Ins symptoms and conditions

I, too, was told, only good things about mirena. I got it after the birth of my son, and had previously had a copper IUD, with it, I still gt my period, but no worse than before. Since getting the Mirena, I'd gained over 30 pounds (with no change in activity levels or diet), and have experienced frustration, depression, and am very self-conscious of this-from being asked if I was pregnant again, etc., as this make a very big difference on my 5'2 frame. I also never regained my libido. My gyn, Just told me last week that loss of libido can be a side-effect of mirena. My periods have been lighter, but still have the emotional side effect. I'm going to check with my ins to see if it will cover having it switched back to the copper one. I'd gladly take a period, than go on like this (as you can imagine how its affecting my marriage.)

Alright, first. I'm under the impression that Ocella is the bad kind of generic for a drug that should not have had the option to be generic. I had been on Yasmin and was happy with the results. I never once blacked out because of a period until I was switched to Ocella because a lack of drug coverage. Since I was starting to go through all of the symptoms above, I chose to take myself off of the pills (that, and the fact that I couldn't visit an OB/GYN because of the ins. issue). Since then, I haven't had a period (did, however have ALL the symptoms of getting one like I did on Yasmin). My only beef is that my body seems to have gotten addicted to the old dose of estrogen that was in Yasmin, and a lack of that amount has made me VERY hard to live with. My poor fiance!!!

I have been taking this Leviquin for 4 days. I have had severe cramps in my calves and feet in the middle of the night. So bad that I get up and try to step em' off but to no avail. My muscles hurt so bad in my legs arms and I have been very sick to my stomach. Do these things go away? I am not taking one more of those pills. I would rather have sinus and bronchitis problems than deal with these horrific side effects!! Any feed back?

I had posted wed. morning that I was getting it taken out, well my doctors office said they had to check with my ins. comp. just to see if they would even cover it which to me meant big money for a simple procedure. After waiting 3 hours for a return phone call I got irritated and my husband helped me to remove it. I was hoping that I would get immed relief from the horrible pains I was having in my upper abdomen and back but it took exactly 12hrs from time of removal to feel better. Today I still felt sick like I could throw up but after I got some water in me I feel much better. I was unable to eat or drink much in the last 24hrs. It didn't hurt at all to get it out and I am glad I did. I feel better just knowing it is gone! Good luck to everyone I hope the people who are suffering get relief soon.

I started taking Lipitor in 2004 and by 2008 was taking 40mg daily. I'm not sure exactly when certain symptoms manifested themselves, as looking back they now seem insidious, but I do know they became bad enough in 2008 I went off the drug myself, especially after reading postings like those at this website. After being off the drug for a month, it was clear to me the most of the symptoms dissipated, but it did have a residual affect. I realized I had suffered a loss of range of motion (ROM) in my left arm (frozen shoulder) and have been in physical therapy for over a month to restored 80% of it. I could not have done this while staying on Lipitor as I was experiencing “deep” muscle pain and weakness. I still have some weakness and pain in my left arm and shoulder and don’t know if it is permanent.

I am Hypothyroid and take Synthroid and am currently going through menopause and am on partial HRT. I took no other meds other than the Lipitor. At one point, I thought my symptoms were stress related, but realized my symptoms were causing the stress. Aside from the muscle pain, spasms, tingling and numbness experienced in my left extremities, I experienced gastro intestinal disturbances, occasional vertigo, some lower back problems and other aching in other extremities (like that of flu symptoms). I also suffered recurrent mental fogs, which I initially attributed to some lack of regular exercise (although I lead a relatively an active life), but that was not the case, as even after aerobic activity the tingling and pain would resume.

When I told my physician I had stopped taking the Lipitor (at that time for nearly a month), he didn't blink an eye. I agree with previous blog; the idea of statins are to lengthen your life, but what kind of life is it when you are in misery and nothing short of ceasing the medication brings relief?

I'm not advocating everyone "doctor themselves. Listen to your physician, but most importantly listen to your body and trust your instincts when it comes to these types of medications. Symptoms listed about scripts described as "rare" are usually not that rare at all. You are not crazy.

