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Review: could Tamsulosin cause Urethral syndrome - acute (Cystitis - noninfectious)?

Summary: there is no Urethral syndrome - acute reported by people who take Tamsulosin yet.

We study 7,538 people who have side effects while taking Tamsulosin from FDA and social media. Find out below who they are, when they have Urethral syndrome - acute and more.

You are not alone: join a mobile support group for people who take Tamsulosin and have Urethral syndrome - acute >>>

 

 

 

 

Tamsulosin

Tamsulosin has active ingredients of tamsulosin. It is often used in enlarged prostate. (latest outcomes from 7,753 Tamsulosin users)

Urethral syndrome - acute

Urethral syndrome - acute (non-infectious inflammation of the wall of the bladder) has been reported by people with prostate cancer metastatic, pain, acne, rheumatoid arthritis, multiple myeloma. (latest reports from 29 Urethral syndrome - acute patients)

On Jan, 21, 2015: No report is found

Do you have Urethral Syndrome - Acute while taking Tamsulosin?

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You may be interested at these reviews (Write a review):

  • Ideopathic hypersomnia from mantle cell lymphoma
    I have an unusual idiopathic hypersomnia surrounded by the circumstance of also having Mantle Cell Lymphoma. I awake each day at around 7:00 am without an alarm after 7-8 hrs sleep. By 8:00 am after a cup of coffee and breakfast, I feel fully awake and 100% normal.

    Around Noon and 12:30, I begin to feel sleepiness coming on. This is nothing like the mid-afternoon low many people experience. A cup of coffee or a little fresh air do nothing.

    By 1:00 pm - 1:30 pm, I feel deeply drugged (like I've taken Ambien) and need to sleep. I sleep 3-4 hours of fairly deep sleep (I don't hear the phone or someone at the door). I have vivid dreams near the end of the nap and about half the time I have auditory hallucinations at the beginning or the end of the nap (I generally don't have these at night).

    When I awake, I feel like it's morning again and need a cup of coffee to get me going again. For the rest of the evening, I feel about 80% of morning alertness and energy levels.

    I go to bed at about 10:30 every night. It takes me about 15 - 20 minutes or so to fall asleep. I get up once a night to urinate, due to slight incontinence from prostate brachytherapy. I generally fall right back to sleep. Even when I sleep more or less than average, or go to bed significantly later than normal, I still feel the 1pm sleepiness at the same time and in the same duration.

    I have tried Nuvigil and it works well enough for me to stay awake during the afternoon if absolutely necessary. I'm feel about 70% of normal, but don't sleep well that night and don't feel fully rested or awake the next day. If I force myself to stay awake, the intense sleepiness goes away around 4:00pm - I feel sluggish but do not need to sleep until my normal bedtime.

    HISTORY:

    Diagnosed with Mantle Cell Lymphoma in June of 2013. I noticed worsening early afternoon sleepiness up to six months before diagnosis. After diagnosis, I gradually became more sleepy and began needing naps of 1/2 hour to 1 hour. By the time I began treatment for MCL (Oct 2012, I was sleeping in excess of 4 hours every day despite getting a good night's sleep. This and the increasing size of my spleen were the determining factors for beginning treatment. During 6 months of chemotherapy (Rituxan/Bendamustine every 4 weeks) I continued to have these naps. After achieving full remission, I received high dose chemo followed by an autologous stem cell transplant in May of 2013. About a month after the transplant, when I gained a little strength back, I needed only a light nap of 30-45 minutes, but gradually the heavy naps returned to the current 3 hr/day level, despite my strength and endurance returning to nearly normal levels. My nighttime sleep pattern has not changed significantly all this time.

    I had an Overnight sleep study that showed no significant apnea, but because I didn't sleep normally at the center, the test was inconclusive. It was followed by an MSLT which showed that I did not have narcolepsy (no early REM). I was then prescribed an auto-PAP machine for three weeks to check my sleep hygeine at home. Minimal apnea was noticed, and most of the episodes were from my changing position triggering a boost in the PAP pressure. I slept significantly worse because of this.

    Because of the clockwork nature of the daytime sleepiness and the correspondence with my lymphoma, I would like to investigate an endocrinological source for my idiopathic hypersomnia but the sleep centers here in Wilmington are not equipped to handle this investigation.

More reviews for: Tamsulosin, Urethral syndrome - acute

Comments from related studies:

  • From this study (2 months ago):

  • The kidney stones are the main problem, I drink more water than the average person that I know. The pain is just unbearable, I can't take much more

    Reply

  • From this study (3 months ago):

  • It seems to me that the anal itching began shortly after I began taking Zetia. My doctor described it as caused by a fungus and prescribed Clotrimazole topical cream. He said to apply twice daily for one month, which I did. I am now into approximately month 3-4 and the itching continues. If I apply the cream twice daily, the itching is under control, but if I don't apply the cream twice daily the itching gets severe. After I started taking Zetia, I noticed frequent stomach gas and some fluid spotting in my underwear. The gas problem is embarrassing in public because it just doesn't stop, and I will have a loose bowel movement. I feel there is a connection between this gassiness and loose bowel movement since I started taking Zetia. Is the Zetia causing a fungal problem in my stomach which is causing the anal itching?

    Reply

    DrLivingston on Oct, 29, 2014:

    (48 y.o. male) it sounds like you may have SIBO (Small Intestine Bacterial Overgrowth). The test for it is very easy and relatively cheap. You need to call a gastroenterologist's office and ask if they use the hydrogen breath test to test for SIBO.

    If they don't, just keep looking until you find one who does, because if they know what SIBO is, but they don't offer that test, they'll most likely want to do an endoscopy, which is invasive, expensive, very uncomfortable (they shove a tube down your throat past your stomach into your duodenum) and take a biopsy, and it's not an accurate way to test for SIBO any way, because SIBO is generally found in the distal small intestine, which is about 12-15 feet deeper into your guts where an endoscopy can't even get CLOSE to reaching.

    Get the hydrogen breath test for SIBO. That will very likely come back positive for you. Bacterial overgrowth in the small intestine creates gas which causes abdominal bloating and gas and either diarrhea or constipation, which depends on the specific species of bacteria that has overgrown.

    You want to get this taken care of ASAP because while about 80%+ of doctors will misdiagnose it as IBS and/or Celiac, it's not and left untreated and CURED, will lead to Crohn's, misery and eventual death, but it won't be quick; it will be extremely slow and agonizing.

    Read Dr. Mark Pimentel's 'A New IBS Solution' and Dr. Elaine Gottschall's 'Breaking the Vicious Cycle'.

    BTW, I'm not a doctor, but I've been dealing with and researching SIBO for 4 years now. The scary thing is, I've heard of people who've had it for 30+ years.

    SIBO is the root cause underlying IBS, which is what both of those books discuss.

    Reply

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