Review: could Topamax cause Tendonitis?
Summary: Tendonitis is found among people who take Topamax, especially for people who are female, 30-39 old, have been taking the drug for 2 - 5 years, also take medication Albuterol, and have Hypersensitivity.
We study 22,595 people who have side effects while taking Topamax from FDA and social media. Among them, 38 have Tendonitis. Find out below who they are, when they have Tendonitis and more.
You are not alone: join a mobile support group for people who take Topamax and have Tendonitis >>>
Topamax has active ingredients of topiramate. It is often used in migraine. (latest outcomes from 24,610 Topamax users)
Tendonitis (a condition that causes pain and swelling of tendons) has been reported by people with osteoporosis, sinusitis, high blood cholesterol, osteopenia, urinary tract infection. (latest reports from 9,549 Tendonitis patients)
On Feb, 4, 2015: 22,580 people reported to have side effects when taking Topamax. Among them, 38 people (0.17%) have Tendonitis.
Time on Topamax when people have Tendonitis * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Gender of people who have Tendonitis when taking Topamax * :
Age of people who have Tendonitis when taking Topamax * :
Severity of Tendonitis when taking Topamax ** :
How people recovered from Tendonitis ** :
Top conditions involved for these people * :
- Hypersensitivity (9 people, 23.68%)
- Arthritis (9 people, 23.68%)
- Blood cholesterol increased (8 people, 21.05%)
- Fibromyalgia (8 people, 21.05%)
- Cardiac disorder (8 people, 21.05%)
Top co-used drugs for these people * :
- Albuterol (10 people, 26.32%)
- Nexium (10 people, 26.32%)
- Clarinex (9 people, 23.68%)
- Climara (9 people, 23.68%)
- Aspirin (9 people, 23.68%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
Get connected: join our support group of topamax and tendonitis on
Do you have Tendonitis while taking Topamax?
You are not alone! Join a mobile support group:
- support group for people who take Topamax and have Tendonitis
- support group for people who take Topamax
- support group for people who have Tendonitis
Recent conversations of related support groups:
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
- Cannabidiol interact topiramate
Chronic Migraines, taking Topomax & propanidol with mild success. Are there any major interactions with cannabidiol (CBD)and the drugs I'm taking?
- Can daliresp cause sever lower back pain and light perioud bleeding?
I started Daliresp tab.and i began having a really bad rash in my private parts .. by the 3rd day i started having awful pain in my lower back with some light blood in my urin, now i have this severe pain and its as if i have a light perioud. i had a comple hysterectomy in 2003,due to overian cancer. i will call my pulmonaligist who put me on this medication on monday the 26th . but i am concern thats why i am asking ...
- Is it possible to suddenly form ulcers after 20 years of tegretol usage
have been using tegretol and Topamax for over 20 years and only now starting to get severe mouth ulcers
- 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.
More questions for: Topamax, Tendonitis
You may be interested at these reviews (Write a review):
- Toperimate has ruined my life!
On Dec 2, 2015 I started taking Toperimate for severe back pain. Within 48 -36 hours I became very sick - throwing up, nausea, blood in my feces, putrid taste in mouth, blurry eyes, difficulty sleeping, confusion and severe fatigue. I felt like I was poisoning myself! After 7 days I felt no improvement to my back pain and was in pretty bad shape. So I made the decision to go off of it after day 7's dose. On day 9, I woke up with severe VERTIGO. I thought I was dying, it was so bad! Was it a brain tumor (I wondered at the time, horrified!)? I didn't know. I believe (actually I KNOW) it was a side effect of the Toperimate, which can cause vertigo. I also immediately began to feel drunk all the time, even when I wasn't "spinning". I had vertigo and the drunk feeling for 1week and then I went to Urgent Care. The doctor was useless and only gave me Valium. No answers, no improvement. I waited 3 more weeks, desperate, and again went to second UC doctor. This one was competent. He diagnosed me with BVVP ( Benign Paroxysmal Positional Vertigo - which us caused by dislodged calcium crystals in my inner ear.) and set me up to have the Epley Manuever through Vestibular Rehab Physical Therapy. My vertigo was (temporarily) corrected after the first PT visit. Although I was thrilled, I was STILL feeling drunk. I've had both an MRI and MRA to rule out brain rumors, etc. everything, thank God, came out clean. Yes! But I still felt drunk 24/7. 3 weeks after The Physical Therapist corrected my vertigo. It fully came back. I was devastated! But I was able to correct it myself by doing the Epley Maneuver by myself at home. I watched a Youtube Video for instructions. I need to mention that I believe I caused the vertigo to return the second time because the night before it returned, my husband used a vibrating massager on the back of my head/upper neck area because I had pain there. I learned from my PT that the vibrations could have again dislodged the calcium crystals in my inner ear. Strange, right? She said often the PTs use vibration to force the crystals back where they're supposed to be. Apparent, the opposite is true too. Well, today is February 2, 2015. I haven't had a recurrence of my vertigo but I STILL FEEL DRUNK 24/7!!!! Thanks Toperimate and it's makers, and the doctor that gave it to me. It was supposedly a "conservative approach" to my back pain, but the question is......will I ever feel normal again? If I do heal from this, I will try to remember to update this webpage again. Good luck to anyone who experiences this problem.
