I don t care symptoms and conditions

Hello everyone,

I have been feeling certain things lately so I thought "let's see what Google thinks it is". I typed in "bloated, tired, swollen legs, increased breast size" and the first site that pops up is this website. I actually thought I might be pregnant because and was surprised to see "Yasmin Side Effects" instead of "signs of pregnancy". I have taken Yasmin for almost 7 straight years. I was off it for 1 summer and probably one other month total in that whole time. I haven't really noticed any huge changes until recently and, like I said, it hadn't even crossed my mind that the things I was feeling could be from Yasmin. First of all, my breast won't stop growing and are so, so sore. I actually just bought my first D bra tonight, after being a C since probably my Junior year of high school. My legs and specifically my calves tend to feel extremely tight and stretched lately. I thought this was from running & exercise in general, yet I've exercised intensely & frequently for 4 years and this is a recent feeling for me. I have noticed for about a year that spider veins have started appearing on my legs. I thought I was just inheriting this from my mother, who has a lot of spider/varicose veins. My sex drive has definitely decreased significantly over the years I've been on Yasmin, but again, I thought this was normal or "just me". I go through periods where I have quite an appetite and can eat bad foods yet not gain weight. Then I go through periods when I seem to have the same eating patterns as normal and I'm exercising normally as well, yet I always feel bloated and fat. Plus, I have no appetite during these times. I also go through cycles where I have horrible stomach issues (I get a "bubbly" feeling, have had really bad cramps on occasion). I thought this was a side effect of coffee but now I'm wondering...

I get my period next week and then I think I'll stop taking Yasmin to see if any of these problems subside. Does anyone know any type of birth control that doesn't cause side effects?

Good luck to everyone!

IT IS GOOD TO KNOW I'M NOT ALONE, LIKE ALL OF YOU I THOUGHT I WAS GOING CRAZY AND SO DID EVERYONE AROUND ME. I'VE HAD MY IUC SINCE JUNE 3, 2008 AND I'M GETTING IT REMOVED IN 2 DAYS, AFTER SEEING THIS SITE. I GOT ON THIS SITE LAST NIGHT BECAUSE OF THE SEVERE MOODS SWINGS AND DISCOVERED ALL MY OTHER PROBLEMS THAT I WOULD HAVE NEVER THOUGHT WERE EVEN LINKED TO ONE THING LET ALONE MIRENA WERE THE SAME PROBLEMS I READ OVER AND OVER ON THIS SITE PLUS A FEW THAT WEREN'T ON HERE. I'VE BEEN HAVING PAINS IN MY FINGERS, TOES, AND BREASTS LIKE I'M BEING JABBED WITH NEEDLES, JOINT PAIN SO BAD I WOULD FREEZE UP, NAUSEA, FELT LIKE I WAS PREG. TOOK 3 TESTS ALL NEG., HEADACHES, SINUS TROUBLE, NERVOUSNESS SO BAD I FELT LIKE I WAS SHAKING ON THE INSIDE OUT, PELVIC PAIN, BACK PAIN, ITCHY SKIN AND MY SCALP ITCHES SO BAD I'VE HAD MY HUSBAND CHECK ME FOR LICE SEVERAL TIMES, IT'S HARD TO BREATH AT TIMES, HAIR LOSS, PAIN DURING SEX, AND NO DESIRE FOR SEX AT ALL. THE MOOD SWINGS ARE THE WORSE, I WAKE UP P-ED OFF BEFORE I EVEN OPEN MY EYES, I HAVE NO PATIENCE AT ALL, I DON'T CARE TO TALK TO ANYONE, I TREAT MY HUSBAND LIKE I HATE HIM. I HAVE A 17 MONTH OLD AND A 4 MONTH OLD THAT I HAVE BEEN TRYING TO HAVE FOR 15 YRS., 10 YRS. OF NOTHING AND 7 MISCARRIAGES AND EVER SINCE I GOT MARENA I HAVE FOUND IT HARDER AND HARDER TO DEAL WITH THEM. BEFORE I GOT THE IUC MY YOUNGEST ONE CRIED ALMOST 24/7 AND I HAD NO PROBLEM DEALING WITH IT NOW SHE HARDLY EVER CRIES AND I GET FRUSTRATED THE MOMENT SHE STARTS. I HATE FEELING THIS WAY, I FEEL LIKE A TERRIBLE MOTHER, WIFE, DAUGHTER, AND FRIEND. I CAN'T WAITE TO HAVE IT REMOVED.