I have been in a serious relationship for 5 years I was on the pill for at 7 years when we got married in June we decided it was time for me to stop taking the pill.. I had my first Gardasil shot and everything was fine just really sore injection site and sore arm. When i went to get my 2nd shot they made me sign all the paper work again to get the shot.. I asked it it was standard procedure to resign these papers and she said no why.. I said because i have done this once and this is my 2nd shot.. She insisted that it was my first. When i got done i asked the lady at the desk and she said she had no record of it and i was like well something is wrong here you may have no proof but i know because remember my arm hurting.. She finally had to call my ins co. to see if they billed me once before.. Lo and behold i was right! I just go t my 3rd shot right about the time my period was going to be here and it has been 2 weeks and I still haven't gotten my period which is really unusual because I am always on time.. I have taken 3 pregnancy all which are negative. However last month my husband and I were really active during that "Window" to get pregnant. I was talking with my mother about it and she said that she had to get a blood test to show that she was pregnant with me.. So i don't know if i need to get blood taken or just think my missing period is because of this damn drug.

I have been taking this since October of last year. not only is it my complete miracle cure, but the side affects vanished long ago. For people who have suffered as long as I can, I'll take some queasiness, horniness, and blurry vision over wanting to die DAILY any time. I love it. Love it love it love it.

Incidentally, I lost my job a few months back and stopped taking it and IMMEDIATELY went back to the worst I ever felt mentally. if you are taking this and would like to stop (or need to cause of lack of ins.) talk to your doctor. My experience with the immediate lack of mood control was awful.

I started taking this med on 6/1/08 after taking Atacand for 4 years (had to switch for ins). Anyway, I feel for anybody that takes this stuff. I started coughing the very next day. I have no appetite because I cough to the point of getting sick to my stomach and aching in my gut. Nothing tastes good. I am totally exhausted. I wake myself up coughing at night and am totally worthless during the day ( I have always been an active person). Can't talk on the phone because of the coughing spells. Go out in public and start coughing out of nowhere. Get stares because people think you have some disease. I CANNOT wait to go to my Dr. in August and tell her she has got to find something else for me! I can't believe this stuff is still being prescribed since I have read some really bad reviews about it.

My Dr. prescribed Seasonale, but pharmacy gave me generic Jolessa. I've been taking it for 1 1/2 months and have been bleeding since after the 1st week. I have mass amounts of constant brown discharge and clotting with daily breakthrough bleeding. I get headaches, cramping, bloating, light headed and dizzy episodes, and my mood has been edgy (maybe from a sexless marriage due to these pills, lol). I've been taking bc for 16 years and have never experienced these symptoms with any other pill I've taken.

Spoke with my doctor's office a few weeks ago and was told that the bleeding can be normal and don't be surprised if it lasts for 2 WHOLE CYCLES that is 6 months of bleeding and clotting! I know what is normal for my body and this is not it! I'm calling my doctor for the 2nd time today and will demand my prescription be changed to either the name brand Seasonale (which my ins will cover) or my previous pill.

Hi all.
I am really dis-heartened right now. I cannot seem to get this thing taken out yet. My husband and I are self-employedso we have to take out our own health insurance. Our ins. company said that side-effects are a "disorder of the reproductive system" and there is a six-month waiting period to have anything done and we have just gotten it. So I went to an after hours clinic that I called waited until today thinking I could get it removed. WRONG!!! :( Today they said they could not remove it. More over, naturally the doc there said that there was no way all these side effects were from the mirena. I was so upset.
To anyone who has had this taken out, how many of your symptoms have gone away? How long has it taken?
Please e-mail me at ****** or private message me and let me know your experiences with post-removal and side-effects that cleared up. I am ready to take action on this mirena as women need to be informed of the possible side-effects of this drug. I have been suffering for 1 year and 10 months.
Thanks for reading!

hi, i've had the mirena in for about 14 months. The first 8 months i had constant spotting, nausea, vertigo (dizzy spells), bloating, weight gain and pimples. The spotting has settled down. i still get a period every now and again. the last one i had was really heavy with clotting. I often get sharp pains and cramping in my uterus but no bleeding. I have also had thrush for the last 3 months that wont go away. has anyone else had thrush on the mirena? My back pain is really bad. particularly my left hip. i haven't been able to sleep on my left side for over a year now. Don't know what to do!!

