Sleeping pills symptoms and conditions

UPDATE: So I made a post on 1/31/09 and hadn't been to this website since about that time. A little over a year ago now. As I stated it was a relief to find this website and it was helpful if anything but definitely the depression side effect remained. I'm 24 years old, and before I was on NuvaRing I was independent, living on my own, had a nice apartment, had a decent job working in the dental industry and was attending college consistently. After I was on NuvaRing I pretty much turned my life upside down. I quit my job for a period, tried to move in with anyone that might take me, thought if I didn't get my degree right away I would be worthless, and thought the only way I could do that was to move in with someone and work part time. I moved in to my mothers which is a really unstable, harmful environment (which is why I was on my own to begin with). I wasn't sleeping at night, I had racing thoughts, what felt like seizures, loss of appetite and ended up losing 25 lbs. I went to the doctor for anything that might help. The doctor prescribed me sleeping pills and lexapro and something for anxiety or panic attacks. Still wasn't sleeping at night (a possible side effect to the lexapro) and was drowsy all day(again a possible side effect). So imagine being SO sleepy all day but getting zero sleep at night. I would close my eyes and it felt like literally I was looking at my eyelids all night until it was time to get ready for work. I felt like I was laying there with my eyes closed all night but definitely not sleeping. I didn't want to die, but it was painful to live. I literally felt like I was fighting demons. I felt disconnected from myself, didn't understand myself at all.

But I'm happy to report that I decided to stop taking any medications such as the lexapro for depression, etc as I felt they were making things worse, and I thought if NuvaRing can give me this horrible side effect, then its very possible that those medications could as well. After much time and conditioning I'm happy to report my life is completely changed for the better. While the experience was horrible, it opened my eyes. No happy pill will ever take the place of a mind naturally and truly at peace.

I have been a professional athlete pretty much my whole life and although in my 50's now I try to exercise 4-5 times a week. However, after suffering a fractured fibula and then developed a dvt in my calf area of the left leg early December, I am not allowed to exercise (running and biking) with my legs anymore. I finally spoke to another sports doctor who suggested swimming, which I have taken up now. This is for me the worst part, no exercise. The side effects I have developed are not much better either:
Can't sleep, which leads to irritability, tiredness and sensitivity as well as being very emotional i.e. feeling depressed. I also have low appetite, but feel like I put on weight anyway (retaining water?) plus I developed high blood pressure. Once when testing my coumadin levels I had 160 over 110 with the coumadin level being too high at 3.7 (should be somewhere between 2-3). Next time my coumadin levels were very low at 1.5 and my blood pressure was just a little high at 144 over 87. Now I have reached the right coumadin levels, I am hovering around 150 over 95. I asked the doctor if there is a correlation, but of course the answer is no. I personally think there is a correlation as I have never ever had high blood pressure before. So needless to say, the doctor wants me on blood pressure pills which I have refused to take, next is sleeping pills and next is you develop too much cholesterol so why not give me some lipitor too! I will try to exercise with swimming and see if I can keep the blood pressure lower and go from there. Just wondered if anybody else have had these crazy side effects?

Can someone please reply to mine a few posts down? I really need some help, and someone's opinion. Please?

Last Night was my 8th day on the Loestrin, and this morning I put 2 and 2 together. I am 21 years old, I don't drink or smoke and have been on BC for the past 3 or so years. My first BC was Ortho and never had any problems with it at all it actually helped with my periods. Since I lost my insurance coverage from my parents, I told my doctor that I would like to continue BC usage at my last annual 2 weeks ago since it was 3 months of no BC and there was no period until that week, which I must say I have had cysts in the past and this was the worst painful period so far. He told me to go on Loestrin since It's the cheapest effective BC so I decided that was fine as long as effective was above the price! which he assured me. Well since I have taken Loestrin I have not had a decent night sleep! I lay there for hours and it will be 3-5am and then I will fall asleep with waking up every so often after that constantly until the alarm goes off. The lack of sleep, fatigue from, and I have noticed some extreme dips into depression with mood swings. I am afraid to continue based on just the lack of sleep. I don't need any other negative symptoms and I cant handle this much more longer. after the second night I told myself to take some sleeping pills because I cannot get into a bad habit and they did nothing! I did always take Ortho at night (no problems) SO I will try a week of taking them of a morning to see if there are any differences before I call it quits on this one, but if I don't see better sleep/or see different symptoms I wont like then this one is just not for me.