I'm almost 25 years old and just had my 2nd child in February. I'm diabetic and also have heart problems and my doctor HIGHLY recommended Mirena. I got it in April 2008. For awhile, I didn't realize how tired and moody I was. Then my husband started commenting on how I never get up in the middle of the night anymore when the baby wakes up, and it's always him doing it. I told him that I was always completely exhausted, and thought maybe it was from all the bleeding I was experiencing. Since I had it put it, I bled for over 2 months. I also started experiencing migraine headaches, severe cramping, and hair loss. I could shower and wash my hair and look at my hands and see large amounts of hair tangled around my fingers. I called my doctor about the excessive bleeding, and they said it's "normal" and will get better. I kept telling myself that... "this can only get better". I also haven't been able to lose a single pound since I started the Mirena. I stay at a consistent 167 pounds (LITERALLY). No matter what I did, or how I ate, I wouldn't gain or lose weight! So, I'd finally had enough with the headaches, the extreme fatigue, and inability to lose weight. I went to my primary care physician and they did blood work to check my thyroid, my liver, kidneys, blood sugars, everything that would typically cause these symptoms. Everything came back normal. So my doctor said it could be that my pituitary gland is enlarged. So I had to do a CT scan and a sinus scan. They told me that I have a sinus infection and gave me amoxicillin. Well, obviously that didn't make most of my problems go away. I'd also been getting into a lot of fights with my husband over the stupidest things, and I didn't even know why! So I decided to take the Mirena out. When I called my dr's office to request to have it removed, my nurse's exact words were "I speak from experience..it gets better" I told her I don't care, I want it out. And that was that. The SAME night after I had it removed my husband commented on my behavior...that I seemed happier and more energetic. And today is even better! I feel like a whole new person! Ladies... if you are experiencing these effects, get it out. It's not worth changing your life around. Good luck to everyone.

I'm a 22 year old newlywed and Yaz has been a nightmare. I was on Diane when I was 16 for a year for cysts on my ovaries, and after my period became regular I stopped it... Cysts came back at 19, took Yasmin, and cleared up again, it also helped with my acne. I wanted to get back on the pill for birth control purposes before my wedding, so I started September 2008. The wedding was in December 08, and about a month later, the side effects started to show up. My eyesight (previously 20/20) had gone back 2 points. I was always very slim, but I immediately noticed my bloating, and by the third month, I had gained 15 pounds. I became a miserable mess, irrationally emotional and anxious. But the major side effect of this poison as I like to call it was something that affected my marriage. Before the pill it'd be very very easy for me to get aroused/wet/in the mood/. Now I am dry, no amount of foreplay will get me wet, and this has lead to bigger repercussions. Due to the dryness, there was of course a sharp pain with intercourse. After trying for so long, and growing more frustrated, I developed a condition called vaginismus, where the vaginal muscles involuntarily clench up and become tense right before intercourse. No amount of trying and coaxing and trying to relax will help, this has become another condition altogether that needs treatment and therapy. I was becoming more and more emotional due to the buildup of these side effects. and geting even more frustrated by my doctors telling me its the 'best pill around'. I decided to stop the pill on my own cold turkey. I was on Yaz from Sept 08 till July 09 and I'm slowly getting my old self back. Its a process that takes time, but this was the best decision I've made. Nobody deserves this kind of distress over a stupid pill. As others mentioned, my period was a lot lighter but with a different and dark, sludgy consistency on the pill. I'm about to start my second natural period off of Yaz and I don't care that my periods are heavier and more natural now, with PMS discomfort. I'd rather live with that than unnatural hormones that almost ruined my life.

