Sleepless nights symptoms and conditions

OMG!!!! Okay, I have had the Mirena since may 2007! Over the past two years I have been through more testing than I care to admit... Severe and constant nausea, headaches, anxiety, depression, acne, sleepless nights, joint pain, no sex drive whatsoever ( my poor poor husband), lack of energy, and just overall moody! I have asked my doctors many times if it could be the mirena causing this.... No! I have also gained about 20 lbs over the last 6 months! I am normally 106 and have never in my life been able to gain weight! This is insane!!! I am calling my doctor today to get this thing taken out of me!!!! Thank you to all the women who have posted! I just thought I was going crazy...

I started taking Lisinopril two weeks ago for relief of high blood pressure. Male, 45, 260 lbs, family history of high blood pressure and stroke. After one week I began experiencing intermittent chest pain, tingling and numbness in my left hand, and sensations like shocks in my head.

I spent several sleepless nights feeling for chest pain, feeling my heart race, expecting my heart to explode and wondering if I should go to the ER.

I visited my doctor and expressed my concerns. She immediately performed an ECG and verified that my heart was functioning normally and that my blood pressure was down. She also indicated that it's not uncommon for vasoconstrictors like Lisinopril to allow stomach acids to rise in the esophagus. This can cause chest pain and affect nerves leading to the brain and to the arm. She prescribed Zantac 150 twice a day and asked me to call her at home 60 minutes after taking the first pill.

I filled the Zantac prescription (one of the $4 prescriptions you can now get most places) and took one immediately. Ten minutes the chest pain was gone. Twenty minutes later the shocks in my head were gone and my arm went from tingly and numb to just slightly achy. Thirty minutes later all of my symptoms were gone. After an hour I dutifully reported to my doc that she was a genius and on my Christmas gift list.

If you're taking Lisinopril and having chest pain obviously let your doctor know about it. Studies indicate that denial is a serious issue and a contributing cause in heart disease victims. Many of my symptoms were classic for unstable angina, which is scary. However, they are also common stomach acid symptoms for first-time users of a wide variety of high blood pressure medications. It's possible that a simple antacid could relieve your side-effects.

Now my goal is to lose 80 lbs so I can get off this medication completely. Working 90 hours a week (the highlights of which are travel, sitting at desks, and eating) isn't going to cut it any more.

22 years old i have had Coltis for 5 years,flair ups pretty much the whole time, i have been on Prednisone a lot this last time has been the WORSE!!! All i can say is i hate it!! i was put in hospital the 4th time steroid thou the iv for 5 days sent home got worse again back to hospital then to try Cyclosporin thou the iv and also the steroid thou the iv. Ten days later they sent me home on prednisone coming off the iv was hard the pain in my legs was unbelievable!!! finally i was sent home on prednisone,coliform anemas,salfak anemas,and salfak granuls,i thought the worst was over but it was far from it... I turned in to a complete loony,crazy women i don't even know myself anymore my poor partner and kids. Having to deal with the pain and everything eles that comes with having a flair up but then also going though the side effects of the prednisone and the coliform was unbearable, i just wanted to die! My flair up was not getting much better and i hated myself as i felt i did not know myself with the mood swings, the crazy flip outs,crying all the time.My partner has been great having to pick me up off the ground and turn the crying reck into someone half normal. I hate the moon face,weight gain, im hungry ALL the time,night sweats,sleepless nights sore teeth,I have come off it now its been 4 days, so now all i need to stop its the coliform then i will be steroid FREE!!!!! i cannot wait!! For my face to go down and to be normal and back to the good old me! I forget what shes like... Coming off the Prednisone has been hard with the leg pain,muscle aches,head aches,mood swings,nausea. Its just hard as no one around me understands what im going though or what it feels like so i just sound like a sookie cry baby or a raving loony. does anyone know how long it takes for moon face to go away??? I wish everyone luck with there battles with Prednisone, its one of the hardest things i have had to deal with. =) your not alone. stay strong and be positive even throu your lowest times.

