Pain meds symptoms and conditions

I have had Mirena since November 2006.(3 years) It was SOOO painful to have it put in, but I know it has to do a bit with the fact that I've never had a kid. I immediately had HORRIBLE cramps for hours and bled for about 4 weeks. Since then I have not had a period at all :) Now, I am 27 yrs old and have NO sex drive, ZERO! I hope that it is because of the Mirena, lol. I don't take any other meds at all. In 3 years I've probably packed on 15 pounds, but I can't say its because of Mirena. Me and my husband are ready for kids, so I'm gonna have it taken out in January. We'll see if it helps with the sex drive :) I haven't had any other side effects really.. overall, I would use it again, just be sure to take some pain meds before you have it put in, cuz that pain is like child birth said my OBGYN.

I've been on the pill for about 7 days, and yes, I know it takes awhile to adjust, but I really didn't expect to be cramping so much, or for there to be breakthrough bleeding every day. The pills are making me bloated and giving me gas; I have to take pain meds each night to sleep since the cramping starts around bedtime. How long should I give the pill before I give up on it?

23th
2009
10:36 PM
MIRENA is the worst thing EVER!!!!!!
I got Mirena as my husband and I were lacking in the sexual side of our relationship because we both HATE using condoms.I have a 31/2 year old son and we have decided that for now we are happy and would like if we didn't have anymore children right now so I talked to my doctor about Mirena.
Let me start by saying that my labor 6 hours with NO pain meds was nothing compared to the pain I had when they put it in. Then the bleeding started right away I was bleeding for 8 weeks then had 1 week free and now have been bleeding for about 8 weeks. I had 2 ultrasounds to make sure it was in proper and everything was "fine" my doctor says everyone's body reacts different.
The symptoms I have are Occasional Cramping,
Sever bleeding,
headaches,
irritation in my legs (same symptoms as RLS),
Depression,
no sex drive,
back pain
Weight Gain (17lbs in 2 weeks)
and the weirdest symptom is hard to explain but its the same feeling in my body as if you were to touch a 9volt battery to your tongue! Every now and then I have little shocks and its so annoying. I have had mine in for 17 weeks and I have an appointment in 8 days to have it removed...Back to condoms it is

Hello,
How long do side effects last after completing steroid treatment? I've been off of pred for 4 months for crohn's first time. I was on 40/30/20/10 for a 6 week period. When I got to 30 my legs went into extreme pain. They felt like they were on fire, burning knees. Went to several doctors. One said steroid withdrawal, one said inflammation of nerves from Crohn's. Neurologist put me on neurontin to get off of the pain meds. I am still in excruciating pain and wondering if it really is steroid withdrawal. I can barely walk at times with extreme sharp pains, like someone is stabbing me in the legs. Can't stand for long periods of time and pain pills barely touch the pain. During steroid treatment, they gave me 3 rounds of Dilaudid in the ER and I was still crying, and I don't cry. Has anybody ever had this effect this long after being off the drug??

I conducted a search for "long term effects of Topamax" and discovered this site, and am so glad to have done so. I have been on Topamax for around 2 years now, at the 200mg level, for chronic, sustained migraines. I have figured out, through tracking, that I will get a migraine lasting 3-4 days during ovulation and again on my period. The Topamax has helped considerably with the headaches, although I do still get at least one per month. It is generally not of the same duration, though, and is fairly easily controlled with pain meds.

I've been a bit worried, though, about continuing the drug for life, as it seems I need to do to control these headaches--thus the search. I, too, have experienced the "mental fog," and general decreased cognitive abilities. I am an extremely intelligent person, a writer, a former English teacher. Why am I unable to pluck words from my brain when I need them?

I've also experienced the tingling and numbness in various extremities, sensitivity to cold, blurred vision, fatigue, and loss of taste sensation. I've also become a royal bitch to my husband and children--although I had no idea that this could be related to this medication. I feel relieved to know this now...to know that I can change and be the person I once was. I don't like myself very much right now, but it's like trying to stop a runaway train. I can no sooner prevent or alter my knee-jerk reaction to things than I can stop that train.

I've been off of the Topamax for approximately two weeks now, and have already gained 5 pounds, although I work out 2-3 hours daily and play competitive volleyball 2-3 times per week for several additional hours. I had initially lost around 18 pounds and kept it off, even when my appetite returned. I'm uncertain, though, why I'm gaining the weight back so rapidly. I'm eating fewer than 1500 calories/day and exercising like crazy. It doesn't make sense.