DON'T TAKE THIS PILL!!!!

I've been on Singulair for more than a few years now. I'm 43, with exercise and allergy induced asthma.....but mild. I also have VERY bad allergies. Talk about being allergic to EVERYTHING outside....that's me. I also suffer from migraines and depression. I've been on every antidepressant out there....still depressed. Now I know why...Singulair. I've tried tons of migraine meds....and I'm wondering if some of my side effects are really from Singulair. I'm moody, I don't care about other people's feelings like I used to, I snap at my kids like crazy,I cry at the drop of a hat....at stupid stuff. And now I'm thinking that my joint pain in my hips is from Singulair. But Singulair was my miracle drug for my asthma and a huge help to my Allegra D for my allergies. I'm asking the doc for an alturnative drug. As soon as I get it I'm off Singulair. ADIOS!

Also reading other people's side effects... when i started the pill i had my period for a month and a couple of days.... THAT ISN'T NORMAL.. i don't care what people say that your body has to get used to the pill... that just does notttt seem healthy to me at all! and i too noticed cellulite on my legs i was horrified!!!!!!!!! so many bad things happened to me because i was on it.. i too was losing my hair.. and still am .... my mom even noticed and was making a huge deal out of it.. whatever i HATE that pill whenever anyone brings it up .. i only have terrible things to say about.. good for you if it works for you.. because i think it sucks!

I am sure that all kinds of people told Kate Miller that Concernedcitizen was a cuckoo or a Merck competitor. I haven't been employed by a pharma company in many years. Everybody ever employed by a pharma company higher than a certain level (practically the mailroom) knows this stuff and what to look for.

I think that I am about ready to say my opinion on how montelukast works and why these problems develop. It will just be my opinion. I need to try to find actual proof but I may forego that and just say it soon.

Hello! My name is Lisa and I had a HORRIBLE experience with Yaz. I took Yaz for 2 months after 3 months of Seasonique. I had switched because Seasonique made me extremely moody (all of a sudden I hated everyone on the planet). My OB gave me a few months worth of Yaz. Within weeks I noticed a strong stomach pain. I contacted my OB and he thought I just had a stomach virus. This pain continued on for several more weeks. I called my OB again and he just said, "The pill doesn't do that." I got a second opinion from another OB and he also agreed.... "The pill doesn't do that." Then out of desperation I made an appt with my Fam doctor and he diagnosed me with Gastritis.... said that he thought my diet was the cause of my pain. Uh, let me mention this.... this stomach pain is so severe you literally CAN'T eat anything cause if you do, 5 mins later you will be in SEVERE pain. To get a better picture of this pain just think of glass shards piercing through your stomach walls (I thought just maybe I was getting an ulcer). My Fam doctor gave me a months worth of Aciphex (which never never never helped at all) and I also saw him twice more in that month (which was my 2nd month of Yaz). He got so frustrated with me... it was Gastritis and if I wanted it to go away I had to be willing to make changes in my diet (I still was not eating and was losing weight) and also be patient enough for the Aciphex to take effect. Finally, out of frustration I quit Yaz. Within weeks my stomach pain was completely gone.
Let me say this to all women reading this. I don't care what your OB says.
There is no need to tolerate any pain from a medication.... especially when there are other options out there. To have a doc tell you to "wait it out for a few months" is ridiculous. To not be able to eat for days or even weeks is dangerous to your health. I eventually googled Yaz + Side Effects and found that the severe stomach pain I was having was a possible side effect and it even instructs you to tell your physician if you experience such pain. Why is it I opted to tell not 1 but 3 docs this and no-one would listen??????? Personally I would like to see all 3 docs lose their jobs because they should have known this.
Ladies, tell anyone you know about this pill. Get the WORD out about this pill. I frequently go on Yahoo Answers and girls are always asking advice on birth control pills and I jump at every chance to spread the word. Let's get this pill OFF OF THE MARKET!!!!!!!!!!!!!!!!!!

