Np symptoms and conditions

I am so lethargic it's not even funny. I can see why the Mirena is 99.9% effective-you're either sleeping or so tired you have no interest in anything, let alone sex. I had a vivid dream last night which I don't tend to have. Also, i've been so blue and can't seem to bounce back from it. I had almost no cramping when I had it inserted but it was expelled immediately. The NP had to reinsert it and said I should use ibuprofen whenever cramping, which seems to be happening more frequently. I've had this only a week and four days. I am concerned that my body may be trying to expel it. Also, I've have to frequently urinate. I have had UTI's in the past but not for a long while. This isn't worth it. I may tie my tubes as I originally planned. After all I have two absolutely beautiful children- my son and daughter.

I had mirena inserted 6 weeks after my baby. I asked my ob about it and said it was great, his wife had it and she has had no problems. I began feeling anxious, depressed, then lashing out at my husband, wanting to yell at my beautiful baby for crying, insomnia, lacking the energy to even clean my house and I am a clean freak, and headaches. I had it removed 2 weeks ago by a NP because my ob was gone. She told me she would remove it but did not think it was the mirena. I told her I had already seen a doctor he had given me depression medicine and I was seeing a therapist. She told me maybe I was bipolar. I told her she was crazy. Anyway, I feel better in some respects. My depression is gone, I don't lash out anymore, I am sleeping better, etc. I have noticed though that I have been having nausea on and off since it was removed and I get very hot (I keep my thermostat on 73 in my house). My headaches seem to be going away but they are still there. I wish I would have read and found this website before getting mirena. I hope it did not mess me up for life.

Hi everyone. I am a medical professional and former user of the nuvaring. It is true, birth control as well as most medicines does affect everyone differently. However, I was an absolute emotional disaster (frequently contemplating self-harm) while I was on this medication. I initially attributed the mood swings to my then current stressful situation. When I finally graduated from NP school and my stressors were alleviated, my depression persisted. Within a week of stopping the NuvaRing, I was back to my old self and have not had any of those symptoms since. It is a rather large dose of hormones so if you're feeling these symptoms as well, perhaps you should contact your provider about a more appropriate method of bc.

I got this thing put in just over a week ago (4/16/09). I wasn't thrilled with the idea in the first place, but I can't take the pill and my husband is sick of condoms. I don't want any more kids (I have 3) but I'm not ready for him or me to get "fixed". Anyway. The nurse practitioner was the one putting it in and she told me if there were any problems she wasn't doing it, she'd wait until one of the gyns was in the office. I had a LEAP ten years ago and she thought it would be fine since I'd had two kids after that, but she said sometimes there was scar tissue from the LEAP and it could be difficult to insert the Mirena. The NP was having trouble getting the big q-tip thing through but the nurse assisting her opened the Mirena package so the NP said she'd try one more time and SHOVED the thing through. OUCH!!!!! Then she put the Mirena in which was extremely painful. I was told I might have a "little" cramping. Yeah, right. For the next three days it felt like I was having contractions on my left side. It was awful. Since then I've had headaches every day. I had a migraine a few days ago and I haven't had one of those in ten years. The headaches are horrible tension headaches that won't go away when I take something for them. I'm still bleeding, but just enough to need to wear something. Has anyone with the Mirena had headaches that have gone away or do they continue until this thing comes out?

I have been using Topamax now for 8 years off and on. I stopped the Topamax about 3 months ago, something I do once or twice a year to try and feel 'normal' again. Then last month I went to see my regular doctor because of numb, pale, swollen, achy fingers, swollen ankles and feet, and for a papercut on my knuckle that overnight turned into a radical staph infection. The NP ordered a full blood panel and the results came back positive for Lupus. I have had so much pain in my hips and knees, more frequent headaches (not migraines), insomnia and vision trouble. The past two weeks I have been super irritable and nauseous. I still need to have a 2nd opinion and/or referral to a rheumatologist, but is all of this related to taking the Topamax? I take 2 Imitrex injections if a migraine comes on and am hesitant to start the Topamax if it has indeed induced Lupus. Am I crazy or is this common??? THANKS for the feedback...SM.

