Pain medication symptoms and conditions

My daughter was being treated for headache pain and eye pain. She was put on prednisone z-pack which did nothing. The pain got worse so she spent 2 weeks in the hospital where they were giving her 1000 mg bags of prednisone in her IV. She finally came home and nothing was found. They did numerous MRI's catscans, you name it. A week after she was home she developed severe pain in both legs we believe is from coming off of prednisone. Does anyone know how longs this lasts, and what can be done about it. She averages 1-2 hours of sleep. She is on every kind of pain medication known to man but nothing helps. Please help!!

My story is long and somewhat depressing. I have had horrible periods my entire life. I have tried birth control pills which caused migraines. I have tried birth control shots which caused 6 months of non-stop bleeding and endometriosis. Finally, I am told that I should try Mirena. I was hoping this would be the answer but it has been just another problem. I have had cysts every single month since insertion. The cyst always develops on the side that is ovulating and then ruptures a couple of days before the period begins (yes I still have periods). Sometimes cysts develop between ovulation and rupture quickly as well. Then the first couple of days of the period are hell because of horrible cramping pain. Yes, the bleeding during the period is lighter, but the periods are lasting anywhere from 9 to 12 days. I have been on prescription pain medication for this now for 6 months. I have no sex life because the pain is there every day. My hair is falling out and I am on the verge of tears all the time. I can not continue like this and have an appointment set up for later this month to beg the doctor to perform an ablation or simply give me the hysterectomy that I have been asking for over the last 15 years. My children are grown and I have no plans to have any more. Why do I need to endure this hell?

I had Mirena placed March 11, 2009 after being post partum for 1 and a half months. It was great. It hurt a little and I cramped for about 48 hours after it was placed.

Now my problem: The first day of my last period was 8/19/09 (5 months into having Mirena) I haven't bled a tiny tinge since that day. So I have been without a period for nearly going on 2 months now. October 11th will be two months no period. Anyways about 4 days ago I took a pregnancy test which was negative. Today I began horribly cramping but still no period. I don't know what to do or who to turn to. I am getting this thing removed hopefully within two weeks. The nurse has to return my phone call within 3 days. Gotta love the military...ehhh I want this out now I feel like I am DYING...the pain hurts from my pelvic bones all the way up to the top of my tummy. I am nauseated and have taken all the pain medication that I can. I might go to the ER I am hurting that badly....I just feel as if I would feel better if I had a period...the pain is like labor pains. Anyone had anything like this happen before????

So glad I found this web page! I just finished a 10-day course of Doxycycline 100 mg. twice a day, prescribed by my oral surgeon after a tooth extraction. Around Day 5 or 6 I started getting heartburn that was not easy to get rid of. At the time I did not suspect the Doxy, because I was also taking pain medication, and thought that was the cause. It just occurred to me yesterday that the Doxy might be the problem. I looked on Drugs.com and read up on it, but nowhere in the listed side effects does it mention heartburn, or any of the mood disorders that other people here have experienced. Luckily I finished the pills earlier today, but I have had the heartburn non-stop ever since. So this time I Googled "Doxycycline heartburn", and I got plenty of results. So, it's not an isolated case. The instructions on my pill bottle were to "take it on an empty stomach", and to "not take any antacids, dairy products or iron within 2 hours of taking this drug". It makes me angry that this possibility of severe heartburn is not listed as a possible side effect of this drug. I'm glad I didn't get any mood disorder problems from it, I already take medication for anxiety/depression. Thanks for letting me vent! I'll be telling my pharmacist about this not-uncommon problem.

I've been on Loestrin for four months now. Previously, I had a hormonal IUD, which was in for 2 months and I had it taken out because I had HORRIBLE HORRIBLE side effects. Cystic acne, had my period the whole time it was in, it stabbed my boyfriend when we had sex, made me incredibly depressed, I sobbed myself to sleep every night, and then the icing on the cake was when it started to slip out, but then got embedded in my cervix halfway through and caused me intense pain that wasn't helped at all by any pain medication, over the counter or under the table ;)

So then I switched to NuvaRing. I had that for two months. First it gave me a yeast infection. It also caused intercourse to be very painful, my boyfriend could feel it when we had sex, and I could feel it at all times. It also made me INSANE. I didn't trust anyone, was a total paranoid freak, and at one point I locked myself in the bathroom screaming and crying because I thought my boyfriend was trying to kill me. I was pretty close to actually hallucinating. I would describe my side effects with NuvaRing as similar to paranoid schizophrenia.