Hi, I had the Mirena for 5years and got another one inserted. The first five years was fine(at least I thought). I had no weight gain,but I had my cycle for 3.5 months. My head would kill me before my cycle would start. I did not not think it was the Mirena. My hair stated to thin at the crown of my head. I went to my appt. to have it removed b/c the 5yrs. were up. I told my doc. about the things that had going on;but she assured me it was not the Mirena. I had the new one inserted and now all hell is breaking loose. I am soooo tired. I had my cycle every two weeks for about 3mos. I feel like I am with child(lol). I always work out I love to work out. I have went from 143lbs from Nov. now I weight 168.5. I will be a walk in on Monday I don't care who take it out it can be the nurse, but somebody gotta get this thing out before I go crazy! I am so glad that I found this website b/c I thought It was just me. I have had all the side effects of all these people. I feel that the doctor. do know , but all about business/profit. God Bless!

After visiting this web site everyday for the past four weeks, I feel the need to share my daughter's (and my families') experience with singulair. My 8 year old daughter was put on singulair aprx. 2 years ago in addition to zyrtec to treat her allergies. Shortly after starting the drug, she developed stomach pain. After a few weeks of chronic pain, I pursued help from our pediatrician. After visits to two different pediatric GI doctors, an allergist (to test for food allergies), and an orthopedic surgeon ( because of sudden leg pain), the results were inconclusive. During this time my daughter also became very sad, angry and fatigued. She also completely lost her appetite and refused to eat much of the time. I attributed all of these symptoms to her stomach pain . In addition, she developed difficult sleep patterns and would often wake-up exhausted in the morning. Over time she also began to have more and more "melt-downs", breaking into crying spells over the smallest provocation or challenge. I recently contacted my daughters pediatrician to discuss what other testing or direction we could take to help my daughter. In the interim of making that contact, a friend told me about this web site. As I read page after page of other parent's experiences, I was in tears. I felt as if I was reading about my own family for the past two years. I say "family" because when one child is living through this kind trauma, everyone in the family is negatively affected in some way. My husband and I felt completely frustrated and unable to help our daughter. Our older children began to resent the great amount of time and energy I spent on behalf of our daughter. My younger daughter who had always looked up to and loved her older sister was sad and confused by her sister's anger and impatience.On March 29th I took my daughter off singulair. Unbelievable. Within 2 days, my daughter's appetite returned. On the second day, she came home from school and requested a corn dog and then some ice cream. She suddenly wanted to eat breakfast again. She started smiling and laughing again. She has suddenly become capable and responsible for doing her homework and chores. She is going to sleep more quickly and waking up happy. The best part is having our daughter back...the sweet, wonderful, happy six year old who I feel like I lost for two years of her life! As a side note-the return call I got from my pediatrician was that he wanted my daughter to see a psychiatrist. That's how close we were to taking another (completely unnecessary) path to helping my daughter. I also recently spoke with my daughter's allergist about our experience. At first he was somewhat dismissive. I asked him to listen to me parent, to parent for just a moment. He seemed to soften and said he would take a second look at singulair and its side effects. I encourage every parent who's child has been so adversely affected by this drug to be proactive. First, please contact the FDA to report your experience. Second, talk to your children's physicians and share, with confidence your experience. Third, share this web site or a similar one with everyone you know. I have been astounded how many children are on singulair just within my own small circle (school, church and play group). I really believe one voice can make a difference. I have to believe that for the sake of all the children still suffering.

