Frequent urination symptoms and conditions

My 84 year old father-in-law took Urimax 0.4 before going to bed. In the morning he was very weak and unable to get up. He expressed great discomfort due to frequent urination through the night. Is this a normal reaction of the medicine?

I had my mirena place in October 2008. I had no symptoms at first, but about 3 months ago that all changed. I'm losing my hair, severe abdominal cramping, fluttering (like being pregnant), severe lower back pain, dizziness, headache constantly at least once a day. I also had regular periods up until last month, when it simply never came. I freaked thinking I was pregnant I had all symptoms (tender breast, missed period, frequent urination, and nausea). So I called my doctor and demanded he order a blood test because with my son the home pregnancy test did not show positive until I was 3 months pregnant. Of course the test came back negative, but I swear I am pregnant, all the symptoms I had with my son I am having now. I know that I'm not but these are crazy side effects from the mirena..Also I didn't know until I read on here that the cyst are a side effect I have one on my right hand that just appeared out of no where about 3 months ago as well..It hurts just to type :)....In the end I will not have the mirena removed, the benefits surely out weigh the risks. Good luck to everyone with the mirena!

Wavy feeling of anxiety in my head (like I used to get from codeine). Fuzzy feeling in big toes. Dry, choking cough when I lay down at night. Now, I am morbidly obese and have bad acid reflux. If I don't take Prilosec every day, I cough. I also have sinus/allergy problems. So I take Claritin-D. And for health benefits, I take baby aspirin. So I'm wondering if it is the combination or if I am getting ready to have a stroke. It's my own fault for being so overweight, but it is frustrating. I also have swollen ankles and legs. And lately I feel like I have to pee too frequently and that I'm not quite able to finish. This worries me because I was feeling like this before I found out I needed surgery to remove an ovary due to a very large cyst. I wonder if I am getting another one.

I had my mirena inserted 3 weeks ago and as soon as they put it in I instantly felt the need to go to the restroom. Every time I drink anything, I am constantly in the restroom to urinate, but I am also constipated all of the time. I have had extreme cramps and my breast are really sore. I have felt bloated and moody ever since I had it done. I have also experienced shortness of breath and felt like I am having panic attacks. After reading all of these responses I am terrified of what else is going to happen. Has anyone else experienced the frequent urination and constipation?

Hi to all,
I have read all comments in complete shock. I am a 53 year old female.
I was prescribed Simvastatin just over 6 months ago (40mg). I am hypothyrod and also have very high blood pressure. About 6 weeks ago I started to have severe (and I mean severe), night sweats. The sheets are absolutely wringing wet as if someone has thrown a bowl of water over me,
The headaches that start within about 30 minutes of getting up every morning radiate from the middle of my forehead right across my right eye and it throbs all day. My throat is sore, my skin very dry, my vision seems very blurred (especially first thing in the morning), and I don't seem to be able to focus very well. My appetite is almost non existent and my shoulder, legs & feet hurt dreadfully and although I hate to admit this I am quite depressed at how I feel.
Three nights ago I decided to stop taking Simvastin and guess what...hay-ho, no night sweats, no cramp and the headache today was much less severe.
I am glad I found this site and for sure I will be visiting my doctor next week to advise my findings.
I think I would rather live on a diet of bread & water rather than go through this again.
Good Luck to all fellow sufferers.

SO I took yaz for a year then I switched to Loestrin 24 Fe last month and the period following I got my period a day earlier than usual and It was heavy the first day then it went lighter until Monday it was hardly there. It was about 3-4 days of a period and I'm worried i might be pregnant. On yaz I had 3 days of heavy period and 1 day of light. two months ago I had sex Two days before my period Obviously i was on the pill and had periods since. There is no fatigue or frequent urination or sickness and I have had at least 6 negative Home tests over this period of two months. I'm worried a little, There was no coming inside and he did not wear a condom and he had urinated before sex. I am wondering If it is the pill switch that is tripping up my period or is it pregnancy?
I'm so stressed and yesterday a rash developed on my face. not red, ichy or burning just little bumps. I'm worried this might the pill or signs of pregnancy. HELP!

I started januvia beginning of October after no luck with other medication but my glucose level remains between 10-12..I haven't lost any weight at all in fact i have increased by about 4 kilos. The worst side effect for me is most nights more frequent urination during the night and also a very foul foamy smell. I had not experienced this with any of the other tablets in the past.I am almost certain it is the Januvia.