Then I was on Ortho Tri-Cyclen, which gave me a migraine every single day which once again was incurable by any drug. So I was only on that for a few days.

Since then I've been on Loestrin. I am not completely happy with it, but I've stuck it out because compared to side effects of other hormonal birth control, they've been relatively mild. If I miss a single pill, I'll get my period, but true to form, they only last three or four days at the most. Before I started birth control, I hardly ever got cramps, but on Loestrin I get pretty bad ones. The worst thing is my skin. When I wasn't on birth control, I had beautiful skin. Maybe the week before my period I'd get one pimple that cleared up quickly with spot treatment, but now I have between 10 and 20 big, red, angry pimples on my face at all times. I've spent literally hundreds of dollars on Proactive, Neutrogena SkinID, Mario Badescu, UV acne "zappers," and many many other face washes, lotions, masks, scrubs, etc, but NOTHING helps. The weird part is that for the first 2 months I was on Loestrin my skin was fine. It wasn't until the past month and this month that it's been a problem.

I'm going to wait it out for at least another 2 months to see if my body gets used to it and my skin calms down, but if these flare ups last longer than that I'm going to have to try something else. I don't want to unnecessarily switch pills because I've had such horrible results in the past that I'd kind of rather stick to the devil I know.

I would also estimate that once or twice a month, I get a killer migraine. I assume it's related to the Loestrin because I used to get them only once or twice a year. The only thing that helps with them is going to sleep, usually with the help of a couple Tylenol PM or 5 or 6 Benadryl or Dramamine. To give you an idea, the first month on Loestrin when I got a migraine, I took 2 Excedrin Migraine, 2 Excedrin Tension Headache, 2 aspirin, 4 Motrin, 2 Tylenol, 1 Aleve, AND 1 Percocet over the course of 6 hours, and it did not help ONE BIT. I hope that this will also improve over time.

My 17 year old daughter is on Yasmin and has been for over a year. She is taking it to regulate her periods and heavy bleeding. We have not noticed any side effects at all. She has a learning disability and a low IQ. She is also on Buspar for anxiety which she has had long before Yasmin. She is also on Strattera for her ADD. Now, after reading and hearing about all these terrible side effects such as stroke, heart disease, kidney failure, blood clots, etc. I am going to ask our doctor about this. I read one post that said if you were on Yasmin and you had to take Motrin you should have blood tests...what kind if this is true? She just had her wisdom teeth out and has taken plenty of Motrin along with other pain medication. This is just way too scary....scared Mom in SC

My neurologist put me on Prednisone for cluster migraines. I started with 80 mg for 2 days, 60 mg/2, 40mg/2,20mg/2. It was so effective at keeping the cluster attacks from coming. I was so thankful to finally have something to stop the attacks. I have suffered with CH for 20 years and other than pain medication to abort an attack I never had anything that worked as a preventative. After taking the prescribed dosage I stopped taking the Prednisone. My neurologist warned me that this drug can be very effective short term but I would not want to have prolonged use because of the side effects. Unfortunately, when I stopped taking it my cluster migraines came back full force. So I went back on taking 20 mg daily. That was a BIG mistake. At first I was euphoric, on a constant high. I had so much energy even though I would only get about 4 hours sleep because my mind was racing from 2:00 am into the early morning hours. I would wake up with night sweats and needing to urinate 3 times per night. My face got puffy, I had terrible heartburn, increased thirst and a decreased appetite. My family was watching me wizz around like the Tazmanian Devil wondering why I was acting so bizarre. I thought I was seeing things so amazingly clear! The worse part of all is the itchy, red rash that started on my elbows, then knee caps. It has now spread up and down both arms and legs. I went to see my GP and I told him that I have never had any skin rash like this before. Could it be the Prednisone causing it? He of course said it was unlikely because Prednisone is used to clear up skin problems. Now having stumbled on to this site I realize that it must be the Prednisone doing this to me. I am unfortunately going to have to suck up the pain of the migraines and let them run their course until they leave me for a few years. I'm so disappointed that Prednisone isn't going to be the cure after all.

