Review: could Topamax cause Bone and joint pain (Joint pain)?
Summary: Bone and joint pain is found among people who take Topamax, especially for people who are female, 40-49 old, have been taking the drug for < 1 month, also take medication Celexa, and have Migraine.
We study 22,567 people who have side effects while taking Topamax from FDA and social media. Among them, 513 have Bone and joint pain. Find out below who they are, when they have Bone and joint pain and more.
You are not alone: join a mobile support group for people who take Topamax and have Bone and joint pain >>>
Topamax has active ingredients of topiramate. It is often used in migraine. (latest outcomes from 24,599 Topamax users)
Bone and joint pain
Bone and joint pain has been reported by people with rheumatoid arthritis, osteoporosis, high blood cholesterol, high blood pressure, multiple sclerosis. (latest reports from 118,740 Bone and joint pain patients)
On Jan, 24, 2015: 22,567 people reported to have side effects when taking Topamax. Among them, 513 people (2.27%) have Bone And Joint Pain.
Time on Topamax when people have Bone and joint pain * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Bone and joint pain||28.81%||22.03%||8.47%||8.47%||23.73%||5.08%||3.39% |
Gender of people who have Bone and joint pain when taking Topamax * :
|Bone and joint pain||87.84%||12.16% |
Age of people who have Bone and joint pain when taking Topamax * :
|Bone and joint pain||0.00%||0.20%||0.59%||6.68%||21.61%||35.95%||20.24%||14.73% |
Severity of Bone and joint pain when taking Topamax ** :
|least||moderate||severe||most severe |
|Bone and joint pain||0.00%||37.50%||50.00%||12.50% |
How people recovered from Bone and joint pain ** :
|while on the drug||after off the drug||not yet |
|Bone and joint pain||12.50%||0.00%||87.50% |
Top conditions involved for these people * :
- Migraine (147 people, 28.65%)
- Pain (98 people, 19.10%)
- Convulsion (68 people, 13.26%)
- Depression (63 people, 12.28%)
- Migraine prophylaxis (60 people, 11.70%)
Top co-used drugs for these people * :
- Celexa (72 people, 14.04%)
- Nexium (71 people, 13.84%)
- Aspirin (70 people, 13.65%)
- Seroquel (62 people, 12.09%)
- Ambien (57 people, 11.11%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
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Do you have Bone And Joint Pain while taking Topamax?
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- support group for people who have Bone And Joint Pain
Drugs in real world that are associated with:
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Can you answer these questions (Ask a question):
- What is the possible explanation for arthralgia upon xolair medication for asthma? (1 answer)
Female, 20 years old with severe asthma is being medicated with Xolair (Omalizumab) over the last six months. Although the patient is getting better she is suffering of severe arthralgia mainly in arms and legs. What is the possible explanation for arthralgia upon Xolair medication for asthma?
- Can nuvigil (vs adderall) be used simultaneously to help wean off 60mg/day of adderall? (1 answer)
I have been on Adderall 30mg 2x daily for years!! I've had it lowered to 20mg, I've TRIED to go months without it (when not working) however I feel I've built up a tolerance level to the point that it's not as effective as it once was. My personal life has detoured WAY past anything an ADHD medication can possibly help as far as focusing on NEEDED tasks etc. I end up feeling wrapped up in what I'm doing at the moment that my anxiety increases due to all that I haven't been able to accomplish. I take various medications for various reasons, depression, anxiety, bulimia etc., and for the most part the doses have varied based on circumstances and current need at said time of prescription.. MY FAMILY HAS A HISTORY OF HEART DISEASE, And realizing that I'm already on the highest Adderall dosage scares me (and THEN as I think about it, it makes my heart race!). I've also noticed increased muscle spasms as well as extreme and intense pressure on my jaw (TMJ). MY QUESTION IS: does anyone have any experience LOWERING their Adderall dosage AND adding Nuvigil? The research I've done to date gives me impression that it could help balance out the more extreme effects of Adderall (60mg/day) but that the nuvigil would or could potentially help with the EXTREME exhaustion I feel as Adderall wears off. Some days I just crash, some days I sleep fine and others no matter how hard I tryyyy, I just CAN'T fall asleep, therefore making the next day worse! IDEALLY I'D LIKE TO BE MED FREE, right now I need them, but am hoping maybe I can speak with my doctor to lower Adderall and add Nuvigil to help wean me off the amphetamines as well as lower dosage intake. YES, a lot of the anxiety, sleeplessness and depression are related to current circumstances in my life, however, where I am is not where I want to be or where I'm headed.. Life is a journey, and all my meds have become a part of a journey I never thought I'd find myself taking. I don't want life/meds to define me, or create a me I no longer recognize, because scarily enough that seems to be a common pattern. As I overcome each and every daily obstacle, I also don't want to be "hooked" on my meds or needing "more" to wake up/sleep/function.. I'd like to work on finding a solution towards weaning off my meds NOW, and work my way off slowly, primarily the Adderall. I'm hoping by suggesting to my doctor and showing him my research he may agree (IF ITS EVEN A LOGICAL COMBO, CLEARLY IM NOT A DOCTOR) nuvigil could help me. I've already started taking less of my anti depressants, trazadone and xanax without discussing with doc because he is always busy.. My next appt I want to go in fully prepared with a plan and an overall goal to REDUCE my Adderall dose, but overall, I'm clueless!!! I have no idea what other meds other than nuvigil "could" potentially help if at all. I could be entirely wrong, Anyone with any experience using one vs other or both simultaneously, or anyone with constructive input, PLEASE COMMENT/SHARE!!
