Urinating symptoms and conditions

My daughter is now 20 years old. she received her 1st gardasil shot in 3/08 and the second in 8/08. She didn't get the last one and will not be getting it. From the day she got the first shot we should have known something. She nearly fainted immediately after both shots and complained of weakness and flu like symptoms. Started feeling poorly in the days and weeks to come. It was the end of her senior year the doctor tested her for mono. and it was negative but she had an extremely heavy schedule at high school. He chalked it up to the stress of that. Between the two shots she started having numbness and pains in her hands,elbows and arms. She continued to feel poorly and terribly irritable in the upcoming months. We saw a orthopedic doctor for her pains in her arms. He referred us to a neurologist. She was beginning her first year of pharmacy school and we put off the neurologist because she didn't have much time until spring break. During her 1st year of school after her 2nd shot. Her personality changed completely. Became insecure, moody, very anxious , constantly complaining of flu symptoms, bladder infections and had a hard time urinating. When my daughter returned home from her first year away at college I knew immediately that she had changed. She had been a very bright, intelligent, independent daughter and came home the daughter from hell. I couldn't believe what I was seeing. She was miserable, disliked pretty much everything. I had been talking with the doctor and friends over the course of the year and they all said that she was in a very stressful field (pharmacy) and college life takes some time to adjust. Then just a few weeks home from college she was complaining of dizziness, light headedness, headaches and saying she was having an episode. I thought maybe low blood sugars.....until I witnessed one. She was having Myoclonic seizures. She could feel them coming on but couldn't move or react. By the time I witness one of them she hadn't slept in 3 days. She was diagnosed within a week seeing a neurologist and having 50 to 60 a day. It took 4-5 weeks to get them under control in and out of the hospital . She has been on many seizure medicines it seemed like if it worked to stop the seizures she had crazy side effects. She was diagnosed with Juvenile myoclonic epilepsy. No one in our family has ever had seizures. I asked about the shot right away everyone said no and it was dropped. Since last July 08 we have been trying to help our daughter get her life back and it has been the worst year of our lives. She was unable to return to pharmacy school. The first fall 08 she was completely disabled. It looked as if she had had a stroke. They were saying it was the meds or maybe she had a breakdown of some kind. I am learning that it was side effects of this horrible shot. This is why I am posting this lengthy message because I wanted to let other people know that you and your daughter are not crazy!! We just started 2 weeks ago investigating the possibility of the gardisil shot being the reason for this madness. We have learned many things and are very sure that it was the shot that change our daughter.. I was contacted by a friend of a friend about a similar girl having the same pains in her arms and the focal seizures. I am learning more and more everyday about similar situations.. If this information can help one person it was well worth the time to jot it down. I will be praying for all of your families out there dealing with side effects from this vaccination.. I will let you know what we hear when we visit the neurologist at the end of the month. Any comments or information that may help us help our daughter can be sent to ******

I am so relieved to has found this page. I had no idea how many people on the NuvaRing were having the problems I've been having. I started using the NuvaRing a few years ago soon after starting to have sex. I wasn't very good at remembering my pill everyday, so I thought it would be a good option. I was so happy in the beginning because I could depend on it.

However, the first major thing that happened a few months later was IBS symptoms, which has put a big damper on my life since. I never know what food item will cause me to cramp and bloat next. It changes every day. I have always doubted this symptom attributed to Nuva until now. I thought my metabolism was changing because I was entering the workforce and exposing myself to new levels of stress.

Next, I never expected that it would diminish my sex drive. I have to convince myself that I'm in the mood, feeling responsible for maintaining a healthy sex life with my husband. That sounds so horrible, and it is. I'm almost never in the mood, not even to masturbate, and I have to keep a calendar to keep track of the last time I pleased my husband. I have not had a real orgasm since before starting the nuva.

It doesn't help to not only be not in the mood, but also when I do have sex, it's uncomfortable, burning, and very painful urinating afterwards. On many occasions, the ring gets pulled out a little during sex, causing a moment of uncomfortable prodding plastic for both of us, and I need to stop long enough to take it out and put it somewhere so I remember to put it back in again. Sex is more comfortable without it after that, but the irritation is still there. It takes a few days to heal before having sex again.

The last straw is more recent. I began to get discharge - a lot - starting the second week in the cycle. It wasn't a yeast infection, as I had a physical and pap at this time and the doctor would have picked it up. There was some itching, but mostly, I've had to wear panty liners 3 out of 4 weeks, including my menstrual cycle. This makes me feel less appealing, and much less interested in having spontaneous sex because I have to clean up first.