I am a 58 year old female Who has been taking Simvaststin for 16 months .
I have been increasingly bothered with mainly night leg pain ( bilateral) that radites to my hips and back. It's like a tooth ache. I too have had to resort to taking pain medication at night to sleep. During the day when I sit for long periods my legs ( especially the thigh area) aches and standing up , walking etc does not alleviate the ache. It is not constant at this point but very frustrating.
After reading the posted notes I am contemplating going off the Simvastatin for a while to see if my symptoms improve.
Any thought?

Thanks!

I just began using Yaz about 4 months ago and I have had the weirdest thing happen. I have massive headaches (never had them before) and this weird pain in me face (right about my right cheekbone) At first I thought it was a sinus infection.. Major pressure and headaches are easy to diagnose. Then when it didn't go away I got scared. An emergency room visit and a neurology appointment later (everything is "normal") I have decided it HAS to be the Yaz. I have also been having weird ear "fullness" Out of nowhere my ears will just pop like i'm going up a mountain...The took me off that and put me on Yasmin. Isn't it the Same pill? Anyway.. has anyone experienced similar symptoms? If so, how long did it take to go away? Thanks!!

am having severe abdominal, pelvic, lower back and hip pain. I went to see my doctor who thought I might have a herniated disk in my back. Having no insurance I had to pay cash for the doctor visit and X-Rays and was told I may be suffering from a herniated disk in my back. X-Rays showed no such thing. I was given a muscle relaxer, pain meds and an anti-inflammatory med. Through the next week the pain began to intensify to the point I had to leave work. I went straight to the ER where I was given steroids and a stronger pain medication. By the way, pain medication has no effect on me so I have been suffering for quite a long time. The ER doctor did recommend I see a gynecologist right away. He thought for sure something was terribly wrong. This was just last night and after reading all the comments above, I am pretty certain this is my problem. Having no insurance my clinic would not see me so I have to go to another doctor who said I must pay $200.00 up front just to get in the door. I have had my Mirena for 2 years and was doing just fine other than having problems with the headaches, zero libido and uuuggghhh, that weight gain thing and a few other problems, but now I am convinced that no woman should use the Mirena. I have already been through all of the with the Norplant. Another horrible contraceptive. If it is indeed the Mirena, I will have to have it removed and most likely will need a hysterectomy. Wish me luck finding a doctor to that with no insurance.

toriintx

I have taken Avelox before with only minimal side effects nausea and diarrhea were the only ones I got but they were enough. I have been suffering from chronic sinus and ear infections for going on two years now. My doctor gave me samples again of avelox on Monday. Last night I had to be rushed to the hospital. After throwing up all day I got a severe headache. I felt dizzy and out of sorts all day but when I couldn't take the headache anymore I tried laying down. With this medicine you can't take any pain relievers so I thought if I just went to lay down maybe it would ease up some. Well it didn't, and before I knew it I was shaking uncontrollably with tremors and could no longer put sentences together. My head hurt so bad I just wanted to stab myself to make the pain go away. At the er they gave me an IV with something to help with the headache.Anyway after taking a Ct scan and not seeing anything on there the er doc gave me the ok to go home and gave me a script for pain meds. I was having hallucinations, anxieties, and could not speak correctly. I am still having trouble making sentences, I am stuttering, which I have never done before. And I can't get words to go together to make a sentence. The Er doctor wants me to follow up with a neurologist. My tremors still haven't stopped and now I sound like the guy from rain man when I am trying to make a sentence. This is pure torture and I feel like I am in someone else's body.

