Extreme exhaustion symptoms and conditions

I have had the Mirena IUD for 2 years. I have notice lately that I have had vaginal dryness during intercourse. I have extreme dry scalp, and I have had about three bacterial infections in that time. I have been irritable for so long everyone in my house has gotten use to it. I am getting the IUD out next week. I am looking forward to the change.

I took Cipro for 3 days back in March 2009. After 24 hrs, I was completely disoriented, had HUGE blisters appear on my feet (they are scars now) and lost my memory. Thank God my husband realized something was very wrong and took me to my Dr (the ER had prescribed the meds) He took me off of it, and my symptoms got better.

Since then, I have had pervasive short term memory loss, loss of vision (periods of blindness), and extreme exhaustion, joint pain, and body aches. My doctor is getting ready to send me for an MRI and EEG- this is after full body X-rays and huge amounts of bloodwork.

My life is not what it used to be. I have 3 small children, and I am terrified to be alone with them for fear of forgetting something crucial. My grades have suffered, and I can barely function.

To all the women still taking this drug: I beg you to stop taking this medication and read all of the posts on this site!!!! Here is my story... I was on Yasmin for 6 years. About 4 years into taking the drug, I noticed a mass on my right side. It was a painful mass that I could easily feel, and it eventually because so uncomfortable that I could no longer sleep on my right side, and it affected basic movement. At the same time, I was beginning to show some side effects of Cron's disease (which runs in my family), so my gastro doctor told me to get a CT scan and an MRI. The tests revealed a gigantic mass on my liver and I was told to see a liver specialist right away. I went to KU Med and was told that I had to have emergency surgery right away, and that I was basically a walking time bomb.... If I tripped and fell, it could cause this mass to rupture and I could bleed to death. He also told me that if I had gotten pregnant while I had the mass, it would almost certainly lead to death for me and the baby. Nonetheless, they cut me open from the middle of my chest clear down to my belly button. They did a liver resection and removed my gall bladder and several lymph nodes. The mass on the scan turned out to be 2 grapefruit-sized benign masses, called Focal Nodular Hyperplasia - most commonly caused from the hormones in birth control pills!!!! Ladies, this was major surgery.... I was in the hospital for 9 days and out of work recovering for nearly 2 months.... and this all took place 2 months before my wedding!!!!!! The MASSIVE stress I endured caused me to have panic attacks and I thought I was going to literally die. Keep in mind that my CT and MRI were purely coincidental. If my GI doctor had not ordered the tests, I would have never known about the masses, and God only knows what would have happened to me.... Anyway, this whole ordeal has DRASTICALLY changed my life and affected all of the people I love, my husband included, who has to endure all of my pain and anxiety. BOTTOM LINE - IT'S JUST NOT WORTH IT! TELL EVERY WOMAN YOU KNOW!

I have been taking Aciphex for about a month when suddenly I started have terrible stomach pains, severe diarrhea, and extreme exhaustion. The exhaustion was so extreme I was sleeping for 2-3 hours a day, not even planning a nap, just crashing on a couch.
I feel bloated and my mouth is dry and feels metallic..in short I felt plain awful!
I thought I was fighting off a stomach flu, but it did not feel "fluish"..I then had one of those light bulb moments..this was the only new medicine I have added to my regular regime.
I am stopping this drug immediately..will let you know if my instinct is on target.

first day on, super shaky, felt like I had drank 20 cups of coffee. First day off of the drug extreme exhaustion, headache and bloating. Taken for a strong case of Poison Oak, which the drug made no change, didn't even slow down the spreading.

Thank God for this site. I thought it was just my sensitivity and exaggeration. I've been on Doxy for 2 1/2 weeks for IBS. Immediately I was nauseated. The instructions were firm in saying to take on an empty stomach, otherwise it wouldn't absorb correctly. None of the side effects websites mention dizziness and extreme exhaustion. I thought it was just me, as I've been so lightheaded and so tired I can hardly function. I want to sleep all the time, but when I try to, it's off and on. I'm up during the night. But when I get up in the morning I feel like I haven't had any sleep. Afternoon naps don't help at all. Nothing, and I mean, nothing, looks or tastes good. I feel like throwing up all the time. I can't stand the sight of certain foods, and don't want to cook because it will make me woozy. I think it's making my already diarrhea worse. I mustn't forget the abdominal cramping.