Our daughter is now 5 1/2 and has been taking singulair since she was two, when she was diagnosed with asthma. She also has a slew of food and environmental allergies. It was not until she started taking Advair that her asthma became controlled. Her allergies still seem to bother her occasionally. I feel since her asthma is under control why take two meds? I did not refill her Rx and we are on day two of no Singulair. She's had headaches for two days and feels lousy. After reading the side effects of this drug I may now have answers to the headaches she'd get often and the moodiness and the sleepless nights and the deep dark circles under her eyes and the diarrhea. We'll see what happens in the next few weeks, although I agree that dose of antihistamine now and then is much better than all this other nonsense!

I started reading articles about links between depression and ddp-4, Which Januvia is a ddp-4 inhibitor. after reading this forum and noticing that people experience depression on this drug.

I had depression as one of the side effects on this drug but what I noticed it was not easy to get off the drug. It took me a week of sleepless nights and anxiety and panic attacks which I never had until i took the drug. I am doing better but from what I read it takes a month for Januvia to leave your system.

So my question would be why would a doctor who knows of family background of depression in family history would prescribe this junk. I would think that if you have a predisposition to a disease that it would be taking into account. What this tells me is that our doctors are not doing their homework on the stuff they are giving us and we are having to do tha t for them. What am I paying for then?

What I got from my research was that lower levels of ddp-4 is seen in patients with depression. I found studies by searching on Dipeptidyl peptidase IV and depression.

Copyright © 1999 Elsevier Science Ltd. All rights reserved.
Dipeptidyl peptidase IV and adenosine deaminase activity: Decrease in depression

References and further reading may be available for this article. To view references and further reading you must purchase this article.

Serenay Elgün, , a, Aytaç Keskinegea and Hakan Kumbasarb

a Department of Biochemistry and Clinical Biochemistry, Faculty of Medicine, University of Ankara, 06100 Sihhiye, Ankara, Turkey

b Department of Psychiatry, Consultation–Liaison Unit, Faculty of Medicine, University of Ankara, Dikimevi, Ankara, Turkey

Received 22 December 1998; accepted 15 May 1999. Available online 17 September 1999.

Abstract
Dipeptidyl peptidase IV (DPPIV) and adenosine deaminase (ADA), two T cell associated enzymes, are known to have a possible interaction and play essential roles in immune system functioning. On the other hand, depression has been shown to be accompanied with some immune-inflammatory alterations. In this regard, in order to make a contribution to the understanding of the ongoing immune disturbances in depression, serum DPPIV and ADA activities were determined in minor and major depressives and compared with healthy controls. Both enzyme activities were found to be decreased in major depressives compared to controls while only DPPIV activity was significantly lower in major depressives than the minor depressives. There were significant inverse relationships between enzyme activities and the severity of depression. Moreover, a positive intracorrelation was found between decreased DPPIV and ADA levels. The correlated decrease in DPPIV and ADA, might be a further support for their possible association. Results also suggest that decreased enzyme activities might reflect the impaired immune state in depression while major depressed patients might have a greater tendency to immune dysfunction than the minor depressed ones.

I was recently prescribed Simvastatin 40 mg by my GP as I have high blood pressure and Cholesterol. After the first nigh of taking Simvastatin, I am suffering from severe dizziness and feel weak. Can Simvastatins cause these symptoms after one dose and has anyone else had this problem?

Hi,
I have been on Cilift for anxiety and depression for 13 years. I also have hypothyroidism so am on Eltroxin every day. I have been on Urbanol for a while but it was not helping the extreme anxiety. I was prescribed Seroquel and have been on it for 3 weeks. My anxiety seems to be far worse, especially in the mornings but it does help me sleep at night. Stilnox sleeping tablets were not working. I have a pain in my chest, severe headaches, tingling feeling in my hands and a 'funny head'. I am on Yasmin as I have the Mirena but it does not work. The Mirena is still fitted. I have now read on this site (thank goodness I came across it) that both these cause extreme anxiety. I have now stopped the Seroquel and plan to stop the Yasmin and have the Mirena removed. If you have any similar experiences please comment.

