actonel symptoms

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.

fermenting in my stomach, symptoms r.reflux hrs after eating bringing up.food, smelly wind, sore bowels, itchy nd burning bottom. Iv put lots.of weight on and have bone and joint pain 24-7. I feel original symptoms were due to emotional problems and depression not being treated, my doc is not interested in.helping cus of budget cuts, I'm.

But also if you are on osteoporosis medications currently, the medication you are taking could be causing your symptoms. 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.

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.

I have been diagnoised with a small hiatal hernia. My question is sometimes I get the following symptoms that last for days even weeks. I have a pain in the center of my chest that hurts when you touch it or push on it. It seems like it is muscular. It also hurts when I take a deep breath, again it seem like it is muscular. When I turn from side to side I feel the pain like a pulling in the center of my chest/breastbone area. It feels like there is something stuck in my throat.

Medications are ether slow to metabolize or be eliminated. Whatever the cause, I develop toxic, life-threatening symptoms on very small doses. 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.

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 have MVP and after every possible heart and lung test, learned I also have a PFO. My MVP is mild with mild regurgitation. My symptoms are severe. I get out of breath easily but all my pulmonary tests are normal. I have chest pains, dizzyness, out of breath very easily, a pounding heart when I lay down. My latest symptoms are burning sensation on my arms and my arms and legs turn purple and get white dots. I've been to two primaries, three cardiologists and three pulmonary guys.

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?

He actually called not long afterward to tell me I have a small stone and a lesion on my left kidney (probably the only place on me I have no symptoms). He does not think this is causing my abdominal issues but I think he is ordering an MRI and referring me to a urologist, or maybe the urologist will order the MRI. Actually, I've had a burning pain on the right side of my back, over my rib area, but think it is a nerve issue. Now, I'm worried. Should I be?

t believe that at my age , this is a huge problem for me. I am taking Paxil and for the last 10 years I was taking Actonel, until my doctor suggested I stop because of medical reports showing after long use, it stops working. I know the 2 problems are not linked, but still remain a concern. Is there a medication to stop me from my late night binges. This is when I eat the most. It seems there would be an appetite supressant that would be helpful.

) Your doctor will order calcium blood tests before your first injection and during treatment. Tell your doctor right away if you have any symptoms of low calcium such as: muscle spasms/cramps, mental/mood changes (such as irritability or confusion), numbness/tingling (especially around lips/mouth or in fingers/toes), fast/irregular heartbeat, severe dizziness/fainting, seizures...

it seemed to bother my esophagus (bumping, reflux) so my doctor suggested actonel. i took one pill a week ago and since have had increasing sensation of a lump in my throat, and like I'm full of phlegm that I can't ever swallow down. I can eat so of course I am swallowing. I'm off all drug right now but throat/phlegm sensations feel settled in, especailly bad at night, and are anxiety provoking.

Thank you for the response. I think I have had about every GI test done. Who checks hormonal endocrine imbalances. Metabolic issues, etc? I have had 4 thyroid nodule biopsies done now. I do have severe Osteoporosis and a new Internist I am going to has ordered a new bone density test. I have been having bad neck, low back and hip pain. I don't think my Endo doctor has been following up on that like she should but I won't take Actonel or Fosomax.

They are given generally prescribed orally and include Fosamax, Actonel and Boniva. They can cause some severe stomach distress as they did for my father. When this happens there are injectable forms of bisphosphonates. Ibandronate (Boniva injection) is injected into your vein once every three months, and zoledronic acid (Reclast) is injected once a year. If approved by your physician these treatments do not cause stomach distress and you do not have to remember to take a tablet.

Actonel, plus Vitamin D3-ANALOG from Denmark for bone re-mineralization (which is not available in the USA yet, but has been used all over Europe with lab proven success), and Crestor for high cholesterol. I had to come to Panama to be diagnosed with Hashi/hypo because my USA family doctor would not run any test except TSH, even though I repeatedly asked him to do the thyroid panel. He said the TSH was normal so no need to test any more.

She started out with Fosamax, and after awhile when side effects start from that one, and Actonel was available, they put her on Actonel and she was on Actonel all the way up until it was stopped at 79. So, I have that in my mind (her being mom and my genes and all), and decided that I want to put off bone drugs as long as I can. If I can reverse this w/o them, than I'm going to.

2. Nearly all parathyroid patients have symptoms; 95% know it--and feel bad. Most of the rest just don’t know it until the disease is fixed. 3. Symptoms of parathyroid disease do NOT correlate with the level of calcium in the blood. Many patients with only slightly elevated calcium and parathyroid hormone will have BAD symptoms and develop severe osteoporosis. 4. All patients with parathyroid disease have calcium levels and PTH levels that go up and down.

Wow you posted on my birthday and we seem to have a few of the same symptoms. I am in need of relief ASAP. This is the type of pain that wears on your nerves and tends to make one a bit irritable. I am 56 and mine also is mostly at night here's my story. I am a 56 yr young female. Who is a Christian and loves the Lord. Before all this occurred and even after some what enjoyed living, traveling, dancing, gardening, being with friends and family to the fullest.

I had 2 shots of Depo Provera and NOW I have just about every symptom of hypothyroid. I go back in a few days to get my test results. I'm so nervous they will tell me nothing is wrong with me, but I'm not imagining these symptoms. I've been dealing with them for awhile now b/c I blamed all the symptoms on the Depo shot. But I've been off the shot for 3 months and my symptoms are getting worse rather than better, so I don't think it's the shot.

I could not walk I got Morton Neuroma which is the nerves under my feet swelled up from taking actonel. I felt like an old lady and it was painful. So now my oncologist wants me to stay on Toxmaxcin. hope i am clear now.

Actonel symptoms

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