I just went to the Dr. for my second Lupron injection and to get some help with the side effects. Menopausal/emotional me, started crying!!! Gawd! I went in with my list of side effects from the last 3 months (and it was long!) and wondered what was worse, the pain of endometriosis or the life changing side effects of Lupron. My Dr. is wonderful and spent an hour with me; he decided to put me on Provera (progesterone or add-back therapy) for a week to see if the side effects improve. If they do, I get my second dose of Lupron in a week. If not, we stop it all and let my body slowly try to get back to normal (although I have never known what "normal" is since endometriosis) and see how the "therapy" worked. He is strongly encouraging me to follow through with the 6 month course as that is the recommended length of time for the best results. I'm 5'8" and have lost 10 lbs. in the last three months, I'm down to 107 lbs. He told me to try and eat more if I could (although my nausea is constant 24hrs. a day) and make sure to take a daily vitamin and calcium for bone loss. He said that he has never heard of blurred vision to be a side effect of Lupron, "But every woman is effected differently." I'm really hoping the Provera works - any kind of relief is better than this! I'm still having 3-4 hotflashes every hour with extreme exhaustion/fatigue, night sweats, daily migraine headaches, nausea 24hrs. a day, life changing mood swings, and shaky hands. He kept reminding me that this only 6 months out of my life - it's not forever ... forever feels like an awful long time when you can barely get out of bed!

Three days into the ultram 200mg, once a day, I experienced a "tonic clonic seizure" what is formally known as a grand mal seizure.

From what my husband tells me it was so severe that he had to call the paramedics. I don't remember the entire seizure at all. I faintly remember seeing 4 heads coming to me down the hallway, and that was all I remember. John, my husband told me that was the paramedics and the fire department. Since they did not see the seizure taking place I was not taken to the emergency room or hospital.

I do remember laying on the bed for 4 days after the seizure unable to move, eat or drink. I was completely exhausted. I've a follow up appointment with my primary care physician on Tuesday, as in required by law to be seen and I believe I may have to sign a paper requiring me not to drive for the next 6 months.

I'm worried to say the least. I'd never had a seizure before in my life and I'm 47 years old now. I'm still experiencing nausea, inability to eat...even though its been just 2 weeks since the seizure.

I have been going through depression and extreme exhaustion and not wanting to be alone in a room since the seizure. The abdominal pains feel almost like when a menstrual period will start, severe enough to make one bend over double and an aching inside as well. Having had a hysterectomy over 7 years ago, I know that is not the issue.

Wow, I thought I was crazy and even thought I was pregnan! The symptoms of this stuff will drive anyone nuts. I have the gas, bloating, dizziness, nausea, lower abdominal cramps, EXTREME exhaustion, difficulty breathing, foggy in the head, pressure in the head/mild, constant headache, lack of interest in anything, loss of appetite, feeling sad and depressed, and an over-all feeling of not knowing myself. All this started on the beginning of the 3rd week of treatment. I really want my Acne to be gone because I am 41 and not loving the pizza face, but this stuff iss making me crazy! I'm drinking alot of herbal teas and juices to try and keep something in my stomach at all times because I don't eat much anymore. I hope that by the end of my 1st bottle, the weirdness, pains, and the feeling of having a vice grip on my head, will go away. If not, I'm calling it quits with this drug! Good luck all.