It just sucks that this has effected me for almost my whole relationship with my husband. Our dates, our honeymoon, our first anniversary vacation last month. All this time, and I find that the only prescription drug I'm on is what has caused me so much stress, sexual tension, and digestive ailment. One can only imagine what all these other happy commercialized medicines have in store for us, and in multiple amounts!

I went to the doctor with complaints of possible mold/fungus in my lungs which got better on it's own - but progressed to a throat infection. Later, my right nostril was runny for a while, which progressed into a blockage/infection of my middle ear. The doctor agreed - I have no compacted wax or anything wrong with my outer ear, so it seems to be a middle ear infection. He prescribes Biaxin XL 500mg for seven days, for my combination of ailments.

By the first day, I had a very vivid wet dream. Awesome, I guess. Then the second day I start with diarrhea, and another vivid dream. Today is the third day, and I slept before work. Had another vivid dream about someone building a house for me - and really runny stool. I can hardly call it diarrhea - more like urinating from my anus. Anyway.

Blockage in my ear went away the second day, but it's back again. I searched the net to explain the diarrhea (hopefully find something explaining the expulsion of bacteria causes this, but no, just a 'side effect' I suppose). I'm going to take some Imodium as soon as I can to battle the diarrhea, and hopefully things will get better by the end.

I can't complain about the dreams though. No nightmares yet, and I enjoy remembering my dreams, so...

hey i have mirena since October 2008 i wish i haven t listen too my doctor...i m constipating,urinating i have a terrible abdominal pain at the left side of it mostly i feel nausea,my vision got worse...
i moved last year from Poland where while breastfeeding my doctor recommended me mini pills but i couldn't get the same thing here...............
...................so theat s how i got it and two months ago i went to cut the string because my husband felt it and while the doctor tried to cut it it fall out and i was so stupid i let him to put me i new one right away how stupid is that.
He never thought that all this health problems have anything to do with mirena but i know they do,before that i was always horny and now i m not.I made my decision i want it out!

I am a 57 year old female and have been on Flomax for 3 years. I have tried twice to stop but my urinary hesitancy was worse. Has anyone had this experience? Does anyone know how to wean off this medication? Doctors don't seem to have the answer.

49 year old male started 4 years ago at 20mg and 10mg HCTZ. some results in lowering BP. 2 years ago MD upped it to 40mg because BP inching up. quit smoking 3 years ago, not one puff since. After MD upped mg the side affects have really kicked in. I experience all the side effects listed on this site with the exception of the cough which I started with but went away after a couple months. I have had stress tests, Holter monitor for heart arrhythmias, mri, blood work, stool samples, colonoscopy, and all sorts of other tests all coming saying I'm ok, yet I don't feel ok, I get progressively worse. After 4 weeks of 5 day a week exercising with weights and aerobics to get in shape to return to racquetball I have had it. I couldn't last 45 minutes my second day out. I felt like I was hit by a truck and it took a couple days to recover.
My MD attributes the issues to aging. I going for a second opinion and third if necessary. I am told by my MD that there are no studies showing these side affects for this medications. However I look at this web site and find it hard to believe that these doctors just haven't seen any evidence of what we are all suffering from. Why don't doctors really listen to patients. We are asked to listen to our own bodies and told we know our bodies better than anyone, yet when we bring up these issues we are treated like children.
No real answers, just questions

I have been taking this drug for almost 4 days, 2x a day at 100mg, i have UTI too, i have been feeling weak, terrible headache, nausea, backache and my eyes would be sore. i just don't think this drug is useful at all. And im 3 months pregnant, my morning sickness went off a week ago but when i started using it nausea is terrible plus backache. i agree this drug needs to be out of the market.