After what I have seen here and on some other sites I'm 99% positive this drug has hit me with several of the side effects listed. I'm a fairly healthy 49 year old woman. I have never had any health problems, no high blood pressure, no heart problems nothing. I went to the dentist in late March with a problem wisdom tooth. I'm allergic to penicillin so I was prescribed Clindamycin (sp) but it did make me sick to my stomach so I couldn't get the entire daily dose down. I had made it thru 90% of the prescription when I went back on 3-31-09 and still had some infection left in the tooth. My dentist took my BP and it was normal. He then said he wanted me on antibiotics for another week, and prescribed Levaquin as "a wonderful drug, it won't make you sick and you only have to take one a day". So I took the 7 day 500mg dose, went back the next week. True, it didn't make me sick. But I did notice my Achilles tendon was really sore and stiff. I also had a re-occurrence of an elbow problem that had healed and was no longer bothering me until then. I also noticed I wasn't sleeping well, and was having vivid dreams, which I attributed to the pain medication (vicodin) he had also prescribed. Went back on 4-8-09 and my BP was sky high!! As I said, never ever have I ever had an issue with my BP including when I was pregnant! He said he couldn't do anything with it so high. I mean a week and up almost 100 points! He attributed it to "White coat syndrome". So another week of Levaquin and back again yesterday. BP was the same story again, this time he didn't even see me but sent in the assistant to tell me to go get on meds with my Dr. So after that, I'm angry and totally confused. So I came home, hit the internet and I'm seeing what changed in that week to make my BP go insane. I'm also seeing other symptoms here. The Achilles tendon, Knee aches, Back ache, Hip ache, difficulty sleeping, and Steven King quality nightmares. I also read somewhere on the net that supplements like MoveFree with MSM would help and I do take that as a regular supplement to help with things just getting a little older as I'm a pretty active gardner. Now I have been off this since Monday and my aches are better today than they have been. I picked up a BP machine yesterday and it's down a little since at the doctor's. I'm keeping a close eye on that for a couple of days before I submit to a chronic disease for the rest of my life. Hopefully the side effects will gradually go away. Has anyone else's symptoms gone away after stopping the drug? How long did it take for them to go away if they did?

ok i'm 27 and I've had Mirena almost 5 months now and no periods since end of 2nd month...last few days I have a strange feeling around the area the IUD would be inside like tingles and just bothersome (as if body was trying to expel it or something...hoping i;m no preggo).....Anybody know what is going on?

I really don't know what to do, I hurt so bad every single day I could cry. I was given Levaquin in March 2008 when I had pneumonia. I took it for 10 days and I hurt so bad still was very sick so I was put on it for another 10 days, so I took the Levaquin for a total of 20 days. I thought all this sickness was from the pneumonia. I had trouble getting out of bed, I could not even bend my knees, my feet, knees, elbows, and fingers were swelled up and I was getting all kinds of cracking in all my joints, headaches, stomach pains, all kinds of muscle pains. When I went back to work, I was telling a girl at work how I hurt and she asked me what kind of antibiotic I was taking, I told her and she said they had it on the world news . I said why is it still on the market. I seen 3 doctors about this and they think I'm nuts! They sent me for all kinds of xrays for all different parts of my body, what is that going to show! Its been a year and I still ache, I keep swelling up, joint and muscle pains, cracking, stomach troubles, problems sleeping, its terrible. I take pain medication for my back, I have 2 herniated discs, and I have to take more pain meds for all these other pains, this is not going to work. I even went to see a rheumatologists and he said I don't have arthritis. So Levaquin done a number on me. If anyone can help, or know what to do let me know!

I am 71 years old, I have been taking 80mg of ZOCOR ( Simvastatin ) for the past 16 years. five months ago I started to hurt in my lower back, hips,Knees,thighs, for two months then it traveled to my shoulders, wrist, hands, fingers. the Dr. gave me a round of prednisone (one shot and 11 pills) the pain stopped and everything was wonderful for two weeks,the Dr. stated that I had avused my body in the years gone by now the pain has started back in my shoulders, wrist, hands the pain is very strong,and my legs are starting to get weak again, I am taking Naproxen 500 mg two times a day and also taking Hydrocodne10mg every four hours also have Oxycodone 10mg to take every four to six hours, I have mentioned the results that I have read about the Statins in this forum but the doctor, does not act like it has any significance. does anyone have any suggestions??? if so please let me know, this pain is killing me, if you have any info. please email me at. ******

Im a 32 year old male that was put on simvastatin 40 mg and cardizem 240 mg. I am now having severe headaches, so bad i cant go too work anymore, dizziness, fatigue, legs feel shaky all the time, cant stand up for long periods of times. Doctors claim its not the medications but its funny i never had these problems until i started taking these medications, after reading what people have too say about the simvastatin on here i am done with that, i cant live my life like this anymore. I have also heard my other medication can cause these problems so im going too talk too my cardiologist about a different one too control my heart. Im glad i have found other people having problems like me, i don't feel so crazy now.