I have been on 150 mg Effexor for over five years.
Although sometimes interested in sex, it is usually out of the question for two main reasons;
1. inability to achieve and maintain erection
2. Hardly any or no orgasm, so really no reward whatsoever to look forward to
If I were younger I would probably stop today, but at age 52 and the fact that my wife hardly complains
pretty much explains my " I don't care" attitude towards sex

I have been taking YAZ for about 4 months. I hate it. I am 23 and started taking yasmine when i was 17. Before that I had 2 week periods with very severe cramping. It would cause vomiting and diahreah. I stayed on yasmine for 4 years and I was extremely happy with it. When I was 21 I had a lyproscopy and was diagnosed with endometriosis. It is the cause for my severe cramping and heavy periods. I then was on a shot called lupron for 6 months then started lo estrin. Hated that, switched to YAZ. My symptoms include weight gain, acne (which i have never had) on my face and chest, severe breast tenderness (felt like my nipples were being pinched with clothes pins or something), extreme mood swings (i spend hours crying and being angry), so tired, depression, intermitent nausea, dehydration, fatigue etc. I also have not had a regular period since beginning. My last official period was in November, I then had some spotting and then I had no period for about 10 weeks. I tested over and over for pregnancy but I was not. I finally had a period and it was like i was 17 again. I am just miserable. The ONLY positive is that I gained a cup size!! I was a 34A now I'm a B! I asked my doctor for yasmine but she said she wanted me to try yaz because it has a lower estrogen dose which is favored for endo. I don't care, i would honestly take longer REGULAR periods instead of feeling crazy. I am going back to yasmine. I like my doctor but I will find a new one if she won't help me. YAZ and Lo estrin 24 were both horrible!

I just got my Metoprolol XL 25 refilled. The druggiest gave me Metoprolol ER 25 . My heart rate is up and i get more PAC, this drug is not working the same . What gives I am going to ask my doctor to put me back on the name brand drug Toprol XL 25 I don't care how much it costs.
the muscles of my legs twitch

Crying, depression, hopelessness, feeling like i'm crazy because I start crying and don't know why, This drug sucks!!!! I have cysts and my doctor changed my birth control from Ortho Tri Cyl Lo to Lo-Estrin to Femco and I don't care if it does work for my cysts or not I feel as though I can't function properly because I'm an emotional wreck. I've never ever had this happen to me before.

I went into Leighton hospital for a simple hernia operation as a day case and before the operation I told the nurse I didn’t want my knickers removed. She said as I was 21st they were not in the way and that was fine I also told her I didn’t want a suppository. I was taken into the anesthetic room and given a massive dose of Midazolam 10mg all in one go according to my medical records.
I then started having a terrifying dream of being gang raped I was in a room full of people and they were removing my knickers in the most dirty, vile filthy and perverted way I feared for my life. I was unable to stop them doing these vile things to me and I was totally humiliated being stripped in public in this way it was the most terrifying experience of my life.

Midazolam is know to enhance sexual feeling and lots of cases of people having these feeling that's why it popular as a date rape drug. My knickers were removed for none medical reasons they claim so they wouldn’t get stained. Any women would prefer to loose a 50p pair of knickers instead of being forcible striped by complete strangers. I don’t know if it was done so people could look at my private parts in order to get sexual pleasure or what. As it’s a criminal offense of Assault and Battery which can have a 6 months custodial sentence I wouldn’t think anyone would do it without they got pleasure out of it. To ask a women while awake to remove her own knickers is one thing but to forcibly strip someone is a totally different thing As I was coming around from the operation I was awake when a nurse lifted my legs and buggered me.

Both the things were done totally without my consent and expressly against my wishes I don’t care how good a reason you had you did it totally without consent and for that reason its sexual assault.

It has now been nearly 2 years since this happened and I still wake in the night from horrendous nightmares screaming and trying to cover my self from the sexual assault my heart rate goes through the roof and I cant breath. My life has changed I am dirty and can never be clean again I have been sexually abused just the same as if I had been raped but its worse than that as I was helpless and had no way of stopping the attack, I couldn’t even fight back. I cant have any sort of sexual relations as I am unclean and cant stand the thought of anyone touching me. I have been buggered and deeply humiliated without my consent has taken place and once again I was unable to stop this happening to me. I feel that some perverted women has had her wicked way with me and once again it was done against my wishes and without my consent.