I WAS TOLD TO TRY NERVE BLOCKS AS AN ALTERNATIVE TO SURGERY. I HAVE A RUPTURED LEAKING DISC AS THE RESULT OF A CAR ACCIDENT AT L4,L5, I HAD THREE INJECTIONS, I WAS NOT EVEN TOLD THEY WERE USING A STEROID. WHEN I STARTED HAVING NIGHT SWEATS, IRRITABILITY AND EXTREME FACIAL HAIR MY GYNO SAID IT WAS THE NERVE BLOCKS. THE NP AT THE PAIN TREATMENT CENTER SAID IN TEN YEARS SHE HAD NEVER HEARD OF IT. THE DEPO SHOT I WAS GETTING WAS NEGATED SO I GOT MY TUBES TIED. I HAVE AN APPT WITH AN ENDOCRINOLOGIST IN JUNE, I GOT IT IN NOV, MY HUSBAND SAYS WE WILL HAVE A CIVIL UNION BY THEN!! THE PAIN RELIEF LASTED 19 DAYS, THE HAIR 2 MONTHS AND COUNTING. THE SURGEON TOLD ME BEFORE HE PUT ME UNDER HE DIDN'T THINK IT WAS GOING TO WORK. I WISH I KNEW ABOUT THE SIDE EFFECTS. NOT HAPPY AT ALL. TREATMENT CENTER SAID BECAUSE OF SIDE EFFECTS I WAS NO LONGER ELIGIBLE FOR NERVE BLOCKS AND CLOSED MY CASE AS A PATIENT. I ALSO HAVE 2 BULGING DISCS IN MY NECK AND CHI FROM THE ACCIDENT. I GUESS I MAY HAVE TO HAVE SURGERY. THIS HAS NOT BEEN A GOOD EXPERIENCE.

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!

Is this normal??? I inserted NuvaRing for the first time August 26th. (During my exam). My NP said it would be okay to start then (although my last period was 08/11), but to use additional contraception. My husband and I have been using condoms since the birth of my daughter 2 years ago - so we continued like normal. Twenty minutes after my appointment, I became very nauseated. The following day I had a severe metallic taste in my mouth and a pounding headache. I became extremely tired (falling asleep at 8:30pm) and got very achy, especially arms and legs. I felt like I was on diet pills or drugs (jetty feeling, trouble spitting out words, racing thoughts). The symptoms would be gone in the morning, but come back as the day wore on. The problems became so bad that I took the Ring out on 08/31. (Holiday weekend, no NP on duty). I called the doctor's office on Tuesday. They said that I probably coincidentally caught a virus. It is now 09/07. My symptoms have become better day by day since removing the Ring, but the metallic taste is now a soap taste and I still have occasional nausea. Shouldn't the hormones be gone by now? How long will this last? Anybody????

After reading these posts, I am glad I didn't change my mind about having the MIUD removed. I have had all sorts of problems since that evil piece of plastic was inserted. I didn't think much of it at first and thought maybe I am just tired because I have my period and cramps alllllll the time. The relationship I was in was bad and thought maybe I was tired and moody because of that. After a couple of months - boyfriend free - things didn't change. I had horrible mood swings, my concentration was shot. My work ethic went down the toliet, I felt like a 10 year old kid with ADD. No energy, back hurt on a regular basis, carpal tunnel came back with a vengence and TMJ (I don't know if that's related but I've never had it before), acne, weight gain, no sex drive, and a constant itching around my neck. I am sure the NP was ready to try to talk me out of it and wait the full 6 months for "side effects" to go away. Well, the last 5 sucked, I really didn't want to deal with this crap any longer, besides with the price of gas, I can't afford the money for the regular buying of feminine products. I am only 6 hours free of this and I am already feeling a little better. I don't have that "pressure" you feel in your belly and a have bit more energy. I am so looking forward to the next few weeks when things start to get back to normal!!! If you have any doubts about this thing....get rid of it. Its really not that bad to get it out, 99 times less painful than getting it inserted!!!

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

Kenalog Warning! Please think twice before letting Anyone inject this drug into you!! I am a new nurse, I had only been working as a nurse for 4 months on May 31st of 2007 last year when I let my NP of 7 years give me a Kenalog injection to my Left elbow for severe tennis elbow brought on my 16 hour days of charting by hand as a new nurse. As with any drug, we should always be on guard and informed, and I feel twice as dumb for being a nurse and letting this happen, but I was so busy and in demand that immobilization of my dominant arm at the time simply was not an option to my employer.

By October of 2007 I had a literal "crater" in my elbow. I went to an ortho doctor and when he walked into the room he looked at me and said I was the worst case he had ever seen. I still didn't believe him until he sent me for xrays and an MRI. I have NO fat left on my elbow. I have total muscle necrosis and wasting away. Basically the Kenalog shot ate away all but 2millimeters of my elbow muscle and the xrays showed so much inflammation and irritation that the doctor was afraid that the bone had become infected as well. So I had to endure a bone biopsy of the elbow 3 weeks ago before he would even agree to do the elbow muscle transfer which I have to have done this Friday.

I was a new nurse and did not even get to work for a year on the floor before loosing full use of my arm and being forced to give up my nursing job. This elbow muscle transfer requires 3-6 weeks of immobilization, then 4-6 months of physical therapy, then another 4-6 months before you can expect your arm to be back to pre-surgery condition.