Hi,

Fist off I'm a fit 38 year old male, not overweight, don't smoke, occasional social drinker.

I've been taking Lisinopril since being diagnosed with high blood pressure in Feb 08, I was started on a dose of 5mg, which was then increased to 10mg and finally 20mg.

The Lisinopril never really got my high blood pressure under control and my Doctor has now switched me to Bendroflumethiazide, only been on those for about a week so have to see how they go.

Lisinopril certainly made me feel terrible:-

Constant Fatigue
Depressed
Foggy
No concentration
Dizzy
Tinnitus
Pounding headaches

if you feel like this then I'd go and see your Doctor and try something else

I am so thankful for this site. I thought maybe it was just me. For one, I am allergic to Sulfa. My doctor knows this, as does my pharmacy. Still, they give me Lisinopril with Hydrochlorothiazide which you should NOT take if you have a sulfa allergy. From day one, I started with anxiety, agitation, nausea and what felt like a racing heart - though my pulse was normal. Day three I called the doctor and they said this was normal as my body "adjusted" to the medication. It has been over two weeks and the same thing keeps happening. I tried taking the meds at night to hopefully sleep through the side effects but no - it just kept me awake. I put another call in today and have yet to receive a return call from my doctor. I hope the doctor calls me and NOT the front desk girl because I have a lot of questions and concerns. Other symptoms I have been experiencing since I started Lisinopril are sever muscle cramping last for over 24 hours, dizziness, heavy chest/racing heart beat, restlessness and less frequent urination. For a 37 yo female who has to "potty" constantly, even throughout the night, going once in an 8+ hour period is not normal! The worst side effect though is definitely the anger and agitation. I feel like I am going to burst out of my skin or die banging my head against the wall. Last night I tossed and turned for 2 hours in agitation. I thought I would surely have a heart attack from the stress. Oh yeah my BP has NOT dropped at all (tho it fluctuates on or off the meds) on the 20 mg dose. Go figure.

My daughter is 7 and was just put on Singular as a preventive medication for croup which she gets when she has an infection. She is not on a daily inhaler nor does she have asthma attacks at school. I asked the doctor for an alternative to the pulmicort breathing treatments b/c the prolonged use of this caused her to have dental issues (8 cavities) and he gave her singular. I am concerned of the side effects in the reviews of this medication but I need some relief for my child. She has been on the medication only 1 day is frequent urination a side effect and can it come on that quick? If there is another medication that doesn't have the side effects apparently singular has please let me know.

I am a 42 year old healthy man that started getting tired of getting up during meetings every hour and a half to urinate. I went to the doctor and he prescribed Flomax. The frequent urination has improved, but the sexual side effects are awful. I first noticed a significant decrease in ejaculate. No big deal. I refrained from ejaculation for a week and this morning, when I had my orgasm I had zero ejaculate. The flomax is in the trash! I can not fix one thing and totally mess up a really good sex life. I sure hope this will not have any long term effects. I'm just trying to honest!!

Hi Iv'e been off of Yasmin for 2 months after a 2.5 year run. When I was on Yasmin I had HORRIBLE cramps before and during my periods, I was tired 24/7, extremely heavy periods, dreadful mood swings, depression, panic attacks, paranoia (I couldn't stay at my house alone for just an evening w/o thinking someone was going to break in my door and kill me). Now that I am off of it, I'm thirsty almost all of the time and frequent urination. I went to the hospital because I was scared of having diabetes since dry mouth and frequent urination are two main symptoms. Thankfully, the hospital staff dismissed it and diagnosed me with a UTI. I still have dry mouth and frequent urination. Now about my period, Last month it came a bit late but it still came. This month I'm currently 3 days overdue for my period (I'ts been 32 days!!) I've never had sex in my life so I know it isn't pregnancy. all I can do is blame this horrible drug and go see my OB/GYN on Monday to see if everything else is ok. Anyone have any reassurance for me?

I have been taking doxycycline hyclate for acne for the past three weeks and find that I am now urinating a lot especially after intake of liquids and it seems as if I empty the same amount that I consume.This is really very annoying and inconvenient.

