Urge symptoms and conditions

To a small population of people, this drug has an immediate detrimental effect to mood. In my case it caused a strong urge to commit suicide within 5 hours. The doctors all said it was impossible. I was inclined to believe them since these drugs are not meant to be effective for days after treatment initiation. However, my reaction cannot be ignored or dismissed.
The prescribing physician (Robert Moffat, MD in Longmont, Colorado) suggested I try it again because he was so certain it was my problem. I did try it again, and I had the same reaction. And so I filed a complaint against him.

Incidentally, I was not taking this medication for depression. It was for nocturnal panic attacks.

I am not saying people should not try it. I just suggest that FOR THE FIRST 24 HOURS WHEN YOU TAKE THIS MEDICATION YOU SHOULD NOT BE ALONE. It probably works great for some. Also see ******

After just one dose of Ambien I experienced my 1st panic attack. I was 38 weeks pregnant and my physician prescribed it since I was not sleeping for more than 30 min at a time because of the urge to urinate as the baby was compressing my bladder.
I took it again thinking that maybe it wasn't the Ambien and I began having daily panic attacks. These episodes didn't last minutes as do regular panic attacks they lasted 4 and 5 hours. My husband, a physician, noticed that my heart was not beating rapidly as it usually would during a regular panic attack, I was actually having bradycardia (low heart rate). He still didn't put the side effects I was having and the Ambien together. After being seen by multiple physicians I was admitted to the hospital for these severe attacks and after having an echocardiogram, a CT of my brain, and multiple lab draws a psychiatrist finally examined me and took my history realizing these panic attacks had never happen prior to my taking the Ambien. He took me off the drug and within 48 hrs this awful hell started to lift. It took me a year to get over the post traumatic shock from this horrible 4 weeks of my life. I gave birth to my newborn and was unable to care for her or even myself while experiencing the side effects caused by this hellish drug.
Meg in Sugar Land

I got the Mirena in Jan 2008. My periods were lasting 2 weeks long (light) every 2 weeks. I had EXTREME fatigue and actually had to go in to take a pregnancy test because my last period came late and I had ALL the effects of pregnancy (had 1 in 2006). I had nausea so bad I actually had to miss work because I felt the urge to be sick, but I couldn't get sick. I had it removed on July 7th, 2008 and felt a difference as soon as I left my doctors office, but now I'm faced with another dilemma. I may be pregnant again! My period never came after I had it removed and have the feeling of being pregnant. My doctor finally told me that my body thought it was pregnant and is going through the motions. I have to wait 2 weeks before I will know if I am or not! I NEVER SHOULD HAVE GOTTEN THE MIRENA AND DO NOT RECOMMEND ANYONE ELSE DOES EITHER! I have a hard time remembering to take a pill everyday, but that is much better than the side effects of this thing. I agree with a previous posting, IT IS EVIL!!!!

The nausea is tolerable, generally short-lived as long as I eat prior to taking the Chantix and drink plenty of water.

I have a sense of...fogginess....detachment, while at the same time, seem to sense clear hidden messages in the way people look at me, in what they're saying to each other, and to me. Yep, it's probably paranoia.

The nightmares are horrible. I dream specifics about deaths of loved ones, in horrible detail. I also awaken at least once a night gasping in terror, unable to get a breath.

The thoughts of suicide are strangely comforting and don't seem wrong at all. I'm depressed, but comforted knowing that I can end it if I really want to. Bizarre and I know it on some level at least.

I'm bruising easily this time. I mean REALLY easily. A small bump results in a hard, raised, dark bruise.

I developed a rash on my stomach that's been there for 3 days but seems to be clearing today.

This is my 2nd time taking Chantix and I'm 3 weeks in. I had the same symptoms last time and expected them this time. I'm smoke free but plan to continue with the Chantix as long as possible. The urge to give in and have one cigarette is too strong post Chantix. I tell myself everyday that the thoughts are NOT me, and that I can let them come and not act on them because it's the drug, not me.

