enablex pi

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.

can someone please tell that which medicine works best for OAB ........VESICARE,ENABLEX OR DETROL LA..........I m male and 29 yrs old ,can i also take detrol la.....Any response should be highly appreciated..........

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?

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.

this when I had my post op Appt I never truely got an answer then I went back to her she gave me some Enablex that never truely help with the no sensation to urinate nor the having feeling when having sex can some one tell me what is going on?

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.

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...

If a person is treating with the PI drugs and fails to get SVR.does it mean that you cant use the PI`s ever again.this is what im gathering from what ive been reading ...looks like its do or you know what....man...sometimes i wonder how i deal with all thie stuff.

Maybe one day they will use the PI as maintenance for the ones who dont respond to SOC and PI drugs.Ive heard of aids people liiving a lot longer now because of the PI`s too.Some are with aids for 25 years and still doing ok. "An apple a day keeps the doctor away, But if the doctor is cute forget the fruit.

I knew it would work! They want me to extend out to 52 weeks, though. I already decided to take myself off the study after the 12 weeks of the study drugs. My job is on the line, I start Grad school in the fall, and I've had just about every side effect there is from the SOC drugs. It would have been nice to get the PI in the beginning, but it didn't happen. I was still detectable at week 16 on those 2, and they are the ones causing me to be so sick! OK, done with my rant.

He was told to do laser PI to prevent the glucoma first. Just wonder if the laser PI is needed and is it will worsen the catarct situation since he plans to have the cataract removed at least 6-9 months later.

I was thinking about this recently. If somebody try's a PI, and fails / builds resistance to that PI, then re-infects somebody else in the general population with Hep C - won't the disease gain resistance to that PI? The new mutation could spread, and become the standard for Hep C (given the new resistance, will make it live longer). Are PI's a short term fix, that the virus will eventaully become resistant to?

Elmiron is the only FDA approved drug to treat IC. It rebuilds the mucus layer of the bladder. I also take Enablex for frequency that is pronounced at night! If you think this sounds like you, ask to see a urologist...there are treatments that will make it better...

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!

Good article on PI drug treatment regimens by IAmTheWalrus http://www.medhelp.

If your talking about the third drug being the PI as info they have not been approved for genotype 2, 3 and 4. If you are genotype 1 some insurance companies will initially deny the PI because it is so costly. Your doctor will have to start an appeal process with the insurance company which may take a little time but usually in the end the PI is approved.

I vote for boceprevir since it has a 4 week lead-in before starting the PI. If you clear in the first 4 weeks of TX, you are responsive to interferon and do not need to add a PI with all its extra side effects and risks.

It has been trending downwards, but appears to be slowing down. I am actually hopeful for the PI. This one is a second generation from Teleprevir and Boceprevir, so I think the hope is it is even better than the other 2. I am hoping to see UND at my next visit on the 16th. The good news is I think I will either have good news meanwhile or go off at 28 weeks at most total. I am actually pretty hopeful for the PI to do it's magic.

Acai berry is really no use, if you want an anti-oxidant, go for blueberry just, it's cheap and does the same thing. There is no proven double blind studies showing any use as a therapy.

Well, to state the obvious, you'd have to have a date for the PI availability in order to time it right. But I wouldn't like to have a tx plan with a date in it that I couldn't trust. However, in general I've wondered too how it would work out to do the PI in the last 4 weeks of tx when the virus is either already dead or on it's last legs, just to make sure and finish it off. That might work well for some potential relapsers.

Vertex knows this and is working on the second generation of PI. I love this link about all the meds in the pipeline and their status. http://www.hcvdrugs.

t give her the RIBA in addition to the IFN and PI. IDIOTS of all of the people to do that too! She almost got to UND for like the first time with it but......without the riba it did not work. Now she cannot take another PI. Trying to say make SURE you are getting all 3 or seriously reconsider...lI'm pretty sure that was what she took I'll see if I can flag her in an email and see if she can post!

The Abbvie regimen contains Paritaprevir, which is a PI, so those who have failed in the past with a PI (Telaprevir, Boceprevir, Olysio) should not treat with the Abbvie drugs. Treating with Harvoni is the AASLD recommended way to go. The AASLD guidelines for those who failed with a PI are copied and pasted below. Go towards the bottom and you will see that the AASLD does NOT recommend the Abbvie drug regimen for those who failed with another PI.

Common Questions and Answers about Enablex pi

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