I was put on Toprol XL 6.5 yrs ago. My heart rate had soared to 130+ and b.p. was elevated. So my family doctor put me on Toprol XL 100 mgs. From day one I felt exhausted. He told me that would soon clear up and not to worry, we needed to be more concerned with my heart rate and b.p. I listened and was a good patient. After a year of total exhaustion and having to quit my job I asked to be taken off Toprol. He said it was the only medication that would control my heart rate and b.p. together. He agreed to reduce it to 75 mgs. After a few months I went back and said it was still too much! My b.p. was better as was my heart rate so he lowered it to 50 mgs. Things got a little better at least I could get out of bed by 10:00! Fed up I lowered it to 25 mgs. and tracked my b.p. Finally I told my doctor and he said as long as my b.p.was better 25 mgs.was ok. By this time though I was having other symptoms, body aches, joint pain, mind fog. He attributed it to arthritis and put me on Vioxx. 2 pills later I stopped due to chest pains. The symptoms I had experienced over the past 2 yrs continued so I sought a new physician. Once again he said Toprol XL was the only medication I could take for tachycardia and high b.p. My b.p. was again elevated so my meds were increased to 50 mgs. he wanted to go 100mgs., I said NO!
In 2004 I was diagnosed with Fibromyalgia, the pain had become so bad now it was debilitating. I had all the full blown symptoms of Fibro, extreme exhaustion, body aches, joint pain, mind fog, depression etc etc. So I sought treatment for Fibromyalgia for 3 yrs. Not so successfully I might add.
I should note that I had none of these symptoms before Toprol XL.

During a recent Gynecology visit my b.p. was extremely high. I told her my story about Toprol. She said point blank, They are NOT listening to you. I think all the side effects you have been having are due to the Toprol XL.She sent me to a Cardiologist. God bless her!!
After many tests he immediately took me off Toprol. He put me on another medication instead. I am having withdrawal side effects from Toprol, shakiness, shortness of breath, heart rate acceleration and mind fogginess. But, anything is better than another day on Toprol. He told me what I was experiencing was normal withdrawing from Toprol. He also assured me there were many other alternatives to Toprol and if the new medication doesn't work there are other options.
I think Toprol XL is the next drug that should be banned!! I pray everyday my life will return to what it was before Toprol XL and that I will not have any lasting side effects from this horrible drug.

hi I'm 28 yrs old and have been diagnosed with endo. i have been taking the Lupron shot since August 07. I'm only suppose to be on them for a year. 2 weeks after my 1st shot, i started getting severe headaches w/ nosebleeds. also, I'm so exhausted all the time. after my 2nd shot i started passing out with severe headaches. i told my doc about it and she took me off the shot til i got a cat scan which came out normal. at the beginning of February 08, i was back in the er room 3x in a matter of 48 hours, thats when an ob/gyn at the hos. gave me another shot of Lupron. since i got this 3rd shot, i started having severe migraines and passing out again along with extreme exhaustion. I'm very angry my doc won't do the hysterectomy. she says, I'm too young. but the shot sends u into perimenopause, whats the difference. i was taking the hormones as well before my doctor took me off the shot but they made me really, really angry all the time. when the doc at the hos. gave me the shot, she didn't put me back on the hormones. this shot is suppose to help me but instead its ruining my life. i have severe headaches and exhaustion with the shot and severe pain without the shot. i don't know what to do. I'm not suppose to have any pain after i get off the shot for up to like months or years i was told. the shot started to where off at the end of January and i had to get it again in February when i was originally suppose to take my 3rd shot. i still have pain in my stomach, it just makes it tolerable. my other side effects r: mood swings, hot flashes, night sweats, no sex drive, extreme nausea, depression, stomach pains, swelling in my stomach, weight gain, and of course severe headaches. this is effecting my life so much. i do not recommend getting the depro lupron shot to anyone. of course everyone is different, but if the shot effects u like this, i recommend u not taking it. i will not be taking my next 1. i will be calling my doc 1st thing tomorrow morning cuz i passed out Friday with my 6 year old daughter here and no one else. i have been so afraid of this happening with my kids here and it has happened. as a mother u don't want your children to have to go thru something like that without no one else around. has anyone else had these side effects? i can live with most of them, but i can't live with the extreme exhaustion and severe headaches with passing out. thank u for listening.

