Insomnia symptoms and conditions

I have been on yasmin for about 5 years. I loved it to begin with but just recently I have been having horrible side effects that i just realized could be related. I just thought i was a 21 yr old with problems. i am having heart palpitations, hair loss, insomnia, anxiety, vision problems, UTI's, lightheadedness and blackouts, and CHRONIC migraines. I am having about 3 migraines a week! they are disrupting my life. it is weird that i was fine on the meds for so long and they are just now resulting in this. I am stopping the pill as of today and i am going to talk to my doctor about other options. i am thinking about ortho tri cyclin lo. i have to be on a birth control because i have had endometriosis and my doctor said it is less possible to come back if i am on a birth control. she mentioned the shot but i have heard bad stories about that too and i don't think i want to go there.

WOW! I have NEVER had a ride quite like this trip. LSD and shrooms ain't got nothin' on these awful little buggers! At least when you ingest a hallucinogen intentionally, you are, or should be, somewhat mentally and physically prepared for the ensuing consequences. I really wasn't down with wigging out on antibiotics while sick as hell. I have mild anxiety occasionally, so I picked up on what was happening physically pretty quick. Until I did tho, I was a bit freaked out. Thought I'd write this for those of you who haven't had any experience with the physical/mental "symptoms" that can occur with this drug. Strange thoughts, detachment from physicality and reality, paranoia, anxiety...all of which can/will trigger actual physical side effects like rapid heartbeat, rising blood pressure, headache/migraine, vision distortion, ringing ears, extreme nausea/stomach ache, insomnia, night terrors/strange dreams, etc. Just keep these things in mind...it's not your imagination. It is the drug. It WILL pass, but it may take awhile. Just ride it out and don't let it get you. You'll be okay, but for me it took about 15 hours after only 3 days of dosing. I feel lucky that I'm so intune with my mind/body. It was a bit scary, but it's just knowing the possible side effects are real and not in your head that will make the biggest difference. This doesn't happen to everyone, and I certainly never thought it would happen to me, but I would rather be deathly I'll than deal with that mind screw and physical pain. Ugh. Terrible drug. I never take conventional meds, and this is why. May the force be with you!

I'm a 56 year old male. I'm taking pred as a trial therapy for CIDP, which can be described as MS "lite". The treatment has been three days of one gram per day methylprednisolone infusion, followed, for the rest of the month, by 20 mg prednisone a day. Then another three days of infusions, etc. It's called "pulse treatment." Side effects have been a bit of insomnia, mainly during the three-day period of infusions, feeling a little hyper, slightly hoarse voice, huge appetite. I seem to be able to control these rather well, and haven't gained weight, so far. I'm told I look a little flushed, but don't have a Barry Bonds face, noy yet anyway. The two side effects that have been problematic: Flatulence. Ever read Confederacy of Dunces? I feel like Ignatius O'Reilly. The most problematic has been the urge to pee, which is most intense a couple of days after the infusions are complete. It's really intense for two or three days, then subsides a bit, but still makes me get up in the middle of the night, something that I've only rarely experienced before. Tests for urinary tract infection are negative. Will do this treatment for a few more months and then get spinal tap and EMG test to see if there's an improvement. Haven't noticed any so far, but that's expected.

Prednisone has messed up my head. I had Bells Palsy (which is paralysis of one half of the face) and can be very scary. I have had some depression before but this stuff made me fall off the face of the earth. I went from someone in control and quite happy to the absolute pits. The depression was quite severe and sudden and I had no ability to stop the downward spiral. It has played havoc with my life. In its defense, it cleared the Bell's Palsy up very quickly but the grief it has caused me through my altered mind state wasn't worth it. Insomnia (eg - no sleep for 6 nights straight) was a trigger and then the mood swings took over and then bang....full blown depression and an inability to focus, work properly or function. I am now on the road to recovery but it has been a pretty turbulent 2 months. Be very careful with this drug....very, very careful.

