actonel pi

I am 3 years post breast cancer i had lumpectomy chemo rads i have taken tamoxofen for 2,5 years now on aromasil i had a bone density scan and was told i had low calcuim levels, now on calcuim sandox and actonel asked if i had osetoprosis and was told no have read around actonel and have not taken it yet as of the side effects please can you advice thanks.

I take once monthly Actonel. While I was pushing the pill through the foil blister, it broke. I did not take that pill for fear that it could cause stomach problems. My question is would it have been safe to take? Also, if I contact Proctor & Gamble, do you think they might replace the pill. If it was a daily pill, I wouldn't worry about, but I just lost a whole month of medicine due to a faulty package design.

i currnetly am taking actonel for my bones the past 3 years and klonopin i per night and take alot of vitamins such as B compex etc. no alcohol consumption but i do smoke half a pack of cigarettes per day no other medical conditions known 6 months ago all my blood workups were normal . ANY IDEAS WHAT CAN BE GOING ON WITH ME ?

Right hip replacement. I'm on requip, lyrica, cymbalta,celebrex, just starting actonel plus vitamins & calcium. thank you. I'm 76, female. I have osteoporosis of the right hip and osteopenia of the left hip. I have peripheral neuropathy (familial), and two bad knees.

I am just tired of taking medicenes that seem to cause other problems. I think I have the GERD from taking Actonel even though I followed the instructions to the letter for taking the Actonel. No longer take it. Just take calcium.

Non-hormonal biphosphonates (such as Fosamax and Actonel) increase bone strength and are available as once-a-week pills. These can also be taken. It is very difficult to precisely confirm a diagnosis without examination and investigations and the answer is based on the medical information provided. For exact diagnosis, you are requested to consult your doctor. I sincerely hope that helps. Take care and please do keep me posted on how you are doing.

If a person is treating with the PI drugs and fails to get SVR.does it mean that you cant use the PI`s ever again.this is what im gathering from what ive been reading ...looks like its do or you know what....man...sometimes i wonder how i deal with all thie stuff.

Maybe one day they will use the PI as maintenance for the ones who dont respond to SOC and PI drugs.Ive heard of aids people liiving a lot longer now because of the PI`s too.Some are with aids for 25 years and still doing ok. "An apple a day keeps the doctor away, But if the doctor is cute forget the fruit.

You might want to ask your pharmacist for more specific directions as far as the timing of your meds. I take Actonel once a month and my pharmacist said it was fine to take it at the same time as my levothyroxine since Actonel is also supposed to be taking first thing in the morning. Don't mix meds unless you get an all clear from a pharmacist.

I have taken fosamax and actonel and have had stomach problems and aching bones. My doctor is thinking about the yearly injection of reclast. How safe is it and will I have more problems with my bones aching - I can't sleep at night a lot from the pain. This discussion is related to <a href='/posts/show/868004'>Atrial Fibulation / Multi-Infarct Dimentia</a>.

I knew it would work! They want me to extend out to 52 weeks, though. I already decided to take myself off the study after the 12 weeks of the study drugs. My job is on the line, I start Grad school in the fall, and I've had just about every side effect there is from the SOC drugs. It would have been nice to get the PI in the beginning, but it didn't happen. I was still detectable at week 16 on those 2, and they are the ones causing me to be so sick! OK, done with my rant.

He was told to do laser PI to prevent the glucoma first. Just wonder if the laser PI is needed and is it will worsen the catarct situation since he plans to have the cataract removed at least 6-9 months later.

I was thinking about this recently. If somebody try's a PI, and fails / builds resistance to that PI, then re-infects somebody else in the general population with Hep C - won't the disease gain resistance to that PI? The new mutation could spread, and become the standard for Hep C (given the new resistance, will make it live longer). Are PI's a short term fix, that the virus will eventaully become resistant to?

Good article on PI drug treatment regimens by IAmTheWalrus http://www.medhelp.

He wants me to see a rheumatologist but an available appointment will be months away. I am 75 and have been on Vytorin for at least 5 years as well as Actonel. My bone scan last year was good for someone my age. What should I do while waiting to see an arthritis doctor? How serious could this be?

Osteoporosis medications like Raloxifene (Evista), alendronate (Fosomax), risendronate (Actonel) and ibandronate (Boniva) all can cause flu like symptoms in individuals that are taking them. I am not sure what medications you are on, but this could be your problem.

If your talking about the third drug being the PI as info they have not been approved for genotype 2, 3 and 4. If you are genotype 1 some insurance companies will initially deny the PI because it is so costly. Your doctor will have to start an appeal process with the insurance company which may take a little time but usually in the end the PI is approved.

I vote for boceprevir since it has a 4 week lead-in before starting the PI. If you clear in the first 4 weeks of TX, you are responsive to interferon and do not need to add a PI with all its extra side effects and risks.

It has been trending downwards, but appears to be slowing down. I am actually hopeful for the PI. This one is a second generation from Teleprevir and Boceprevir, so I think the hope is it is even better than the other 2. I am hoping to see UND at my next visit on the 16th. The good news is I think I will either have good news meanwhile or go off at 28 weeks at most total. I am actually pretty hopeful for the PI to do it's magic.

Well, to state the obvious, you'd have to have a date for the PI availability in order to time it right. But I wouldn't like to have a tx plan with a date in it that I couldn't trust. However, in general I've wondered too how it would work out to do the PI in the last 4 weeks of tx when the virus is either already dead or on it's last legs, just to make sure and finish it off. That might work well for some potential relapsers.

Vertex knows this and is working on the second generation of PI. I love this link about all the meds in the pipeline and their status. http://www.hcvdrugs.

t give her the RIBA in addition to the IFN and PI. IDIOTS of all of the people to do that too! She almost got to UND for like the first time with it but......without the riba it did not work. Now she cannot take another PI. Trying to say make SURE you are getting all 3 or seriously reconsider...lI'm pretty sure that was what she took I'll see if I can flag her in an email and see if she can post!

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