Kidney stones symptoms and conditions

60 YO male: three weeks on .4 Flomax

I went on it because after Parathyroid surgery for kidney stones, I was still having symptoms. Mostly a painful urgency to pee, with only tablespoons coming out. That would last for 3-6 hours. I started out with pyridium (the pill that turns your urine orange). That seemed to help, but I was still having some lower-right abdomen KS pain events with the urgency. The urologist suspects I still have some stones that have yet to come out.

My prostate exam and PSA were good. No signs of cancer. I don't think the size of the prostrate was measured or whether BPH was an issue because of the obvious Parathyroid issue.

I started taking .4 Flomax, got the lightheadedness that evolved into a feeling of being slightly high most of the time. And feeling mildly relaxed.
Flow was improved, maybe a few less pees per day. Still peeing at least twice a night; good stream, good quantity.

Not a runny nose, but a thicker discharge. This week (3 weeks in) the nose is better.

Lower volume and clearer ejaculate. After the last ejaculation, I went right into an urgency and lower right KS pain event that lasted 6 hours. I was uncomfortable, but OK on Tylenol and pyridium. My events frequently happen on Saturday/Sunday. I have tried to figure out what, if anything I might be doing to cause or break this cycle, but there seems to be no correlation. I was hoping to get rid of the painful and disruptive urgency episodes, but so far they are still here every week or so.

Dreams have been a bit weird.

I have a swollen knee and toe, but this could be due to some hiking while on vacation. I saw the posts about painful joints, but can't make a direct connection yet.

Since Flomax three weeks ago, there seems to be a low level feeling in my lower abdomen. Not a pain as much as a presence, a tension. I think it's in the testicles, but you know how that is; accidentally smack one and the pain feels like it's inside the body.

I have been on Advair 250/50 for 5 years for asthma. I'm a 48 year old female. I have experienced severe hoarsness and my voice is rough sounding. Some days I am so hoarse that others have a hard time understanding me. I have had 5 kidney stones in the last 5 years, never had one before taking Advair. I had the last one a month ago and it was so large I had to have surgery. I experience nausea about once a day. I seem to always have a headache. I feel tired all of the time. Over the last year I have developed high blood pressure. I have gained 20 pounds. I have rashes on my upper arms that comes and goes. I experience mood swings. The Advair does control my asthma, but these side effects are too much anymore, especially the hoarseness. I am going to ask my doctor for other solutions.

I was prescribed methadone for chronic pain associated with partial paralysis from the chest down, 5 Macerated Discs, and a slipped disc right against the spine, preventing surgery as a cure. Believe me, the partial paralysis begins ONLY on the right side, and ONLY from the leg down, so the back pain is horrible!
Methadone has SLOWED the pain, but has not cured it in the least. Morphine helped, but I was so irritable to be around, I was losing family, so I tried changing to Methadone, and so far have not been very impressed! Highly addictive, cancels out any Hydrocodone, Oxycodone, Morphine-based meds, so if your treated in the hospital and they treat you with any of those meds, they will not work for around 3-5 days, and then not well for another couple of weeks. I was in the ER for Kidney Stones, and was given, over a period of a couple of hours, 20cc's of Morphine straight into my IV, and was still wide awake, and was only on 60mg of Methadone per day. I WOULD NOT recommend this as treatment to chronic pain, even though more and more pain clinics and Neurologists, or even rehab specisicialists are changing to it, because the AWFUL SIDE EFFECTS. I still have not found my medication of preference, yet, but Methadone definitely is not suitable, for me. Though everyone is different, for me, the Methadone has increased the pain level due to, when I am NOT on it, I feel awful, so I wake up having to dose myself, and can not sleep until I have stopped taking the meds long enough to cause pain.

Kidney stones pain,swollen feet and lower legs,joint aches. taking 200 units a day
100 am and 100 pm

TERRIBLE took first dose yesterday morning my gf loves to swallow almost gagged last eve how can 2 pills change that much almost passed out bout noon nooooooooooooo more of this crap still have kidney stones will deal with it

i was prescribed LEVAQUIN 500MG for an infection from kidney stones and ever since i have taken it which is 3 days now i have absolutely no energy and no appetite and forcing myself to even drink something to keep from dehydrating..i've never taken this medication before and I'm not gonna finish it..i have 6 days of it left but i can't go on feeling like this..i can barely get out of bed..i talked to my daughter about it and she thinks its just cause the kidney stones took me down this time moreso than before and if i would eat and drink i'd feel better..i don't think so..i'm done,i wanna feel good not miserable for the next 6 days..i just hope the symptoms go away soon...