I began taking Adderall when I was about 16 yrs old.My doctor prescribed me 30 mg of Adderall RX. At first I would take it ALL the time (more than I was prescribed) and my grades improved tremendously..but then all the bad side effects began happening. I would get horrible back pains, had trouble swallowing (felt like I was swallowing a ball of dry food - usually happened late at night) Insomnia that kept me up all night. Another side effect that led me to stop taking the meds all together was that I felt like it was slowing my brain down. I couldn't construct sentences as easily as I once used to, and I felt like a ROBOT. I was numb to everything, my friends even started noticing my change. I was just a different person on this medication and not my usual bubbly self. So I stopped taking the medication daily and would only take it when I really needed it - for example, SAT'S, test, etc. When I got to college I began taking it as well for tests, long lectures, etc..but I started getting horrible migraines at night - not even Tylenol would work.. I used to have to lay in complete darkness and try to go to sleep. HORRIBLE. Anyway..has anyone found any remedies for the side effects you feel later on in the day when you start "coming down" from the medication? Tylenol doesn't seem to work..also, is it okay to be on sleeping pills and adderall? My doctor prescribed me both but I really felt like she was just handing out meds just cause she could so I didn't take them.

Alright, listen. There is a light at the end of the tunnel for those who have found this site. My story was posted on June 20th. I would have to say that I cannot trust any doctors for anything since then. This web site has saved me money from the idiot doctors and my insanity. Really. It is so scary that when you go to the doctor they will never investigate your meds you are taking and will send you through many tests and prescribe you medicine that you don't need. I went through 4 different doctors multiple times that prescribed many different things with no effect to my condition. I went off Lisinopril and went back on Diovan and it took 8 days before I noticed any improvement. During those 8 days I got more depressed because I didn't feel any better. Then my symptoms started going away. My anxiety and coughing started to decrease. By the second week i did not need the help of sleeping pills to knock me out due to the anxiety at night and the gagging and coughing decreased.Since then I am almost back to normal. I still though have some symptoms of coughing, but not that bad. If you found this site and taking Lisinopril, please take note that your doctor is probably wrong. You are not going to die. Get off the da#m med and start living again. It may take longer than me. Don't get discouraged.It may take more than a month or so. Stay strong. I am pissed off and would love to beat the s&it out of the ones that created Lisinopril. I know we are the small % that has the effects, but get it off the market. People are dead from this med and the others are going though Hell......I feel for the ones who have had family members that have died from allergic reactions. I had an undiagnosed throat swelling that took me to the ER. I know what it was now...Take care, stay strong, get off Lisinopril, enjoy the rest of your life...

I've been on the fentanyl patch for almost 3 years. I started on the 25 patch, then went up to the 50. Now I've weaned myself back down to the 25 patch. I was put on it for chronic back pain caused from a car accident.
I'm determined to get off this drug, so any and all suggestions are welcome!
In the last few months I've been experiencing some odd side effects that seem to be becoming worse by the day. Firstly, it seems like I can feel the effects of the patch more so, like when I first started using it. I also started experiencing nocturnal problems, my legs in particular felt like they were burning up and the muscles were really tight. If I stretched them it only seemed to worsen the problem. The only solution, weirdly enough, seemed to be jumping into the tub for a half hour.
In the last couple of weeks I have been experiencing MY FULL BODY HEATING in the middle of the night, as though it's the middle of summer in the middle of a big heatwave. I move around on the sheets and try to find a cool spot. I manage to sleep for only minutes at a time. For awhile this was only happening the second day with the patch (I only wear it two days at a time). Now it's the first and second. It's disrupting my sleep and I'm exhausted. My doctor gave me some sleeping pills which worked rather well but now I've run out and I really don't want to start depending on another drug.
I NEVER should have started on this drug and though it does work and work very well for chronic pain, I still highly recommend finding any other option out there for dealing with your pain. The withdrawal effects are horrendous. The first time I went through withdrawal I could not believe how terrible the symptoms were. Vomiting, diarreah (never could spell that one right, lol), and the pain was amplified times 100. My Doctor seems to not understand how scary it is to even contemplate getting off this drug, the withdrawal is that scary!
I managed to get down a patch size by cutting a tiny sliver of the plastic backing on the patch (NOT THE PATCH ITSELF!!!! The backing that you remove!) and sticking it on the patch before transferring the patch to my skin, so in essence, I was blocking out part of the patch and just made the plastic a little bigger until I had finally blocked out half the patch at which time I went down to the 25 patch with zero side effects.
I'm on percocet for the fallout pain and take up to 8 per day, although some days I can take as little as 3. After I'm off the patch I'm determined to get off of this drug as well and learn to manage my pain in a different way.

