Bladder Disorders :: Trimethoprim 300 Mg For 7 Days - No Improvement
Mar 31, 2014
The doctor prescribed me Trimethoprim 300 Mg for 7 days. I am having it since last 3 days now but nothing has improved.
The dipstick test showed blood in my urine...though I have been having some other health issues as well...but this medicine was prescribed when the urine sample had blood.
I am worried that I might be having the wrong medicine, as nothing is improving.
I need to understand, how long should I wait for the improvement signs. I am worried. I feel dizzy after this medicine, and my health is getting worse.
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I been peeing for the past couple of days like two times every two hours what can that be ?
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I have been diagnosed with Chronic Prostatitis and prescribed a 28 day course of 200 mg Trimethoprim tablets along with 2.5mg of Oxybutynin for the same period. Started the treatment several days ago having taken 4 tablets of each drug.There are no immediate side effects apart from a slight dizzyness. Having read the posts about the bad reactions to this drug,it has given me great concern over the long period I have to take these tablets. Are there any other readers to this website who have taken this drug for the same period of about a month ?
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I've started to get really thirsty, and I drink a lot of water everyday. I have to go to the toilet about every 10 minutes, and the pee is clear. Maybe I should drink less, but I get really thirsty so I can't. I'm really tired to, but I don't know if has to do with it.
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I believe I have an UTI. I am VERY clean when it comes to "Down There" It concerns me because It hurts when I pee, but at the very end. It also has a funny smell, as if you left urine to sit for days. Also, sometimes afterwards, my clitoris is waaaay more sensitive to movements and the way I walk. I've done some research and I've found that cranberry juice and water helps flush out the system. What do you think I should do? (I'm a virgin by the way, if that helps any) Thank you!! Also...I've used a different brand of soap when I wash down there.... Do you think that could've caused it?
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I am a 72 year old women and at night when I wake up to pee I have to strain to finally go. It only does this at night. Any ideas what causes this?
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I've had two bladder neck stricture surgeries at two month intervals after open RP and recently a urethral stricture.
Uro recommends daily dilation for a year using a Cook Medical dilation balloon catheter.
Recently had blood/clots in the urine which cleared after up after 3 hours but now I have a lot more irritation getting the catheter past the urethra stricture.
Uro says any further Urethrostomy would be serious as he has already cut close to the sphincter ...does this also rule out Urethroplasty?
Has anyone found that daily dilation works long term or does the stricture eventually close in.
I noticed that after waiting 3 days for a new catheter to arrive it was then very difficult to insert it. ...as opposed to daily dilation.
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I am 22 year old. My question is that I had a baby 3 month ago, and noticing when I go to the bathroom, my urine smells really bad, and its cloudy (smells like port-a-potty). I also experienced that I can't hold my pee.
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I Had a repair to mucosal part of rectum a week ago.. i am quite a lot of pain at the moment every time I try to wee the rectum comes down and a keep popping small stools which cause lots of pain I now cannot empty bladder properly and have a uti i seem to I In more pain not less. I have just gone on all fours on floor to try and wee and poo was there for 30 mins with pain from rectum and bladder. I eventually passed wee and poo....now still in pain at 3.40 am. So fed up ..don't know what to do with myself. Thinking of going on a liquid only diet to take strain.
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Please tell me is my period flow normal. I used to get 5-6 day periods, heavy for 2 days, medium for 2 days, then light for 1-2 days until it tapered off and ended. It was this way even when I was on birth control.
For the past few months now, I have been getting 3-4 day periods, where the first day is really just some spotting indicating my period is going to be starting. The second day is my heavy day. The third day is medium light. The 4th day is light. I'm still on birth control. I am 30 years old now.
Also last month, my period color was dark brown and I also had some black colored clotting during my heavy day. I know some blood clots are normal during menstruation, I had them all my life. But this blood clot was black. Again this month on my heavy day, I had black colored clot. It was a dime size clot. Size was not large. Is black color clotting anything to worry about? I do not see red blood these past two periods like I am used to seeing. I am seeing mostly brown and/or black.
And how can I increase my menstrual flow. I am worried that my endometrium lining is thinning and can cause a problem when I do try for children.