I am a 61 yr. old female former smoker diagnosed with COPD/emphysema. I was put on ADVAIR 500, along with using a nebulizer with albuterol and bromide to "inhale" several times a day.I also was on oxygen. I quit smoking and worked at getting my health back and to the surprise of the doctors went back to playing tennis several times a week.After reading about the side effects of the high dose Advair I had my Dr. reduce the amount to 250. It has been almost a year now that I have been on Advair. I have noticed some of the side effects mentioned here. The leg cramps, and leg spasms have been horrid. I also have had blurry vision. And lately I seem to not be able to sleep even if I am tired.I am going to see if my Dr. will let me drop to the 100 Advair level. Lately I have been intentionally skipping Advair doses to see if I notice any difference in my breathing. I almost forgot- since going on the meds listed above I have had kidney stones, an emergency appendix surgery and now high bilirubin count. I cannot find any info on those problems if result of medication ADVAIR. Even though I smoked for a number of yrs. I was very active and not over weight. The Dr. thinks thats why I am back to playing tennis. Has anyone else had a gastro problems ??Thanks A.

My 6 year old daughter is taking topamax. Since the time she been taking it she has forgotten who she was and everyone around her, she went for an excellent student to not be able to do simple things like reading writing and math. She does even seem like the same child. She is very emotional and I just want my little girl back.

Does anyone know how to purge this crap out of your system? I've only taken a small number (5) for kidney stones. I had 2 of them back to back...I'm completely clear now -thank god!
I took the last one 10 days ago and the side effects just won't go away...I drink lots of water and finally went to a homeopathic doctor for help...My urologist was of no help. I'm scared that it'll never go away...Can anyone help?
Robert

I've been on Topamax since Sept 2007 and the only side effects I have had were at the beginning were the tingling in the hands and feet when I was brining my dosage up. Soda tastes awful but I no longer drink it and that is a godsend after being a heavy drinker of it for years. I do find there are time when I can't find the right word to say, or I forget what I was doing, but I deal with it. I have lost 20 pounds since being on the medication. After being on it for 6 months the tingling is gone, I usually counteracted it by drinking plenty of water in the morning, that got rid of it. The drug has taken away the migraines, and regular headaches I have suffered from for years. It has also stabilized my moods and taken away my anxiety issues. I'm 36 and have never felt better. Topamax is definitely not for everyone. For those that are suffering, please do contact your doctors and try to get off the medication.

I have had problems with kidney stones but thank god, no prostrate issues..
My first stone occurred in the fall of '05. My doctor at the time - the nastiest old bastard that ever graduated med school, prescribed Flomax to help the stone pass.....I took one or two and the stone passed in a few days..I don't recall any side effects from that instance.

Fast forward to Jan '08...I had another stone that made itself "known" to me for weeks before being diagnosed.......That after a trip to the ER.Lotsa' fun, everyone should go!.....I took Flomax about three times during that period and had some nasty side effects - reflecting many that have been previously published here. I got dizzy and nauseated at times.....I also suffer from panic/anxiety disorder.Flomax made me a basket case!......The "roaring" and "ringing"in the ears was and still is problem..... I passed that stone in early Feb.....
At the end of Feb the BIG ONE (1cm) decided to drop down the ol' ureter. My present urologist (Yeah the old buzzard finally retired!) gave me options, as stones of that size are real mothers to pass. Take pain pills, Uricit and Flomax......Or insert a stint and wait.....The final option was lithotrypsy. Lithotrypsy is an outpatient procedure that breaks up the stone into smaller pieces while still in the body via vibrational waves...
I had the procedure and most of the particles were flushed out.....I recommend this procedure for a quick but costly fix....
The doctor warned me that there would be smaller particles that might take weeks to work their way out........Well, that's what happened..Just when I was recovering from all the medication - Flomax included, I had another piece start working it's way down..It's still mocking me as I write this.
I took Flomax - out of desperation for three days for the purpose of flushing out this one last particle. My patience with this stone and it's aftermath was at an end! I wish I hadn't taken them.......The dreams, anxiety, rushing in the ears, dizziness..The whole thing! I had three capsules left and ground them up and threw them out today!