- Urea urine increased while taking topamax
I was on Topamax to lose weight. It worked for me, I lost weight but my blood urea increased. I have to stop taking it.
- Massive aggression within first 4 days at 50mg (1 response)
am only taking 50mg and have only been taking it for 4 days(this is the evening of the 4th day)as a preventative for migraine headaches that I have suffered from from 16 years. I have had pins and needles in my hands and feet as well as spontaneous crying fits since day 2 and Major aggression since yesterday. With normally an insurmountable amount of patience with my 1 year old son, I outright yelled at him last night. This is unacceptable. I have never felt such quick and sudden rage over nothing before, well, over anything before.
- Ceftriaxone reynolds syndrome & tenditis
Ceftriaxone intravenous, after a week hypokalemia hospital visit waited a week went back to the CDC physician he said that drug had nothing to do with it. I am allergic to 99% of antibiotics I can only take a z-pack for two weeks and then run into allergic reactions. We started back on the Cefriaxone as soon as it entered my system heart pain burning sensation every nerve had to be iced. Also the Reynolds was so bad my hands turned white the blue numb. Now pain in wrist and upper arm. The cdc physician knew I was allergic why!
- Seizure disorder med problems (1 response)
Velafaxine 150 mg. 1 per day.
In process of switching from Topiramate 50 mg. 1 pill in morning & one at night (going off of this because of kidney stones) Was on this medication approximately 10 years.
Lamotrigine 2 25mg pills in morning and 2 - 25 mg. pills at night.
On the 3rd day of the 2nd week of switching I started the nightmares. I took a one hour nap and had a nightmare that seemed like it went on the entire time. Even if I slept for 20 minutes I had a dream or nightmare. I've sometimes been known to have vivid dreams but never this constant in my entire life. Also, very seldom do I have such terrible dreams. So many in one evening. They are an occasional thing, not an all night long thing.
Also, I have sinus trouble occasionally. The same day the nightmares began I got a terrible headache behind my one eye and under my eye. I have no drainage yet anyway. Not sure if this is during the start up of this medicine, but if I had known it could cause trouble with sinus I would never have started it.
I was put on this as a quick back up plan when the medicine we agreed upon - Levetireacetam made me feel drunk feeling and I had to be careful just walking around my homes and steps.
More reviews for: Topamax, Tendonitis
Comments from related studies:
From this study (2 days ago):
This has been going on for years. Also had neck surgery in 2011 now my hands will go numb from time to time. also my feet and legs go numb also. Was diagnosed with DDD and also my knees with CMP. Do have that sensation of dizziness or like being "drunk" but I don't drink.
From this study (6 days ago):
thin, fragile, wrinkled, spotted skin compared to clear, smoothe, firm, unblemished skin before taking these meds.
From this study (1 week ago):
I am currently experiencing constant muscle contractions in my abdomen and jerking movements in my neck and midsection. My neck will pull back by itself... Or while I'm standing I'll involuntarily bend over. I'm also having balance issues. I feel very unstable walking and am experiencing some tremors.
Post a new comment OR Read more comments
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.
DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.
You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.