I don't care about the weight, though. My chief concern is the return of my cognitive function. Has anyone experienced a return to their prior cognitive state after getting off of this medication?

My mother just died from all of the secondary effects of prednisone. She was diagnosed with glaucoma 4 years ago but no one ever did a sed rate blood test to find out that she had giant cell arthritis. So once they found out, they treated her aggressively with 60 mg of prednisone. She swelled up immediately and had terrible pain in her legs. Then she became diabetic with big sugar swings that couldn't be controlled. Then s he got thrush in her mouth and couldn't eat or drink. Then she became dehydrated. For pain they gave her constipating pain meds and this caused a bowel impaction. She had tremors and then she had mental confusion. Then her skin started splitting everywhere but wouldn't heal. Then she started losing fluids from her skin. Then her bowels got impacted again. Then her colon ruptured and she got sepsis. Her sugar levels went haywire. Her heart wouldn't slow down, her skin tore up worse, she lost more fluids. And finally she got pneumonia and fever. She died in my hands after so much s suffering - it was just ungodly.

I hope she's ok now and happy and having no pain and is in God's loving arms.

I will never forgive this doctor.

Please be careful with this drug. It is so incredibly dangerous.

I had Implanon inserted on Feb. 08. I just had it removed about 1 month ago (Jun. 09). This was the WORST birth control experience i have EVER had. I gained over 60 lbs. over a year's time, I was eating less and working out normally, i still kept gaining weight. I would be on my period for months at at time, although i never had any cramps, i developed anemia. I was the worst person to be around, I was always irritated and had lots of trouble sleeping. Occasionally, I would have terrible muscle pains in both arms, felt like loss of circulation. I was always tired and very depressed. I hope anyone who is considering this birth control to reconsider other options. After i had it removed my body went haywire! My red blood cell counts spiked and developed shingles(I am only 22)! Not only that i had the MOST painful period of my life, cramps so bad i had to be put on pain meds! My body is finally getting back to normal, and I feel like a whole new person!!!!!

Hi. I had mirena inserted about 2 months ago. It was pretty painful getting it put in and i had a lot of cramping the next few days, but i didn't take any pain meds before it either. I would highly suggest taking at least 3 ibprofen before you are scheduled to have it inserted. Anyways, I have been having to wear pantyliners every day since. I have brown milky discharge that smells terrible as well. I sometimes get very light stomach aches but that is about it. It is very nice having a birth control that you don't have to think about but, do you want to have discharge for months at a time? It is your decision. I am hoping this will stop soon! Hope this helps.

hello i am a 28 year old mother of three i am going to school to become a nursing assistant just started my clinical.i have not been feeling good for the past 4 weeks went to my doc and asked for them to test my urin they took it and only did the dip stick instead of sending it to the lab the doc called me about a week later and told me everything looked good i said to him are you sure i feel like i have a uti so he told me if i am still not feeling well come back in in about a week so a week passes and now i am having pains in my back and trouble going to the bathroom so he does a (ua) i go to the lab to give urine and he put stat so the women said it should be back by tomorrow i called my doc the next day the receptionist says yes your results are in so i told her i am coming down cause she couldn't give me the results over the phone so i get ther and she tells me well it came back abnormal which i knew didn't have to pay $80.00 to tell me that i was the one telling the doctor that so anyway she tells me the doctor is in with another patient that i will have to wait i said oh no i feel like i am dying i am having so much pains in my kidneys so she said ok 1 min she got the doctor he called me down to his office and said well it looks like you had a uti and now it seems a little worse than that it might have traveled into your kidneys so i said i told you a few weeks ago when you said my urine came back fine i was in a lot of pain so now what he told me he was going to put me on levaquin 500 mg for 5 days and lets see how that works and to come back in in 2 weeks to take a repeat ua so i said ok got the prescription filled $50.00 later went home and read all the side effects and was so scared to take it but i was in so much pain and hearing about the actress who died of a ut i was so scared but i took it even know in my heart i knew it was not going to respond to me ok well let me tell you i almost had to quiet school i can hardly take care of my children just to walk up the stairs to go to the bathroom feels like i have been running a marathon for 10 miles we are a young couple and parents of 3 and i am a homemaker till i finish school so we live on my husbands pay check which really is living week by week nothing in saving cause we need every penny for bills and food but now i have been in so much pain not sleeping a wink cause i am so afraid of the nightmares that he has been home and not working which means no money is coming in at all i mean how do you tell your children well sorry i have nothing here and no money to buy you juice boxes for school i just really wanna give up i feel like i became a failure to my husband and children if i wasn't so sick he could be working and at least we can have the basics how do i tell them that we are almost out of oil and might not be able to have hot water i mean my life seems ruined all because of this drug i can not believe it i wish every day if i do fall asleep mybe it would be in my childrens best if i do not wake up but then feel like how can i even think that they love me no matter what i don't know i just can not even believe that my life turned around like this in the matter of a week how can this happen i really need help if anyone is out there please help i just wanna end it but i know deep in my heart my kids need me what to do