I have Bipolar Disorder and was put on risperdal for 3 weeks. 3 weeks only! I had to be taken off of it. It was an amazing drug that really helped me with what I was going through, but it made me eat like crazy! It felt like I was a wild animal when food came around. I would smell someone elses food and be unable to resist the urge to eat soooo much or think about anything other than their plate. I got so embarrassed by the way I behaved when I was around food that I began to eat in private. They put me on ability now and I feel just as good as when I was on risperdal but now without the food problems.

I got Mirena put in on July 5, 07...never had a child but Dr. said since I was 36 and not planning on having children, Mirena was a good alternative to the pill which I had been on since I was 19. On the pill I had very light 2-3 day periods and with diet and exercise, could lose weight. Now, almost a year on Mirena...the only good think that has gone away from when I was on the pill is the migrane headaches that I was starting to get on a monthly basis...but, in their place...I have gained weight, tired, have acne, cramps erratically throughout month, never know when my period will show up...some months it does not, some months it lasts 4 days (like last month), and I always feel bloated - esp. in the abdomen. I've even wondered on occasion...am I pregnant?? why do I feel so bloated?? One other weird thing, since I started running this year, I get this weird sensation that I have to go empty my bladder...this also occurs while doing intense stomach crunches...but it is not incontenance..nope never have bladder problems...it is just this funky feeling - sometimes almost a burning feeling around my uterous. Have not seen anyone post this - but it did not happen before Mirena when I ran or did sit ups...now it does - doubt this is coincidence.

Some of these symptoms truely could just be simply the result of ovulating again - that is what my Dr. told me...that on the pill I never released an egg...so now my body was getting used to ovulating again. Well...if that is the case, I just can not stand it anymore...I get it removed June 26th - next week so hopefully I'll be able to post back that these symptoms are gone or have removed. Going to go on the pill again...which has its own side effects...but I sure did not have as many when I was on it. Husband has offered to go under the knife to take care of him...but I'll see how the pill does again. Hoping to reclaim my life and actually lose weight as I've been dieting and exercising while on Mirena to no avail!

I guess I owe my boyfriend (possibly ex-boyfriend now) an apology. I'm in my first week of using the NUVARING and already I've engaged in some erratic behavior. I cry several times a day and feel the urge to throw screaming fits. I am 29 years old and in no way am I a tantrum-throwing type of woman. My 2nd day on NR I became extremely angry with my boyfriend for talking to a girl and I left him to find a ride home from the club. I have been someone completely different from myself these past few days and I couldn't figure out why. I've also been very drained and sluggish. I am so glad I found this page. So I'm not bipolar, NUVARING just makes me crazy.

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've been taking Budeprion for the last 3 months and the only pleasant side effect has been that I've lost weight. The reason I've lost this weight is because from the minute I wake up to the minute I fall asleep, I'm nauseous and have awful headaches. I have to take at least 4 advils a day just to get by. Even more terrible is that I've started having the urge to hurt myself, something I've never had on any previous medicine (I've tried 3 different ones before this) and the bulimia that I thought I'd stopped is worse than ever before. I'm in college and can't afford to pay for the name brand. I don't know what to do.

I started taking Yasmine in 2005 and almost imeemdiatley I started to have severe anxiety, depression, no sex drive at all and worse of all extremely bad migranes especially a few days before getting my period and during. My life had to be put on hold when I had my period because of the migranes. I stopped taking the Yasmine 3 weeks ago because I just couldn't take the migranes anymore. I have noticed I have gained some weight, my skin and hair feels alot oilier, and my hair has been falling out more than usual which is kind of freaking me out, don't have mood swings. My sex drive has gotten better which is a relief. I still don't know if my migranes will have gone away during my period. I'm just curious can anyone tell me if these side effects (hair loss, weight gain, oily skin) will go away after a few months.
When I went off another type of pill I actually lost weight, why is this one different?

I started taking two 160mg tablets of sulfameth a day about a week ago in conjunction with prednisone and hydroxyzine for a bad case of contact dermititis. Yesterday I woke up with a crazy fever, pressure in my sinuses and headache. I got off work and went to sleep at 5:30pm. Around 9pm I woke up covered in hives. The fever had broke, but this was a new beast. The hives started out all over, but there were not many. Over the next 24 hrs they spread so that now I am mostly a giant red splotch. It itches like hell and for some damn reason I feel wired. I can't get to sleep. I keep pacing around.