Been on it for almost 5 years, 400 mg a day. Don't know what the official word is on long-term use, but I have had the following problems: recent weight gain and long-term extreme exhaustion/fatigue. Although I haven't changed the dose in years, the fatigue seems to be getting worse. I am on other meds, so I don't know if it is for sure the Lamictal causing these effects, but there is a good chance. I'll see as I lower the dose, under doc supervision, of course. Take care, all.

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've been on the NuvaRing for about a year. And I'm quiting this week.
This has been the worse year of my life and did not know until this past week that it had to do with the NuvaRing. I started looking up side effects & reviews of the NR because I was getting worse and the Nuva Ring is the only medication I take. I'm glad I started looking stuff up. My side effects I have been having I can not live with any longer.
They are:
The day before and the first day of each period I always have the following symptoms - Sever leg aches that only heat can help ease (but not get rid of), a lot of pressure in my head, my eyes feeling very heavy, unable to get my words out right, and extreme exhaustion, I usually stay in bed for about 2 days.

I've gained 20 pounds this year,
Very bad depression.
Social Anxiety - (I've always been a people person, but while on the Nuva Ring I could not stand to be around people. It would make me so anxious and I wanted to scream. Thought I was going crazy)
Very Irritable
Frequent Constipation and gas (never had this problem before)
Brown spot on my face
Not able to sleep through the night
Breast increase by 1 cup size (but no soreness)
Lack of energy all of the time
NO SEX DRIVE, I've got the best husband in the world, but for some reason it makes me not even want to be touched.
My allergies/sinuses have been worse than ever since I've been on the Nuva Ring.
Hair loss

I just thought that my life had gone really bad and that I was losing my mind. Once I started looking up reviews of the Nuva Ring I found that a lot of woman are having these same symptoms.
I've read that some women have pain with sex..... the little my husband and I have had sex, it wasn't painful. At least that part was good. ha ha
I'm thankful to have an understanding husband that is standing by me and is taking care of me as I go off the ring.

I DO NOT recommend anyone to use the Nuva Ring.
The only thing it did good for me was make my periods a lot lighter.
I think I will go back to dealing with heavy periods and clotting. At least I'll be normal the rest of the month. (I'll just pray that my periods will be good)

i have been taking Yamine for about a month and a half, after being on a generic pill for a couple years. I didnt know if these symptons i was having was caused by yasmine, but now i think it may be. I have been getting lightheaded, blurry eyes, shakiness, hot flashes..almost like a panic attack, and i have become very dehydrated, even though i have been drinking alot of water. I even went to the doctors for these symptons and they still don't have an answer, so i think it may be yasmine.my newest sympton as of yesterday is chest pain. also i feel like my heart is beating fast all the time, and i feel fatigued way too often, which is causing me to eat more, becauase i am starving way to often, and if i don't eat i feel like i am going to collapse. Also my sex drive has gone to non-existant- is that common? I workout all the time, and eat pretty healthy, so i don't know what else these symptons could be coming from. Is anyone else experiencing these sympons?

I have been taking lisinopril for 3 years. My cardiologist believed I had a virus that attacked my heart. He prescribed lisinopril for my hbp. It has worked to lower my bp but I am experiencing all or at least a majority of the symptoms that everyone is complaining about. I have on multiple occasions stopped taking the medication but experience extreme exhaustion to the point that I can not function. I did not notice anyone having a problem stopping the medication. Please if you have any information let me know my Dr. does not believe me. Thanks.