Flomax is hell on earth and I regret ever taking it. If I'd read this board on Sat I would have thrown them out then and just dealt with it, well I didn't and I'm suffering again.....Will it ever end?

Has anyone else experienced a bitter metallic taste in the mouth as well as an unpleasant smell to the urine as well? I also have this irritating urge to urinate but the flow is moderate........I was doing well without any medication when I got impatient and took the Flomax. How long will this be in my system I wonder.... Sex drive? I have none now.......Kidney stones really take it out of you, that mixed with the Flomax has put me on the sexual sidelines.....*sigh*.
Robert

Constant ringing in the ears after taking flomax for several months.Any help or suggestions would be greatly appreciated.

side effect: bleeding at urethra

For a long-term sinus infection that has drained my energy, I took my first pill in the Leva-pak about noon today with a large glass of water. Ate lunch. Planned to vacuum, but it was difficult to get into and around in our garage (we made a space for a car to go in now that mornings bring frost outside.) So I ended up moving things around in the garage. Major moving around, some stuff heavy. I was thrilled to have energy and strength to actually do something at last and to think of how long I had been listlessly surviving and at times even bedridden before this magical pill.

About 8:30 I came in to pee and found my undies bloody. Bravo, I said to myself, 10 years post menopause and I got my period again. This is the drug of youthfulness: energy and menstruation. Fortunately I still have a few sanitary items around for female friends who visit, so I got to be one of my friends.

But it seems that the blood is coming from the urethra, not from the vagina. And I have some discomfort there. So I recalled that the drug pakage said to drink plenty of water and realized that I hadn't had any more drinks since about noon or 1. I drank another glass of water and headed back to the garage.

I finished up the garage (who said I'm obsessive?) about 9:30 and came in to find out more about the new drug. I saw that the pack said right on it that drinking plenty of liquids PREVENTS THE FORMATION OF CRYSTALS IN THE URINE. So I drank 2 more glasses of water, thinking maybe crystals have formed in my urine and are cutting into the tissues of my bladder and urethra making them bleed. Guess these crystals must be softer than kidney stones or maybe much much smaller, because I've seen the pain folks get with kidney stones, and I would not be sitting here reading your experiences and now typing up my own to share with y'all if I had as much pain as kidney stones cause!

Anyway, with those two more glasses of water, I came online to see the deal with urethral bleeding caused by Leva-pak, and what do I see. Well, the first website I went to said about reading the pharmacist's paper that came with the L-pak. (My doc calls it L-pak, and I hope it's not gonna be L for me as it has been for most of y'all.) Now I wondered if the pharmacist had even put one in. Went and looked and sure enough, there it was, and it said to drink plenty of water "to prevent the formation of crystals in the urine." No further info about those crystals or their side effects. Some words about bleeding but totally vague, like does drinking water cure bleeding?? Who knows?

That paper the pharmacist put in my bag also said that one of the side effects can be "excitement". I thought, that's my side effect, and I am very happy about that. Garage is too. Hubby is too. Life is good. Leva-pack is good for me, for us for the world.

Anyway, back at the puter, eventually I found y'all and your many stories of pain and suffering caused by Levaquil. But, lo and behold, NOT A ONE OF YOU HAS MENTIONED MY BLOODY SIDE EFFECT. That goes to show what drinking plenty of liquids can spare you. Save ya a quarter wasted on sanitary pads you coulda given your female guests. Save ya from washing blood out of your undies again. Save ya from worrying about whether to call the doc (pharmacist is home in bed by now and tomorrow is Sunday. It figures.) And whether to take another pill.

Sheesh, it's a slow business trying to type up my story for ya, now 11 and time for more water, I figure. Be right back again...ok. I see the bleeding continues but it's a LIGHT DAY.

