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How effective is Actonel for Arthritis - osteoarthritis (Osteoarthritis)?





Summary: 7 Actonel users have rated its effectiveness for Arthritis - osteoarthritis.

Overall ratings: 3.1/5
Long term ratings: 3.2/5

This is a review of how effective Actonel (risedronate sodium) is for Arthritis - osteoarthritis and for what kind of people. The study is created by eHealthMe and is updated continuously.

You are not alone: join a mobile support group for people who take Actonel for Arthritis - osteoarthritis >>>

What is Actonel

Actonel has active ingredients of risedronate sodium. It is often used in osteoporosis. (latest outcomes from Actonel 17,608 users)

Arthritis - osteoarthritis

Arthritis - osteoarthritis (joint disease caused by cartilage loss in a joint) can be treated by Celebrex, Meloxicam, Mobic, Naproxen, Tramadol, Ibuprofen. (latest reports from Arthritis - Osteoarthritis 33,176 patients)

On Dec, 21, 2014: 7 people are studied for taking Actonel in Arthritis - osteoarthritis




Actonel effectiveness for Arthritis - osteoarthritis


Long term Actonel effectiveness for Arthritis - osteoarthritis

Actonel effectiveness for Arthritis - osteoarthritis (number of people):

not at allsomewhatmoderatehighvery high
Overall01420
Long term
(1+ years)
01320

Age of people who take Actonel for Arthritis - osteoarthritis * :

0-12-910-1920-2930-3940-4950-5960+
Arthritis - osteoarthritis0.00%0.00%0.00%0.00%0.00%0.00%28.57%71.43%

Who find Actonel more effective for Arthritis - osteoarthritis?

Age of people who find Actonel more effective * :

0-12-910-1920-2930-3940-4950-5960+
Arthritis - osteoarthritis0.00%0.00%0.00%0.00%0.00%0.00%50.00%50.00%

* Approximation only. Some reports may have incomplete information.

Find out which drug is more effective in real world to treat:

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Can you answer these questions (Ask a question):

  • Does anyone experience heart palpitations causedby their acid reflux ?
    I have had acid reflux/Gerd for 4 years + Was not believed that symptoms were real for a while as had no heartburn and a diagnosis of Fibromyalgia which even now some medics think is imaginary...it's NOT!!! Following a demeester score of 45 ( very high confirmation of acid reflux) and discovery of a large hiatal hernia, ( a classic physical cause of acid reflux) I had hernia repair operation and LINX anti reflux surgery. Throughout the four years a major symptom of my acid reflux were heart palpatations. They started at the same time I started with reflux and cleared up after the surgery. I have been reflux free palpitation free and antacid free for four months. then I was put on Gabapentin for back spasm and the reflux returned along with the palpitations. Medics keep insisting this is just anxiety yet eat a food that gives me reflux also starts the palps which is the indicator of the reflux as I do not have heartburn. Comes on when relaxing and eating watching tv ( no anxiety present) and when I am sleeping peacefully ( no anxiety present) my heart wakes me up and fires off into tachycardia. Recently a doctor has said it is now known that acid reflux irritates the nerves in the solar plexus area and that triggers the palps. Anyone else experienced this? Are there any studies on it at all? Thanks all.
  • Do you have lower gi pain from taking risedronate sodium?
    I have been taking Fosamax for years and have developed significant lower GI pain. Am wondering if taking Actonel would have less side effect.
  • Can i take ibuprofen with acronel
    I have pain in my pain and tail bone. pain in the tail bone related to a fall,
    pain in my spine related to osteoporosis.
  • Is there a support group in the us for people with insulinomas? (1 answer)
    SUPPORT GROUP IN UNITED STATES!!!

    Hi, the only support group that I've been able to find for people with insulinomas is located in the UK... just wondering if there is one in the US. I had pancreatic surgery to remove my first insulinoma in 2012, we're thinking there's another because I'm still having problems with hypoglycemia... if anyone know anything, PLEASE CONTACT ME!!! :)
    I know there can't just be a support group here for FERRETS!!! people are kind of important... I hate this song, but "Don't worry, BE HAPPY" is okay, I guess... I'm trying to force it upon myself. Things will get BETTER!!!
  • What is the current treatment for larangospasm?
    For two years I have been fighting with larangospasm. I have been hospitalized twice and treated with prednisone as well as nebulizers with albuterol. I had botox injections into my vocal cords last July 2013 and have a straw hanging around my neck for straw breathing. The last "attack" lasted one hour last week and I get approximately two a week now. With the botox injection I could not talk or drink water without it being thickened for six weeks. Is there any other alternative that I can try?