I am going to copy the address to this page and personally drive around to local family practice offices and discreetly drop piles of them everywhere. I pride myself on my medical knowledge and background having worked one way or another in the medical field all of my life. I take into account every aspect of a new medication after a life altering labor and deliver drove me to have a bright shiny new Norplant installed before it had time to be researched and tested properly, i'm still awaiting the final outcome of that young, uneducated, made out of fear of unimaginable horror and lack of RELIABLE READY INFORMATION ABOUT ALL OF IT'S SIDE AFFECTS. I believe every person is different and no one person will tolerate the same information the same way.
Except for the Mirena apparently. It seems almost UNIVERSALLY bad for a women's body and was MOST LIKELY conjured up by some ill treated ManBoy.
All that being said to the women who were in NO way warned of any of the negative side affects,(most likely older women who finally found mr right but under no circumstances want to go back to diapers sleepless nights and college tuition worries...) Thank Goodness for the WorldWideWeb and access to information. I am over 35 and have a family history of heart disease, there are very few options for birth control for me. This seemed like some sort of modern day miracle and while I suspected someone having as *significant* of a period as I, should probably...have one regularly...I too was *woo'd* by the prospect of a shorter, lighter, possibly infrequent period. However I was not warned that the other 3 weeks of the month I would rather be dead than alive. Turns out my body is smarter than I am and just days after finding this site and putting it all it finally passing the *MirenaBlock* ...I made an appt for a check and my body had spent the last 4 months attempting to push it out.
I'm never lucky enough for the *magicpills* to work, to those who are *KUDOS* but don't belittle those women smart enough to pursue a logical explanation to a sudden change in every aspect of your life. Information is knowledge and if you look most of those *BITCHY* women who called you babies have has the *device* installed less than 6 months...lol Kharma's a bitch and I think the Mirena has pissed off *Mother Nature* good luck lol and yes...I too within HOURS ...felt better and I EMBRACE the wonders of modern medicine daily...just not the horrors !

Like all of the ladies that posted. I had the mirena put in place 6 weeks after my daughter was born, she just turned 1. I have had nothing but problems. I have not had one period since this thing was inserted only discharge and a odor, which i have never had a problem with. I had to be placed on paxil for depression and anxiety, I have sleepless nights and not because of the baby she has slept all night since day one. I have no sex drive and when i attempt its painful. I am 22 and active and weighed 170 the day i gave birth and in 6 weeks i had only 5 pounds to go to be at my original 130lb pre baby weight..I now weigh 180 lbs. Iv tried all the old tricks, i quit sodas, fried foods and switch to water. i was working out with no response. I found this site last night and called my doctor first thing this morning but im a full time student without insurance and he told me it would be $200.00 which is a lot when your a parent in these times. so i called planned parenthood they will remove it for $ 50.00 and that includes a pelvic and a pap, so i can try a new method. Now that is the student rate but even at regular it is cheaper then the alternative.
good luck ladies, i can honestly say i feel your pain

I was diagnosed with Ulcerative Colitis in Aug of 2005 and in remission for 9 months. I came out of remission in May of 2006 and have been on prednisone since then until right now. I would go on high dose of steriods, try a new medication, and try to ween off and get sick right as I went off the steriods, so I'd have to do this rollercoaster all over again. For a year now, I have been on steady, high doses between 60-100mg daily with no break. I tried to go below 20 and got really sick again and have run out of medication to try, so I had my colon removed. Right now, we are trying to ween me off the prednisone (since i dont need it for my disease anymore) but have to go over 3-4 months and very slowly since I've been on it so long to prevent the body from doing all the fun things it does when you stop prednisone cold turkey, like a coma and stuff. I'm SICK of the side effects this drug has had on me! I have had countless sleepless nights, heartburn, night sweats, weight gain (i went from 140 lbs to 215 lbs right now), the moon face to where i can't even recognize myself, red face, weird skin, sensitive teeth, thinning hair, hungry ALL the time, stretch marks, all the weight is in my stomach, the buffalo hump, high blood pressure and high eye pressures etc. These are all the side-effects that have been horrible on this miserable drug. I'm sure there are a lot more I am forgetting, but these are the ones that come to mind. Hopefully they will go away once I am able to finally get off this drug!