My Mirena Removal....
So i posted here a few weeks ago after I found this site. I had EVERY side effect listed and was so freaked out that i immediately made an appointment for removal.
For those of you reading and wondering what the removal is like..
Well, NOTHING like the insertion. I was so so nervous and it was over before we actually started. The DR was surprised that i was back in his office to have this removed. He then proceeded to do an ultrasound to be sure it was placed properly before removal. And yes, all was OK on the position of it. I explained to him my reasons and he looked at me like he had never heard this before. I honestly can not imagine with all the women he sees that NONE of them have complained. But...as I was getting dressed afterwards, I took a good look in his office. There was Mirena literature ALL over the place. In fact, that was the ONLY thing he was advertising. Not to mention...they made me pay up front with the insertion back in Nivember...billed my insurance and I still have yet to receive my reimbursement. Oh yeah, and that...they charge more than the actual Mirena costs, then they bill your insurance for the price they know they will pay and the DR then makes about $150 profit. Nice.
Ok, back to my side effects post Mirena. The removal was not painful at all. I did spot for about a week- nothing too heavy but it was clotty and def there.
A couple of days after the removal it felt like I was coming out of my skin something terrible. I figured this was my body adjusting to the lack of hormones. I also had some headaches.
It has now been 2 weeks and the spotting has disappeared. I also can see the bloating of my stomach is starting to go away. It looked like I was about 4 mos preggo while I was on it. I also have an increased sex drive. And sleep-- well let me tell you, I have not slept this good in a very long time. I am actually sleeping more than 6 hours now and the night sweats have also discontinued.
I can't believe EVERY time I come to this site and look up Mirena ALL the people that have posted their experience as being negative. Yet, the DR looks at me like I am crazy! I have been seeing him for years and I have never complained about something like this. I really am so happy that I have it out and wish I would have done my research on this prior to insertion (which was one of the most painful things ever!)
So..for those of you out there that are either contemplating having it inserted...I say NO WAY. And for those of you out there that are nervous about the removal or not sure..I SAY YES, DO IT! For our bodies to be reacting this way, it is clear to me that it should not be inside of us. Listen to your bodies...they really do speak to you and let you know when something is not right. Forget about the DR saying it is safe or he has not heard of any of these side effects...YOU be the judge.
Good luck! And I promise it gets better once you get that lil' demon out!
Mona

I am getting mine removed FRIDAY!! And Friday can't come soon enough. I am kinda bummed tho for having to go back on the pill but I can't hack this ANY LONGER!!! One of my friends works for a GP and I went to him because of some of my side effects. The flu like symptoms minus having the flu (had it for at least 2 to 3 mos now) NO sex drive (causing trouble with my marriage. Hubby is taking it WAY to personal), swelling in my hands, feet, legs, and face. (my face will feel flush and BAM I'm swollen!!) VERY BAD MOOD SWINGS!!! Very Bad isn't the word for it!! There are no words to explain my moods!! ANYHOW..... I sent this to my friend to read and she pulled it up at work. Well the GP said that this isn't a reliable place to go for information on the side effects. "There are NO positive side effects to anything." Which is true BUT he seems to think going to Web MD or some sight like that is more reliable than here. And that this sight shouldn't scare me and he wouldn't urge me to have it removed after reading this. (OH YEAH I forgot to mention joint pain, I have HORRIBLE joint pain in my hands, wrists, elbows, knees, ankles, and feet. The worst of it is in my wrists and elbows) Back to what I was saying. To that (this sight not being reliable) I say go to Web MD and post there too! I pray that I can get back to me after this comes out!! I hope it don't take too long either! I MISS the old me and HATE the new me!! But FRIDAY HURRY UP AND GET HERE. And for anyone who has had it removed........ anything I should be repaired for??? Thanks for your time!