I went to the ER and they said it was probably the sulfameth. They told me to discontinue use and put me on a higher dose of prednisone, zantac and diphenhydramine.

I am almost sure it was the sulfameth. I have been on prednisone before without anything like this happening. I have never taken the sulfameth before this and I rarely took the hydroxyzine they gave me so I doubt it caused it.

The reaction to the sulfameth is seriously 100 times worse then what they gave it to me for. I would rather have just not gone to the doctor and suffered through what I had before than deal with this. It's a sleepless, itching hell. I will never take a sulfa drug again.

I can only wonder how bad it would have been had I not already been on prednisone when the allergic reaction hit. So 24 hrs into it and the hives are getting worse. Hopefully the prednisone and benadryl will end it soon.

I have posted before but wanted to update. Singulair ruined my life for nearly 2 years, but I did not realize it was the reason until about 2 months ago. About 4 months after being on singulair, I sought treatment for severe depression and anxiety. My docs/psychs thought that it was a delayed reaction to the death of my father a couple of years earlier, so we did lots of therapy and 3 different psych meds trying to help me adjust. After all this (and one suicide attempt), I was finally just starting to accept that I was a miserable excuse for a human being, and I should get used to the fact that my life was going to suck from here on out. Then, I developed GERD and could not see my regular doc. The new doc told me to research all my meds (I was taking FOUR a day at that point, including the singulair...I am 27...) to find out if any could be the cause. That was when I found out what singulair can do, and that it could be the cost of my problems. My doc checked my charts, and sure enough, I started taking it shortly before I developed all of these "psychological problems". I've been off singulair for 2 months and my psych meds for a month (had to wean off). I finally feel like myself again after two years of hell!!!! I still have a slightly foggy head and problems concentrating sometimes, but what can I expect? I've been on mind-altering drugs for a couple of years. I hope things continue to improve. Never again will I take any drugs without doing *thorough* research (not just reading the hand out that comes with it..when I started singulair, there was no information about all these problems on the leaflet).

Strattera was terrible. I do not recommend this drug or any other drug that just came out. Adderall and Ritalin and such might be more likely for abuse but those have been around for years and years and at least you know the worst that you can happen to you.

Strattera made me depressed and tired. Made me concentrate even less than normal. My heart rate would be at about 125 beats per minute and I'd be sweating buckets when normally I'm cold easily and prefer hotter climate. The next minute I'd be freezing cold with chills all over my body. Nausea was extreme as well as the urge to vomit. The thought of food made me sick. It gave me blurred vision.

I wasn't able to do anything but sit at home and hope it would pass.

DO NOT TAKE THIS DRUG.

Thank God for the internet. Seriously.
I am really trying to give Mirena a fair trial, however, some of the side effects are worrying me.
I have been having hot flashes (I just turned 40), my mood swings are disturbing, and my breakthrough bleeding happens often without warning. I also have the weight gain. However, to be fair, I don't know that I can really attribute my weight gain to Mirena. This is pretty important; has anyone else out there experienced addiction feelings? To cigarettes? Alcohol? I have never had strong urges for drugs and alcohol, however, I have lately... Again, can you really say that Mirena is to blame?
The upside is that my periods are, blessedly, light. This is a definite upside for someone who had heavy periods. I also don't feel the strings, nor does my husband. After reading some of the postings on this site, that concerns me.
Thank you.
MaryKay

Cystex relieves my pain, burning, and frequent urge to urinate. I also feel that it helps control the infection. While taking Cystex I noticed that I do not have regular bowel movements. After taking this medication for a few days I always need an enema.