What makes this worse is the hospital refuse to sack this woman or name her so she can be brought to justice. She has no excuse for what she did its her job to ensure she obtains consent before she touches anyone and simply asking if its ok and explaining what she wanted to do is all it took but she didn’t do any of these things just simply buggered me. As she didn’t seek consent I can only conclude that she is a lesbian and obtains great sexual pleasure from this act of sexual abuse. No decant caring nurse would do this terrible thing without first obtaining consent.

In the last 2 years I have lost over 11st in weight due to this incident. If I go out and see a group of people it can bring on panic attacks were I think they are going to strip me again my heart races and I cant get my breath. The attacks can happen watching television if there is anything similar to what happened to me. My life is a total mess I am depressed and often go into a world of my own for a week at a time. I cant talk about what happened without getting flash backs.

The hospitals attitude is once you give consent to an operation they can do what the fucking hell they like to you. For senior management to refuse to give the names of the perverts that did this is unbelievable. The senior management at the hospital refuse to answer any emails and have not bother to even apologize for the sexual assault they claim it was all done above board but if you bugger someone and remove their underwear without consent there is no great area its assault. The GMC have ruled that these things were done without consent so there is no doubt that in the eyes of the law a crime has been committed but still the hospital refuse to name or discipline the nurses who have done this to me.

I want all doctors and nurse to read this and I hope they will then think before they do anything to a patient without first obtaining consent they must remember that people are not just pieces of meat but have feelings and fears and are very vulnerable. Maybe reading this they will understand what effect their actions can have on someone. To them removing underwear is nothing but to many this has the effects that I have described. Many modern women might not mind but there are thousands who feel like I do.

I noticed my time in hospital that most don’t ask consent or explain what they intend to do they think they are gods better than the rest of us and can abuse patients and get away with it. I believe that most of the violent attacks on staff are because they don’t explain what they are doing and don’t seek consent. It take a second to say I want to take some blood is that ok.

I do accept that the whole incident was done for all the right reasons and nothing untoward happened but this doesn't make any difference to what I felt and what I still feel a lot of the feeling I believe are enhanced by the drug Midazolam that they used and it show they have considered the side effects of this drug. Midazolam can lead to the patient experiencing daydreams with a sexual content.

I have been on prednisone since February. I was giving it in the hospital and
it helped increase my appetite. I was very dizzy but the Dr. in the hospital said it was from not having enough fluid. It was 80 mg and then cut down to 20 mg. I then had a lung biospy and found out that besides the hemolytic anemia I was diagnosed with earlier I had some lymphocyctic intertial pneumonitis. The drug of choice for treatment is prednisone. The prednisone was upped to 80 mg again and I, of course, had to take insulin on a sliding scale. It was okay for a while and then the EYE PAIN began. I never knew my eyes could hurt so much. I went ot see the optometrist who sent me to an opthamalogist and checked the pressure which was high. I told the dr. I was taken back to 40 mg. The eye pain was better and weaned but after a couple of weeks it hurt like nothing else. so they placed me on 20 mg then 10 mg then 5. I don't know if anyone else had a problem with this and it would only relate to female my period is so heavy and so irregular that I get it like 2 weeks on and 2 weeks off. I,also, don't know if it's the change. I am 45. I did lose weight and I have a puffy face but I think I always did. I am in pain. I know I cry and try to make myself do things. The one thing I do feel is that my brain is gone. I can't thnk like I used to and I don't care.

I did have to go back up to 80 for a while and then decrease and now on 15. The pressure is good now in my eyes and there is no pain for the most part.
I am going to a dr. who my lung dr. is referring me to to see if they can do another medicine since he worked with some othe pt who had this. I hope so because this prednisone is worse than what I have.

Over the past few years I've had 3 different doctors convince me to try Yasmin instead of my very old fashioned but tried and true Demulen. I'm a military wife and we move a lot... I told each doctor that I really feel awful on Yasmin but none of them believed me. Last month I let the third doctor convince me that I should be on Yasmin. The same old side effects started within days...bitchy, depressed, irritable, frustrated, scared, short fuse, etc... I stopped after 1 month and have an appointment tomorrow. I don't care if any doctors believe me....it IS the Yasmin. I've tried it 3 times. Stay away from this POS drug. Oh yeah, I had yeast infections the whole month.