Thank goodness I googled insomnia and Yasmin- I finally feel like I'm not insane. Started Yasmin about 4 months ago, boobs have grown by nearly a cup size and are now tender all the time. The worst thing has been insomnia though, but for some reason I never thought of the link until now, at 1.45am, and I have to be up in 4 hours. Just an average night on Yasmin. I'd put it down to finding my job quite stressful, but now it's all starting to make sense. Will be going off this pill soon.

I know that so many of you have said it but I will say it again: THANK GOD I'M NOT ALONE!!!! I thought that I was going mad! Im a 27 year old mother of 3 and decided to get the Mirena because it seemed soooo easy. What was not to like??? 5 years of worry free sex?!?!? Sign me up!!! Well, I had it inserted Sept of 08 and it did not hurt as much as I anticipated (that was a relief). First of all, I bled what seems like nonstop for the first 5 months. Right when I was thinking about having it removed due to the bleeding, it stopped! Suddenly! That made me very happy. But yesterday, as I laid on the couch, in pain, watching my kids destroy the house and helpless to do anything to stop them due to pain and lack of energy, I started thinking really really hard. I said to myself 'self, something is not adding up here'. It suddenly dawned on me that my chest pain, intense lower back pain, my right side hurting so bad that sometime I can hardly stand it to walk, coincidentally started shortly after having the Mirena inserted. The more I thought about it the more it made sense! You see, I have never been a sickly person (thank God!) hardly ever had a headache. But for the first time in my life, I felt as if my body was falling apart!!! I woke up every morning feeling as if I was ran over by an eighteen wheeler! I mean, sometimes I can't even function well enough to get through the day. This is causing so much stress on my children, my fiancee, my school, and work! Everyone (including my DR) thinks that its just stress and that I have too much on my plate. I accepted that for a long time and struggled to simplify things. My Dr. has tried Naproxen for my chest pain, muscle relaxers for what he thinks are pinched nerves causing my backache and stiff neck. But dude, seriously... its getting worst! And besides I do not want to take 50 pills everyday just to function! SO here I am researching side effects and BAM!!! So many women are experiencing the same symptoms. So 1st and for most, thank you all for sharing your experiences. Now I know what is ailing me. But Im not sure that I want to take it out because I love the freedom that comes with the Mirena. I will talk to my doctor about ways to manage or eliminate my symptoms if possible. Does anyone know of another worry-free birth control method? Other than abstinence :-)

It's been a while since I've added a post. I had the Mirena removed on Feb. 14/09. I have been feeling great, except for some bad spells while PMSing and ovulating. My last PMS wasn't half as bad as the first one without Mirena. I think next month I will be 100% again. My hair is growing back, have a sex drive again, my joint pain is gone, I am no longer depressed and anxious, I don't hate my husband anymore.. (maybe just 1 or 2 days last month..LOL), and I'm not binge eating anymore and have lost 16 lbs! Not sure about the insomnia yet, as I am taking sleeping pills still.. But I am so happy to be me again!