I am so relieved to have discovered this site. I suffer from reoccurring UTIs. Two years ago I was prescribed Bactrim and within two hours felt all of the symptoms of a very serious virus, or so I thought.

Recently, I switched medical providers and was again prescribed Bactrim for my UTI. Within 4 hours I began to experience chills; the chills soon turned into a fever (fluctuating 100+) and night sweats. The symptoms continued throughout the night and into the next day when I started to get tingling skin, body aches, a severe headache with pressure behind my eyes and ears (which got worse when I bent over or stood up), vomiting, restlessness and insomnia.

I started to make a correlation between my first Bactrim incident and second. I called my Dr. to describe my symptoms and she said I most likely was suffering from both the UTI and flu. But, she recommended I stop the Bactrim dosage and call her in a few days to let her know how I was feeling. After missing the second dose of Bactrim I am starting to feel human again.

There is no doubt in my mind that this was the Bactrim. The symptoms came and went too quickly to be a virus. I still have a slight headache, especially when I stand up too quickly, but it's improving.

Thank you all for posting. No more bactrim for me!

Took it in August this year.

Developed raging anxiety, insomnia, memory loss, muscle twitches, weakness, nausea, lost myself, my job and almost my husband.

I'm on Benzos now.

Thanks Cipro and your makers, you took my life from me

I have been taking a low dose for only 5 days and I am ready to quit. I am either in a rage of anger or crying non-stop. I am severely tired and more moody than I have ever been. I was doing SO much better before on Effexor. The doctor switched my meds due to the insomnia and anxiety that I still had on Effexor, but it was nothing compared to this.

I have had rheumatoid arthritis for 20 years,controlled reasonably well with a combo of methotrexate, naproxen and enbrel. I do a 10 day course of prednisone several times a year for bad flares. I absolutely hate taking prednisone because it turns me into a crabby, edgy, insomniac who can't stop eating. It makes me bloat and that REALLY makes me nuts because I've done so well at weight watcher's, I don't need that nasty, upset stomach over full bloat feeling. And the "roid head" headache thing ? I'm on the phone all day at work so that's bad, too. The insomnia is the worst, really, because I just lie there awake. When I stop taking it I return to normal within 2 days. I only do it when I am absolutely desperate - I already lost some tendons in my left hand to arthritis related damage so I tend to use the prednisone when the fluid builds up in the right hand or if I'm really too sore. I'm also aware that long term prednisone usage is a one way ticket to osteoporosis / osteoarthritis, so I really have to feel like I cannot deal before I take it. It's a hate/hate relationship.

I'M SO GLAD THAT I FOUND THIS WEB SITE BECAUSE I JUST DIDN'T KNOW WHAT WAS WRONG WITH ME. I THOUGHT I WAS JUST FALLING A PART. I HAVE HAD THE MIRENA FOR 14 MONTHS AND I HAD HEAVY BLEEDING FOR THE FIRST 8 MONTHS AND THAT ENDED. I HAVE SEVERE HEADACHES, INSOMNIA, DEPRESSION AND NUMBNESS AND TINGLING IN MY FEET. SOME MORNINGS I WAKE UP AND IT'S LIKE I CAN'T GET OUT THE BED BECAUSE I HAVE JOINT PAIN. I'M ONLY 38 YR OLD. I HAVE NEVER HAD ANY OF THESE PROBLEMS BEFORE THE MIRENA. ONE LAST THING I HAVE ALSO LOST THE DESIRE FOR SEX! IT'S GONE. I'M IN THE PROCESSING OF TRYING TO GET THIS THING OUT OF ME. ASAP . LADIES THINK TWICE BEFORE YOU GET THE MIRENA.

