me what problems your arthritis has caused you? Do you have any

joints

> starting to deform? I have a finger with a small hump on it, and my left

> ankle is getting a little whaky. I am trying to be smart about taking

meds,

> but I always have said that when I start to see/feel joint changes I would

do

> something. Well, I am there now... and I still can't bring myself to take

> anything more severe! So, there is my delimma. Since we see this drug

issue

> the same way I am asking you what you would do if you started to see joint

> changes? I have had this disease for over 6 years now, but I was diagnosed

in

> 1999. Thanks for any advice.

>

>

>

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I have also seen the paraffin units at some major department stores, Bed,

Bath & Beyond, Linen & Things. Homedics is a brand that makes them. Hope

this helps you in the quest of finding a unit!

" )

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Wal mart or those type stores have them, don't know what type you're looking

for tho

Re: [ ] Vioxx

> where did you get the paraffin unit from. do you know a website that I

can

> check?

> Janet

>

>

>

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Homedics has one that is not expensive. It about $30. I got it at Bed,

Bath and Beyond. I have also seen them at WalMart. It is such a comfort.

I don't think it probably has any long-term benefit--but great for quick

pain relief. I do it before I go to bed.

Ks Di

Re: [ ] Vioxx

> where did you get the paraffin unit from. do you know a website that I

can

> check?

> Janet

>

>

>

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I got my paraffin unit from Isometrics online. Its a Parabath brand, cost

$150, and my rheum wrote " medical necessity " on the script. Even if

insurance hadn't paid, I'd tell you its worth every penny. I keep it on all

the time so the wax is always hot, whenever I need it.

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I love Vioxx, but it destroyed my stomach. I now take protonix daily with

the Vioxx. I had GERD before I started taking Vioxx--so if you have a good

stomach--you might not have so much trouble. I was on 50 mg Vioxx at the

time. I am now down to 25.

Ks Di

-

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