Right off, my main suggestion is if you are experience these symptoms, just simply tell your doctor you don't like the side effects and to prescribe something else. I just finished taking Prevpac which contains Biaxin. I never did get diarrhea or stomach cramps. Day 1 and 2, I did not much of any problem. Day 3 I had a headache all day and then at night my hands and feet were freezing, I couldn't get warm. In the morning, I felt nauseous and my heart was racing. I made it to work, but then got the shakes and had a trouble concentrating. I ate extra food which helped a little. But I think it was on night 4 when I went to the ER in the middle of the night because I woke up with a strange taste in my mouth, then my heart started racing. I felt sick, wide awake, dizzy, faint and generally didn't feel well, so I panicked. I stuck with the medicine because the doctors told me that the side effects were not from the medicine. My general doctor gave me generic Xanax which calmed my nerves (I only took it a few times throughout) and sleeping pills, which I did not take take. All my doctors (the ER doctor, my general doctor and my gastroenterologist) told me that these drugs are not causing my symptoms: anxiety, nervousness, shaky hands, cold hands & feet, racing heart, etc. I resorted to Reiki and Meditation, which helped somewhat. Every day at some point, I get the shakes, jitters and anxious and still some problems at night. On my twelve day, my daughter suggested drinking a large mug of warm milk with honey and cinnamon in it (I added a little carob powder too) about 45 minutes before going to bed. She said it would help with nausea and I would sleep better. It was the first night that I had a good night's sleep. My daughter told me she also had a similar side effect and went to her doctor the next day and asked for something else. I just finished the 14 day therapy. We'll see how long it takes now for me to get back to normal. I'm going to print out these posts and hand them in to my doctors.

I have many of the same symptoms as everyone else... miserable stomach pain, diarrhea, terrible headache and heartburn. this drug is awful. I've never had this sort of reaction to an antibiotic before. Today is only day 4 and i'm afraid to take the pills. Has anyone heard that the side effects get better as your body gets used to the drugs?? I'm in the middle of taking exams and I was worried about this throat and ear infection interfering with my studying. I think I could have managed the infection better than these drugs.

Been on Lisinopril for a month and wake up at night and can't get back to sleep. I always sleep great. On the weekends I used to be able to sleep till noon if I want. But Now. Felt like I was having some kind of panic attacks. My doctor put me on sleeping pills. Now I wake up and hour or two before I need to and feel like I drank a pot of coffee. I am going to stop taking Lisinopril for a couple of days and call my doctor...

Hi All, I am here for the first time in desperation trying to ascertain if my problems are Advair related. I have been on it for over 20 years (started as a study patient). I probably would be dead if it hadn't come along - seriously - and I had been on prednisone a lot. But, to add a voice to what others are saying, I can't sleep, and always wake with the most terrible headache, along with other general aches and fatigue. I was coping so so until I was rear-ended and developed some neck issues. Now I live with never ending headaches and fatigue and a tendency towards depression. Pain killers and sleeping pills get me through the winter months and then in the summer with lots of activity outside I rebound so that I can go through another yearly slide downward. What is really a killer is that I can't get going in the early mornings and have been hassled by my employer who has determined by a psychologist that I am a malingerer because there is little proof of physical illness! If I didn't have a history of having been, and still being, a very hardworking and persistent individual I would think I was going nuts (I'm 60). If anyone has a similar story, please comment further. Thanks

I just had my Mirena removed after 3 years.. I had it removed on Thursday, 2/12/08. The last 3 days have been WONDERFUL without the Mirena. I can finally sleep without taking Ambien. I am not eating constantly. I am much more happier. I was soo miserable and depressed before. My hair was falling out, my face was constantly broke out. I went from a size 10 to a 16 in less than a year. The only thing I have noticed since the removal is extreme fatigue. If I sit on the couch for more then ten minutes i want to fall asleep. Which is actually okay for me after relying on sleeping pills for so long. Overall I would NEVER get the Mirena again. I hope this helps people. And please know there is an end in sight. Within 3 days I feel so much better and my family has noticed a drastic change in my attitude, which is what matters most :)

my mother was raised a month ago to 50 mcg, and since then she has eye muscle spasms around her eye,
she has rupchured discs in her back, which doesn't help with the pain, she also has restless legs, i see how she sleeps, and her legs can never stay still, she sleeps a ton, and has static hair, and also hair loss. if you have any of these symptoms please let me know