- Can mrsa cause chronic intestinal pseudo obstruction?
I had a small bowel obstruction caused by adhesions from an appendectomy carried out 20yrs previously and had grumbling pain ever since but been labelled a malingerer by my family GP until one day at work when I started with terrible tummy ache and sickness like I'd never known, fetching up bile with force. I hated going to hospital after yrs of being called a moaner but after a day of rolling round in pain, temperature of 103 an dehydration, my Mammy insisted we go and I was seen straight away - to my shock I was in theatre within 3hrs with a serious obstruction.
I never really recovered... The obstruction returned after 2 days and a portion of necrotic bowel was removed, then further fever and cellulitis then MRSA and deaths door.... Isolation in high dependency (intensive care) wound break down, ventilated and all related issues that come with that - chest infection, pneumonia, bed sores. Total time in hospital 8 months. Negative pressure dressing on laparotomy wound, colostomy, picc, 4 rounds of vancomycin, minor flirt with heart failure (just water related) an eventually everything healed. Had a large incisional hernia to repair and some corrective work to the horrific scarring but then the neuropathy started plus problems eating, spewing up after any solid food, more than a few forks, diarrhoea and sickness or constipation nausea and pain driving me mad, tried all manner of drugs, nerve blocks, physio, floating tank, acupuncture, opiates, non opiates, spinal cord stimulation, an now a consultant just had a 'eureka' moment and said were you treated with vancomycin when you had MRSA? If so I'm pretty sure you have chronic intestinal pseudo obstruction and is 90% sure but wants to take a muscle biopsy to be certain. I've had so much surgery and bad news in the last 10yrs I'm terrified of germs, hospital acquired bugs and anaesthetics, is there any other way? Or can I have this test done awake - conscious sedation? I had it before during spinal cord surgery so I know what's involved and it's better than GA as I know what's going on, who is doing what to me etc...
Does anyone with a medical background know about this ailment/disease? Does it sound feasible that MRSA or it's treatment could have caused this? I was surgically debrided up to every other day when the vac pac/negative pressure machine and dressings were changed and the doctors told me I lost a great deal of tissue and had a lot of nerve damage due to the infection.
Any patient perspectives on this illness would also be very much valued in helping me make a decision, moving forward. If all this is going to accomplish is to attach a label to the pain but not actually change anything, after fighting it for 10yrs now, avoiding hospital as much as I can, I really can't see the point of exploratory surgerys and biopsys now when it is known that I have this propensity towards adhesions and a new wound means a potentially new adhesion growth site.
If it helps, the appendectomy happened when I was 10yrs old, the MRSA when I was 30 and I am now 40.
- Does topamax effect sexual desire and cause weight gain (1 answer)
I have taken topamax for 10 years and have been gaining weight steadily every year. My doctor says the medication is not the reason because Topamax causes people to loose weight. I have also voiced my concerns to him that since I started taking this medication I have no desire for sex. He says this medication would not affect this. Please help so I can get him to change my medication.
- Omeprazole or pantoprazole?
I take an oral contraceptive, Diane-35 ED, which is not in the list of drugs to choose from on this site.
Recently, the medication I was taking for my stomach ulcer (Omeprazole) became unavailable in my country of residence and was replaced by Patoprazole. I started taking it yesterday morning and by midday today the side effects were unbearable. I am nauseous, have diarrhea, and a very severe headache. This didn't happen with Omeprazole. Do you think this is a drug interaction or is there some difference between the two that I am perhaps sensitive to?
More questions for: Topamax, Bone and joint pain
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Comments from related studies:
From this study (2 weeks ago):
diagnosed with sero-negative spondylarthropathy and ankylosing spondylitis
From this study (11 months ago):
I am on Remicade once a month since July 22nd of 2013. Had a great response until I hurt my low back again. Then the back pain just worked it's way right up my spine to the neck. I have had neck fusion one level...several bad discs. A knee replacement, a shoulder reconstruction etc. The numbness and tingling in my left hand and buzzing in my left ear are driving me nuts. A recent hearing exam showed I had nerve problems there as well. Don't know what to think. Had a brain MRI it showed normal. Now thinking a spinal tap in order?
From this study (1 year ago):
Have constant pain in knees, feet, toes, hands, arms, neck and back. Cannot sleep because I wake up constantly with shooting pain in neck, feet, knees, including tingles and numbness. Left side is worse; includes some drooling and paralysis at times. History of colitis and recent IPIN neiplasms found in pancreas head, neck and tail with dilated bile ducts as well as dilated pancreatic ducts and swelling of gallbladder. Constant nausea, off/on vomiting, major pain in neck and back, as well as abdomen which has included constant pain in upper right and left rib cage area. Knee pain has increased dramatically, especially while sleeping (??). Migraine history severe; hospitalized many times and is constant. Hx of anemias, malnutrition, malabsorption, fecal incontinence, low mono#, low eosinophil, high Granulocyte and Gran %, low Vit C, Low Vit B6, Low Lymphycites, High Baso%, High Baso#, Low WBC, Low Transferrin, High Cardio CRP, Positive ANA, High GGT, abnormal fecal fat, hypoalbuminemia, low calcium (always), low anion gap, low protein...many labs always abnormal, could go on...always fatigued and in pain.
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