I am a 52 yr old woman who was rushed by ambulance to the hospital on Sunday 4, 2009. I awaken with a horrible ripping pain in my lower left side and back. It reminded me of labor pain although it was worse because I knew I wasn't about to have a baby. I could barely walk and the pain kept me bent over, and burning in agony. After being x-rayed and diagnosed I was told I had a very tiny kidney stone, along with a UTI. I was told they could manage my pain better if they kept me overnight, with hopes I'd pass the tiny stone by urinating in a little strainer cup, to catch the stone. I've not seen the stone yet, and this is the 3rd day. Anyway, I awaken in the hospital after being knocked out by pain medication, with an excruciating headache, as if someone was putting pressure on my neck and back of head. I also noticed a big red rash on my forehead. The nurse gave me benadryl, and continued my doses of Bactrim, and Flomax. When I was released the next day I was given a prescription to fill, Bactrim 2X 3 day therapy, Flomax, and Vicodin. Recovering at home I've had an excrutiating headache the entire 3 days.. I had nausea, felt chills, had no appetite, and felt dizzy and as if I'd throw up every time I got up. I ran a low grade fever of 100*. After reading this site I know that it had to be the Bactrim that caused all those horrendous side effects.This is the fourth day since I was diagnosed and I still have a UTI, and will be calling my doctor in the morning, thanks to post like these.

I have been on Flowmax almost a year. It solved the hard to go problem almost immediately. I do not have any problem going to the bathroom and usually make it through the night now without having to get up. I do not have a particularly hard time getting an erection, but I have notice a much lower ejaculation and less satisfying climax. But age could also be a factor for me at 64. For the most part I like what Flowmax did for me. Before the doc put me on Flowmax there would be times I had a hard time urinating and it was scary. For me I will have to continue using the drug.

This post is in regard to a form of albuterol known as "Xopenex" or levalalbuterol. From what I've read, many pediatricians are using this instead of Albuterol for infants and young children. It's the drug of choice because it supposedly has no side effects. This may be the case for most children BUT not my three year old daughter. Her pediatrician prescribed nebulizer treatments of xopenex and pulmicort, twice a day for six weeks. We managed to stick with it for four-five days- It was a nightmare! My daughter wouldn't eat (and this is a child who isn't a picky eater at all) or drink much at all and went for 12 hours one day without urinating. She was so horribly moody that you couldn't stand to be around her. She cried and screamed about everything and she is normally a very cooperative and happy-go-lucky kid. She also became aggressive towards me and others which was also very unlike her. The worst part was at night. She would have horrible screaming fits when it was time to go to bed. When she finally fell asleep, she would jerk and twitch most of the night. Several times she woke up after sleeping for about three hours, screaming at the top of her lungs. I would try to console her and she would yell louder and pull away from me. If I tried to touch her, she would swing at me as hard as she could. She seemed terrified of me and my husband. It would take me forever to get her calmed down enough to go back to sleep. If someone had videotaped these episodes, blocking out her face, NO ONE could ever have convinced me that this was my little girl. Her personality was so changed that I wanted to cry. I knew what it was doing to me to watch her and I couldn't imagine what was going on in her little head. I called my pediatrician and she brushed off my concerns. She said "Three year olds have temper tantrums." I told her that I understand that but not usually at three thirty in the morning. I took my daughter to MY doctor and he said he thought it could most certainly be the drugs. He suggested that we use the pulmicort alone one night and the xopenex alone the next night. We were surprised to see that she had reactions to both the drugs. One night she tossed, turned and twitched and the next she woke up in a terror. We stopped both medicines and ALL the symptoms ended. She will NEVER use these medicines again unless there are no other options! And we will not be back to our pediatrician!

I just found this site. I have had all the mentioned side affects too, but I have so many health problems besides the Diabetes I am on the Lisinopril for, that I never know if the symptoms are from a med or a health problem I have. My BP was never very high but my dr put me on this "to protect my kidneys" and said I HAVE to take a BP med to do that, or my kidneys would stop functioning. MY PROBLEM now is, I cannot get my Diabetes under control. I have been thru 2 drs and the last one just told me to get lost when I refused to go on insulin injections. At this time I do not have another dr yet. My Psoriasis has flared up again and my skin on my face is so dry I have red/scaly patches on my nose and down all around my mouth. My skin is getting drier and drier. It seems like I am drying up. I have been drinking lots of water and putting salves/lotions on my face and it is not helping. My daughter called me last night and told me to check out my BP medicine as she read that some can cause high blood sugar. My blood sugar keeps jumping all over the place. It drops to 165 then may go up to 225 the next day. Has any one else had problems with this medicine and Diabetes?
I am 63 yrs old and am in poor physical condition because of Lymes Disease and other health problems. So I do not know which of these symptoms are from this medicine or from other health problems I have. I did find out that the Diabetic medicine Metformin depletes you of B12, so I am now on spray B12 500/equal to shots. NOW I read that this medicine will deplete you of Potassium. Please let me know if you have Diabetes and this medicine makes it worse.