Hi. I was on Topamax for about a year for severe pain in my foot. I had nerve pain on the front outside part of my foot so bad I could not walk. I am also a sufferer of chronic migrains and have been hospitalized several times a year for them. I stopped having migrains - didn't realize until now that it was probably the Topamax. I didn't know why they stopped and didn't know that Topamax was used for that. I took it for just over a year. 100 mg a day at bedtime. I lost 40 lbs, the pain in my foot went away, and I haven't had a severe migrain since. I have been off of it for abou 1 1/2 years now, but want to go back on it because of the weight loss and some other nerve pain I am having with my ciatic (sp?) nerve. I did experience tingling in my leg and toes and soda was flat. I didn't know what the leg tingling was from until I read this blog. I can deal with soda being flat because I really don't need the sugar!! I love Topamax. It worked GREAT for me!! The pros far outweigh the cons for me. But everyone is different!!

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.

I took Lisinopril 10 mg for about 10 days. My doc had told me that 5% of those tested developed an itchy cough, and to stop if this happened to me. I stopped as soon as the cough developed. That was more than a week ago. I haven't been able to get a night's sleep since then. The cough is dry and hacking and continuous. Coughing can also come at any time during the day. Sometimes a coughing attack hits when I already have a cough drop in my mouth.

I feel just the same as I've felt when experiencing a sinus infection, with nighttime drainage and sinus headache.
When I called the doctor's office, I was advised to take an over-the-counter cough med. It hasn't helped. I am exhausted.

This seems to be a case of the "cure" being worse than the initial problem.

I posted a few reports on this site a few months ago and just thought to let you know how I feel after 10 months off Jasmin: well I feel great and back to my old self again.
Do not despair Ladies, if you want to go off Yasmin, please do it. Here is an account of what happened to me when I went off Yasmin:

1/ finished my last pill and waited for my periods.
First 2 months: periods came regularly/ SYMPTOMS OF VERTIGO AND GENERAL UNWELL FEELING WENT.

2/3rd and 4th months: horrible muscle pains with cramps, and very sore upper right arm: I went to see a physio who advised that I should carry on (even if I could hardly walk) walking once a day (10mns) and swimming for 20mns a week, and he also gave me a 'theraband' (elastic band) to exercise slowly my right arm. Although it gave me pain, I persisted and I did the swimming once a week and the walking once a day.
EAR CONGESTION : no improvement /
HEART MURMUR AND PALPITATIONS / no improvement

5th and 6th months: pains in my calves stopped but muscles were still weak, I carried on walking and swimming
EAR CONGESTION: SLIGHT IMPROVEMENT
HEART MURMUR AND PALPITATIONS/ NEARLY GONE

7th and 8th months: I started to gain more strenght and more stamina in my regular exercises.
EAR CONGESTION: NEARLY GONE
HEART MURMUR AND PALPITATION / GONE

9th and 10th months: BACK TO MY REAL STRENGHT AND I MANAGED TO CARRY A HEAVY RUCKSACK ON A WALKING HOLIDAY IN ANDALUCIA / Since I came back I've been really energetic! full of good humour and in an excellent mood.
I still do my regular exercises to keep my muscles in good shape.

So ladies, please do not despair, it will happen to you also!
And since I went off Yasmin, I have decided to leave my body alone and will never put it under drugs anymore.
Also, I have not seen one doctor since the end of June last year !! SO YASMIN IS THE CAUSE OF ALL YOUR TROUBLES AND PAINS.