I am so annoyed that this medication is still on the market.
What is it going to take for it to be banned??? It took me almost one year to get my life back together. The side effects from this medication are horrible. Only the people who have gone through them know how severe it is. I had anxiety, insomnia, chills, numbing in the hands and feet, palpitations, vomiting, tremors, twitching, vision problems and the list goes on. My body was out of control. My blood tests were even coming back with all sort of problems thyroid, high blood sugar etc. When retested a few months later, everything was normal.
It took me lots of hard work to get myself back to normal. Thanks to Chinese medicine/acupuncture I now have my life back.
Please don't take Avelox!!!!!

Well hi all. I see we have some new ladies on here since I was here last. I had my Mirena removed on Feb 14, 2009 after it nearly ruined my life and my marriage over a nearly 3 year period. Feel free to read my old postings. My Mirena symptoms have been gone for months now. My chronic pain has been diagnosed as Enthesopathy. It may or may not be related to the Mirena, but I'm getting treatment from an internist, not a moment too soon! I was at the point where I couldn't go on another day. The interesting thing is, Enthesopathy is a disease of the ligaments and tendons. I couldn't figure out why I had little to no pain whatsoever when I was on my period, and my pain and mood and depression got progressively worse as my period approached. I wouldn't be surprised if the Mirena is involved in this. Anyways, I recently did some research and discovered that during our period, we release a hormone called relaxing, which relaxes our ligaments and tendons (among other things). So it's nice to finally put things together and make some sense of it all.
Since the removal of the Mirena I have energy again, I used to be so sluggish I would cry, sex drive is back, I'm not crying all day and am very happy, not angry at my hubby, no more insomnia, and my hair is still growing back. I didn't realize how much I had lost until it started growing back and see all this 1-6" -long hair.

It is wonderful for the pain. I have shoulder arthritis and costochondritis. I get 3 shots a year. One in each shoulder and one in the chest. I get the hot feeling, insomnia, pain worse for about 3 days. Then I get an itchy feeling in my chest like it is healing.

I'm 24 and just recently finished my lupron treatment for endo. I'm still having some of the side effects and have yet to start my period again. I honestly would've rather had surgery again for endo than go through months of the side effects. The memory problems, overall fogginess, night sweats, insomnia, mood swings, hot flashes, and just the stress and complete crappy quality of life I've had most of this year has completely affected all aspects of my life. It's not easy at work, at home with my husband- surgery took a day or so to recovery from and this has been a nightmare for months and months. I'd really think about it and research the benefits for you vs the side effects before doing it. If there are any other options- I'd absolutely consider them.

I think that I finally figured out why I am so physically and mentally sick. I received the mirena almost 2 years ago and I was a true advocate of the product...I love it!! About 6 months ago I started to have panic attacks and anxiety (i have never experienced this before) it was so bad that I barely made it to work everyday and could no longer handle being out in public. My PCP placed me on different types of anti-depressants (which made me depressed). Currently I take Budeprion which has decreased my anxiety but I do not feel like myself. The past month and a half I wake up with the feeling of morning sickness (the numerous pregnancy test say that I am not), have headaches, low energy levels and little motivation. I was pretty sure that my hormones levels must be "off" but my PCP and OB insisted that there is no way that my symptoms have anything to do with my hormones because my child is almost 2 years old and I am 29 years old. I have gone through numerous tests on my gallbladder and other organs to find the cause of these symptoms that I have and Everything is Fine. After reading the stories on this website I now know that I do not need anti-depressants and I am not going crazy...I just need to get the Mirena removed.

In addition to all I mentioned in my posting before, I am now having burning skin feeling and my shirt can't touch my skin sometimes without it burning, hurting.

Has anyone heard if this drug leaves your system or not???