After reading many of your experiences, I feel the urge to tell my story. I got my Mirena put in back in June 2007. My doctor had been encouraging me to try Mirena because I was having such problems with my periods while on the pill and I had tried different types and brands and nothing seemed to be helping me. So, finally after about 2 years of her telling me to try it, I did. Since I have not had children, she said I needed to have it put in while on my period so that my cervix was more open. I called her on the first day of my next period and got it put in. It was very painful to be inserted, and the horrible cramps lasted about 48 hours, but then went away. My period also got worse during that time, but then completely stopped two days later. I didn't get my period again until two weeks ago, which stunned to me. My doctor had said that I may have spotting the first couple months, but then that would stop and I would no longer get my period. Since it has been 6 months since I've had it, I thought it was very odd for me to suddenly be getting my period again. Along with the actual menstruation, I got the cramps, headache, bloating and everything else wonderful that comes along with a full blown period. I only had menstruation for 3 days (the shortest period of my life) but the cramps have continued constantly for the last 2 weeks. I decided I should look up the side effects of Mirena to make sure it wasn't abnormal. I got the same information from their website as I did from the pamphlet I'm sure we all got from our doctor - saying that only a very small percent of woman have any side effects at all. So, I thought I was making things up. But the more I thought about it, the more I realized all the things that have changed for me since I got it put in. That's when I stumbled across this site and found I'm not the only one and I'm not imagining all these things! I gained 30 lbs in the first 3 months - I blamed it on stress because we had just put our house on the market, however I had never in my life gained THAT much weight in such a short period of time. I am now over 200 lbs and I'm only 5'3". I have been desperately trying to take the weight off, but it won't budge and I'm only continuing to gain more. It is getting to the point where my weight is starting to cause other health concerns. Also, I have not had a single good night of sleep since I've had Mirena. I again blamed it on stress (but to be honest, I've lived through much more stressful times in my life without the tremendous weight gain and insomnia). After several weeks of trying OTC sleep aids, I went to my doctor and she gave me a 10 day supply of Ambien. The first 2-3 nights it helped, but then that also stopped working and I was back to sleepless nights. I found there is an herbal supplement that helps me sleep, but it only works for a few hours at a time, which obviously is better than nothing. I have also had cramps on and off throughout the last 6 months, sometimes they are very sharp stabbing pains that make me buckle over in two. I have also realized that I may be having depression - I don't feel suicidal, but I get very down very easily and stay that way for much longer than I ever have. I have actually had such horrible down days that I've called my husband at work crying and begged him to come home. I have never in my life done that until Mirena. I'm sure that I have more symptoms, but I have been able to persuade myself that they are "normal" or explained them away otherwise. I think that Mirena and the OBGYNs must be in cahoots. I was not warned about any of these problems - I was only given the small pamphlet and told it was so wonderful. I think there are a lot of other women out there experiencing all these side effects but their doctors are telling them it's normal or blaming it on something else. And they aren't realizing it is Mirena that is causing all these problems! I have an appointment for next Tuesday to get mine taken out and I cannot wait! I am finally going to be able to sleep again!

I am getting mine removed FRIDAY!! And Friday can't come soon enough. I am kinda bummed tho for having to go back on the pill but I can't hack this ANY LONGER!!! One of my friends works for a GP and I went to him because of some of my side effects. The flu like symptoms minus having the flu (had it for at least 2 to 3 mos now) NO sex drive (causing trouble with my marriage. Hubby is taking it WAY to personal), swelling in my hands, feet, legs, and face. (my face will feel flush and BAM I'm swollen!!) VERY BAD MOOD SWINGS!!! Very Bad isn't the word for it!! There are no words to explain my moods!! ANYHOW..... I sent this to my friend to read and she pulled it up at work. Well the GP said that this isn't a reliable place to go for information on the side effects. "There are NO positive side effects to anything." Which is true BUT he seems to think going to Web MD or some sight like that is more reliable than here. And that this sight shouldn't scare me and he wouldn't urge me to have it removed after reading this. (OH YEAH I forgot to mention joint pain, I have HORRIBLE joint pain in my hands, wrists, elbows, knees, ankles, and feet. The worst of it is in my wrists and elbows) Back to what I was saying. To that (this sight not being reliable) I say go to Web MD and post there too! I pray that I can get back to me after this comes out!! I hope it don't take too long either! I MISS the old me and HATE the new me!! But FRIDAY HURRY UP AND GET HERE. And for anyone who has had it removed........ anything I should be repaired for??? Thanks for your time!