Lauren- May 2005 through August 3, 2007: The following is my daughter’s story which I put on paper so that she could bring it with her to the gynecologist in case I couldn’t be with her. I didn’t want her to forget anything. Someone suggested that I post it to a website:
The most recent issue seems to have started when she first went away to college in the fall of 2005. She came home one weekend with a stomach virus (vomiting, nausea), but it seemed to never completely go away. She was taken to the ER a few times, just to be treated for dehydration and sent home because there was 'nothing wrong with her'...Over the next few months she seemed to constantly feel sick, nauseous, fatigued, and get a lot of headaches. We took her to her primary care doctor, who did blood work and treated her for heartburn, acid reflux, etc.. During this time, she actually had appendicitis and had her appendix removed. After that she continued to feel sick. So we moved on to the gastroenterologist who ran many tests: cat scan endoscopies, more blood work, and were told that they couldn't find anything wrong. Then we started with a nutritionist to help her eat healthier and hopefully reduce the nausea which subsided occasionally but never let up. Nothing there helped. Then it was back to another gastroenterologist with no results. Over this time, anxiety was hitting her big time. She was finishing up finals in her first year of college and was constantly skipping classes because she was too nauseous to get out of bed for her 8:00 classes. Home for the summer - no relief. She decides she couldn't go back to her college for her 2nd year so she enrolled in community college - not exactly the plan, but at least she was on course with her classes and doing well. Still stressed and nauseous, we started with the neurologist who prescribed many medicines and ordered an MRI, which showed nothing (no problems, not no brain!). Back to the primary care doctor who finally diagnosed her with Irritable Bowel Syndrome, which fit the current symptoms of nausea, severe diarrhea while vomiting and the finale: passing out. So, back to the state college for 2nd semester of sophomore year. But the medication for IBS was making her too sleepy to get through the day, so she discontinued it. The symptoms had subsided a bit but towards the end of the school year got worse again - just in time for finals, again. During that semester at school, she sought counseling at school which seemed to help her stress level, but she still had daily ‘melt-downs’, so the therapist sent her to a psychiatrist for meds. The doctor started her on the lowest dose (25mg) of Zoloft. As she started to feel a bit better, they increased the Zoloft over the next few months until she was at 100 mg. Home for the summer, the symptoms came and went, but about 2 weeks after she started the 100 mg, she confided in me that she was feeling depressed and actually had thought of 'not caring if she died'. We immediately took her to the psychiatrist upstate who had treated her at school and whom she had seen once since she left school. (She had also continued with the cognitive therapy at the college.) The doctor told her to start weaning off the Zoloft, but start Seraquel (another seratonin-based drug). She also said she was going on vacation and Lauren needed to be seen often as she switched medications, so she advised us to find another psychiatrist closer to home to monitor her progress. So the new doctor put her on Wellbutrin, continued to wean her off Zoloft, and continued her on the Seraquel. He also ordered blood work and a fasting glucose-tolerance test (all of which came back normal/negative). The symptoms got severely worse over the next 2 weeks: constant nausea, vomiting, dizziness, weakness, fainting. On Monday, she spoke with the psychiatrist and he told her to stop all meds. We continued to believe that the recent symptoms were caused by either the psychotic meds themselves, still in her system or the withdrawal of the meds. By Tuesday night, she had been vomiting for almost 24 hours and I had to take her to the ER, not because I thought they could figure out what was wrong, but to re-hydrate her because she was becoming dehydrated. After 7 hours, and more blood work, x-ray, EKG, she was released and proceeded to get nauseous on the way home at 4AM. BUT, a very nice nurse came in while Lauren had fallen asleep and asked me why my daughter was on so many meds. I basically told her the above story and she asked me when Lauren started on birth control pills. I told her that I took her to my gyn. in May of 2005, before she was going off to college and we told him about the terrible menstrual cycle (heavy bleeding and 1 day a month home with cramps all through high school) and he put her on Ortho-tricycline low. At her 3 month check, she told him she was losing large amounts of hair. He changed her contraceptive to 'Ov-con 35'. In November, she complained of nausea and he switched her to Yasmin. She has been on it ever since. The nurse asked me if I was aware that every symptom that Lauren has had since October of 2005 could be a side effect of oral contraceptives!! She told me about a book to buy, written by Dr. John Lee about hormones and imbalances. She told me not to stop the b.c. pills abruptly, because since they are synthetic hormones, and with what her body was going through, it might put her into an hormonal chaos, similar to a full-blown menopause! So we are now reading the book, waiting to do saliva- testing and trying to see a gyn. to help us. Her own gyn. has a personal family emergency and is on a temporary leave of absence (as we found out when his office canceled her yearly check-up twice in the last 10 days). We are trying to get her in with one of the other doctors. She cannot start a 3rd year of college still feeling ill!
Added to the above is the fact that my husband’s sister called to see what was going on with Lauren after she got a phone call from her mother. It turns out that my niece, Heather (age 23), has been making the rounds with the doctors and having testing done (MRI, blood work, etc.,) because she has been nauseous and passing out. Guess what medicine she is taking…..Yasmin!