More questions for: Actonel, Arthritis - osteoarthritis

You may be interested at these reviews (Write a review):

  • Had nms in 2005, will trileptal increase chance of recurrence?
    In 2005 I had NMS, which was not detected by my drs for 4 months. I'd been on Lexapro & Seroquel for 2 yrs, but was weaned from Lexapro & placed on Lamictal 3/05. Began getting low-grade fevers, which I was told were not caused by the Lamictal. I quit taking it anyway, fevers (along with uncontrollable shivering) continued & got higher. By 5/05 my temps were reaching 105 deg F. Husband said I became combative, refused to go to hospital. Early June/05 he came home to find me wrapped in blankets, with a temp over 105 F. He tried to place me in a tub of cold water, said I was rigid & screamed when he tried to move me. I was in the tub, speaking "in tongues" (his description, I have no memory of this). He called 911, took me to hospital. I woke, no idea where I was or why. After a lumbar puncture & 2 days in ICU I went home. The fevers continued...2 weeks later he came home to find me wrapped in sheets, towels, blankets, with the heat on full (it was in the 90's outside) he called ambulance again. I awoke to find myself under an ice blanket with nurses pushing large vials of dantrolene into both arms, several liters. Another LP, a stint in ICU...this time they told me it was NMS. The dr who dxd me said he was surprised I was alive, & not a vegetable, as my temp had peaked at 109 deg F. I suffered brain damage; short-term memory loss, brain can't control my body temp, my blood pressure went up. An arteriogram showed completely healthy heart & arteries, no plaque at all. I lost all body fat as well as some muscle mass. The fevers continued even after stopping the Seroquel. I visited my PCP for a checkup in 9/05, temp was normal. I started shuddering, my temp went up a full degree every 5 minutes. PCP admitted me to ER, my heart rate was over 272 B/M; they stopped my heart 3 times to "reset" it, which didn't work. I spent 3 days in hospital. Several months later my P doc tried me on Lamictal alone; I got Stevens-Johnson syndrome. I stopped the drug as soon as the signs appeared. I've been untreated, except for Neurontin & Primidone, until my manic episodes became unlivable. 3 weeks ago I went 8 days with no sleep, became psychotic. My P doc gave me Trileptal, which has evened my moods, but I've been getting low-grade fevers (highest was 103.6). Would having had NMS in the past make me more prone to falling to it again with the Trileptal? It's the only new med I've taken in over a year.
  • Sepsis hallucinations misdiagnosed
    I was admitted to the hospital at 10 p.m., with a total bowel blockage caused by scar-tissue adhesions. I had first gone to the ER at 3 a.m. that morning, but the ER doc misdiagnosed my condition as constipation. I was in extreme pain and also too weak to tell my husband when he first came home that I needed to return to the ER. By the time I returned, I became violently nauseated, and vomited repeatedly. Then a gastro-nasal tube was forced down my nose and into my stomach. I began hallucinating at approximately 5 p.m. the following day. I did not realize I was hallucinating, and thought my experiences were real. Some were quite coherent, such as believing there was a book sitting on table at home with a photo on the front showing a sculpture in white marble of a woman's hands holding the Bible, with barbed wire wrapped around her hands. I thought the sculpture had won the Nobel prize, and the book was the biography of the sculptor, whose mother had gone to extraordinary lengths to keep him safe from the Nazis. Some may actually have occurred during dreams, and were wildly improbable, but I don't recall ever going to sleep. At one point, I thought I was at a rest stop on the NJ turnpike, and saw the Nobel-winning sculptor there, working on a wood sculpture. The sculptor turned out to be the maintenance man on the hospital floor. I pulled out the naso-gastral tube three times, but was unaware that I had done so, although I do remember believing that I was buried beneath peat moss and feeling suffocated as I clawed my way out. I also thought I was at a party being given by a law firm which had sold its building to a school for gifted children, but I (also a lawyer) had been deposited there by my nurse and her boyfriend, who were supposed to have taken me to the OR. Some scenes from a book I had been reading made their way into my delusions, which were so real to me that I actually called some of the people involved later on and asked if the events had really happened. The hallucinations began before surgery and continued afterward. When I awoke from anesthesia, I thought the hospital staff was painting the doors to my upstairs bathroom, a project I'd been involved with before the blockage struck. I asked them how they knew what colors to use. They thought I was joking, and confirmed that they had gotten the colors right. Finally a neurologist was summoned, and I told her I was on the passenger ramp at La Guardia airport (instead of in a hospital in NC), and that I'd been born in Havana, Cuba (instead of Baltimore, MD.) I