I am a 53 years old female diagnosed with diabetis for about 5 years, now. Currently, I take 1500 mg of metformin to treat the diabetis. A year ago this month, my bp went up to 164/88. That's when my doctor put me on 5 mg of lisnopril. The 5 mg dosage brought my bp down to about 140/84, it never went down to 120/80, even after using for one year. I can say that since I've been on this medication, I have been extremely fatigue. Several times I told my doctor about the tireness and that I thought it was due to the Lisinopril. She just sort of disregarded my complaint. She said that what I was feeling was due to menopause and the diabetis. About three weeks ago my bp went up to 171/88, so she decided that it was time to increase the dosage to 10 mg and to put me on hormone replacement therapy to reduce the fatigue. I told her that I didn't want the 10 mg of Lisinopril because I believed my fatigue was due to it. She insisted that it was best for me and that HRT would help.

Well, what I've done was decrease the dosage to about 2.5 mg on my own. And what I notice was that my energy level seems to be returning. I been feeling better and my goal is to start taking the 2.5 mg every other day until I can completely stop taking this stuff.

Today, I noticed that my arms felt a little heavy like and my heart seems to flutter a bit. I would like to hear from some of you that stopped taking Lisinopril, what were some of the symptoms that you experienced and for how long. I know that getting off a med can be dangerous, but staying on them can be just as dangerous, too.

Hello , My name is Naisha I was giving Lupron in 2002 and I would NOT TAKE THE DRUG if I was you . I would do anything to have the Endo back then feel the way I feel from THE LUPRON it is a drug from HELL. I would of never taken Lupron if I was awear about all the side effects that the shot had and YES everyone body is different but I see to many caes that went bad . If you like to read story about what alot of the side effects our look up the website-http://www.ipetitions.com/petition/Depot-Lupron/signatures-5.html. You know what the sad part is I still had to have an Hysterectemy buz the shot was not working at all for me I would still feel all the pain without the bleeding , Only if I can go back to the day My Doctor said only thing I can do now Naisha is we can try a new Drug they have out called LUPRON to help control the Endo buz I was to young for a Hysterectemy at the time I was only 25yrs old with one kid and my INS will not appove it HE said. Here is all the side effects I'am having for that dama LUPRON , headache , hotflashes/sweats,nausea,weight gain/loss,joint disorder,nerous system,depression,skin rash,breast swell -tenderness. . So what all the side effects my Dr check me because they was thinking I had Lupus that was rule out so I now have Fibromyalgia and I am only 29yrs old , and I can go on an on . But I am scared to death because I got pregnant atfer my last shot and what will end up happening to my lil girl every year I seem to have a new side effects. Please check that one website and see if you think twices before you go on LUPRON I would take the LUPRON shot back anyday if I could.

well i havent started the shots yet but by what i am reading here i am not so sure i want to get these shots!! they found my endo a couple months ago and i have to have the shots but i really am scared!! i have much pain and problems now but it seems like the shot is going to make me worse!! i dont know what to do!! does anyone have any good sites for me to go on and do some research on these shots? someone help i dont know what to do!!! fara

I was put on Loestrin 24 a year ago after I told my Dr. that I was getting more and more migraines every month during my period. (I've had them since I was a kid, now 27, but they were beginning to come more and more frequently in recent years and most often during my period.) The pill seemed to be working like magic, my migraines lessened more and more and I was experiencing less mood swings and depression than I'd had in the past near my period. My periods have been 3 days tops and very light. I thought I had found my miracle BC and felt like the $60.99 I've been paying every month (no Ins!) was well worth it. WELL.... this month is a totally different story. I got period on Monday, when I was supposed to, and I still have it today, Saturday. I have never in my life had a 6 day period until now...esp since Im on this "3-day period" pill. Mon-Wed was the same as it's been for the past yr, light and a breeze as far as periods go. Wed night I had practically no bleeding and thought my period was at it's end, like always. Well I woke up Thurs around 3 am covered in blood. I then went to the bathroom and proceeded to "gush" blood for lack of a better term. I've never experienced such a heavy flow. I've been wearing a tampon AND a pad for the past 3 days now because I'm soaking thru tampons and leaking A LOT onto pads. I hadn't experienced any pain until today (day 6!@!@#!@!) and can't believe I'm still bleeding and so heavily! I did call my Dr. just yesterday and explained my situation and how abnormal this all is for me and was told to continue taking my pills as directed and "see what happens" next month! If I'm still bleeding like this tomorrow, the 7th day, then I seriously think I'm going to go to the ER. I'm freaking out and can't understand what in the world is happening to me out of the blue. I've had normal, regular periods ever since I started menstruating at age 11... 16 yrs ago! Has anyone else gone through anything like this????