I have posted before and have been on the mirena going on three years. My symptoms started about April of this year; severe anxiety with all the symptoms: chills, panic attacks, even in my sleep, insomnia, depression, numbness and tingling in my hands and feet, shortness of breath, chest pain, the works... My doctor put me on celexa and my psychiatrist put me on klonopin to sleep. Note: I had never needed these types of medication or any kind of mental specialist ever, in my life. I have one daughter she is 2 and a half, and a very happy home.
My anxiety has gotten so much better since I have been on the meds. but the paranoia kept me from taking them for at least a month.
I can't say the mirena caused it but my doctor says that it is possible. A hormonal imbalance can be caused by your bc, The longer you take it the greater the risk.(for some women)
I have horrible mood swings still... and my sex drive is ok, but not what is used to be, but she did warn me of this before-hand. The acne and weight are my biggest problems now. I cannot stop eating, and I am not depressed, just so very very hungry even an hour after a big meal. My doctor said this is because of the hormones. Your body thinks its pregnant and will react as such, so as we all know; all of our bodies react differently to a pregnancy, morning sickness, swelling, sex drive, these things are all different for different women. It has not been a picnic for me and for others I know that it may be an ideal bc. I will have mine removed this coming week and will update if I see a change.
Thanks for reading.
emg1223

I was prescribed Bactrim for 10 days due to ear/throat/cough issues. After day 2 I had 102 fever, chills, sweats, extreme fatigue, and headache. After day 3/4 I started feeling severe doom and gloom. After day 5 I had insomnia and began having vision problems and felt like my eyes were "loose" in their sockets. I went back in, and saw a different practitioner, and reported my symptoms she thought it was my blood sugar and checked me for diabetes (which it wasn't). She ran more lab work, and chest xrays. Nothing came of it. On day 6 I began feeling a burning and itching sensation on my face, and throughout my head. Nothing helped. During all of this time I could not eat, and was extremely nauseated. I got online, and found all of my symptoms of Bactrim side effects. Needless to say, the bactrim is in the trash. In addition, last year my husband was prescribed bactrim for bronchitis, and ended up in the hospital. At the time they told us he had Scarlet Fever, but when we both went in this week, they stated it was an allergic reaction to Bactrim. He looked like he has a sunburn from head to toe, with a rash. He had 105 fever, and was severely dehydrated. I wish we would have been told that last year. They gave him a zpack this time, saying he was allergic to bactrim. I will never take this medication again, or have my family on it.

I was prescribed tramacet which did nothing for me.. Ralivia was useless.. but Tridural, which is a type of Tramadol, is working for me very well. I take 300mg slow-release tablets every 24 hours. It is, however, extremely dehydrating at first, and gives me difficulty urinating. I used to be up 7 times a night to pee, and then sat there and had to concentrate to pee! I just thought I would ask if anyone else had the following problem with Tridural: I had been taking it in the afternoon, and I was extremely lethargic and sluggish midday when it began to wear off. I also had insomnia at nighttime. After suffering like this for a few months, I finally clued in to what was causing this lack of energy, and I decided to experiment with the time I took my pill. When I took it before bed, I was wide awake at 5am ready to clean the house! When I waited till morning to take it, my pain was too severe to get out of bed, and I was sluggish again (from withdrawal). Finally I set my alarm and took it at 4:30am, and by 7:30 am I am feeling terrific and am full of energy all day long. I just thought it was important to share this since the time of day really made a huge difference to my quality of life.
By the way, I am using Tridural for pain from "Enthesopathy" or migratory polyarthropathy. In my own words, all of my tendons in my body are weak and very painful. I have trouble walking and carrying my little kids, and some days I feel like all of my limbs are broken and I can't even function or be around my kids, they find it too upsetting.

I was on Prednisone a couple years ago and it gave me severe insomnia, I ended up tapering as quickly as possible, I was so wired I couldn't function. My son was started on it today, and I was a bit worried about letting him take it, he has asthma and is in the middle of a flare up that started 5 days ago and isn't getting much better. So we started the Prednisone tonight, and within an hour he almost had an accident with diarrhea which is not like him at all, he is a 30 minute on the toilet taking his time kind of boy. Now I'm worried it's going to be a long night, and worry that tomorrow nights dose will be worse?