I am 31 years old and I FINALLY have relief from the pain caused by endo. I have been dealing with this crap for about 14 years. I have only been on it for 1 month. The hot flashes are TERRIBLE!! But I guess it beats the pain. I have been reading some of the other people that have posted their side effects. Some of you are saying that you have been on Lupron for 1 year or even 2 years. My Dr. says you can only use if for 6 months. I guess I should've asked more questions. Any suggestions on what to do about the hot flashes - other than put a fan in my face??

To this day, I am not sure if Nuvaring is the cause of all my problems. But after reading about the side effects and finding many commonalities in my own experience, I took it out today and will not continue using it.

I've been on Nuvaring for the past year. Just before I started using it, I had an episode in the gym where my heart started racing very uncomfortably and I felt like i was going to faint after running. Two visits to the ER and numerous specialists' visits later, they concluded I have generalized anxiety disorder.

Over the past year since that incident, I've become much more anxious than I ever remember. I've gained about 20 pounds. I get headaches all the time. I'm CONSTANTLY tired, to the point where it doesn't matter how long I sleep, I still don't want to get out of bed. Most of the time, I don't want to have sex. I have spells where I feel like I'm about to faint (but never do). Of course, the doctors attribute this to my anxiety, and I'm pretty sure that's what it is since it doesn't seem to be anything else really serious.

Like I said, I don't know if the Nuvaring has had a hand in putting me through this ridiculousness, but I'm not taking any chances. I read somewhere the Nuvaring isn't good for people with anxiety problems because it just makes these problems worse.

At least if these symptoms continue for a while after I've stopped the Nuvaring, I'll know it may not have been it. However, every month I feel my best the week of my period. Coincidence???

Wow to the 10 year old story above. I'm on here because my 10 year old started Advair back in Sept for a nagging nighttime cough, asthma associated. Then his grades started to tank. He has aced his SOL's in math/science, but, this year has a D in Math! Today when we met with his teacher and found out he had been 'daydreaming' and seemingly 'asleep' in class, thanks teach for letting us know before now, we finally put it together, the new med. So, he has complained about being tired and having some sleepless nights. We put our kids to bed at 8:30pm and we don't run them to death with sports, etc. We couldn't figure it out. But, I can tell you, beginning tonight, no more Advair for him. We'll see by next week if this was the problem. Scary that this isn't rated as a 'side effect' of the med.

I began having right hip pain a month after the mirena was inserted. I assumed it was from running. All the doctors I have seen for the past year stated I strained a muscle. They ordered MRI's and physical therapy. I have completed all, but still have the same hip pain-over a year now. Has anyone had hip pain due to the mirena? And did your hip pain stop completely after your mirena was removed? I am considering getting it removed. Although the doctors tell me they are not connected, I can't help but think there is a coincidence.

I had my Mirena inserted 6 weeks after I had my son (14 months ago) at the suggestion of my o.b. (she was using one also).... had I known then what I know now, my post partum birth control decision would have gone in a totally different direction! Insertion was very painful! Sex with my husband was awkward at first, mainly because he could feel the strings (they are wires!!!) poking him during deep insertion... After several weeks of getting used to the mirena, the nightmares started in! Sleepless nights, tossing, turning, dreaming about my fears and insecurities, and waking up sore... feeling like I had been run over by a truck! Moodiness and quick tempered feelings also came with the little devil... wanting to kill my husband and children over the littlest things like not eating all their dinner or not picking up their laundry...stupid stuff? My husband kept asking me why I was so angry, mean and hurtful...these are not traits I usually possess! I had become a bundle of tired, bitchy nerves! Then I had a trip to the emergency room, thought to be an appendicitis at first.....but no! I have a golf ball cyst on my right ovary, compliments of the mirena!! Now I have to have monitoring of this cyst until it bursts or is so painful I cant take it anymore and have to have it removed!!! Needless to say, I booked an appointment a few weeks ago and and have my mirena removed three days ago... I know it is going to take a while before I am "normal" and heal myself from this awful cyst, but I cant wait to love myself, husband and children again...if you are thinking of getting this inserted in your body, think again!!! Your doctors will not tell you what these women have experienced and gone through!!! Don't be a part of a class action suit down the line, money can't replace your health and well being :(