I am a 50yr old female... was prescribed Lisinopril 10mg for bp.. after a few weeks I started getting a funny hard to explain feeling with my heart beating a certain way.. don't know how to explain it.. fluttering maybe.. feel it pounding. So after I realized it could be this pill I stopped it.. I moved out of state from my dr... and not ins. yet.. however I watch my bp and when it got alittle higher I thought I will take 1/2 one.. which takes BP down to normal, but after doing this here and there.. that same feeling in my heart started..
Has anyone experienced this feeling?? I don't seem to have the other side effects Thank God.. but this one scares me as I don't see anyone mentioning this feeilng..

I love this little pill I took ambien 10mg for quite some time and it really worked for me the only reason I stopped is because my ins. doesnt want to pay. I will say this, that if I did something after taking ambien like puting things away the next morning I had a tough time remembering where I put them ( like my keys, books ect.) and my family thought that after taking it that I was an actual pleasure to be around they would often ask me to go take my pill

I went on accutane 5 months ago and it was a great decision. The side effects can be nasty though. I had really bad lower back pain (I literally felt like an old woman. Bending over was so painful as was moving in general). It is not as bad now though. Mood swings are another side effect. I am irritable on the medicine. But even so, I consider that a small price to pay to get rid of painful, embarrassing acne. I feel so much more confident and happy in general. The doctors are really careful when they put you on the medicine. montly (pain in the ass) blood tests, monthly check ins with your dermatologist, etc. If you have serious cystic acne (i'm not taking about a break out here and there) I would consider accutane as an option. talk to your dermatologist. Accutane works for almost everyone but beware of the serious side effects it can have: Depression, nausea, irritability, headaches, raised triglyceride and cholesterol levels, and suicide (at least according to the labels), among other side effects. If you feel depressed or suicidal tell your doctor and get off the medicine. But don't rule out accutane because of it reputation. I think it gets an unfair rep. Just use common sense just as you would on any other med. Good luck!

I'm 36 and I've been on Yasmin for 2 years for my hormone imbalance and POF, and have never experienced anything I've read on these posts being on it. I lost weight on it, my mood swings went away, my skin never broke out and I was able to have periods again. Yasmin made me feel great.

I've been off it for 4 weeks due to a medical ins. issue and I'm starting to have cronic fatigue problems where I can't fight falling asleep at odd times of the day, my period wont start, I had some really bad bouts of depression, I get dizzy easy and my hair started falling out more than usual having long hair.

I had my thyroid checked and everything is fine. I'm not on any other meds, nor do I have any other health problems.

I have been experiencing neuritis symptoms (pins and needles} I have been taking 40mg of zocor along with a niacin product on the advice of my Dr. I am going to stop all the meds and see if these symptoms disappear..I forgot to mention I was on lipitor for years but ins. stopped paying for it and was switched to zocar one month ago.