I have been taking 40mg lipitor for over 9 years now.

I have had back issues since an injury to one disc (L4?), and had microdiscectomy in 2001? Took about two years to actually get close to normal.

The last few years, I have had multiple issues with shoulder pain, wrist pain, elbow pain, lower back pain, Upper rump muscle pain , and now both hips are killing me (the shoulder, upper rump muscles and hips are by far the worst). And I am now so weak in my lower back muscles, that it feels like I will (and do) pull out my back.

I have seen NO many doctors I can't even name them all. I have had operations, multiple injections (cortisone) taken pain meds, etc. Nothing has helped and in the last year and a half, I have gotten steadily worse. To the point where I can't really do much of any activity. Sleeping at night is painful. Can't lie on left shoulder, and can't lie on either hip for more than a few minutes. If I fall asleep on my side, the pain wakes me up. When I try to walk, 80% of the time, I end up with a pain in my upper right rump (sacroiliac area), that I MUST sit down to get the intense pain to go away, which it does. But comes right back when I walk again.

I have had x-rays, MRIs etc, and never reveals all that much. Disc issues, yes. NOt much else.

Recently, I have begun to get a nasty clicking (catching) on my left jaw (joint?). Not really painful, but something definitely wrong. My dentist sent me to his Chiro. I went and liked him right away. I had gone to another chiro for years and I believe in them. But this one is the best I have seen.

Anyway, one of the FIRST things he suggested, was that it was POSSIBLE that the Lipitor is causing all of my problems. Put me on COQ10, and doing multiple adjustments and treatments. I will be seeing my regular doctor 5/26, and my chiro wants me to see if he will take me off lipitor and put me on Niaspan instead.

I guess my question is: Can Lipitor be fine with me for so long, and then in such a short period of time, turn me into a compete wreck from the pain and wasting away of my body/muscles? I've told doctors for over a year now that there is SOME connection as to all these issues and pain. One Doctor, of course, gave me the "you are getting old" bull. Yes, I am 56 yrs old. But I understand the process of getting old, vs the complete failing of ones body.

Also, IF it is the Lipitor, can it possible all go away? Or should I expect some damage forever?

One more thing, the last ortho I went to the other day for a second opinion, wants me to do a EMG, to see if there is muscle damage. I was not planning on doing it, but wonder now, should I? He was not doing it because of lipitor, as he never even talked about that to me. I had shoulder operation and have not had the results I feel I should have had.

I am a 38 year old male suffering from a combination of occipital neuralgia and migraines. For 20 years, until a year ago, i would endure pain that was only manageable with narcotic pain relievers (imagine all the gamut of such kind). I would have neck and head aches typically 3-4 times a week, accompanied by vomiting, dizziness which would put me to bed for the entire day. Work and family suffered in magnitude comparable to my own suffering. So then I finally saw my GP for that. The pain meds went up the roof, imitrex, maxalt was added to the equation with only marginal side effect. I saw a neurologist. He had me do an MRI and put me on Topamax starting from 25 mg, which I upped to 200 mg within 6 weeks. Past the initial side effects, the headaches subsided, the frequency reduced and i was able to enjoy weeks at a time with no episodes. Stayed at 200 mg for 5 months. In the meantime, the MRI came back positive for some brain inflammation. False positive they said, does not fit the clinical picture. Second MRI, same positive, this time proceeded with LP, which was negative. Third, MRI still positive; making the neurologist uncomfortable. While dealing with MRI results, the topomax had yielded positive results as far as pain management was concerned. But little by little I noticed that I was becoming more irritable, more impatient and more forgetful. Someone would have to remind me of something several times before it would even register in my mind. I empathize will all the posts that mention feeling like having Alzheimer's. I didn't care in the meantime. As long as I didn't have to deal with the pain it was ok with me. But the situation became worst and worst. I couldn't concentrate on anything, the mere task of remembering to do something was insurmountable. I would wake in the middle of the night and find myself staring at the bathroom mirror for no reason. I would have terrible panic attacks which i control with valium. But yet i continued on with topamax convincing myself and being convinced by other people around me that i just had a "personality disorder". Finally, work begun to suffer. I was loosing track of meetings, deadlines and when this happens someone knocks on your door (boss) telling you that something just doesn't click, something just doesn't feel like a personality quirk. Other people playing doctor would slap on my face that i just had ADD, that I should take something for that and get on with my life. But something was wrong. Pain or dizziness or lack of concentration etc are all electrochemical processes in your brain. It turns out that topamax was helping my headaches but it was not slowly deteriorating other cognitive abilities. Finally, the neurologist decided I should wean of the topamax, stepping down from 200 - 150 and then we go to 100 and so on. I dread the re-occurrence of the headaches. I am waiting for them to happen again at some point as I drop the dosage. But in the end of the day, I'd rather be in pain and in control of my life rather pain free and absent minded.