I have had the Mirena in for about 8 mos.I love having no periods.But that is the only good thing I have found!I am 5.7" and weigh 186.I was 145 before I had my son.After I had him I was going to the gym every day and even had a personal trainer.It seems No matter what I eat good or bad I cannot lose the weight.I thought maybe it was just because I had a child, but Ive found other woman are having the same problem.Just cannot lose a pound.Until they get it removed.Before I got the Mirena I was already pretty emotional but now its ten times worse!And the acne, OMG!!! I have it so bad I am using face stuff everyday nothing is working.I have it on my face,arms,back and butt.Absolutely hideous.I feel like crap.I cant even walk in front of my husband without thinking he is thinking something bad about how I look.This has upped the depression,I am feeling like everything is screwed up in my life (but its not) its just my perception right now.I have found that the doctors look at me like I am lying to them, like its all in my head.I should print everyones blogs and show them to my doctor! It makes me mad that the medical industry will present something so perfect and screw how it effects peoples lives.I had to pay cash for the freaking thing too!That makes me even more pissed off.I want this thing out so bad.Now my husband and I are talking about vasectomy because its much easier then a tubal.Its sucks that we had to come to that.

I had my Mirena IUD put in May 1st of 2007 and all the side effects that came along with it......the constant spotting, acne, itching breasts (which I thought was due to new bras that I had just purchased), nausea, depression (which I had to go back to taking Wellbutrin), no energy; tired all the time. My biggest side effect which I have not found any others to have is Allergies. I know it sounds crazy, but I have never had problems with allergies until a month and half after getting the IUD, extreme allergy symptoms, swollen glands, neck pain, very shortness of breath; to the point that I was down for a whole day here and there, I am having to take Allegra; had to get a steroid shot. Now that it is cold, I thought I would be getting break from the allergies, nope. I joined a gym hoping that it would help in giving me energy, nope.........I have talked to my Dr and the nurses that work with my gyno and they act as if I am making this stuff up. It is very frustrating when you know that your body has done a complete 360 in the wrong direction and everyone seems to think your crazy.

Well I am having my IUD taken out as soon as I can!

I was on Yasmin for the last 6 months before this one. My doctor was out of the Yasmin and gave me Yaz to try. After being on Yaz I have finally realized something. While I was on Yasmin I could NOT stop eating. I would eat a full dinner and then ten minutes later, even though I knew that I was full.. would go into the fridge and eat something more.. and then an hour later.. and so on. I have gained about 30 lbs. I just thought it was some weird depression I was having since I am slightly depressive anyways. Well.. now that I am on the Yaz....I feel completely different.. I do not have the out of control urge to eat, eat, eat. Finally I feel normal again. I am also not bloated with my stomach sticking out like before.. so I don't feel so disgusting physically. The Yaz is having its own little side effects...but for now I am doing a "wait and see." This is because they put my on Yasmin to help me out because I have a high testosterone level and it is supposed to not increase that like the other pills do.. it uses a different kind of androgen.. I definitely do NOT want to go back to the normal testosterone pills since they cause my testosterone levels to surge over the "normal" limit. Sigh, hopefully Yaz will work.

I have been taking Flomax for 5 days. My urine flow was about the same for the first day or so, and I believe I have been getting up as many times as normal. The urge to go seems like it is less, however.

The first day, I noticed no sperm (only clear liquid) after ejaculation. this happened twice. the rest of the days were normal.

I do notice that I get dizzy sometimes after standing and feel like I have sortness of breath.

I took saw palmetto for a year and it is worthless (one pill per day), as my doctor told me it would be..