I'm 56 y/o with hx of MVP,SVT and was on Inderal for 23 yrs. until after taking RED BULL energy drink threw me to AFIB that sent me to ER and got admitted overnight ,that problem got resolved until about few months ago i started having on and off palpitations again and my doctor put me on 50mg METOPROLOL and take extra dose for frequent palpitations but i noticed that the more i take METOPROLOL the worst my symptoms gets with some dizziness, sleepless nights ,occasional chest pains,joint pains so i went to my doctor again ,had stress test, 24 hr. monitor, and everything was normal, i was then referred to a Cardiologist-Electrophysiologist who told me i was taking to much Metoprolol that i should cut it to 25mg , He planned to put me on 30 day holter monitor to see the activity of my heart but on the other hand being a nurse i tried to monitor myself, i still have the same symptoms but less since i cut down my dose but i decided to stop the Metoptolol completly and put myself back on Inderal for about a week now i'm telling you it was alike a night and day symptoms of increasing palpitations are less and i feel much better , hopefully i treated myself and goodbye Metoprolol.

I'm 56 y/o with hx of MVP,SVT and was on Inderal for 23 yrs. until after taking RED BULL energy drink threw me to AFIB that sent me to ER and got admitted overnight ,that problem got resolved until about few months ago i started having on and off palpitations again and my doctor put me on 50mg METOPROLOL and take extra dose for frequent palpitations but i noticed that the more i take METOPROLOL the worst my symptoms gets with some dizziness, sleepless nights ,occasional chest pains,joint pains so i went to my doctor again ,had stress test, 24 hr. monitor, and everything was normal, i was then referred to a Cardiologist-Electrophysiologist who told me i was taking to much Metoprolol that i should cut it to 25mg , He planned to put me on 30 day holter monitor to see the activity of my heart but on the other hand being a nurse i tried to monitor myself, i still have the same symptoms but less since i cut down my dose but i decided to stop the Metoptolol completly and put myself back on Inderal for about a week now i'm telling you it was alike a night and day symptoms of increasing palpitations are less and i feel much better , hopefully i treated myself and goodbye Metoprolol.

i had Mirena inserted on the 28th of September, i usually check my waist measurement every week since i had my baby- i lost 4 inches after delivery and exercise, i was so shocked this evening to find out i gained 2 inches on my waist in two weeks! i have been asking myself why i am so gassy these days, am always sweating, sleepless nights and i noticed my stomach looks like am pregnant. am so shocked! and the most scary part is that my baby developed skin rashes all over her body, right about the time i had mine inserted. i have tried all kinds of cream, changed her laundry detergent (mine as well), skin care products, but the rashes wont dry up. my baby`s skin was flawless before i had this mirena. i always dress her appropriately, moreover the weather is not hot for her to develop rashes. i feel so guilty that i put her through the discomfort,am getting the mirena removed to confirm my suspicion but i know already that mirena is the cause as there is no other possible reason. its unfortunate that the professionals won`t tell you the truth and i specifically asked if it will affect the baby because i am breast feeding. i am so glad i did this research to validate my sanity, even though the harm has already been done. thank you all for sharing your experience.

This is my first month on this pill, and i started my period two weeks before i was suppose to start. I've had AWFUL mood swings, and there have been a couple of sleepless nights due to cramps. My periods usually last no more than a week, and I've been on it for close to two weeks, and might I add that it is VERY heavy. My face hardly ever breaks out ( knock on wood ) and now its broken out everywhere! Randomly throughout the day, I feel like i could just collapse at any given time. I got on the pill to regulate everything, not make it worse. Hopefully this is just my body getting use to it!

My wife just got her injection almost a month ago. She has a new doctor. The doctor gave her a 3 month supply, in 1 shot!!! She still has the pain, also back pain, constant on/off bleeding, depression, mood swings, headaches, hot flashes, nausea. I want to know, is she suppose to get such a large dose at one time? It seems that her body is fighting the medicine. Now she is taking another hormone in addition.