I'm a 46 year old male. I started 10 years ago with Lipitor 5mg, after one year increased to 10mg, insurance company made me switch to Zocor 10mg. After switching with another ins company had to go back to Lipitor 10mg, had to switch again to Zocor 20mg, then my doctor took it to 40mg along with 1,000mg of niacin. Switch again to Lipitor and back to Zocor, all this transpired within a 10 year period. I have always been extremely active and very muscular. One day I noticed twitching in the upper part of both arms. When I visited my doctor, his first words where stop the Lipitor now. Within the next three months I had extreme body tremors, full body muscle cramping, extreme night sweating (would soak the sheets) and had a vibrating (it was like a humming sensation) sensation in my whole body 24/7. It's been two years now since I stopped taking this poison and I now suffer with a great deal of muscle loss in my hands, forearm, upper shoulders, butt area and feet. I have difficulties with balance, holding my bladder when I feel the urge to urinate, severe pain, difficulty lifting my arms to my head and difficulty with my speech. The sweating and vibrating feeling has gone now however my quality of life is not anything to talk about. If I new then what I know now about this statin drug I would have never takin it. If any one knows of any ways too reverse these side effects, please e-mail me at ******

MY WIFE HAS BEEN ON PREDNISONE FOR 4 YEARS HER FOR FIRST SIGN OF ASTHMA SHE IS 25 NOW WE HAVE BEEN IN AND OUT OF THE HOSPITAL WITH NO INS. THEY TESTED HER FOR EVERY DISEASE AND FOUND NONE THE DOCTOR SAID THE BREATHING PROBLEMS ARE CAUSED FROM SEVERE ALERGIES WE CANT GET THE ALERGIE SKIN TEST DONE ON HER BACK BECAUSE THE DOCTOR SAID SHE HAS TO BE OFF THE DRUG WHEN SHE STOPS THIS DRUG HER ALERGIES CAUSES HER TO HAVE BAD ASTHMA AND BREATHING TREATMENTS DONT WORK WHEN SHE STOPS THIS DRUG SHE ALSO BRAKES OUT IN RASH AND IT TURNS INTO A BRUISES SHE CANT GET OFF THIS DRUG WE NEED HELP SHE IS A MOTHER OF 2 AND HAD A MISCARRIAGE 7 MONTHES AGO HOW CAN SHE STOP TAKEING THIS DRUG?

I started taking Neurontin about 4 years ago.My neuroligist started me on it for Polyneuropathy(nerve damage in my feet and legs)He started me out on 300 mgs. (taking 2 three times a day) It was a miracle drug at first,since my feet had been hurting(burning,stinging,numb toes and balls of feet felt like I had been walking on sharp rocks bare footed and they were bruised)for 2 years.Then they started hurting again after I had been on it for 2 weeks.So he increased the dosage to 400mg taking it 2 three times a day and same thing happened.So he increased it to 800 mg. 2 three times a day.I started getting blisters on my tongue and alot of swelling in my feet,ankles and legs,so he decreased it and that all went away.So he slowing started increasing it and those didn't come back.
I went to another dr. because I moved and he decreased it because thought I was taking too much.And the pain became worse.Well I had ins. whenever I was taking it before and then I didn't have it anymore after about 8 months of being on it.It is so expensive so I had to cut way back on it because I couldn't afford to take the full dosage I was suppose to take.And that is how I know it works for the pain.While I was cut back on it,the pain was almost unbareable.I am taking 300 mg. 3 in the am,2 at noon and 3 at bedtime and my feet and legs still hurt,but I know from experience that if I wasn't on it I would be in unbearable pain.
I am on alot of various drugs.I also take Lamictal 25 mg. 1 four times a day for the neuropathy.And I also have fibromylgia.I seen where alot of people have fibro and it is being treated with this drug.It doesn't seem to help my fibro.Or maybe it would be alot worse if I wasn't on it.Don't know.I take Elavil 100mg. 1 at bedtime,Zanaflex 4mg. 1 at bedtime for the pain and fibro,Synthroid 0.1 mg. 1 a day,Pravachol 40 mg. 1 a day for high cholesterol,Metaglip 2.5-500 mg. 1 a day and Avandia 4 mg. 1 a day for diabeties and Vicoden 5 mg. & apap. 1 every 6 hours for pain.
The Neurontin seems to interact well with all these drugs.
I have dry mouth and some confusion which affects my ability to think and carry on multi-tasks.I am trying to get on my diability.I applied twice and was denied and I got a lawyer and we went to court before the judge 2 weeks ago and it will be 3 to 4 months before I hear if I am getting on it or not.