Ive been on meprozine or just plain demerol for 5 years now i do not take more then 1 pill in 24hr and then i try to put days in between doses i have OI a brittle bones and kidney stones and this is the only pain medication period that i can take with out having a bad reaction. as far as mood swings i don't have any if any thing it keeps me calm but it will only stop the pain if you take it on the first on set, if you wait and take it till the pain has gotten worse it simply wont work at all. there is one side effect it keeps me awake lol im the only person i know who can take this and stay a wake all night

I am a 52 yr old woman who was rushed by ambulance to the hospital on Sunday 4, 2009. I awaken with a horrible ripping pain in my lower left side and back. It reminded me of labor pain although it was worse because I knew I wasn't about to have a baby. I could barely walk and the pain kept me bent over, and burning in agony. After being x-rayed and diagnosed I was told I had a very tiny kidney stone, along with a UTI. I was told they could manage my pain better if they kept me overnight, with hopes I'd pass the tiny stone by urinating in a little strainer cup, to catch the stone. I've not seen the stone yet, and this is the 3rd day. Anyway, I awaken in the hospital after being knocked out by pain medication, with an excruciating headache, as if someone was putting pressure on my neck and back of head. I also noticed a big red rash on my forehead. The nurse gave me benadryl, and continued my doses of Bactrim, and Flomax. When I was released the next day I was given a prescription to fill, Bactrim 2X 3 day therapy, Flomax, and Vicodin. Recovering at home I've had an excrutiating headache the entire 3 days.. I had nausea, felt chills, had no appetite, and felt dizzy and as if I'd throw up every time I got up. I ran a low grade fever of 100*. After reading this site I know that it had to be the Bactrim that caused all those horrendous side effects.This is the fourth day since I was diagnosed and I still have a UTI, and will be calling my doctor in the morning, thanks to post like these.

I was prescribed Ultram for chronic back and neck pain because I had been on Vicodin for a long time but did not want to be on a strong narcotic long-term. Ultram is effective, but i have been on it almost a year and if I run out and don't happen to have any more, after about 12-24 hours I start sweating and I feel weak and can't sleep, plus legs twitch uncontrollably. I guess all pain meds have their problems.

Very high tolerance for medications incl 60mg morphine, 20mg oxycontin 4x day, however, I just cannot seem to tolerate Fentanyl. Have tried it two times in past, both the 25mcg and 50mcg. The first week or so is great, after that the side effects are more than I can tolerate. All of these side effects were extreme and unbearable not just mild. They affected my ability to function and sent me to bed on more than one occasion. Extreme fatigue, nausea, sweating, anxiety and weakness. I felt as though I had a very bad case of the stomach flu. Both occasions I stuck it out for 2-4 weeks till I finally had to quit using it. Any suggestions as to why would appreciated. Some of my side effects aren't even listed in brochure.

I was put on Levoquin after 4 days of Bronchitis. My body was not responding to the antibiotic so they added Prednisone. I continued on both medications IV for 8 days. After the second day, I developed a severe pain in my groin. I mentioned it to the NP treating me and she said, "we will worry about that once we get the Bronchitis under control". The pain continued as the medication continued. After the Bronchitis was resolved, the pain in my groin was terrible. My doctor sent me for CT scans and and MRI. The next thing I knew I was in the Orthopedic Surgeon's Office talking to him about a total hip replacement. He said the test showed very mild degeneration and he was not sure a total hip replacement for me was the answer. I opted not to have the hip replacement. Diagnostic Testing continued. Finally, my doctor told me that the combination of Levoquin and Prednisone caused a tendon rupture in my groin. He said it would heal but would take a long time. It is now 8 months since I took those medications and my hip is more painful now than ever. I am on pain medication and it does not help. I see my doctor today and we will discuss other options to relieve this awful pain. I walk with a cane and I feel like I will never walk normally again. It has totally disrupted the activities of my life. My doctor tells me to stay off my feet as much as possible to rest the tendon, this is impossible as I am a registered nurse and I am on my feet constantly. This has destroyed my life!