I was put on Singulair two weeks ago and since then I have have experienced everything from hyperactivity and insomnia to flu symptoms and loose bowel movements. I contacted my doctor after 3 days because I was having tingling in my hands and feet, flu symptoms, cramping etc but no fever and otherwise fine...He said the benefits outway the side effects so take half. I continued to take half. The cramping reduced and so did the other physical type side effects, but I started feeling like Superwoman. Instead of sleep I sterilized my house, wrote emails, tended to laundry, etc...and then continued my normal day with a smile and pep that I would not expect. I really had no desire to eat. The thought just made me cringe. After two days of no sleep and hyperactive state I decided I am done. I stopped taking it...and I took my son, 6, off it as well. He had been taking it for 4 years and was presenting with signs of hyperactivity. It has been one week...he turned yellow, became more hyperactive, talked about how the man in his room is gone now. He had struggled with sleep since he started Singulair but there were no side effects at the time that listed bad dreams, hallucinations, hyperactivity etc...It has been one week and we watched our son turn yellow as he withdrew ...he could have been spider man break dancing on the ceiling for the first few days. His teachers and even the bus driver had sent home warnings about his behavior "can't sit still" ...the last 3 days of school he has been on "green" which means great behavior. I do not think anyone should give this drug to kids...and it should not be given in sample forms either to any doctor trusting patient...without a full discussion of these side effects. I feel like I just went thru hell and put my son thru hell.

I have been on Wellbutrin SR for 1 year now. 100mg once in the morning. Have had 18-20 lb. weight gain, more anxiety(take alprazolam at night to help me sleep due to anxiety).I also at times hear a faint "door bell ringing" and am very short tempered towards my family.. Massive insomnia. I am trying to wean off and start over, but am experiencing major heart palpitations/anxiety along with alot more sleep issues. I don't know if my weight gain if from wellbutrin or alprazolam? My doctor said it was neither and it was because i'm in my 40's now. Wrong!!!!!!!!!!!!! Something is not right.

I am a 35 year old male in perfect health. last week i received two Kenalog injections in my trap muscles to to treat muscle spasms{trigger points) from a pinched nerve in my back. When I went home later that day as I layed down I begin having severe heart palpitations. I went to my doctor and my blood pressure was very high 169/94 with a heart rate of 127. For the last week I have been experiencing anxiety attacks, insomnia, hot flashes, sweating, nervousness jittery, very emotional. I had my heart checked out and had bloodwork drawn all normal. I was put on lopressor 50 mg 2times per day and xanax to help me sleep at night. I am crawling out of my skin! I can feel my heart beating all hours of the day and night! It is driving me crazy!! I regret getting the injection!!! The doctor told me it could take 2 months before the steroid leaves my body. I hope I will not have any lasting affects of the drug! I am very nervous these symptoms will not go away! I also am experiencing headaches and burning in my stomach. I am also always hungry and yet I am losing weight.Im thinking about seeing an endocrinologist. Im scared!!

My dad had taken Avelox 400 for 5 days prescribed by a doctor for Bronchitis. He is a cardiac patient as well. After 1 week he developed the following symptoms in the order: high fever, Swelling in the ankles and knees, mild jaundice, thick sputum, rashes all over the body, difficulty swallowing food, conjunctivitis affected like discharge from the eyes, poor mental co-ordination, skin tearing in the lips, diarrhea, difficulty passing stool, anxiety, confusion, low blood pressure, insomnia, slightly impaired vision. I only hope and pray he recovers soon. I really do not know why this drug is administered to people when there are other alternatives which are milder. This drug has not done any good to anyone.

I've been on and off singulair for several years. I had a horrible bout of bronchitis that then triggered bronchial reactive disease and I now have allergic reactions to certain chemicals (some spray deodorants, etc.) Singulair worked so much better for me than advair, I was thrilled to be able to talk and breathe. As a teacher I would sometimes have to stop the lecture to get my breath again and drink some water if I inhaled the slightest amount of chalk dust or something.