I too suddenly developed frequent urination for doxcycline.

My experience with Norvasc is headache, stomach pains, depression, and nausea, frequent urination, and my chest feels very heavy about 15 minutes after I've taken the pill.

EVERYONE PLEASE READ!!!! GARDASIL HAS DESTROYED MY LIFE! I am 24 years old and a year and a half ago I was graduating college and planning to be a professional dancer and go to law school...I was perfectly healthy and energetic! In February of 2007 I received my first Gardasil shot. After a few days I started to feel as though I had a Urinary Tract Infection and was also feeling more tired than usual. The doctor gave me an antibiotic and sent me on my way.

In May of 2007 I received my second Gardasil shot and yet again, a few days later I started to feel like I was getting another Urinary Tract Infection. I went to the doctor numerous times between the second and third shot...all for bladder and urinary tract pain. For months I was on different antibiotics and they were not making the pain go away. After visiting a number of urologists, I found out that the urine cultures had all been coming back negative - showing no sign of an infection, so the antibiotics were pointless. All tests that I had run, both blood and urine came back normal. It is not standard procedure for a doctor to call you if your test results come back normal, but there was clearly something wrong, so I searched for a urologist who would believe me that I wasn't making up the pain I was in.

In August 2007, I had a cystoscopy done (they took a scope and went into the bladder to look in the bladder wall) and they concluded that I have an incurable bladder disease called Interstitial Cystitis. This is a condition where there becomes a defect in the bladder wall causing it not to have the protective mucus layer inside of it. The pictures of inside my bladder show red, raw skin, obviously showing the severity of my case of it.

There is no evidence as to what causes Interstitial Cystitis, and there is no proven successful way of treating it. The initial signs are exactly the same as a Urinary Tract Infection (painful bladder spasms, painful urination, body aches and back pain). The main difference is the fact that it is not an infection. There are thousands of people with Interstitial Cystitis who are misdiagnosed as having chronic Urinary Tract Infections.

I received my third Gardasil shot in October of 2007 and that is when EVERYTHING fell apart. The bladder pain became constant and there has not been one minute in a day since that shot I have not been in unbearable pain. This is when everything else in my body began to crash down as well. The other health problems and side effects from the Gardasil that I am having are constant sore throat, vicious migraines, vision changes, back pain, body aches, joint pain, sinus problems, vomiting, constipation, dizziness...I could keep going on forever!

I have tried all of the conventional treatment for Interstitial Cystitis and have gotten NO relief from the pain and other side effects. The doctors didn't know what to do, so they put me on OxyContin and a diet consisting of no acidic foods. That has now posed its own set of problems seeing as now my body is addicted to the narcotic, and I have gone from 5'6'' 125lbs to 100lbs over the course of a year due to the diet. I am extremely malnourished and have to take B12 vitamin shots once a week due to the severe anemia. I am 24 years old, and feel like I am 100. I can not live a normal life, I am going to lose my job from numerous absences, I lost my fiancé and am not able to have an intimate relationship anymore, I am extremely depressed, I have to have my family clean my apartment because I am too sick to do it, I can not do social activities because I am too tired and in pain. This vaccine has DESTROYED my life! I am desperately seeking out someone else who is having bladder problems due to the Gardasil so that I can contact an attorney. This needs to be OFF the market a soon as possible so that it does not run any other lives! Gardasil has caused some deaths, but in my mind, I'd rather die than live with the pain I am having. I did notice there are some posts regarding girls getting urinary tract infections... PLEASE PLEASE PLEASE have your urine cultured because there is a good chance it may be Interstitial Cystitis!

I am desperately looking for someone who is having some of these symptoms so that I can go to a lawyer and get something going before things like this happen: Numerous states are pushing to make it mandatory that girls receive the vaccine before they enter the 6th grade. We can not let this happen! We all need to stick together and somehow fight this and get out lives back!

Let me know if you are IN - and also what you thought about my post!

You can email me at ******

Bless All of You!

*~Amber~*

Anyone having frequent urination with the mirena? (I feel like I did when I was pregnant)

I spent the weekend reading about the development of Singulair. The early studies recognized that the first phase of the acute asthma response bronco-constriction was probably not caused by leukotrienes. They identified histamines and prostaglandins as the probable sources. I don't think that changed because the Singulair literature states that it should not be considered as a treatment for that. Leukotrienes were a source of inflammation caused by eosinophils and mast cells present in greater numbers (than normal) in airway tissue. So, it was beneficial to find a way to decrease that.