Was prescribed this antibiotic at the er for an ear infection. Had been taking for five days with no feeling of relief from the pressure and pain. on the fifth day I noticed I was shaking and shivering but sweating at the same time. My ears and nose became very clogged, my eyes turned bloodshot and felt a lot of pressure. I was very dizzy, had a very dry mouth was drinking lots of water and urinating a lot. Began to have a panic attack because the symptoms I was experiencing, after about five hours of this I started to feel a bit better. I did not relate this to the drug at first but after I took my second dosage that day I began to feel the same symptoms intensify, only my throat began to swell and I had trouble swallowing. I immediately took two benadryl as I realized I was having a serious allergic reaction. Went to the doctor the next day and was prescribed a different antibiotic, so eight days later I am finally feeling better! Will never take this drug again!

I've been taking Januvia for 8 weeks, and have experienced muscle cramps with shock-like pain running down my leg into my heel; upper and lower GI spasms; night sweats with sleep interruption; and I gained 5 pounds in the first 4 weeks which I can't attribute to anything else. I've also taking metformin and glyset for several years, and although I've experienced the night sweats, they've greatly increased in intensity.

I took Lisinopril for only 11 days and stopped due to the horrible night cough - ALL NIGHT LONG !! Wasn't getting any sleep, it was awful. I know I had some earlier minor side effects, but they were not as bothersome and went away - like diarhhea, urinating a lot, minor muscle aches. But this cough was something I couldn't put up with. The night after I stopped taking, I slept thru the night!

I have been on Lupron for 9 months. I go to the gym regularly (3 times a week) to counter bone/muscle mass reduction. I feel sore and achy all the time, and have regular hot flashes. I never sleep the night straight through anymore. I drink a lot of water to handle the flashes, so I am urinating all the time, it seems. The biggest problem is the 25 lbs I have gained. Fortunately my PSA has stabilized and I will go to an interval without the injections to see how long the 0.0 PSA will hold. I hope to lose some of this weight to bring my blood pressure back down to my 110/70 from the current 120/90.

I have been taking flomax for a couple of years now. The benefit has been urinating a few times less a day. I don't sleep well. Lately, I have been have mild, not real painful, like a dull pain headaches. I do get dizzy upon standing more frequently lately, I do not recall the dizziness until just recently. But my big side effect is loss of erection during sex and/or voluntary erection. I never had this problem before. I workout five days a week, three cardio days and two days in the weight room. I also take lisinopril for blood pressure and lovastatin for chloresterol. Great to hear other men are experiencing these same side effects.

Has anyone noticed that when taking Levoxyl you have some irritation after urination. I seem to have a nervous feeling in the urinary tract and after urinating it seems like I have a sensation of irritation. I have had tests for infections but nothing showed up, I am considered Hyperthyroid because of my dose of 150 mcg which is where Endo. wants me to be. I would appreciate anyone who has any input. I do not know if levoxyl makes your urine more acidic or not.

Hi All, Been either on Maxide or one of the cheaper substitutes for about 3 years now. aside from increase in urinating for a few hours after I take it I notice no side affects. Seems to work. If I am going out I skip it for a day. It does not seem ciritical to miss once in awhile at least in my case.

prayers to all
Richard

hi i am a newcomer to this site and i have been on prednisone for 3 weeks and actually i took my last pill todayi have also been experiencing side effects like, little sleep, aching bones and muscles, acid reflux/hearburn, quite often urinating and hunger..actually hunger is the only side effect that i don't mind having as i had very little appetite before and is underweight for my height so i actually hope to gain a little weight..how long does it take for the side effects to leave your body and if i only took this for 3 weeks will it leave any permanent damage, like bone problems?????

I've been taking 10mg of Lisinopril since 1/06 just before going to bed. I, too have experienced dizziness and fainting. Many nights when I've awakened to urinate, I've felt like I've been drunk (and I have not had any alcohol). However, last Friday night I woke around 1am extremely dizzy. I fainted after urinating. I've since readjusted my schedule of Lisinopril and am now taking it early in the morning. I'm also taking it with a full glass of water, have STOPPED taking potassium supplements and I am trying to drink more water during the day. I've not had an incident since I've readjusted, but remain concerned about the drug.

For those who become increased in thirst and urinating after taking Prednisone, you might want to check for your sugar level in your urine or blood.