I have two experiences with Prednisone to share: I am a 52 year old woman, married, no kids. One year ago I came down with a serious case of shingles on the top and inside of my left eyelid. What started out as a bump that looked like a pimple or a bite on a Friday afternoon (and I don't have acne), spread across and under my eyelid by Mon, morning, up into my eyebrow and down the side of my nose. My eye felt like there was glass in it every time I blinked. I got to the doctor on Mon, the dermatologist on Tues and the opthamologist on Wed. All confirmed shingles. I have never felt anything to excruciating in my life! The dermatologist prescribed a 3-week descending dose of Pred starting with 6 pills a day. I was also given Gabapentin (a nerve blocked), Acyclovir, a muscle relaxant, pain medication and two separate eye drops, one of which was also low-dose Pred. After the 3 week course of treatment was done, I had to continue for another week, but with lower doses.
Side effects: I did not notice any side effects except that my appetite was seriously jacked up! I ate anything and everything -- and then some! Food was my best friend and I hogged everything in site! In hindsight, when I try to assess myself and any changed, I guess I do have some attitude issues in that I am quicker to anger, quicker to react and respond and seem to "snap" a lot quicker.... Oh yeah I am also on antidepressants.... I now have one droopy eyelid due to the nerve damage from the Shingles and permanent damage to the cornea and tear ducts.... However I am not really sure how much of that is due to the Shingles and how much is due to the Prednisone.

My 89-year old mother was hospitalized in August for emphysema and chronic lung disease, she was down to 81 lbs. They treated & released her and she was on a descending dose of Prednisone for a week. She needed to gain some weight & gained 3 lbs! This was very good.... She is still smoking and her doctor will NOT insist she quit (I think they have given up). They put her back on a 2-week course of Pred again last week. Her appetite is back up Yeah! but she has some serious attitude and anger issues. We are only 1 week into the 2 weeks and I don't know how our family is going to stand taking care of this evil old woman during this Prednisone treatment, and afterwards. I'm sorry I ever let the doctor put her back on it--- however she is gaining weight and getting (falsely) stronger, which she needed.

MY STORY

My Mirena was removed on 29th May 2008.

I had the Mirena put in four years ago,I had terrible pain the day after, it was that bad I was going to go to the hospital Emergency to get the thing out but I put up(the worst thing I done in my life, Im paying for it now) with it and it and the pain got a bit better,had a lot of bleeding (spotting) for the first six months and then it finally went away. For the first year I thought Mirena was Great but then the problems started.I started to gain a lot of weight,facial hair,Very sore breasts, I also had a lump removed from my left breast a couple of years ago, but I didn't know until recently that it was most likely caused by Mirena. Some of the other problems I had, My stomach bloated, I look like I'm six months pregnant ,I have a cyst on my left ovary,dry skin,acne,strange depression,headaches,and the Worst of all I had to have my Thyroids REMOVED on 1st Nov 2006 and I'm pretty sure that was caused by Mirena as well, so now I have to take thyroid Medication for the rest of my life,I had the Mirena removed as soon as I done some searching on the internet for my unexplained medical problems, mainly my weight as I had weighed about the same my whole adult life and now I had put on a few stone and now I have to try and lose it,as for my thyroid I have trouble getting the Meds right its a real pain,blood tests all the time.I just don't feel I have much left in my life,depressed,sick all the time. I eat well as I have high cholesterol so its not that I over ate,I noticed you do feel a lot more like eating sweet things. I found a site called ****** and found out there are thousands of woman,girls with the same problems as myself and that there is a class action law suit going on to Sue. Its worth having a look at this site it helped me a lot.I feel so bad I don't go out anymore I don't see friends or family I'm to depressed about my weight now. I am in the process of trying to find out if there is a Class Action Law Suit in Australia.If anyone knows of a Class Action in Australia could they Please let me know. After having the Mirena removed about 6 weeks ago I thought I was doing ok only a bit of spotting,but about 3 weeks after having it removed I got my period and the pain was unbearable,I was in agony stomach cramps and I bleed so much I thought I was going to die from blood loss,also the scariest was the huge blood clots,very scary,must of been four years of period in 1 week I couldn't believe how bad it was, I felt really sick and weak,but thank goodness its eased off now after a week. I just hope now I might slowly start and feel like my old self. Im also on medication for heart palpitations,I get Heart palpitations (SVT) a few times a week,I had my heart palpitations just after my thyroid removal op and was put on ecg and my heart rate was 176 Beats per Minute I was rushed to Intensive Care and I had to have an injection called Impending Doom (It makes you feel you are going to die) to slow my heart rate,it worked and I was kept in intensive car for 3 days,very scary thing to go through I hope I never have to go through that again,my heart palpitations got worse while I was on Mirena and now I also take Magnesium to help control them as well as Metoprolol which I have been on for some years and I recently read that if you are on Mirena it increases the side effects of Metoprolol.