Well, now I've read this whole webpage top to bottom, and I feel pretty worried about taking enough of this Levaquil stuff to get exploding tendons and total nerve damage and pain and suffering and crippling and insanity and death by anaphylactic shock if I take another one.

I probably will take another one, just being sure to drink plenty a water too. Excuse me a sec while I go get another, as it is now after 10....okay I'm back now.We'll see as time goes along about taking any more. And if I am a good scout, I should come back and provide the REST OF MY STORY in a few days.

I saw that someone here said that Cipro is a fluoxosomethingorother too. I don't know why the doc didn't pick Cipro for me today instead of the Leva-pak. Maybe the last drug rep in his office gave him some good lines about the advantages of L as opposed to C, who knows? Anyway, if Cip and Lev are in the same family, I must say that as a postal employee, I am ready to take Cipro at the drop of a hat if our new machines spot anthrax in the air where we work. Sounds like those postal employees who died would have survived if the docs had recognized what was wrong with them and given them the Cipro early on. At least, other people who showed up sick afterwards with anthrax exposure got Cipro, and most of them survived, I heard.

The upshot is that I hope we don't take away the fluoxisomethingorothers until we find somthing better. Law suit perhaps, but not to deny the life-saving drug from EVERYBODY because some folks have bad side effects. Instead, we should find out how to test each person for having trouble taking it. You know, put a little drug in with some of their hair and a little in some of their blood and a little in some of their pee and see if it curdles or grows sprouts or something to show how each patient will react to it. Then tell each one what to expect from the various drugs available for that person's ailment. Then the patient can decide which side effects he wants to sign up for or if he just wants to stick with his original ailment.

I have not decided whether I will take any more of these pills. I will observe my crochety side effect and watch for any new ones that may pop up before I make my decision each day. I am very very concerned about long lasting muscle and tendon pains. I have not been able to hike now for about 3 months due to loss of energy, strength, and confidence. And I sure don't want to miss 3 more months trying to get over exploded achilles, burning knees, seizures, or nerve damage etc.

As a postal employee, I never do any research into cures for ailments. I am fairly experienced with ailments. I cannot provide you with any good excuses for not seeking to find cures for our health troubles.

I feel lucky to have been born when and where I was. I waited until central heat, air conditioning, cushioned seats in heated, air-conditioned autos(spare me from buckboards on unpaved "roads"), and penicillan. That penicillan brought me through pneumonia in 1947. Had I arrived 5 years sooner, I doubt it would have been available to me. Hmmm, I wouldn't a been available to share my story with you folks this evening either. So I must say a blessing for all those who try to improve my health when I go to them for help with my various complaints. Sure, money may be highly motivating for some of them, but Donald Trump and Bill Gates found ways to make money without going into medicine or research and drug development or doctoring.

So far, that's my story, my red flag today.

May THE FORCE be with each of you as you search for the best solutions for your ever-new mind and body problems. May we seek wisdom widely and recognize that what used to work for us often won't work any more because our bodies keep changing. We are along for the ride and hope to make it as pleasurable as possible as we round each curve and surmount each hill.

God bless us all, each and every one.
Christmas is coming...Tiny Tim's words echo through the years.

I've only been on a few days and already experienced the flat soda effect... that's the whole reason for soda.. I like the fizz... not cool.

My doctor warned me about the tingling, it's a sign of low potassium, so she said to start eating more bananas... so no tingling yet.
Also consume a lot of water to reduce risk of kidney stones...

So far I've only experienced the flat soda that I know of..

Has anyone out there had an increase in urination? I started Yaz in Feb. and since then I've been peeing like a race horse. My OBY said it was probably an overactive bladder, typical for a peri-menopausal woman. I had tests for bladder infections and they read negative. I was in the middle of relocating my family across many miles and I just put up with the symptoms. Now I find out there is microscopic blood in my urine and I am scheduled for a slew of tests probing for tumors, cancers, polyps, etc. in my bladder and kidneys. My Dad had bladder cancer so I'm pretty scared. However, I am starting to wonder if there is a Yaz connection. I hate the thought of returning to periods where I couldn't leave the house because I was bleeding so much but all the risks here are scaring me. I don't have an OBY here yet but assuming I am not harboring cancer or an other disease (i.e., kidney stones) I think I'll go off Yaz. I already have horrible migraines and acne so I'm wondering if it will all get worse. My headaches are the same (2-3 times a month) with Yaz and my skin is better. It's been pretty good for water weight but as I said, I am in the bathroom way too much.