The cysLT1 receptor was identified as source of the signals that tell the cells to produce leukotriene. The receptor, a gene, consist of 337 (they think) amino acids. They modified a compound that would bind to that receptor thus blocking the cells ability to produce leukotrienes. This compound is very specific. It was formulated to bind to the "model" receptor. This compound will not even bind to cysLT receptor sub-types. (That is the good thing.) There is an enormous amount of research that discusses the genetic variability of the chemical reactions that occur in the leukotriene (calling it this for simplicity) pathway. We are also seeing that a number of researchers would like to use gene profiles to predict whether patients will respond favorably to different asthma/allergy drugs. ALL PATIENTS HAVE A RIGHT TO KNOW IF IT IS INHERENT THAT SOME PEOPLE WILL NOT RESPOND TO SINGULAIR OR RESPOND ADVERSELY.

There are many studies from the 1998 era that conclude that montelukast is not effective for everyone. Those researchers stated that it can be predicted that those people who are going to respond favorably will do that within the first 14 days or so. That conclusion would be consistent with a genetic component for efficacy and safety of Singulair. Those doctors concluded that those who did not respond within that time frame should not take Singulair for fear of harming them. That makes good sense.

The Italian researchers wanted to know if there was more going on than blocking leukotrienes in the action of montelukast. They set up a "test tube" study regarding montelukast, the cysLT1 receptor, and some t-cells that they selected. Why? Researchers always have something on their minds. They observed the death of these particular t-cells.

Montelukast is a quinoline. We basically know of quinilines and quinolones as compounds that were invented as broad spectrum antibiotics. They work because they interference with bacterial DNA so they cannot replicate themselves. Montelukast is a quinoline modified to bind with the cysLT1 receptor (a gene) and prevent that gene from activating. That's consistent with what a quinoline/quinolone does.

So what does montelukast do in blood plasma if it does not bind to the receptor because of genetic mis-match? (If montelukast does bind, then a chemical reaction has occurred and the liver will break down the by-products. Montelukast metabolized in 10-12 hours.) What happens if it doesn't bind? How long before it breaks down? Does it produce toxic by-products?

I want to know what happens to lymphocytes such as t-cells just because montelukast is a quinoline. Maybe nothing but what's up with the Italians researchers? I want to know if montelukast has the capability to interfere with lymphocytes who can clone themselves. That could be a good thing under circumstances when these lymphocytes are causing inflammation. But it could be a bad thing in the case of normal individuals with no problems.

I want to know if the bad side effects are due to the fact that the body has to break down and metabolize a quinoline that did not bind to the receptor for which it was created. The side effects of Singulair are strangely similar to what is observed in the quinolones such as levaquin. I have not as yet been able to compare montelukast as a quinoline to levaquin as a quinolone. I am hoping to find something on these categories. There may be no reason to worry that they cause similar damage. But frankly, I think that there is. There is some terrible chit happening to some people. The scariest is the neurological damage.

All of these questions would be in the everybody pharma knows to ask category. I don't know where the answers are. I haven't found them as of yet. Maybe there are no answers. We have to remember that Singulair and Vioxx were released in the same year. They have continued to be drugs under the current executive management of Merck. If the Vioxx marketing promoters had their ghost writers, why not the Singulair marketing promoters. The genetic component appears to be widely accepted but we haven't heard one thing about even that.

I think that it is sad that maybe the marketing of Singulair as one stop shopping for asthma/allergies may have destroyed the original concept. I really think from reading the original work that they knew that they couldn't engineer a drug for one size fits all. Everybody gets harmed when information is withheld.

Shame on the allergist who yelled at the mother who wanted to discuss issues. Does he know exactly who is allergic to Singulair and who isn't? Get him a dunce hat. Just because Singulair is marketed for allergies does not mean that you cannot be allergic to it. See the power of Madison Avenue? The ad agencies focus group these drugs to death. The ad agencies cleverly craft the product information. A good piece of legislation would be to prohibit consumer drugs ads.

