enablex and headaches

I have been on Ditropan, then Ditropan XR (or EX, don't remember which is correct) and after about 10 years that didn't work, so my doctor put me on Enablex and that works pretty well. Then I got a new Dr. and he wanted to switch me to Vesicare. That didn't work well, either, and I began having episodes of incontinence and urgency again. It's almost open enrollment for Medicare Part D, and the plan that is the most affordable otherwise doesn't cover Enablex at all anymore.

On celexa, tried oxybutinin and myrbetriq. Gave me anxiety. Is enablex a good choice? Side effect of celexa was frequent urination. Eneblex only one that didn't cause anxiety, but side effects are bad. Anybody?

DETROL LA should be taken once daily with liquids and swallowed whole. The dose may be lowered to 2 mg daily based on individual response and tolerability. Refer: http://www.rxlist.com/cgi/generic/tolter_ids.

She put me on antibiotics and gave me enablex and detrol (neither which have worked). I went back in for a recheck and the repeat urinalysis was exactly the same as before. Doctor sent the sample out to a lab to see if it was bacterial related and I was told that I did not have an infection. She set me up with a ultrasound of the right kidney and it came back normal. OKay so now (as in the past) I have had intermittent right flank pain.

I'm not sure how to describe what I'm feeling or even if it's real or imagined from nervousness. My left side only...leg from about knee down, not feet and my left lower arm/hand feels "weird"...mostly at night when I get in bed and lay to watch t.v. I think my left hand feels weird when I'm typing, not fingers. I have no "pain" , numbness, tingling...just a weird, mild feeling. Sometimes a small shakiness.

I have had several episodes of not being able to make it to the bathroom and have also wet the bed several times. My doctor gave me Enablex and the episodes stopped. I stopped taking Enablex and the bedwetting and not making it to the bathroom happened again. The doctor started me on Vesicore and again the episodes stopped. Have you ever heard of this happening after TUMT? I had the TUMT so that I could stop taking Flomax.

Well if you were a guy I would say enlarged prostate gland if you had surgery and a lady then I would say you will go and run water and drink plenty of it. If you still cant go you need to go to the emergency room you may have stones blocking there.

I have had good luck with ice packs and/or hot compresses. I have been diagnosed with interstitial cystitus and irritable bowel characterized by chronic constipation. My gastroenterologist believe this symptom is bowel related...I have never discussed it with my urologist, but as suggested by helstrom I will! corndog, a urologist diagnoses and treats interstitial cystitis. IC is chronic inflammation of the bladder lining.

I have had just a couple bouts of dizzyness and vertigo especially upon looking up and reaching up that I have noticed this past week. I have also noticed my headaches that I do get are more like in the back of my head/neck and radiate to my temples if this helps. They tend to feel more like a stiff neck than a headache, they don't feel like other banging, throbbing migraines that I have had in the past.

he has done urodynamics and also looked into my bladder through scope and said that nothing is wrong with my bladder and urthera,he first gave me vesicare for a month than enablex but condition still remains the same ,then i went to another general phyisican he sent me for x-ray of my lower back,results came out negative.my urlogist told me to go to neurolgist...

(about three years ago) I was ok for awhile and, now the severe pain has returned....which meant I had to return to my urologist....He gave me elmiron and vesicare to treat the IC....the Elmiron never helped my pain and, the Vesicare took my blood pressure from 113/72 pulse 68 to 153/103 pulse 122...I contacted my urologist and, he stated...that's not true ... neither of these meds would cause your blood pressure to go up...well, I called him back four days later...

My doctor did a urinalysis and it came back negative. He put me on Enablex which has yet to help at all (2 wks. ago). I am at my wits end trying to find a solution for what is going on. In addition to the urination problem, I also have tingling in the scrotum and trouble with the head of the penis retracting inward in an uncomfortable manner. Prior to the surgery, I was totally healthy and had no urological issues. I would be very appreciative for any help. I am getting desperate!

i have bipolar and is thinking about taking a acai berrry pills is it safe with my conditon i take depakote, effexor & enablex

The uroligist put me on Enablex which has been working, and I am due to go back in two weeks......yesterday, I started feeling almost swelled up at the opening of the bladder.....I am embaressed to ask, is it possible that my bladder is dropping....it just doesn't feel right, and I don't know if I should just wait for the appointment at the uroligist, or call the gynecoligist?

For two months Detrol LA was added without any change in my symptoms either. Now I have been given Enablex 7.5 mg and after a week I am still waking up every 2 hours with the sensation of pressure in my bladder. I am very frustrated and would appreciate any suggestions.

I did a voiding rate test during that time (pee into cup device and measure flow) and it looked ok. The whole time my voiding seemed slower and with less volume in my own opinion. I ended up seeing a 3rd urologist due to a move. He was shocked that I hadn't had more tests. He first did a cyctoscopy (camera into bladder by way of catheter). He said he could see that the pelvic floor seemed tight, but I was free from lesions or other stuff.

I am 47 years old and am scheduled to have a hysterectomy this Wednesday and I am very confused on what to do. I have fibroids in my uterus, I just had a biopsy on my cervix 2 weeks ago due to abnormal cells (it was OK) and I have a complex cyst on my ovary. I have had a crampy pain on that side for 4 months. I am prone to ovarian cysts as they come and go for me though not always complex like the one I currently have.

Just wanting to say hello, give you a cyber hug and wish you peace with your thoughts and wishing you some middle ground where you get the quality of life and structure you are use to, and love, but are not stressing out your body while doing so.

I never had an accident, but I was so worried it was just around the bend I made sure I had a water bottle in the car and a set of underwear and jeans in the car in case it ever happened.

t getting any better. He also has a strong sensitivity to light and is always cowering away from it and covering his eyes. Please guys is there anyone out there who recognizes these symptoms or can offer any advice. I am actually writing this from along side his bed in hospital where they are telling me it's a gastro bug ! (I don't agree).

I have be diagnosed with a high reumatoid factor count but do not have any joint pain at all. I do suffer from dizzyness, headaches, memory loss, and blurred vision. No other results are coming back from my blood test besides the high factor count. Wondering if anyone has had these same issues.

I'm 10 weeks 4 days and for several weeks now I have headaches that come and go everyday as well as backaches (lower and higher). Has anybody else experienced this?

iv had pressure before but this type was and is completely new. I suspect it has something to do with either my spine\ nerves or\and the aorta artery. sometimes like these last couple of days it feels like there is a kink in the aorta right where the neck and skull join. Then there is my allergy to wheat. Again since I was about 12 years old i have had problems with wheat however i did not know then that is what it was.

Hi I'm cue 19 Feb and I get heads his seems like every day and I just started getting heartburn about 2 weeks ago and I can sleep for days if someone would let me.

Enablex and headaches

Common Questions and Answers about Enablex and headaches

enablex