I began taking 10mg per day of Crestor on 19th May this year. I received the documentation regarding side effects and read it. After two days I had tingling pains in my legs and I was checked for further cardiovascular problems, and cleared. I enquired if Crestor may be the problem but I was assured it was not.
I had a CT scan and then subsequently an MRI of my lower back looking for restricted blood flow but after seeing a neurosurgeon this was ruled out as the cause of the tingling. There was some degeneration of the back but not serious blood flow restriction. At about this time the Crestor dosage was increased to 20mg. At this stage I had back pain but it was not thought to be related. I enquired again if it might be Crestor but was assured it most unlikely.
Pain in my back increased dramatically one night shortly after and was so intense not only could I not sleep, I simply could not get myself to think of anything else despite intense mental energy to try to do so. I was on the verge of calling an ambulance, but walking around and applying heat seemed to relieve it slightly and I lasted until morning. Doctor thought it was a locked facet joint and sent me to a physio. She helped considerably and I assumed this was the problem. However, the next day it returned. Upper body strength was fine but from the middle down was just plain sore. The physio worked on my back again, and suggested I get a back brace which I did and I struggled on with that as a help.
The pain shifted from my back to the top of my hip and I went back to the doctor to check my hip. He assured me the pain was on the top of the hip, not the groin area and was unlikely to be my hip. I began taking over the counter pain killers for the pain which was hitting about 8 out of 10 spasmodically. The physio was mystified and suggested it may be kidney stones, and so I went back to the doctor to check that out. He had already taken a urine sample which had no blood at all. The pain shifted to the hip and upper right leg. By the time I was able to see him, the pain was quite severe and I was sure it was my hip. He was not sure, but prescribed Panadine Forte for the pain and sent me for an Xray of the hips.
I was very distressed about this, as it appeared I would not be able to continue working. The hip Xray showed perfectly normal hips but the pain was even worse, by this stage in the right thigh. In desparation I saw the doctor again and agreed to try and “tough it out for a few days” using pain killers, another round with the physio, and as much rest as possible. The physio was so convinced it was not muscular but rather a possible kidney stone she sent me back to the doctor. While waiting to get to see him I began looking at the side effects of Crestor on the internet and after checking with the doctor I stopped taking it on Aug 1st to see what happened. Within a day I began to improve but I still thought it might be kidney stones (possibly a big one blocking a tube completely and therefore no blood) and my doctor ordered a CT scan of the bladder area which confirmed that both kidneys were working just fine.
Slowly over a week and a half the pain is completely gone, the back is fine, the hips are fine, the groin is fine and I feel so much more like living. I am now absolutely certain it is Crestor that has caused the whole problem. The docotrs have now prescribed Lipitor in it’s place, and I have the tablets but as yet I have not begun taking them. I am a bit fearful of doing so, but I will begin in a few days time. However, if I get any repeat of the muscular problems I have had I will stop immediately.
I decided to document this as I realise this is important feedback concerning a relatively new drug. I don’t know how this is conveyed to a national data base, but it seems to me this is a serious side effect that has very nasty consequences. Was it that my kidneys were objecting violently to the drug? I don’t know. But it caused me great distress and this is surely a concern.

I have had migraines for 4 years almost on a daily basis and nothing has worked. Finally started Topamax, the first week iI felt like i had a stroke, my speech was slurred, I couldn't concentrate, I was exhausted couldn't make complete sentences, numbness in hands and feet and every thing tastes bad., I had been on 4 pills a days to start so decreased to one-i believe it it 50 mg. worked well then headaches began again after 2 weeks, so increased to 2 then again in a few weks to 3 now i have had only 3 migraines in 3 months. Still have the numbness and taste aversion but I have never felt better as far as migraines. My new problem is I am having a lot of digestive issues including cramping and constant acidy, bubbly,gassy, bloating feeling and no gas x, pepto or anything works??? Is this a side effect or something unrelated??