I have been on Lyrica for almost 2 years for nerve damage and fibro. I have gained approx. 60 pounds since starting it and now have arthritis in my back. I finally took myself off because the side effects outweighed the benefits. I ha a hard time concentrating at work, dizziness, severe weight gain, bloating and frequent urination. I also have IC (bladder condition), so the frequent urination was also killing me.

I am a 32yo male and a Paramedic and it has been a living hell for the last two years. Here are my side effects and then my story. Anxiety, anxious, Irritable, high heart rate, leg calf pain, horrible sleep, bad nightmares, depression, suicidal thoughts, thoughts of hurting people, hate being around people, fear of heights (I used to rock climb daily), dizzy- if I move my head too fast or spin around with my son, weight gain(could be unrelated) arm cramping, frequent urination, and mood swings from crying to anger in just a few minutes. Not like me at all! First few years looking back, I was just became irritable and short with people. The last year has been horrible depression and anxiety along with the other side effects. I like many of you who have written here have had many of the exact same side effects. I had a stressful job at times and worked 24 hour shifts. I have always loved people, and enjoyed meeting new people. Not any more!! Two years ago my mother who lives 3.5 hours away asked me why I was in such so anxious all the time. She said, you are not the laid back and carefree man I know. I thought it was just due to some stress about being recently married or the job. The changes took time and I did not realize them or see them. Looking back, others knew something had changed.
Knowing about medications for my job and how to research them, I looked into every possible side effect and how Singulair worked before I started taking it. Looked good in 2004 with no major side effects. A little over a year ago my father became sick. He was going to battle cancer, but before he could, he would find out he needed a heart valve replaced. He got the surgery, went into cardiac arrest at home a week later, and was given CPR by my mother. A local police officer shocked him and got the heart out of V-fib. I slept with him in the ICU almost every night. He died a week after that and my wife was 7 months pregnant. Talk about stress. The baby came and I stopped working to raise our new little boy. I became short with my wife and started to pull away from being around people. I started to have bad dreams with twisted and morbid outcomes. I had suicidal thoughts out of nowhere and would wonder, where did that come from. Just as soon as they would come, they would be gone or I would think about something else. I got dizzy all the time and started to get carsick if I wasn't driving. I used to be able to read while riding backwards or sideways in the ambulance without a problem of feeling sick. That was not like me at all. I would snap at anything and became almost OC about everything. Thinking all this time the last year that I was just depressed about loosing my father whom I was very close too. Our little boy ended up having some medical problems and the insurance company would not pay the bills. More stress! My wife an EMT-Intermediate blew out 2 disks in her back on an ambulance run, more stress again. More insurance problems. I became a basket case! More anxiety, more depression, never got a full night sleep, mind racing, calf pain soo bad I would ask my wife to rub them, arm pains and finger joint pains at night. I also had a high heart rate of 100 almost all the time. Heart palpitations and a few times it felt like my heart was empty off all the blood and would beat very hard in the middle of the night lasting only a few seconds to a minute. Weight gain, moody all the time. I thought just due to all the normal stress in life.
Two days ago I went for a hard hike and came back with a pounding headache. Excedrin always does the trick for me. Not this time! I had seen a second of a news where the anchorman was talking about Singulair. Googled "Singulair problem" and found this site. I freaked out!! Almost all of you are talking about all the problems I have had as well!! This medication is making us go completely mad!! Tried to go to bed two nights ago and my mind was just racing. It has been Singulair the whole time. The only medication I take. It has made me nuts. My head was pounding the worst I have ever felt and my heart was coming out of my chest. I was awake since 3:30am and read the story of Cody Miller. This poor boy had no chance with this drug. He brain was not fully developed like an adult at just 15 years old. He wouldn't be able to fight the suicidal thoughts like I can. I have been to a lot of hangings, suicide shootings, and drug overdoses. I have seen plenty of death.
I called his mother a few hours later and explained to her that by them going to the media and getting the story out, prompted me to look into Singulair side effects. And that they just saved my marriage and my life. I explained to her that she did nothing wrong by giving Cody the medication for his allergies. It works great for the asthma and allergy symptoms for me. But, it ruined the last year of my life! I felt like I was going to have a stroke shortly after talking to her. I had my wife check my blood pressure and it was 154/100 (normally 120/82). Got grandpa to watch the boy and went to the ER. After my lab results came back and talking with the doctor, we decided it was a panic attack and who knows what the side effects of coming off this drug will be? I had stopped taking it the night before. Thanks to all of you who posted here and thanks to Kate and David Miller for speaking up. You saved my life. This medication got worse over time for me. It got worse as the stress level went up. I have been off it for two nights and already feel much more calm and was sleeping fine, until the little boy woke up and wanted a hug, or bottle. I hated almost everyone, I was short tempered, anxious, OC, and wanted to hurt people for no reason. I want my life back. I want the old me, the care free happy go lucky guy! I already feel better and will write hear as the days and weeks go by. I will never take Singulair ever again!! Not one stupid pill!! Look to those close to you and see if they notice changes. Even those of you who have been on it for three years like me. The drug company knew what was up the whole time. Bad men and women who want money over telling the truth. Maybe not everyone taking Singulair will ever have the side effects soo many of use have been living with, but to those of you that notice changes! Throw this medication away now and never touch it again. Get your life back!!! Be the old you again. I will go back to Albuterol (the only medication I used to take). Read the stories about the two year olds and the five year olds that cry all the time and are angry all the time. Little kids tell it like it is. It's not until they get to work for large drug companies as adults due they lie about side effects and wait years to publish paperwork saying that post marketing research shows all these negative side effects. They knew all along.