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'm 23 years old and had the Mirena put in 6 weeks after our first daughter was born. The first 2 weeks of having it were fine... other than a little struggle implanting it all was going well. Exactly at the 2 week mark I wound up in the ER with what I thought were a bladder infection, hemorrhoids, and swollen lymph nodes in my hip-flexors. Now none of this has been linked to the Mirena, so it could be a fluke, but none of the doctors could figure anything out! My urine sample was clean, my pap was normal, they couldn't find hemorrhoids, and it was a frustrating un-diagnosis. The doc sent me home with pain meds and a local numbing cream, but using the bathroom hurt so bad I had to bite down on a towel to pee! Taking a poop... HA... I've been putting it off for days because I feel like my rectum will tear open! Has anyone else had any of these things? Maybe I'm just ill with a strange disease, but this site has me curious if it isn't the Mirena!

I had Mirena inserted Nov 2008, one year after my miscarriage. Everything was great at first. I had it inserted on my lunch break and went back to work with no problems. Periods were shorter and lighter. Now, 6 months later I've noticed problems. About 2 months ago I was working over night and felt a sharp stabbing pain in my abdomen. I went to the bathroom and was bleeding a lot. More than a period. I went another hour, and the pain was almost unbearable. I left work and went to the ER. They said I looked fine, that Mirena hadn't moved and nothing was torn. Gave me some pain meds and sent me home. I've had short sharp pains ever since.

I was diagnosed with depression my 6th grade year, when my grandfather passed away. I've been battling ever since. So, when my depression got worse after Mirena, I didn't think much of it. But the past month or so, my thoughts have been like some other users have described. I've had very scary thoughts, and boughs of uncontrollable crying for no reason.

My periods have stopped, with some light spotting every month. I do still have cramping, but no bleeding. I'm thinking of making an appt with my OBGYN and having it removed now that I've read all of these posts. I had no idea of any side affects other than interfering with menstruation. If you don't have Mirena, make sure you research more than I did. If I had, I probably wouldn't have gotten it. I really wish I would've researched more options because now I'm beginning to regret my decision.

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.

i went in 4/15/09 to have the mirena put in...it wasn't scheduled with my normal ob...she was super nice but i wasn't dilated at all and i hadn't taken any ibuprofen or anything and it felt like i was going into labor...it was the most painful experience i had since i had my 8 month old daughter...anyways, she said she couldn't get my cervix to open enough and that my uterus was tilted and she didn't want to hurt me anymore so she said to reschedule for a week later with my doctor and to take 4 ibuprofen plus a darvocet before my appt...anyways a week goes by and I'm super nervous, i took the pain meds as i was told and my doctor came in and discussed the mirena with me and he actually took a tiny tiny needle and numbed my cervix which i didn't feel at all...i love my ob he's wonderful... anyways...two minutes later it was in...the process wasn't very painful...a little uncomfortable but no pain really...anyways, about six hours later the numbing agent started to wear off and the cramping was horrible, which I'm used to however because thats how i cramp with every period, but its been three days and i'm still cramping like i did the first day...not really bleeding, just like a yellowish thin discharge (that smells awful) its starting to make me feel dirty and after reading all of these comments I'm starting to wonder if the mirena is right for me...i'm 5'7'' and 125-130 lbs, i don't' want to gain weight, thats my biggest concern and the pain also...im not sure if i should have it taken out or leave it in for the first six weeks, till my check up appt...some of my other side effects are...very tired like wore out, i was moody and depressed to begin with but now its just worse...no acne or hair loss but like i said it's only been four days...does anyone have a suggestion for another method of birth control other than the pill....? please help i need some feed back...if you're going to comment back in response address me as sjm....that way i know you're talking to me...thanks much...sjm

also by not giving me the bupropion that made it worse my period started the next day,no pain meds,no buproprion not even tampons in the facility...horrible