I have had Mirena now since August 29th '08. I was one of the people that was lucky enough to not experience any pain what so ever when it was inserted. Not a single bit of discomfort at all!!! I did have my period though so that may have had something to do with it. But ever since I've had Mirena I've gained 12 pounds, my husband and I fight all the time, we have been together for 15 years and haven't fought this much as long as we've been together, I'm always depressed lately which is weird for me at this time of year because until Christmas I love this time of year!! I've had a few anxiety issues, I don't sleep at night, my poor kids I snap over the stupidest things, the fatigue oh my the fatigue. I've had sleeping problems for many years now but I can't even sleep on sleeping pills most nights either and I could before. The last couple of weeks now I've experienced gas (I mean gas very regularly) out of the blue didn't think that had to do with Mirena but then I started reading this site, some days I'm constipated others I don't stop going. It seems I get the "spotting" one week straight done for a few days then here it is again. My husband feels it when we have intercourse. If and when we have intercourse these days it's not enjoyable for me and not him either, he can tell it's not enjoyable for me, let alone he can feel the thing. I have a very clear completion (normally only get acne at that time of the month and only a couple), lately I've broken out along my hair line, getting pimples in spots I didn't know you could get them. And with the weight gain and acne it makes me feel real good about myself. I look like I'm pregnant again some days. And I'm bloated all the time. Oh the one I almost forgot about the hot flashes, I'm 31 years old having hot flashes.
I was thinking that my body just needs to "adjust" to this thing inside me, but after reading this why wait and make it worse with more symptoms I don't have yet?! Like the cysts, I guess as far as I know I don't have them yet.
I just want to feel like myself again. I'm a happy person, normally motivated to clean my house, normally don't feel like I have a grey cloud over my head, I hate feeling like I have a scowl on my face all the time. These are the memory making years for my kids, do I want them to remember the always crabby yelling mommy? No I don't. Well I'm gonna go cry now and call my doctor to have it removed. Thank you for having this site it's made me feel like I'm not going crazy and it's not just me! And you know what I will respond back in a few weeks after having it out and let you know if I've gotten rid of any the "side Effects" the doctors claim have nothing to do with Mirena!

My 15year old daughter has just stopped taking Yasmin due to severe depression, anxiety attacks, uncontrollable crying, suicidal thoughts and chest pain with erratic heartbeat. I thank God that we figured out the connection to Yasmin. She has been spiraling down so quickly, I thought I was losing her. While she does not relish the return of heavy, long periods, she is so ready to have her sanity back. Her counselor and gyn confirm the strong likelihood of these being side effects of the Yasmin. I was ready to put her on Prozac and sleeping pills because the situation was so desperate! While I was on Yasmin for years with no adverse effects, there ARE people who are desperate because of this pill! The hundreds of posts are too numerous to ignore the REAL truth. Is is worth it to "just try it out" for a boob inflation? You are taking a serious risk, sweetheart!

Okay, I don't have any side effects, but I do want to know something important!
I'm 16 years old and i REAALLLY want someone (who knows about the Yasmin pill!) to help me out with this one. Tomorrow i am going to the doctor with my mom. I have irregular menstruation. Like 2 or one week before it's supposed to come. I also get cramps, which are just enough to hold out...But the thing is, i just want to get the Yasmin pill. I heard that it clears your skin (although i don't have acne or anything) and it can make your breast bigger.. I have like a A-cup and bigger breast are nicer.
But now I read these bad experiences and I'm just scared to start it.. But still i wanna try it, 'cause I can stop right after it starts to become bad, right??
Please give me a good and useful answer!

Thanx!
A confused girl

Moderately high cholesterol and BP 150/90. Was put on Lipitor 20mg and after a week felt more fatigued than usual but nothing much more than this. Had stress test and angiogram which showed 60-70% block in one artery as well as arrhythmia. Cardiologist bumped Lipitor up to 80 mg which I took for 2 weeks. But by then I was suffering most of the effects described in these postings: aches and pains, giddiness, nausea, extreme weakness and fatigue. I took myself off Lipitor and even after one day my head started to clear aches started to diminish, though urine still a reddish color suggesting a lot more flushing out required. And, best of all, the arrhythmia reduced from moderate/severe to mild (which it always used to be before taking Lipitor). This drug is not for me. I'd rather take my chances without it and rely on strict diet, weight loss, etc. It is surprising that the possible side effects are so understated in the manufacturer's descriptions.

