Uroxatral and side effects
Common Questions and Answers about Uroxatral and side effects
uroxatral
If that is the only feature you're concerned about Uroxatral is less likely to affect ejaculation.
I am 58 yrs old, have BPH and had not taken medicine for the condition, as symptoms were not that bad. While in S. America in November, I had pain which was thought to be from kidney stones. I was given scopolamine. The doctor didn't ask about BPH and I didn't know that the med had side effects related to prostate. It became hard to urinate any more than small quantities at a time. I began retaining fluids, something that was determined after I returned home to US.
I have had an ultrasound of the prostate which checked out fine and have been tested for chlamydia and gonorhea, which both came back negative. I am currently taking uroxatral and avodart daily, and am curious as to why I am still having symptoms. Is it possible of being overmedicated? Or is there something that has been missed? If so what other possibilities are there?
There is another class of medications, such as Uroxatral, which can help shrink your prostate and improve your symptoms. the results of this class of medications, however, often take many weeks before they make a major differences. Ultimately, flomax and drugs like uroxatral can be combined to give maximal medical therapy for BPH. Sometimes men continue to have problems and may be candidates for surgical intervention to improve symptoms.
t know what triggers this problem and there is no cure. Uroxatral is an excellent option and you have gotten at least a partial response-- good. There is no risk of cancer or other serious impairment or long term damage to your pelvic organs. Symptomatic relief with Uroxatral, and possibly antiinflammatory agents give many men some relief.
I can't use Flomax or other alpha blockers due to side effects -- disturbed sleep. Uroxatral even caused me to sleepwalk 15 feet from a nap on the sofa one evening, waking when I fell flat on my face in the next room! Separately, due to a Vitamin D deficiency my doc found, he put me on 50,000 units Vitamin D per week for 8 weeks, followed by biweekly doses. And guess what...the Vitamin D almost instantly "cured" the BPH.
I am 55 yrs old female and went for a physical and was told i had high blood presure, that day it was 144/92. I had a blood test and it showed high cholesteral 257. Doctor put me on 10 MG Lisinopril. I took the tab for 5 days on the fifth day my heart was pounding so hard in my chest and i felt like someone was sitting on my chest. This happened a few more time over the next week and it would go away after a few min.
22 days on sovaldi-olysio-no side effects,not even a headache.And to this life long non responder who has done and failed with everything that has been on the market,this combo is working.Cant believe I am getting better and not suffering like I did with all the previous poison.Its like Dr. Bones McCoy from Star Trek brought this stuff back from the future.
I woke this morning with aches and pains and have been experiencing a headache on and off all day that is when I am not SLEEPING. Honestly I am not complaining especially since I had expected much worse. My question is do the symptoms change or/and get worse as treatment continues. I would assume they do get worse since the meds build up in your body. I have 3 kids ages 16,11,and 7.
Did you taper off the vibryd or quit abruptly? You can't just switch from one medication to another even in the same class and avoid withdrawal -- these meds are not easy to stop taking and it must be done carefully. Unless you completely stop taking a medication before starting another it's impossible to tell if your symptoms are a sign you're suffering withdrawal and quit too quickly or are side effects of the new medication.
You definitely need to get some high quality moisturizer and start lathering your body with it. Also note – hot water dries out the skin. If possible, you might feel better if you skipped a daily shower when possible.
The nausea stinks big time. The Pegasys folks are pretty clear that this particular side effect doesn't last and in my case it didn't. After about a month it went away. Try to eat small, frequent meals. Anything you like. Cold food is better than hot food.
The known, serious side effects of tamoxifen are blood clots, strokes, uterine cancer, and cataracts (see Questions 5–8). Other side effects of tamoxifen are similar to the symptoms of menopause. The most common side effects are hot flashes and vaginal discharge. Some women experience irregular menstrual periods, headaches, fatigue, nausea and/or vomiting, vaginal dryness or itching, irritation of the skin around the vagina, and skin rash.
seek immediate medical attention if you develop any serious symptoms or side effects. and that these side effects may only occur infrequently, BUT SOME MAY BE FATAL.
would this statement not really get you thinking.I never had any serious deseases but thought that the hep c would kill me. how irronic. those serious side effects are all that occur in our bodies, for some of us. I never experienced any thing like this before on the treatment.
It could be a side effect of the methadone or even an allergic type reaction to it. I remember when I took Macrobid (antibiotic) for a urinary infection, I had a high fever (102.3) every time I would take it, so I called my doctor's office and they told me to stop it immediately because I was having an allergic reaction to it. As it turned out, my father had had this same type of reaction to it a couple years before.
I had many side effects. Headaches, severe heartburn accompanied with hiccups. Blisters and discoloration all over my tongue and back of my throat. By day 6 my feet and ankles were badly swollen and it was getting difficult to swallow. My doc said I was having a systemic reaction and to quit immediately. We are going to try Subutex now and I hope it works.
On all the info I found, the only side effect I had that was listed was headache.
Hi I'm new to this site. In Jan. of 09 I had cervical fusion, in Dec. of 09 I had lumbar fusion. In Aug. I started the treatment (Pegasys Interferon and Ribavirin).I was wondering is treatment intensifying the aches and pains from the surgeries and I've developed several rashes.I go to see my GI on the 17.
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