I just got the Mirena fitted 2 days ago... I wish I would've found this website prior. I feel jipped because the doctor did not warn me how badly the fitting would hurt. So, while it was being fitted, I moaned and did everything possible to not scream. It hurt soooo bad!! When I got home, I had very bad cramps and, about every 5 minutes, I would get sharp, unbearable pains in my stomach. It felt worse than labor contractions. I called the doctor and he prescribed some pain meds but the cramps have persisted. I would like to get this monster removed but I'm scared that the removal will hurt as much as the insertion.

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 started taking simvastin (the lowest dose) about 6 months ago with amazing results when it came to my cholesterol. After about 2 months I started getting headaches. I went off the drug for about a week and the headaches went away. I went back on the drug and 3 weeks later the headaches came back. This went on for a few cycles. This last time I went off the drug was February 7. I have not taken it since and I have had a headache since then. This time it has not gone away. I HAVE NEVER had headaches before taking this drug. And all I know now is that for the last month my life as I knew it completely changed. Of course the Dr. put me on some pain meds for the headaches that made me sick, sick, sick after 3 days. I just can't take the pain meds as they are worse than the headaches themselves. HAS ANYONE HAD THIS and if so how long did these headaches take to go away.

Hello, I have been on Lamictal 25 mg 2 times per day for mood stabilizing since Sept 2008. For the past five months I have had extreme lower back and hip and leg pain. I have been being treated for the pain and so far no one has been able to find the cause. I am currently going to pain management because I am in drug and alcohol recovery, pain meds are not and option for me and just had my 2nd epidural spine injection with no relief. I am so GRATEFUL I found this site. God works in his own way. I am calling my doctors now. Thank you all and God Bless.

PS I have never even looked up my drug side effectives before let alone post on a site.

My experience with Merena has been this. .. Some bad cramping here and there and lots of discharge. I am also more tired then I ever was before. I always want to sleep. Almost like the way I want to sleep when I am pregnant. That is how tired I feel!
As for the sex, my sex life has actually gotten better. I am on an anti-anxiety med that gave me little to no sex drive. Once I got the IUD my libido came back. I am also always bloated nomatter how little or much I eat. It is quite uncomfortable for me. Last time I went to the OBGYN she could not find the strings to the mirena so she sent me to get an ultrasound. The Mirena is still in but the strings are way up high. Does anyone know how they will get it out when it is time?

i had my mirena placed on 12/9/2008 and its now 12/13/208 and i already want it out! every since ive had it in ive had really severe cramps and my legs have been really numb. its so bad that i cant even pick up my 2 month old son cuz it hurts so bad and i also have had really bad nausea. i called m obgyn and they said its normal and just called me in some pain meds.

Hi Ladies, I am glad to have found this site. I got my Mirena inserted on July/08. I was very nervous and anticipated the pain, however with the 2 Tylenol that I popped prior to the appointment and the wonderful nurse I had the pain was bearable, nothing more than a bit of cramping and a little pinch and it was over. I figured we had got off to a great start, except for the uncomfortable feeling of having a foreign object in my body that lasted about a month. My partner complained that it poked him during intercourse but he understood our WHY to having this done, I was determined to make it work. Now Im a 28day cycle girl that is regular...lasting only 4-5 days. Since Mirena has been in my life I am bleeding for up to 2 weeks long, seems like my periods get longer and longer! I have experienced bacteria vaganosis, along with yeast infections. Yuck! Weight gain of 15lbs, minor stomach pains and the mood swings. This is starting to affect my life and its very frustrating...Im sitting on the fence with what to do. I go to my doctor next week and will have made up my mind by then, I cant take it anymore! Even if it were not for the irregular, looong periods, I think I would hang in there, but am tired of constantly feeling wet! and not being able to touch my partner!