I have taken Levenquin for years - so far nothing bad (at least that I have noticed). I have had cohn's, fibro, CFS, UTI, kidney stones, COPD (from having my immune system suppresed by crohn's treatments), diabetis (caused by Prednisone), high blood pressure alternating with very low bp (ranging from 234/142 down to 53/36), racing pulse then very low pulse (ranging from 156 down to 29 bpm) and some of these (pulse and BP) can be all in one day (both caused by Prednisone).

Thing is - I just turned 29. I have been dealing with these since I was 18 or so. I have often taken Levaquin with Prednisone and other antibotics.

The only thing that seems to concern me this time is extreme sweating - It is hot enough in the deep South without this med. I am noticing now that since the diabetis is under control (without meds now), I am very shaky and low sugars.

Also, if this causes racing pulse - I am in big trouble. I was given this med for a UTI, along with Prosed (which contains Atropine - from the Belladonna plant). Atropine was given to me in the hospital when I had the pulse crash of 29.

Just praying that I won't deal with any side effects like this.

Oh and I see insomnia- I am dealing with that enough now! If this is similar to Cipro - I should sleep well though LOL

I've been using the nuva ring for about 5 months now. At first my doctor told me that my body had to adjust, but I am experiencing more and more side effects with each cycle. I am experiencing:

severe headaches
brown dischard (the whole month)
depression (I don't care about anything or anyone)
moodiness (I am insanely angry. I think I could honestly hurt someone)
Urinary (kidney stones and frequent Infections)
No Sex Drive (I don't want sex, don't even want to think about it, its yucky!
Aches and Pains (back, neck, legs and chest)

I didn't realize all these symptoms were associated with the nuva ring. I was about to see a mental health professional, as I am scared I could hurt myself, husband, children, or someone. I have never been so angry in my life. I feel INSANE.

You know, it's very irritating when people post "STAY AWAY FROM THIS OR THAT" etc ... just because *they* or someone they know had a problem with it. I've been on Topamax for about 4 months now - up to 300mg/per day, only side effect is the metabolic acidosis if I overexert in the heat (which is damn annoying) - I haven't yet reached tharaputic levels because the weight-loss hasn't kicked in, so I'm liable to get close to the 800mg per day dosage. All this AND I'm prone to kidney stones to begin with! So please stop all the screaming about how freaking dangerous it is just because it didn't work for YOU, hell, pennicillin KILLS people too but you don't hear people screaming about how terrible it is, do you?

I took Levaquin 750 mg for 2 days. The first night it made me sleepy and drowsy. The second night I took it, I was high. I felt like I was a zombie. I sat in front of my computer rocking back and forward. And al I wanted to do while I sat there was take more and more and more levaquin. I wanted sit there and eat them like they were candy. That urge was so overwhelming. So, I hurried up and I flushed them down the toilet except for 3. Knowing that they were there, I wanted to eat those 3, so I flushed them.
That was the worst night of my life. I said to myself if this is how high suppose to feel. I don't ever be high.
This drug need to be taken off the market.

Hawthorne helped with my bradycardia:

In addition to the other link I posted about supplements that have helped me enormously during this time being on/coming off of Yasmin, wanted to share something that has alleviated alot of the problems I was experiencing with bradycardia (unsually slow heartbeat -at/under 60 bpm that became ectopic-where it would skip beats) because I think there were alot of women who have reported concerns/issues with their hearts.

I am still presently using this in tincture form along with schizandra and have noticed that the arrhythmia I was experiencing has almost completely disappeared. Here is some information about its healing properties:

Phytochemicals: Caffeic Acid, Hyperoside, Oligomeric Procyanid, Vitexin, Ursolic acid, Rutin, Flavonoids, Quercetin

Medicinal properties: Hawthorn contains a variety of flavanoids that appear to be responsible for the cardiac actions of the plant. Hawthorn has been used for heart cardiac insufficiency, bradycardic rhythm disorders and angina pectoris. Hawthorn increases the blood flow to the heart and restores normal heart beat. Hawthorn is also used after heart attack to help recovery. Hawthorn dilates blood and assists in reducing high blood pressure. Studies have shown that hawthorn increase the contraction strength and the stroke volume of the hearth. Howthorn is only effective if taken for a period of minimum six weeks.
Hawthorn flowers and berries are astringent and are used in decoction to treat sore throats and digestive ailments, such as vomiting and diarrhoea. Hawthorn is also used as diuretic and to treat kidney stones.

