As for myself, I am a patient suffering from severe osteoporosis. My doctor, realizing I cannot afford Forteo ($950 per month!), has suggested I try to find how I can take the equivalent, generic version, which is Bonista.
Please, if anyone can tell me how to get ahold of this medication, any address, emails of sellers, etc! I would be so grateful!
This discussion is related to <a href='/posts/show/1230787'>Bonista-side effects</a>.
I have been on Forteo daily injections for 1 year and I have experienced considerable joint pains which did not exist prior to treatment. My left hip and knee, my right knee and my hands have been getting worse each month. Has anyone else experienced similar reactions?
My doctor told me that I have Osteoporosis and wants me to try Forteo an injection for two years. Has anyone tried this drug and what were your side effects, if any. I don't want to make my stomach problems worse than there already are.
I have severe osteoporosis and am trying to take Forteo. I started out with half dose and have worked up to a full dose. The full dose 2 days in a row was disabling. My doctor suggested every other day. So I let the previous trial work its way out of my system for 5 days and tried another full dose. This is three days after the dose and I am weaker each day. I move in slow motion. My doctor is puzzled. Anyone had a similar experience?
Just was informed that I have osteoporosis. My doctor wants me to use Forteo, an injection that you use for two years.
I have found articles to suggest that high-dose bisphosphonate therapy (40 mg/day for 6 months) offers a significant improvement in patients with fibrous dysplasia of the skull. Do you believe that since my fibrous dysplasia has remained static / unchanged in almost 4 years that bisphosphonates would possibly be helpful to a large degree?
Also, what do you know about the risks of taking a high dose of this drug such as Fosamax?
The head and neck surgeon who follows my case has always shunned the idea of surgery, eventually though he realized my quality of life is poor due to my constant headache and he told me that he had an idea, to send me to an endocrinologist to be put on bisphosphonate because there was literature to suggest major improvement in symptoms of people with intractable headache/fibrous dysplasia.
Hi-- When you say Medicare, I assume it is Medicare Part D, administered by an insurance company like Blue Cross, etc? If so, you might be in for sticker shock. I had a similar experience w/ Forteo, via Part D, they wanted $5K for 3 months. I went directly to Lilly, and qualified for pro bono meds for 2 years, the limit of tx on Forteo. My understanding is patients with cirrhosis get priority. Other Gilead experienced persons, and there are a few here, can tell you more.
Hi - This isn't a diabetes question, but I still hope maybe you can answer my question. I have monostotic fibrous dysplasia of the skull with intractible headache (a benign bone tumor). I've known about this for 3 years but have had very poor treatment results with the therapy. Seems like a neurological question, right?
Medications themselves can be classified as antiresorptive or bone anabolic agents. Teriparatide (Forteo) is also approved for the treatment of postmenopausal women who have severe osteoporosis and are considered at high risk for fractures. The medicine is given through daily shots underneath the skin and you can give these shots even at home. Another advantage is that it can be given in patients who cannot tolerate oral biphosphonate drugs.
Thanks for your feedback. My case has baffled most doctors. I drink alot of water, eat a healthy diet and don't smoke or drink. The only meds I take are for my bones (Forteo) as I found out that I had extreme osteoporosis in Nov. 2008. I have had my circualtion checked several times and it is reduced in my "weaker" foot. There is no blockages and I have no rare diseases....
My problem is only becoming worse and noone knows why....
Painkillers (NSAID tablets, morphine, patches) are of course one logical intervention. Bisphosphonate (example zoledronic acid) injections every month may help with the pain, and also reduce the chances of fractures etc. Radiation therapy to the affected bone too is an effective way of managing pain. In women with ER or PR positive cancers, hormones are beneficial in bone mets. Next-line chemotherapy too may be an option. Please discuss all options with your oncologist.
The probable treatment plan involves hormone therapy with Femora (Letrozole) pills to suppress growth of estrogen receptor (ER) positive cancer cells, a monthly infusion of Zometa (a bisphosphonate) to delay bone complications and participation in a National Cancer Institute trial of Avastin (bevacizumab), a drug that might halt progression by blocking blood flow to the tumors.
I am in the process of many test now and the only abnormalty found so far is an elevated level of calcium in my blood, a result of Forteo injections. My blood pressure is perfect! Can you give me any idea what is happening to me and if there is anything I can do to help myself this mystery is solved?
He scheduled a CT for confirmation. The CT confirmed the non-union. He wrote a prescription for Forteo, and the use of a bone growth stimulator, stating that if, after an additional 8 weeks there is still no sign of bone fusion, he would do a bone graft and replace the hardware.
I feel as though he is not listening to my complaints of pain, edema and the inability to sleep secondary to the pain and discomfort.
I do not/have not ever taken estrogen replacement. I did have Aredia/Forteo injections for the treatment of the osteoporosis. The lump/mass is my breast was found to be "prominent glandular" tissue....no sign of mass/calcification...the "lump" under my arm and in my right groin come and go. My ribs under my arm (upper part) of my ribcage is very tender.
s, but this has exponentially been exacerbated by Arimidex. For the past 2 yrs I have been taking a weekly bisphosphonate (Alendronate), plus twice daily Calcichew/Vit.D to help prevent further bone loss.
Tamoxifen is prescribed for pre-menopausal patients, the AI's for post-menopausal. As I had a full hysterectomy some 19 yrs ago, I could go straight on to Arimidex.
In fact, everything was normal except for his neurological problems. So they sent him home and told him to try Forteo. Well, Forteo has a side effect which is increased risk of bone cancer, so he stopped it. And I put him on Strontium, which is a supplement that builds bone density.
Strontium is used in Europe and a pharmaceutical company has a patent on Strontium Ranelate, which is Strontium with an artificial substance linked to it.
I do hope some Neurology experts are able to throw more light on this, particularly what you should expect in future from the bisphosphonate treatment and about palinopsia.
For almost 2 years, I have been, and continue to be, treated for Fibro, Osteoarthritis, Senile Osteoporosis (daily injection of Forteo), high blood pressure and low/none vitamin D, and periods of low white cells. Was checked for the usual, RA, Lupus etc. Nothing showed up. Previous health-worked fulltime around 50 hours a week or more, constantly going and doing, did many family dinners, active runner, won divisional 5k first place and masters and weight trained. BMI is around 20.
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