Review: could Ditropan xl cause Vaginal burning sensation?
Summary: Vaginal burning sensation is reported only by a few people who take Ditropan xl.
We study 1,927 people who have side effects while taking Ditropan xl from FDA and social media. Among them, 4 have Vaginal burning sensation. Find out below who they are, when they have Vaginal burning sensation and more.
You are not alone: join a mobile support group for people who take Ditropan xl and have Vaginal burning sensation >>>
Ditropan xl has active ingredients of oxybutynin chloride. It is often used in urge incontinence. (latest outcomes from 1,959 Ditropan xl users)
Vaginal burning sensation
Vaginal burning sensation has been reported by people with vaginal mycosis, vaginosis fungal, vulvovaginal mycotic infection, birth control, fungal infection. (latest reports from 927 Vaginal burning sensation patients)
On Dec, 29, 2014: 1,926 people reported to have side effects when taking Ditropan xl. Among them, 4 people (0.21%) have Vaginal Burning Sensation.
Time on Ditropan xl when people have Vaginal burning sensation * :
Gender of people who have Vaginal burning sensation when taking Ditropan xl * :
|Vaginal burning sensation||100.00%||0.00% |
Age of people who have Vaginal burning sensation when taking Ditropan xl * :
|Vaginal burning sensation||0.00%||0.00%||0.00%||0.00%||0.00%||100.00%||0.00%||0.00% |
Severity of Vaginal burning sensation when taking Ditropan xl ** :
How people recovered from Vaginal burning sensation ** :
Top conditions involved for these people * :
- Pain (2 people, 50.00%)
Top co-used drugs for these people * :
- Adalat (4 people, 100.00%)
- Arthrotec (4 people, 100.00%)
- Crixivan (4 people, 100.00%)
- Combivir (4 people, 100.00%)
- Allegra (4 people, 100.00%)
* 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.
Do you have Vaginal Burning Sensation while taking Ditropan Xl?
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- support group for people who take Ditropan xl and have Vaginal Burning Sensation
- support group for people who take Ditropan xl
- support group for people who have Vaginal Burning Sensation
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Hi ,My name is Pauline Newman I live in Adelaide,South Australia,I have NF1 & NF2,I am 5th generation carrier of the NF Gene,I have literally thousands of lumps,bumps & café au-lait marks all over my body.My question is are NF1 & 2,cause Narcolepsy or EDS, I have also recently had an MRI & ultra sound which has shown up a Plexiform NF, I am in constant pain because of scoliosis,and I am Totally wheelchair reliant, I have 2 Harrington rods alongside my spine & have had a T4-L4 fusion & T12 osteotomy, As a result of my spinal condition I have Rhuematoind Arthritis,fibromyalgia and low vitamin D levels & iron deficiency.Is it possible that these medical conditions are all linked to NF?
20A Shearer Ave Seacombe Gardens.. SA 5047
- Has anyone had issues with vistaril causing ibs flare ups? and does vistaril help ic symptoms?
I have had IBS for almost 20 years and was diagnosed with IC about 12 years ago. I have been on Elavil for about 2 years and it was causing weight gain and I was starting to not sleep well at night past few months even when I take 3 of the Elavil at bedtime. So I asked my doctor if there was something else out there and he recommended Vistaril. I started taking it on Dec. 17th, 2013 along with Cymbalta and I stopped taking the Elavil. I started having weird dreams and waking up with headache everyday and not sleeping well on the 25 mg he put me on, so he said to double and see how that works. It didn't seem to help, so I was determined to figure out which drug was causing weird dreams and headaches and some nausea. I stopped taking the Cymbalta on Jan. 13th and saw no relief, so I stopped taking Vistaril on the 16th. On the 16th I had one of the worst IBS attacks I've had in over 5 years which also threw my IC into a flare up, a really bad one! I eliminated everything but water the 16th-18th and started taking the Vistaril again on the 17th. I DID NOT go back on Cymbalta. I have been in excruciating pain since the 16th, even with use of pain meds, heating pad and TENS Unit. I ate a somewhat normal bland meal last night and was up in middle of the night with another IBS attack which continued the next morning, to the point I almost didn't make it to work again. I have never had an IBS attack last this long. I went to Urologist yesterday and got a treatment for my IC, but still in pain today. I don't think the IC Flare up is going to go away unless the IBS stops. Any suggestions? Anyone have issues with Vistaril?
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- Is it safe to take ditropan while i have been diagnosed with hyperparathoidism. iam waiting to have my operation but i cant sleep at night due to getting in and out of bed to pass urine ever hour
I have been diagnosed with hyperparanoidism.i am awaiting my operation.in the meantime I am not able to get enough sleep at night because I have to keep getting in and out of bed every half hour to empty my bladder.my doctor has prescribed Ditropan for me to take.is this tablet safe for me to take with my condition. thank you.
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You may be interested at these reviews (Write a review):
- Oxybutynin chloride and chest pain
A urologist prescribed Vesicare (and Estrace cream) early in 2013 for urge incontinance. When hospitalized for cellulitis (never had it before) in May (2013), I took lots of I-V Clindamycin. The hospital had Ditropan on their formulary, and the urologist switched to it (it was cheaper)--and I continued taking Oxybutynin throughout the summer (2013).
Before 2013, I had had rare episodes of chest pain (not proven angina) no more than once a year. While on Vesicare and Dipropan, the frequency of chest pain increased to once a month, then once a week, then twice a week, then every other day (by late summer). In July I had a treadmill-EKG (with radioisotope) in USA and my family-practice-physician said it was normal and that my chest pain is NOT heart-related. He took me off Indocin and I have since quit taking Meloxicam and aspirin (no NSAIDs now). I returned to where I live overseas in early August and continued to have chest pain with increasing frequency. In the city where I live, it is too hot in the summer, and too cold in the winter. I saw an American doctor (overseas) in mid-August and my heart rate was irregular (I've never been told THAT before). My blood pressure is usually perfect, but this time my diastolic BP was the lowest it's ever been (about 50). My EKG was said to be normal (except slow rate). My normal pulse is about 60. The doctor said the low diastolic blood pressure was my body's way of helping me "beat the heat," and she suggested I lower the dosage of Oxybutynin from 15 mg daily to 10 mg daily--at least until the summer heat abated. [She was concerned about possible synergistic effect of anti-histamine (Claritin) and anti-cholinergic (Oxybutynin).] Having no return of urologic symptoms (which were severe a few months ago), I have since lowered the dosage of Oxybutynin from 10 mg daily to 5 mg daily.
I am 68 (had total thyroidectomy in 1978, 3 C-sections in the early 1980's, and two total knee replacement surgeries in 1998 and 2007). I had elevated anti-TPO in 2012 and a new dx of auto-immune thyroiditis early in 2013 (but 98% of my thyroid tissue was removed in 1978).
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i was diagnosed with ms five years ago when i went blind. recovered and was in remission for 3 years when all of a sudden my upper abdomen bloated and i developed a rash on my belly. have seen doc. had bladder scans and was catheterized to drain bladder. nothing came out. have done bloodwork and waiting for results. waiting for ultrasound
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