This is the list of most of the medicines (besides the 3 oral contraceptives) that she has been on during the last 27 months because of the side effects of Yasmin, and no doctor suggests she stop her oral contraceptive pills for a few months!
Prochloroperaz (5mg), Topamax (25mg), Prevacid (30mg), Zofran (4mg), Omeprazole (20mg), Amitriptyline (25mg), Amitriptyline (50mg), Inderal (60mg), Propranolol (10mg), Amitriptyline (10mg), Sertraline (Zoloft) (25mg), Sertraline (Zoloft) (50mg), Metoclopramide (5mg), Sertraline (Zoloft) (100mg), Seroquel (25mg), Wellbutrin (150mg), Dicyclomine (10mg), Compazine (severe reaction: Extrapyramidal), and other anti-nausea meds in 4 trips to the ER (one due to the reaction to Compazine!)

EXTREME EXHAUSTION ALL THE TIME

I really don't think anyone too young should take this product. I have only taken it for about 3 days (I know I probably sound like a hypocondriact because I haven't waited long enough to see if the side effects subside) but even in the first couple of days I felt really weird. I felt like I was sick with mono or something. I felt really tired for the first half of the day and then at night I was awake. My change in mood has made me feel a little out of it. Also my acne got much worse just in 2 days. Instead of it just being a bad it was like every new pimple was beneath the surface of my skin. I also take doxocyclin with yasmin but it doesn't seem to do much. I also feel really lathargic and odd. Very tired and my head just seems to be floting.

I know I have only been on this for 3 days but, I have work to do and I can't let this pill bring me down in that. I have to be alert and know whats going on in order for me to do my job. I don't want to be someone who still has side effects long after just starting to take this pill.

I can't say much else but I that I don't want to risk my sanity for this. I really don't think I need it now. I am only 15 and I just want other young people to be aware of the side effects. Although I was not perscribed Yasmin for pregnancy reasons, just know that taking this so early may cause problems. Anyway, good luck to all and I hope whatever BC you choose it is right for you and your body!

I have been on NuvaRing for 2 years 8 months. I have been seeing a doctor for the past 20 months for a series of unresolved symptoms:

1) extreme exhaustion
2) unexplained weight gain/inability to lose weight
3) Gall Bladder attack
4) High Inflammation based on CRP (C-Reactive Protein), predictor for heart disease, alzheimers, stroke, cancer, etc.
5) Loss of mental focus - Constant brain fog.

Other symptoms digestion problems, bloating, zero sex drive.......

It just occurred to me this weekend that it might be the NuvaRing. I had a gall bladder attack in June of 2005, with no symptoms and not a typical profile for someone to have an attack. In May 2006 my husband and I took a trip to Hawaii and I skipped my period by inserting a 2nd ring when I removed the first. I did not feel good the entire trip (bloating, extreme headaches, sensitivity to sun, stomach upset), and even had a skin reaction to the tag on my swimsuit (sign of high inflammation). I have been through cancer tests, bone marrow test's, tested for autoimmune disease (all thankfully came back negative) and there is no explanation for the high inflammation I am experiencing. My inflammation/CRP levels are 2x what Lupus and Rhumatoid Arthritis patients experience.