Never really having stuck with any other type of birth control before, I started using the NuvaRing about 6 months prior to my wedding. I had consulted my Dr. about it asking what would be ok for me knowing I am forgetful and didnt want to take the pill everyday. He said the NuvaRing was my best option and proceeded to tell me some of the pros and cons about it. As a very persistant bride, I didnt really listen, just said "Great, sign me up!". Well the months go on and I never really had the urge to be with my soon to be husband, I just assumed it was because I was too involved with the wedding plans and everything else. The wedding day comes, everything perfect as I wished, then there was the night of the wedding... NOT everything I wished, I was "tierd", but I did what your supposed to do the night of your wedding and got practically nothing out of it. The entire week of the honeymoon, I bet we had sex MAYBE 5 times, 5 times!!! Thats how much you should be having in one day on your honeymoon. I just ignored it and figured it was the sun and alcohol, big mistake! We have now been married 6 weeks and probably have sex twice a week if we are lucky. My sweet new husband has been very good about this, any other guy would probably kill their wife by now for this. Finally, our solution, one of my best friends who is a nurse was listening to me wine a complain about all of this. I mean, what girl who loves their husband and is attracted to him wants to have no sexual desire, not me! So after she finishes listening to me, she starts to tell me all of the horrible things she has heard about the NuvaRing, she in fact was about to start on it before she heard all of the negative symptoms. She has heard of many relationships falling apart due to this "oh so wonderful" birthcontrol. In fact, some people have said they used to have sex 5 to 6 times a week and once they started this it went down to maybe once or twice! Not how I want to live my life or marriage. I suggest to all of you out there that are either researching the NuvaRing or have been on it, DONT DO IT!

My husband has been on Advair for about 1 month now and he is 24 years old. He has been experiencing worse asthma attcks then ever with constant mucus. Chest pain and pain in his pinky,unable to sleep at night at all. His eye sight was perfect but rescently he had to see an eye doctor for bluriness they perscribed him glasses.Will his eye sight stay blurry for good does anyone know?How can they give this crap out to people without warning them first about side effects?My husband even asked his doctor about side effects before taking it and the liar told him there are none. What kind of world has this become when Doctors can perscribe death in a disk? DO NOT TAKE IT EVER I URGE EVERYONE PLEASE FOR YOUR SAKE AND THE SAKE OF YOUR LOVED ONES.

I've been on various pills over the past 8-9 years, including OrthoNovum, OrthoTri-cyclen, Orthocyclen, Estrostep and others. I basically switched every year because I had constant break through bleeding.

By contrast, Yasmin is by far the worst birth control I have ever been on. I'd been on it around 2 years, maybe longer. I am a level-headed, career minded woman. About a year ago I started to suspect I might be bi-polar or depressed.

Here is a list of the side-effects I had while on Yasmin that have disappeared since I stopped taking it 3 months ago:

-Depression
-Suicidal thoughts
-Paranoia
-Anxiety
-Nausea
-Decreased libido
-Intense Anger/Rage
-Irritability
-Increased thirst
-General disinterest/lack of motivation
-Acne
-Break-through bleeding
-Irregular periods
-Overly sensitive/swollen nipples
-Yellow discharge

I only had the above symptoms during the time I was taking Yasmin, not before and not after. This stuff is vile.

If you don't have any side-effects from this pill you are lucky. But I still urge you to pay very close attention. It is very easy for these symptoms to slowly grow over time until one day you wake up and don't even recognize your own self.

Since I stopped taking hormonal birth control I feel normal again, which by comparison means even the worst day is 10x better than a single day on Yasmin.

I had been on Yasmine for about two years with no complications until last week. Last week my heart began beating extremely fast just while sitting at my desk typing. Later on in the day my chest began feelign tight and I had an "anxious" feeling in my upper body. At the same time my lower body felt completely weak- as if my legs could not support my body weight if I were to stand. Evenso, I thought nothing of it and just assumed my normal one cup of coffee just so happened to have a strong effect on me that day. The next day the anxious feeling and weakness had subsided but my left arm and hand were tingling. It felt as if they had fallen asleep and now had that "cotton" feeling. The next morning I lost all feeling in my left hand except for my first three fingers. This is when I began trying to figure out what on earth I may have eaten, where I had been, had i drank too much coffee, etc.

I rarely drink alcahol, don't smoke, have no family history of heart problems, etc. I don't take any other medications, I don't take vitamins, I dont eat strange foods, and exercise regularly. The only thing I could possibly change is my birth control. I immediately quit taking Yasmine and all problems disappeared in two days.

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