This is so scary!! I was just looking up "my son says he hates himself" on google, because I was concerned, as I deal with depression and wanted to find out if a little boy saying this (6 yo) is normal or if it may be signs of depression. Weirdly this link for singular came up.
My son DOES take singular for his asthma and has been taking it for about a year on and off. I have tried to take him off because I hate feeling like a pill pusher, but then his asthma flairs up again. So I put him back on it.
But today he has just been whining and crying (he is still crying and screaming for me loudly now!) and I began to get VERY concerned that my son was exhibiting signs of depression. If this is true, we may need to file a lawsuit against the drug companies as there are too many similarities and coincidences with this singulair. It wasn't even a THOUGHT or consideration that the medicine could have been causing this. I just thought that he was growing up and just goind through stages. Now I feel stuck because I don't know whether I should take him off and risk his asthma flaring up, or keep him on and risk his depression gene flaring up. This is VERY scary....

I have been on prednisone for 5 1/2 months now, I was hospitalized starting in February until like the 25th of March for a bad exacerbation(sp) of my ulcerative colitis. I have taken prednisone for 9 1/2 months out of the last 17 months. I have experienced everything from growing facial hair I don't want to loosing what hair I do in a short period of time. Most of my hair loss started after I weaned off the prednisone about one week ago, or lets say it got much worse. I also while on prednisone got have got to experience the lovely side effect of pysicosis(sp) and am on meds to couter react what it has did to me. This is a evil and horrible drug, I hate it with a passion for all the harm it has did to me. I now have joint pain, restless sleepless nights, night sweats, tremors, not to mention the rapid weight gain. And to top all this off I am still not in remission, so this drug was used all in vain. Please be careful using this awful drug and if you have to use it, only use it for a few weeks at the time and not long term...the side effects can be horrendous and sometimes like in my case permanent to some extent. I do wonder about the hair loss, it has been worse this time than ever...I hope it stops soon.

Hi again , just wanted to update I am now on week three since the removal and I no longer have backaches, and I am feeling about 80% better there are still the sleepless nights but they are not as often as before. Life is good and getting better. My sex drive is coming back as well as my energy level . I will repost at month 2 . Good luck to the rest of you there is a light at the end .

This is my story. My daughter 14, the most precious child ever born. She has a wonderful disposition always happy, loving, and determined to succeed in whatever she does. She just brightens everyone’s world.
She suffers from severe seasonal allergies and mild asthma. She takes approximately seven allergy/asthma medicines a day during peak season. Over the past two years she has been taking Singular as one of her medicines. Being 14, sick of taking medicine she would not take the Singular on a regular basis. Approximately four months ago “MOM” says, if you take nothing else take your Singular it will work both for the seasonal allergies and your asthma. She has been taking this regularly four the past four months.
She became paranoid, she became a compulsive eater and bites the skin on her fingers. She would eat and chew on her fingers at the same time, until she choked. She had so much anger, she could not even go to the mall without temper tantrums.(As a child she never had any tantrums ) Always afraid. Severe depression set in. She would cry at a moments notice. She would say, I have a very sad life, sad very sad, nothing makes me like this, I’m just sad. She felt she should go live with the homeless people. I asked her why, she didn’t know, she felt maybe that’s where she belonged. Nightmares and sleepless nights.
She needs help quickly. Before calling the Doctor, I went on the internet and entered Singular and depression and I found 1900 entries, all people telling me what I was experiencing. Could this possibly be the answer for us? I called her Dr and told him what I thought, he said he has never had anyone that this has happened to. He hoped it was the answer, but really didn’t think is. He said if it wasn’t the answer she would need therapy, mood stabilizer and Prozac.

Its day four off Singular, she smiling, no tears today, no temper tantrums, looking forward to school next week, wants to play volleyball next year, singing in the car,
I hear that happy voice again.(Hi, Mommy!!!!!!) Every once in a while a glaze comes over her face. She isn’t a 100% back, but I know it is coming.

To all the people that don’t have the happy ending, I will pray for you and hold you in my heart forever.

June 2, 2008