I was on synthroid for 10 years after getting treated with Radio Active Iodine. As the years went by my period was all all over the place. They were heavy the first three days and lasted 9 days or more days. I spotted all the way through the month. Other times I was so late that I thought I was pregnant. I had PMS two weeks before I started and was irritable. I had low grade depression. I had anxiety and heart palpitations. My skin was dry and rough. I went to the doctor and had my blood test. He checked for TSH and T4 and T3 levels. He insisted they were normal and that something else is wrong wth me (he wanted to give me sleeping pills, anxiety pills, depression pills) and that it had nothing to do with my thyroid. He sent me to an endo to get a second opinion and he said my levels were normal too. I ended up going to a holistic doctor (paid over 1000 dollars for two visits plus meds) that checked under my feet (yellow) and my reflexes. She checked my reverse T3 and my free T3 and T4. It turns out that my body was not converting T4 to T3 the way they said synthroid (T4 only med) should. My diagnosis was hypothyroid. I was put on Armour and felt the difference in my skin. It was softer and moist! My teeth felt strong compared to before I felt like my teeth were getting loose. My stamina last longer and can run on the treadmil 45 min at six miles per hour. I am less nervous and my low grade depression seems to be lifting. My days are brighter and less anxious. My hair is falling less. I know I have a long way to recovery because my Adrenal glands need some healing and I am still being optimized. I might still need to be raised on the dose that I am in. I will never go back to synthroid! My period has improved drastically as soon as I started on Armour! I am down to 4 days of period and less heavy. I still spot on day 5 and 7 but it is nothing compared to what I went through when I was on synthroid (T4 med only). My gynecologist wanted to burn my uterus to control the menstrual flow. He said that he could also pull it out. It seems like main stream doctors are more interested in treating the symptoms than looking to see what is the problem that is causing the symptoms.

I have been on celexa for 4 days I know its not a long enough time for the meds to "kick In" but i am terrified and waiting for something bad to happen. I have struggled with terrible panic attacks since my pregnancy in o6-07 and they have lingered on and gotten worse. I was ok and happy to finally take the initiative to get better, I don't like even taking Tylenol so tis is a big deal for me. I was prescribed 10mg and have been only taking 5 of the 10 to wean myself into this drug.. I wish i could know what to expect and all i feel is nauseous, weird and shaky and last night i couldn't fall back to sleep i felt a lil dizzy is this normal?? I hope i don't have any vision loss also!

15 years ago, at the age of 35, I had a major heart attack. After testing, the doctors decided I needed a quadruple bi-pass operation, followed by Lipitor, among other things. I was taking 20mg (the doctor ordered 40mg), but due to financial reasons I took only half. Everything was just great for 15 years. During a routine annual physical this year, my doctor noticed that my liver enzymes were off the chart high. He immediately had me discontinue the Liptor, but stay on all of my other medications. One month later, my liver enzymes were normal, and so was everything else; however, my cholesterol had climbed to 204, and I eat no meat, eggs, or other dairy products. They say my liver damage is permanent. Having had 4 lumbar surgeries and 1 cervical surgery to fuse disks in my spine, I have always attributed my back and other muscle pains to that. Now that I have been of the Lipitor for 3 months, I have not noticed in decrease in pain in these areas.

Responding to chap56:
If you have a problem with Ambien CR, then don't take it. Wanting to take it off the market for other people is totally over reacting and rather selfish though on the surface it would appear well-meaning. We don't need you to act like a nanny for other people, for whom Ambien is a wonder drug, like myself. And no, I don't work for the makers of Ambien, I've just had insomnia for many years.

Im only 16 years old and ive been on levaquin for about 3 days now. My doctor told me off the bat that the only thing wrong with the drug were some "theories" on cartilidge damage, how ever, now i see for myself, and for many other people that is not the only side effect. He told me that no one under 18 is supposed to have it but i caught a severe case of sinutitus, and a uti which ive had for 2 months and nothing was working, so he put me on levaquin, once a day for 7 days. Ive now been having the following symptoms and im extremely scared!!
1. Constant fatigue
2. Extreme Migraines
3. Nausea, vomiting
4. Rapid heart beat (and chest pain)
5. Stiffness in joints and horrible pain...
6. Constant anxiousness, to where i cant get to sleep
7. Dizziness

Is there anyone i can talk to who's had these same problems? please email me or something im scared and i don't know what to do my mother doesn't believe me and she says its just a head cold....

******

Please help me!!