Other facts: Hawthorn was first mentioned by the Greek herbalist Dioscorides during the first century AD. It went out fashion as a medicine until the 19th century, when it was used to treat heart diseases. Hawthorn originates from Europe and Western Asia.
_________________
Yasmin 12/05-8/06. Side Effects: Hiatal hernia, vision changes, congestion ears, chest pains, heart murmur, palps and bracycardia, ectopic (skips beats), melasma, bronchitis. B12, Folic Acid deficiency.

Vitals--35 yrs old male, 210lbs, 5'6". Three years ago, I had an agruement with my wife over dinner and brought on stress resulting in soreness in my left arm. I went to the hospital and stayed there for five days. I had an enlarge heart and a BP of 215/110. I didn't have a heart attack but was told to change my lifestyle. I was initially placed on atenol(however you spell it) but my doctor told me lisinopril was better.

I have family history going against me, my father has HBP and has had two mild heart attacks, 47 & 57 currently he's 61 and was treated by angioplas for those heart attacks and his father had four heart attacks and died at 85. Diabetes in all over my family, only in seniors.

Here's my deal, I have anxiety issues, I'm just a high-strung person. Since the two years, being on this stuff. I've noticed weakness in my left elbow at times, tingling feeling, and sometimes in my legs. I've developed this year, pain around my gall bladder and stomach pains. I don't have gall stones was checked out. I have also after six months of being on this stuff developed gaut in my big left toe, where I couldn't walk for a week. I have mini-attacks of gaut from time to time. And to add to the misery, this week, I passed two kidney stones.

I do feel tired all the time and my sex drive has weaken a bit, and let me tell you, my wife is hot and I love her to death so that's not the problem. I do get depressed from time to time. I don't get the cough as everyone has stated, but two years ago I did get pnemonia over the summer.

It's been a rough go, but let me offer hope to all. I've been trying to lose weight but been holding it on for some reason. I would recommend the most sensible solution, and we know what it is.

1. Diet--No matter what--fast food is crap-repeat after me-fast food is crap. Soft drinks are bad, yes even diet soda. Drink water and water and more water. Water is not boring when you cut fresh lemon or lime slices and put them in your glass or pitcher. Fruits, Veggies, low-sodium foods(throw away the salt shaker). Eat plain oatmeal with fresh blueberries in the morning. Zero fat yogurt perhaps as a snack. No meat. As much as I love prime rib, I had to give it up. Maybe meat once a month, or a small portion the size of your fist.
2. exercise--this is a no brainer. Just walk on a treadmill, once a day for 10-15 minutes while watching TV. Increase the minutes as months go by, but check with your doctor.
3. mediation--Half a hour daily, clear your mind, pray to God, or think about Hawaii, whatever it takes to relax.

Take care all,

John

My Urologist prescibed this drug for me after having kidney stones removed, he also said I had a slightly increased prostate.
The side effects of this drug are horrendous. I've had dizzines, sore throat, running nose, constipation, insomnia and by far the worst of all is the itching. I have scratched until I have drawn blood. Anti-histamines give no relief. The only way I have obtained some relief from the itching is by holding ice cubes to it. I will never take this drug again no matter what!

hi everyone. I was put on yasmin in june for cramps. It works great on my cramps and my cycle. The only problem is my cycle is so light that i cant use tampons but i hate pads

The problem i am having is ever since i have been put on it i have no sex drive at all. I dont like it if my boyfriend touches me in a sexual way, but the minute he leaves for work i am all over him. Everytime we try to have sex it burns and is really painful for me. It got worse after i had kidney stones and surgerys. My boyfriend and i havent had sex in 4 months. I love my boyfriend and he is patient but i know he misses sex.

I get more sad for no reason and a medicine i was put on for paying attention in college it would only make me sleep 3 hours. My doctor is putting me on a medicine to control my anixous feelings.

My boyfriend wouldnt believe me until he read this site about yasmin and sex drive. I feel really bad that i dont like to be touched and all i want to do is sleep.