I was recently on Prednisone for 2 days with 60 mg per day (3 pills of 20 mg) and I started to have severe lower backpain. I went back to see my doctor and found out that my sugar (or glucose) level was high in my urine (and the sugar level was same to that of a person with diabeties) and I stopped the medicine right away. I have been monitoring my sugar level for 5 days now and it is still high now especially 1 hour after meal (i.e >200 whereas a normal sugar level should ~ 80-110).

As some of you, I had anxiety, sleepless, swollen face after taking the medicine for 4 days but now these have stopped. However, the high sugar level still remains the problem of concern.

Do any of you know whether the high sugar level is temperoray problem AND how long the sugar level will come back to normal (being thirsty, blurred vision or sensitive to light can be the results of high sugar level).

Please advise.

I have been on prednisone for weeks at a time due to asthma. In 2002-2003 I had been on it for a total of 3-4 months (shortest being 10 days and longest being 6 weeks) I gained 10 lbs in 5 days laying in the hospital bed...from 154 to 164 and then up to 172 within the next week. I was swollen in the face and belly and I could not sleep. I was not even tired so it wouldn't have been so bad except I was so hungry that no sleep meant that I was up longer and had more hours to eat and eat and eat. I became disoriented and would start little projects and only finish half before I moved to another...very strange and emotionally unstable. It took a long time to loose the weight because I broke my foot . I am sure that the prednisone was responsible for weakening my bones...I just stood up and my foot broke. I didn't fall or bang into anything nor drop any object on it.

My dog is now on prednisone for the second time. The first time she was on it she became extremely hungry and ignored all of her normal restrictions...she would eat the trash, get into any wrappers and even ate an entire dish of candy. She was 10 at the time and well trained not to behave like that. She is now on it again for a brain tumor...her belly is so swollen that it is scaring me. She is disoriented, very thirst and always hungry. She is urinating constantly and she seems depressed. I am going to call the vet in the morning about these symptoms. We worked hard to get her weight down because she has arthrits and it helps her to be in shape. I feel that this drug is going to fatten her up beyond control. I know she is truely hungry because of my own experience and it was difficult to control my appetite I do not want her to feel starving all the time on top of the mood disorder. Does anyone have any suggestions.
Thanks, Jenn
P.s. she will not eat carrots or any thing like that, I already tried

Hi - I have been on prednisone now for 4 weeks due to a rash from an allergic reaction to sulfa. I started on the paks of 6/5/4/3/2/1 which I was on twice. That didn't work so my dr increased me to 60 mg for 2 days/50 mg for days etc. That didn't work so now I'm on 40 mg for 4 days/ 30 mg for 4 days etc. I'm not feeling confident that this will work either. The only side effects I had until this last dosage was the excessive sweating, increased thirst and urinating. However since I started taking this last dosage of 40 mg for 4 days I have developed the "moon face" which is horrible and insomnia. I haven't slept in 4 days. When I do fall asleep I wake up with the sweats. Also my vision has started getting blurry at times too. This stuff is scary. My dr didn't tell me about any of this - I have learned it from reading the drug effects and this website. I appreciate knowing I'm not alone. I hate being on this drug but it when I'm on the higher dose it does stop my itching which is driving me crazy too. I have been having mood swings too but I'm not sure if that is the drug or just from the stress of all of this. If this dosage doesn't work I don't know what else they can do but I don't want to have to go back on Prednisone again. I'm afraid what side effects will happen next and I worry about the long-term effects too. And please tell me the moon face will go away after I stop Prednisone... Thanks for listening.

I've been using nuva ring for a little less than two months. At first I LOVED it!! Finally I didn't have to think about a pill every day. But in the last few days I have developed serious inflammation and burning in and around the vaginal area. Sex is like torture, not to mention urinating. Look, if you have problems remembering your pill, nuva ring might be perfect. Just don't ignore the early warning signs like i did and know that vaginal infection, discharge and headaches are some of the most common side effects.

I was treated with radiotherapy for prostate cancer 4 years ago. My doctor at Radiotherapy Clinic of Georgia recommended taking 2 (.4 mg) Flomax capsules daily.
I stayed on that dosage for over a year, much to my misery. Furthermore, when urinating, I was unable to control bowel flow. In addition this dosage caused urgency to urinate more frequently. I am currently cutting back to 1 pill every three days. This is not recommended by anyone. I am just trying to cut back as much as is I feel comfortable about. Since I seem to be unable to control my bowel flow that occurs when urinating, I have developed bleeding from the rectum.