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just wondering if anyone here has a reverse T3 problem and if so, how long did it take before you saw an improvement in symptoms after taking medication?
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I'm 30 yrs old and i have a left-eye amblyopia. I undergone squint surgery last year's August. My eye barely improve and i really feel very down because i was expecting my eye will be at last okay but it didn't. The surgeon said it will require my right eye (which is okay) if i want further improvement in my left eye. I want to know what's will be the downside once my right eye get operated. Please help! My surgeon doesn't talk too much aside from telling me what else i need to do. I really wanted my left eye to be aligned correctly as greatly as possible. I suffered too much.
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Just wondering how long it took people to get any kind of improvement in their colitis symptoms with renicade. I had my first loading dose today and the dr said it would take some time to see any kind of result.
Also did you experience any itching or headaches after? About two hours after i started expiencing itchy eyes and started to get a headache, now 8 hrs after the infusion finished my hands, arms and face are itchy. My eyes are still itchy and my headache is still there.
I had an allergic reaction to 6mp but it was far more intense itching than this.
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I've reluctantly started Zoloft (SSRI antidepressant), being encouraged to do so by my GP due to the depression of diagnosis and the possibility I also have fibromyalgia.
(Pain isn't just limited to joints and fatigue is crippling) ie: I've slept 18 hours of the last 24 and still so very tired.
I'm having awful start up side effects which I understand will pass and understand there will be no benefit until 4-8 weeks, if at all.
I've tried Lexapro a while back with no real success.
Has anyone had any improvement at any level with ADs? I really hate mucking around with my brain chemistry.
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I was virtually deaf in one ear and very little hearing in the other ear, have worn hearing aids for 25 years. Recently (all happened so quickly, within 6 weeks) got diagnosed with Otosclerosis in both ears. 6 weeks after seeing doctor, i had the op. I had a stapedectomy/stapedotomy on 04/01/2016. Noticed a faint improvement in hearing when lying on the ward after the op, could faintly hear trolleys being moved about. But nothing drastic...... I've had dizziness, (not room spinning dizziness) which now only remains if i read, do jigsaws, scan shop shelves from side to side etc, weird! I've been through the heart pulsating, creaking, the rain dripping onto a metal plate sound etc.
I've had no real explanation of what to expect, i didn't really ask the surgeon any questions as i wasn't sure what would happen after and was unaware i'd have so many unanswered questions come up.
I assumed, and read some on the internet, and was told by a friend who'd had it done, that once the packing was removed, i'd be able to hear. Had packing removed 6 days ago, i'd built myself up SO much, that i stood and sobbed when i still couldn't hear! Surgeon looked a bit puzzled, but he said he wasn't worried at this point and to see him again in 6 weeks and that it'd be fluid behind my ear. He said i need to have some popping before i'll hear.
So, here i am now, with no change in my hearing for the last 6 days. I'm sure when i swallow, i sound as if fluid is in there? I also get like a thunder noise mainly in the morning when i wake up and my throat moves. But what's worrying me most after reading up on the internet again, is when i put headphones on, i can hear the music, (have to have it on loud to hear it), but the loud thumps/beats in the music make my ear crackle like a loose wire on a radio. I read last night that this is because the op hasn't worked and the prosthesis needs tightening/shortening/revising. But then on the other hand i've read that this may be normal?
If i go to do a burp movement when i have music in the headphones, i get a millisecond of a loud noise, but then it goes again as my throat can't seem to hold the noise open if you get what i mean. I have soooo many questions but don't want to bore you with them, maybe later. So, should i be hearing by now, is the crackling loose wire sound normal, and if you have any other advice that might stop me worrying please. I'm just sitting waiting day by day thinking today might be the day that i hear.
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I have taking Amiodarone 200mg for about 35 days for my AF .However, I still get irregular occasional especially after taking hot food. The improvement to my condition is marginal. Can anyone advise me if I should continue with Amiodarone. Also,I have been on warfarin for the past 3 years . Due to the interaction of Amiodarone with Warfarin, my doctor has reduced my Warfarin dosage from 4.5 to 3.5 to maintain my INR between 2 to 3.
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I m diagnosed neurocysticercosis on left optic nerve n m having blurring of vision.
Drs have put me on steroids past one year ,but no Improvement is seen.