I also just heard about the Singulair side effects. I am a 58-year-old female with recurrent sinus infection and general allergic reactions. I had testing at my ENT's last spring--I was allergic to nothing specific. It was thought that I am generally sensitive to lots of different things. Well, the ENT put me on Singulair and I never put two and two together until now--- I became extremely anxious and depressed, couldn't sleep, my legs were so restless at night that it was unreal. I also had frequent urination and bladder spasms, low pelvic pain, etc. Over the winter, I stopped taking the Singulair and gradually was able to get off Lunesta and an anti-depressant. These were the worst months of my life---I went through all kinds of urinary and gyne testing to no avail. The urologist couldn't give me any answer---just that he though it might be a neurological issue so I also spent a lot of time and $ getting CT scans and MRI's to no avail. I really thought I was losing my mind---it was half a year during which I was definitely not my usual healthy, upbeat self. I will never touch Singular again!

I have been taking this drug for a week and two days. I am able to fall asleep easily but I have been waking up every night since I started this medication with terrible anxiety and my heart beating fast. I have also had some stomach cramping and frequent urination. I developed an upset stomach three days ago and haven't had a bowel movement since. I have also had really bad headaches.

I took Aciphex for 3 days and stopped. Two days later I awoke with a very scary irregular heartbeat that lasted for 2 hours and accompanied by frequent urination for the two hours. I was petrified. I thought I was dying! Now I am scared to take any more Aciphex. I only have GERD or Dyspepsia infrequently. I will try to find a natural remedy. I also had a headache every time I took the Aciphex. I did not have any bowel changes that I noticed but I was only on it for 3 days. I had none of the other symptoms mentioned.

I have been on Yasmin for three months now. I just finished my third pack, actually on the placebo week. The first month I had no symptoms or reaction to the pills and I got my period the first day of the placebo week. The second month I had unprotected sex and began to have cramping, lower back ached, nauseated, frequent urination, and at the end of my second pack I did not get my period. On my third month, much of the same symptoms and now I am two days into my placebo week and am worried I might be pregnant. I have taken the pills religiously and have not missed a pill. Please let me know if anyone has had any of these same symptoms and possibly missing two periods in a row! Thank You in advance.

LOW POTASSIUM LEVELS,DIZZINESS,NAUSEA,VOMITING,FEELING FAINT/FAINTING,MUSCLE CRAMPS/SPASMS,FREQUENT URINATION,FLU-LIKE SYMPTOMS,TIREDNESS,WEAK,HEART PALPATATIONS; I AM ONLY 30 AND FEEL LIKE A 70 YEAR OLD WOMAN.I HAVE TO HAVE MY POTASSIUM LEVEL CHECKED ALL THE TIME BECAUSE IT KEEPS BOTTOMING OUT AND I WILL PASS OUT AND MY PRESSURE GETS TO LOW.BUT I NEED A BLOOD PRESSURE MEDICATION WITH A DIURETIC.WHAT ELSE CAN I USE I ASK YOU?