BEST OF LUCK (DO NOT BE AFRAID OF SUFFERING AFTER YASMIN!)
Sylvia

have had asthma for as long as i can remember. i am now 35. i started taking ad-vair about 3 yrs ago. i have since gained alot weight and have tried dieting,exercising to no avail. i also have phlegm all the time, at first i thought that advair was the best thing since sliced bread but now not so sure. i have the " moon face" always sleepy, always coughing, gained weight, moody, tender skin, if i do skip a dose i get sore on my behind just like with prednisone. it has the same side effects as prednisone i don't care that the dr.'s say it has a low dose of steroids i can't tell it and neither can my body. also have noticed my spine curving, numbness in my hands, fingers and arm for no reason. it is like when you bump it in just the right place it has the numb feeling but i didn't bump into anything. if i had i would have had a bruise, because i can barely touch something and bruise. i have tried getting off of it but then i wheeze and can't hardly get out of bed because i can't breathe so i need decide if the side effects are worth having, or if i can get over the withdrawl effects. if anyone has any suggestions please let me know.

I HAVE BEEN ON ADVAIR FOR 5 YEARS STRAIGHT. I HAVE HAD ASTHMA SINCE I WAS 17, DURING THESE 5 YEARS OF USING ADVAIR I HAVE GAINED 65 LBS AND HAVE HAD CHRONIC BRONCHITIS AND CONSTANT PHLEGM THAT NEVER GOES AWAY. I HAVE WHAT THEY CALL A "MOON FACE" AND ALL THE WEIGHT I HAVE GAINED IS AROUND THE MID SECTION. I AM ALWAYS TIRED, SO TIRED I CAN'T EVEN PLAY WITH MY CHILDREN. THIS IS THE FINAL STRAW! I AM ADVAIR FREE STARTING TODAY. I TRULEY BELIEVE IT HAS MADE MY ASTHMA WORSE THAN EVER, I HAVE A CONSTANT COUGH AND THE PHLEGM IS ALWAYS THERE NO MATTER WHAT I TAKE FOR IT AND BELIEVE ME, I HAVE TRIED EVERYTHING TRYING TO RULE OUT THE ADVAIR AS BEING THE CAUSE OF MY SIDE AFFECTS. I DON'T CARE WHAT ANY PULMONOLOGIST SAYS ABOUT IT BEING TOO LOW OF A STEROID TO CAUSE ALL OF THESE SYMPTOMS. I KNOW WITHOUT A DOUBT IT IS THE ADVAIR. IF YOU USE ADVAIR NOW, MY ADVISE TO YOU IS TO GET OFF OF IT A.S.A.P. BEST OF LUCK.

TO GUEST 36372,
Your post really annoyed me. I am sorry that you find the new forum annoying but you know what this is the only website that has helped me. When I found this website I was just about ready to end my life. If it was not for these woman on here telling their stories I would have thought I was just going plain crazy. There is a BIG difference between side effects of a medication and a whole life altering experience, which for us is what it was. A horrible experience. People on this site are going above and beyond to help each other out. If you are looking for just side effects well go search somewhere else if we are Annoying you so much. And just so you know that is why Sarah started the forum, so we can still be there for each other without annoying petty people like you. YOu make me ill after reading all of our post and having the nerve to say we are annoying. Maybe I am being rude right now but personally I don't care, you didn't have to attack people that are just here supporting each other. I hope for you, you don't have to ever encounter what we are going through. Because any person that was, would not sit there and call us annoying or have a problem with our conversations. Sarah is not advertising anything or making money from this. She is doing this from the bottom of her heart. On the lighter side maybe I am starting to feel better because your post really irritated me and for the first time in awhile I actually felt like speaking my mind like I use too. Well thanks for that.

I was given Topamax about 2yrs ago because I have epilepsy. It seemed to be working pretty well at first, all I had noticed was that I lost about 10 to 15lbs and that the medication seemed to be controlling my siezures fairly well-and who was going to complain about that right? As time went on both my family and I began to notice that my weight wasn't the only thing I seemed to be losing. I'm only 20 and I'm losing both my memory and my hair. At first I just seemed a bit more flighty than usual, and I was finding my hair everywhere-but at this point its really just impossible to deny the difference in me or the amount of my hair thats consistently in my hands, sink or tub. I don't care how thin I am, it's not going to be worth anything if I end up without any hair.