Alendronate therapy
Common Questions and Answers about Alendronate therapy
boniva
I have had a continuous intractable headache behind my forehead which has not responded to the usual headache therapy regimen. It is believed to be monostotic fibrous dysplasia of the skull. 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.
I took my first dose of Alendronate and then experience significant muscle pain for the next 4 days. Does anyone know if I should expect this to happen each time I take it or is it something to happen for the first few times until my body adjusts to the medicine?
Do you mean Fosamax (alendronate)? If you do, its for treating bone problems like Osteoperosis by adding bone mass and slows bone loss. I use it for Osteopenia.
The prescription drug Fosamax (the generic is alendronate sodium) is a medication which has been prescribed to hundreds of thousands of postmenopausal women to treat osteoporosis and help increase bone mass thereby reducing the chance of spinal or non-spinal fractures. Fosamax has also been prescribed to increase bone mass in men with osteoporosis. Brand name Fosamax is manufactured in the United States by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
I am also taking Aromasin for bc. Stopped alendronate (I am osteopenic due to 30 yrs of prednisolone and Arimidex) in case this caused the oesophagitis. Would appreciate your advice.
thankyou,i am with contact of my doctor ,he said there is no solution for damaged vertibras,but calcium and vitiman d and alendronate sodium/cholecaiciferol tablets will help spine and bones from further damages but what to do with prednisones i cant stop them because of asthma and taking of them will damage other bones isnt there any other solution instead of prednisones, i know there is nothing accept these because my doctor told me:(
The authors examined the effects of high-dose oral alendronate (40 mg daily) for 6 months on 3 adult patients with intractable headache due to fibrous dysplasia of the skull. Each patient had disease processes not amenable to surgery. The patients underwent clinical follow-up at 1, 3, and 6 months. Their pain levels were documented at each visit by using a visual analog scale. All 3 patients demonstrated a significant decrease in pain levels and became independent of scheduled analgesics.
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.
s heart, already a bit iffy due to something missed in that first hospital episode, may have been damaged by too-fast, unmonitored thyroid replacement therapy, and finally challenged too much by that immense dental work--all in the space of four months.
This does not sound like good medical practice, to say the least.
Also, would it perhaps be possible to add some alendronate, or something else to help her bone density and still be able to benefit from the thyroid medication? Thank you so much!
t working together properly, either. So in addition to the vestibular therapy, I had therapy for Convergence Insufficiency. When an object was within a certain distance from my face, my eyes wouldn't work together to keep the object in focus.
There are other issues related to convergence where the eyes don't work well together.
Good luck to you. That's great that you'll have an eye exam with someone experienced with head injuries. Let us know what you learn...
went to therapy - alot came out about mymom death when I was young. I just wasn't sure about how much I have repressed. MY WHOLE LIFE IS REPRESSED. I journaled this morning and it came to mind with a major cry fit..that as a child, I did everything I could-for 5 long years up to the age of 14 to make it all ok. But then she died. It just hit me this late in life that I couldn't fix that or protect it in anyway. Has anyone ever been in this type of a position?
How is it that therapy is suppose to help you deal with why you used when all therapy does is make me want to use? I have been able to numb all my emotional feelings through opiates, even though my pills were used and prescribed for all my surgeries, it was my outlet, as sick as this sounds, hearing the words another surgery was like a free pass to opiates. Then of course it lead to my opiate abuse.
I want to get back into therapy and NOT be on medication again. Just wondering if a Psychologist or Psychiatrist would be better.
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.
Alendronate one tablet once a week for my Osteoporosis, Calcium 600 + D3 too. then I have Telfast 800 mg for my Allergie Rhinitis, Metformin 2 x a day 'cause I'm DM type 2, Simvastatin 10 mg - for cholesterol and Vit. E 400 IU. I took five years of Tamoxifen then changed to Femara because I have had Lumpectomy in September, 2003. Praise the Lord I am cancer free now. BTW I have also Rectozorin for my Hemorrhoid. It bleeds because I'm always constipated.
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