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My Surgery was July 7th (3 months back) to repair torn ligaments and tendons and also to align my ankle. I have a metal plate on one side and 6 screws on the other. I have been going to PT 3x a week for the last month and I feel like I am not seeing any kind of improvement. They keep telling me that I am making progress and I am walking and wearing sneakers but the pain is and has been so bad. I am also back at work with some limited restrictions. Standing is painful and I find I have to shift my weight around a lot. I am getting to a point where I am always in pain and I don't know what to do. I can't really talk to my family anymore cause they just dismiss me...pretty much since I started walking in two shoes they figure I must be well and I don't know how to tell them that I don't feel well. I still have a lot of swelling but they say that it is all normal. I feel like I really shouldn't be back to work but I had no choice. How do I deal with the chronic pain all the time...I can't keep popping pain meds cause I just fall right to sleep and I need to be able to function at work and not be in so much pain that I am just angry all the time. Am I foolish to think that I will be better soon?
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After what feels like a lifetime of side effects and then nothing, I think things are looking up. Had a great day today, and I haven't said that in a while, particularly on a Monday. I have counted hours, days and weeks. Like everyone else I have questioned my dose and the medication on many occasions and felt like giving up a million times. To everyone who encouraged me to keep going and give it time, thank you, because it does get better in its own good time. I have no doubt that there will be ups and downs to come, but hey, I think I'm going to make it! Yes it really has taken 20 mg this long to start to work on my head , so keep at it during the early weeks. I hope everyone is letting a little more light in every day.
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For the past year i have had many strange symptoms in varying degrees, good days/bad days, good weeks/bad weeks.
Here is a list of my symptoms
Lack of energy, Extreme tiredness/fatigue,feeling faint (although never fainted),dizzy on and off but always dizzy up to a week before my period, one very bad period of 4 months vertigo. Jelly legs,shaky inside, feeling weak as though I've had the flu or something but I've not even had a cold this year.Palpitations, feeling detached, feeling like i'm about to loose consciousness (very odd feeling) the feeling you get just as you are about to go to sleep, Brain fog.Sensitive to light, eyes often become bloodshot. Headaches/migraine. Sometimes feel so cold inside & cannot seem to warm up.Periods of insomnia, bladder irritability especially in week before period, episodes of what i now call bladder fizz where bladder so irritable it feels like i have fizzy liquid in my bladder cannot sleep through this sensation sometimes accompanied by the feeling of a red hot needle going up the urethra (would be interested to know if anyone else gets this & any remedies please? A pain I get on either side low down about where pubic hair begins pain seems to radiate to back & sometimes down into the thigh on the side of where the pain begins, doesn't seem to coincide with ovulation & randomly happens (ibuprofen usually takes it off after a couple of hours) Bloating & times of excessive wind.Monthly cyst like spots on jaw line, hair sprouting on chin & upper lip (invested in a home laser scanner) Hair beginning to thin at temples.
Food cravings for something salty & chocolate particularly before period.
I am almost 53 so after reading forums on here have come to the conclusion that its menopause & not some mysterious illness, thought I might have Chronic Fatigue Syndrome, just didn't realise there were so many different symptoms of menopause.
Last year I did have very bad night sweats & hot flushes but they have reduced greatly, I take vit 6, eat plenty of fresh fruit/veg/salads, chicken, fish, flax seeds/chia seeds.
I'm so pleased to have found this forum & to find i'm not the only one suffering through this and not going mad, hope this might help someone else.
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I was prescribed a 3 day course of Trimethoprim for a UTI I took the first one on a Tuesday night and by Wednesday morning i had a numb left knee, the next day i couldn't walk, phoned my GP asking if i should continue on the antibiotic because it seemed obvious to me that i was having a bad reaction to it. I was told to continue the course but wish i hadn't, the pain on Thursday night was unbearable in my left leg, i couldn't move it and it was hugely swollen. On Friday morning i went to hospital and was there for 5 days on more antibiotics and painkillers. it's been 5 weeks now and i still can't walk on my left leg i still have pain and it also started in my right hand too. Before taking Trimethoprim i was a healthy 43 year old woman with no health issues. I'm now waiting to see a Rheumatologist and am terrified my leg won't recover.
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