After reading the comments on this website I am going to discontinue taking singulair. I used to be this skinny person and never, ever worried about my weight. At the age of 37 I had a rip-snortin' major depressive episode with insomnia that had me miss 3 days of sleep (this is on no medication of any kind) and panic attacks and suicidal thoughts and impulses that I'd never had before. Imipramine was my first prescribed med (in 1991) and worked like magic. It cheered me up, calmed me down and made me sleep. I went from 135 pounds to 155 pounds in just several months. I finally got switched to effexor and trazodone, but there's really not been much weight loss. I'd hover around 150-160, but then with singulair added in the last several years I am 170 lbs. I can't believe I am a fat person now and do not over eat. I can't go off my psychiatric medication because it runs in our family and if I taper off I am...uh...crazy. My insomnia is tenacious when I am without medication and then that makes depression and anxiety worse. I never want to have a panic attack again.

I just ran out of my singulair prescription about a week or two ago. I am breathing and speaking fairly normally and my husband and I now have to pay for our own health insurance which is exorbitant and I just didn't feel like renewing the prescription in order to save money. I was pondering my weight gain today and just decided to google singulair and weight gain and I just can't believe it.

I have also experienced hair loss, but my hair is so thick it still looks basically the same. My husband and I have noticed over the last several years that I lose lots of hair after I wash it and there is a mass of hair in the shower stall.

My memory may have been adversely affected by taking singulair. I thought it's just getting older. I am 55. It's been the last several years that I have started to have problems remembering things. I have always had to work with my husband in helping him remember things (it's been life long with him: he is an absent minded professor. He has a genius IQ, is an M.I.T. grad, is an excellent engineer and can't remember his mother's birthday, what plans we have for the week-end, no matter how major, etc. to save his life.) I feel like I am becoming more like my husband in being hopeless and helpless about remembering what's happening from one day to the next. It could very possibly be the singulair. There has been a marked difference in my memory over the last several years. It is embarrassing. I sub for the school district and once showed up on the wrong day at a school and another time didn't show up and they had to call me up and get me out of bed to go to work. I also teach piano and never used to forget who was coming when. Again, I don't know if I can blame this on singulair causing memory loss, but there would be times when someone would knock on the door and I'd be surprised to find a piano student standing there. I feel like I am getting Alzheimer's. My grandmother had it for 17 years. My mom has always been afraid of getting it but she is 80 and is just now starting to show signs of real forgetfulness. I explained to her what my lapses in memory are like and she is shocked to hear that they are similar to hers. My mind just will completely go blank. I will have this thought, get distracted, and just a moment later will struggle to remember the previous thought and there is just a void, peace, blankness, white screen in my mind. Maybe it is getting older, but maybe it's the singulair. Since I'm just recently off it I'm going to pay attention and see if my memory improves or if it is just old age.

Also, my joint problems have been nearly ruining my life the last several years. I don't know if this is exacerbated by my singulair use or not. Bursitis in the hips runs in my family like crazy. We re-sided and painted our house several years ago and my bursitis started to flare up and has been bad since then, but it's also about the time I started taking singulair. I had to quit a sales job this summer because my bursitis has become so bad. Sometimes I can hardly walk. It is nearly unbearable. I get cortisone injections every 6 months, but need it every 2 months. I wonder if my discontinuation of singulair will ease my joint pain? I'm going to track that as well.

For me: weight gain, hair loss, joint pain, some dizziness are possible side effects from singulair.

Thank you to everyone who has contributed to this site. I am never taking singulair again.

hair loss, neuropathy in my right leg, complete exhaustion, numbness and tingling, stabbing pain in my back that wraps around my chest, headaches, depression, paranoia, stomach pains, chest pains, tremors in my head, pain down my neck, pain in toes, blurred vision, tearing pains in feet, very weak, moody, pain in face, really bad symptoms week prior to period, cracking sound in joints, -- Have had symptoms for three years and just had a neurologist confirm today that all of these problems have been caused by my doctor prescribing avelox and prednisone!