So if you have had any bad experiences with Mirena please let us know,it will help others with their problems, hopefully. I just wish I never got Mirena and my advice is DON'T its not Worth the risk,if the Doctors had of told me about the BAD side effects I would NEVER of had it put in. Sorry about going on so long, Good Luck to you all,

Thanks Net.

google mirena-side-effects.****** (a mirena help,info site)

UPDATE

I have had it out nearly 3 months now my painful breasts feel normal again,I haven't lost any weight yet, but will soon hopefully,I do feel a lot better but still get some of the symptoms back just before my period.

I get sooo mad when i think of what Mirena done to me and all the other women and how bad some of their side effects have been. I get mad when i read some of the other ladies stories and the terrible things they have gone through ,

Perforations,Miscarriages,IUD's lost in their body,

Hystorectomy,and the rest. I want to wish them all the best, and we WILL get Better and Bayer ,Mirena will PAY some day for what they have done to US..

Well...i'm only 17 years old and i have been trying EVERYTHING to get rid of my 2 week long heavy period and extremely severe cramping. I have been on 3 different kinds of oral BC and i would still bleed for 2 weeks. So i tried the Mirena IUD and that was the worst idea of my life. It went in fine but about 10 minutes later i was in a extreme amount of pain (and i have a very high pain tolerance, broke 3 ribs and didn't cry) i called my gyno back and he prescribed me a pain medication but it didn't work. After trying 3 different pain medications and an antibiotic i had enough. I went to the hospital and was prescribed percocet and that helped. I went back a few days later and had it taken out so now i am trying the NuvaRing. I put it in and a few hours later started cramping and having back pain. The next morning i had very bad nausea and cramping. Its about a week later now and i am experiencing headaches, nausea, quite bad cramping, bloating, tiredness all the time and i just don't feel myself anymore. I am calling my gyno back to see what he suggests but i'm looking for any ideas or suggestions until i get a hold of him. Thanks

Monthly wicked migraines, right before period starts. Sometimes lasting on and off for 2 1/2 days. I had one so bad I had to go to the ER. I've never had problems with migraines before in my whole life. A few were very bad and makes me not want to do anything all day. I went to the neurologist just to get a pain medication for this.

Also was diagnosed with allergies last summer because I had 2 bad sinus infections.

Recently I have started to have acid reflux every night and now sometimes in the mornings. This sucks!! I am getting this removed.

I did several internet searches over the past several months and all these symptoms are caused by progestin (levonogestrol). This is not worth it.

I've had this thing in for over a year now, but all these symptoms appeared after getting this thing in.

Ive also been very moody around the time of the month, super irritable and bitchy.

My gyne suggested to take another drug to counteract, (basically prozac with another name) but that's like taking speed to counteract a downer. No thanks!!!!!!!!!!

I got this thing put in because of heavy periods, but it is totally NOT WORTH IT!! My health has suffered because of this.