I have been on an anti-inflammatory diet for 6 weeks, and the results were actually worse at the second test. So in trying to deduct what could be causing the inflammation and other symptoms it finally occurred to me that - BINGO maybe it is the NuvaRing! I read the potential side effects and was shocked - gall bladder disease, heart disease is one of them. I have been off for 2 weeks, and I already feel like a new person. I have not been tested again for inflammation (will happen in 2 weeks), but I am almost positive that is the cause.

Don't let this be you, do not let symptoms go as long as I did before realizing what you are doing to your body. Maybe the NR works for some people, but judging by the number of responses on this board, not many!

About six months after my daughter started taking yasmine. her moods changed, her personality changed, she was is a state of depression and was having panic attacks regularly.she lost an excessive amount of weight and was thinking about suicide. I asked her doctor and a gyn if the yasmine could possibly be causing these side effects. They both said no. So she started getting treatments for depression and anxiety and was put on medication. Paxil. This medication seemed to be helping at first but then she started having the same effects as before and she was still taking the yasmine. in the last 3 months she has been taking the birth control shot and has not taken yasmine or paxil and is now doing great. I'm really disappointed in her doctor's because a lot of her misery could have been avoided if we had been told this earlier. My daughter was on Yasmine for 2 years before I finally decide to check the side effects from the internet myself. Now she says she feels so much better and is back doing things with her friends again is having a fun teenage life. Never again will I let her use Yasmine!!!!

Horrible dry, hacking cough day and night. Started within 3 days of starting the medication. Extreme exhaustion (possibly due to lack of sleep from all the coughing). By early afternoon, all I want to do is lie down and sleep. Of course, I can't because I start coughing. Pain in my upper back and arms, some pain in my legs as well. Sometimes dizziness and a feeling of being light-headed also. At times, I feel very near collapse. After six weeks, on this medication I have been taken off it and put on Norvasc. I started taking it this morning. I'm hoping the side effects of the Lisinopril will soon subside. I'm 65 and feel 85. I felt good before starting Lisinopril.

Flu-like symptoms raised temperature, swollen glands, aching joints, rapid heartbeat, interrupted sleep, nightmares, night-sweats, raised basal temperature and body temperature, sensitivity to cold, immediate change in menstrual cycle.

Oh my god! I just called my gyn to put me back on Yasmin because I was on TriNessa (just as evil as Yasmin). About 3 years ago I had my daughter after trying for 8 years to get pregnant (I have PCOS). My periods were irregular and I was concerned about ovarian cancer as my chances are higher due to the PCOS. My gyn suggested yasmin. I took it for about 3 months. During which time I bleed almost constantly. The doc said I needed to give it more time to even out. I started having severe leg cramps and rapid heart rate. One night, I started having really strange chest pains and was vomitting, needless to say I was concerned of a heartattack. My family doc sent me for a stress test to check my heart, it came back ok. I even mentioned to my doc that I was feeling more depressed and that the leg cramps and heart problem seemed to start with taking Yasmin and he just dismissed it!! My heart palpitaitons and leg cramps stopped when I stopped Yasmin but my depression contined with the new prescribed pill TriNessa and even more symptoms occurred such as extreme exhaustion (I can't seem to get enough sleep), unmotivated, antisocial, aggitated, tearful, no sex drive, weight gain, bloated, heavy periods... I just feel horrible and unhappy. So to any one who is getting off Yasmin do not, I repeat do not take TriNessa! Now that I realize that my other symptoms are validated with the use of Yasmin, I'm not going to take that either! Does anyone who has PCOS know of a good BCP to take to regulate your periods without making you insane?

I was on Yasmin for a year and a half with no real problems. I was off for 2 months and then went back on. Since then it's been horrible. I had a panic attack last week and have been experiencing intense anxiety, numbness in my legs and extreme exhaustion. I went to the ER after the panic attack and they wanted to put me on anti-depressants. It didn't make sense to me because I had never felt that way before and it came out of nowhere. It occurred to me that it could be the Yasmin and I'm so glad I found this site. I'm waiting for a call back from my gynecologist, but no matter what she says, I don't plan on taking Yasmin ever again.