believed myself to be a member of the ruling party in Cuba (pre-Castro) and during an outdoor ceremony, an earthquake had struck, causing ancient monuments to come tumbling down. Later, I was bobbing in harbor waters near a huge ocean liner, with plastic bottles and other detritus floating by. The foregoing are only a small sample of the multitude of hallucinations. Occasionally, I was only an observer of astonishing events, but usually I was a participant. I recognized my husband and friends, but told them about many of these events, believing they had happened. The neurologist diagnosed clonazepam withdrawal. My other doctors later said this was unlikely, as I took clonazepam in small amounts on an erratic schedule, and was not dependent on the drug, although my prescription called for 3 mg. daily. Physician friends said my symptoms were more likely the result of sepsis. I did contract a urinary-tract infection from the catheter, and was being given antibiotics. Additionally, the nature of my underlying condition, and the delay in diagnosis and treatment, may have contributed to the sepsis. Hallucinations occur in only a very small percentage of sepsis sufferers, and in only a small percentage of those withdrawing suddenly from clonazepam. However, I do fit the profile of those who do experience hallucinations with sepsis, being female and aged 62 at the time of this description. After the three-day period, I returned to normal, although believing that my hallucinations had been real persisted for some days afterward. I recovered quickly from the surgery, although the pain persisted for a while, and I was walking easily (dragging my IV with me) through the hospital halls. This was the ONLY symptom I had. Not all the hallucinations were unpleasant -- in fact, they were highly interesting -- but they were incredibly complex. I still remember all the details, better than I remember what actually happened yesterday. Except for the urinary-tract infection, I had no other adverse effects from hospitalization -- no fever, chills, nausea, sweating, headaches, trembling or anything of that kind. The bowel blockage and the surgery were of course not fun, but in a way the hallucinations were fascinating. My own feeling, and that of the doctors who know me and my medical issues, is that my experiences were caused by sepsis, not clonazepam withdrawal, and the antibiotics I was given are probably what saved me.
  • Non effective for pain effective for positive nausea (1 response)
    Have been taking this product for a little over a month and the nausea is getting worse but the pain is not. This seems to be causing more problems. This side effect occurs with or without food, and with or without a full glass of water.
  • Marijuana effect on oa pain
    I have severe OA ( hips, knees replaced) cervical and lumbar spine require fusing both shoulders need replacing.This is Ortho doc talking not me. I get no relief from non-steroidal anti inflammatory or only short relief from steroid injections. oxicodine does work when pain is intollerable but Fear of addiction keeps me from using. I have found that POT is by far the most effective pain reliever of any pharmaceutical I have taken, by far.A few puffs of high grade pot and no pain for the day!! A wonder drug !! only down side and I've been smoking this on a daily basis for some time is a fondness of tasty cakes !Amazing to me how a country based its pot drug policy on lies from some stoge in the 1930 named anzinger. pot is no more a gate way drug to heroin the a pot roast.
  • Plaquinil use shortness of breath
    Approximately 4 months after starting Plaquenil, I observed I was experiencing SOB while lifting the patient I was caring for, also had severe muscle weakness. I had been out of the country for several weeks and thought I might have picked up something while in The Dominican. I was also losing weight without trying, A positive consequence as far as I was concerned. Generally I expect to see side effects when beginning a drug so it took me 9 more months of being tested for PFT's sleep studies, pulse ox while sleeping, many and various blood testsand cardiac testing. I was so sick of testing especially when all tests came back in normal limits. One day in a point of desperation I looked on line and there it was buried toward the end of side effects of plaquenil and most specifically for women in my age bracket in the 60% range. It can take up to a year for these to develop! I found my answer and immediately stopped the plaquenil, reported my findings to my doctor.

More reviews for: Actonel, Arthritis - osteoarthritis

Comments from related studies:

  • From this study (3 years ago):

  • I took Actonel for about 2 yrs. Blood work was done after 1 yr and again after 2 yrs. Within 1 yr the white blood cell count dropped by 0.8 (significant for me).

    Also, there was a change in the bone marrow and blood clods developed in one leg.

    I am very upset that Dr. recommendet taking it. If I had been informed how bones stay strong naturally, I would never have taken this very bad stuff.

    Stopped using, but now won

    Reply

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