Basically I can not work as a nurse for a year, and will not be able to type, write, sign my name, use my cell phone, drive a car, wash my hair, or even pull up my own pants after I go into surgery this coming Friday.

And no, Doctors can Not be sued for an improperly delivered Kenalog injection if the intention was good and the shot was in the right place and did not hit the bone. I have been turned down by 3 lawyers.
Please be careful and try physical therapy, ice and immobilization first!

I to have a huge dent in my right butt cheek. I would be interested in a class action suit. This is ridiculous! It has been about three months since I received the shot. Has anyone noticed their dents getting better with time?

I have been taking Lisinopril 40mg.for about 4 months now for high BP. It works very well for the BP issue. Since I have started taking it I have had the dry cough, but its not so bad that I would have change anything because of the fact that it IS helping my BP. I have also noticed that I have been getting the numbness in my arms mostly my left. My Nephrologist mentioned that its Steal Syndrom caused from my Fistula Creation (dialysis access). After reading these posted side affects I think its from Lisinopril. ALSO, in the past 2 months I have been getting acne. First thought it was from my diet, but I have not changed anything in my diet. Its almost like my body is trying to get rid of something in my system. This is not the ordinary acne problem, this is on my face, back of my neck(hairline), on my shoulders and back. The "acne" gets very bad and when I get something out of the sores it has a very strong metallic type smell. Also, I am experiencing the itching, which has been getting worse the past few days. As of today I will NOT be taking any more Lisinopril. I am certain Lisinopril is the cause of all of my problems. Has anyone experienced acne from this product??

Thanks,
Shawn
36yo, Minnesota

I am 35 yrs old. My son was born 7/2/6 I got the Mirena inserted on 8/31/06. Right after I had my son. My body doesn't react well to the birth control pill and did not want to get pregnant. My Gyn said there is a slow release of hormone so I wouldn't even notice any changes. My period was off but I just had my son. In March I went to my primary and she put me on Zoloft since I was experiencing anxiety, a constant flush, and insomnia (kinda feel like your going crazy at certain times of day). I never had these before giving birth (and its not the stress of my son). They did blood work it came back fine. I took yoga, acupuncture and Zoloft, nothing is working 18 months later I went to my primary office and seen a nurse practitioner and she said take the Mirena out-she herself had certain side effects that I had. My Gyn says that is not the cause, it could be the Zoloft. How confusing is all this. I am really considering having it removed soon. I want to feel myself again. I'm sure my husband does too. Anyone with info. on after the Mirena is removed and how I might feel would be helpful. At least I have idea what might lie ahead even though every one is different.I am so glad I found this site. Ladies take care of yourselves. There will be happiness again.

Anyone else have shoulder pain and/or rib pain? Almost like a gall bladder attack? Have taken it twice and both times have had a severe pain for a short time, helps cough though..Is this just me or a common side effect? Also the itchiness..

As a follow-up to my posting of 10/10/07, I have had my Mirena IUC removed and went immediately on Errin Tabs (mini-pill). All of my previous side effects have gone away - meaning I was right on the money thinking the Mirena was causing them even though my Dr. and the NP both said these were not side effects: weight gain, hair loss, fatigue, dizziness, and the horrible joint/bone pain. I haven't bled since I started the mini-pill which was great since the non-stop bleeding with Mirena. I feel like my old self with that thing out! Best of luck to all.

When a class action lawsuit is filed, let me know....this drug should be taken of off the market immediately. We started all of this with an OB/GYN that prescribed this “miracle pill” and now have had to go not only to our primary doctor, but also a psychiatrist, gastrenologist, college campus counselors, psychologists, psychiatrist, and the campus medical doctors; All the while, accumulating enormous doctor bills. All the doctors say, "No, Yasmin won't cause those problems" (except the college campus doctors..wonder why? Hmm.. could it be that they are not in private practice?)....well, I beg to differ. Everyone needs to give this website to their doctor so the doctors can hear from the patients that have taken this drug, and not listen to the pharmaceutical companies that are pushing this drug to be the "miracle pill". Maybe if enough people complain and go to the media, we can get rid of this drug!
My daughter who is 18 was put on Yasmin because of irregular periods, hormonal imbalance, etc. We were told it was the new “miracle pill”. It will make you loose weight, regulate your periods, clear up acne, you name it, it will fix it. Yeah, right.
She started taking this pill in March 2007. She was off at college but called to tell me she was experiencing horrible headaches, behind the eyes. She complained about her stomach hurting, but we just figured it was the stress of freshman year at college. Then she said she got where she couldn’t eat when she went to a restaurant. When she came home in May for the summer, I noticed a total personality change. For example, she was always a neat freak, and now she wouldn’t clean her room. The first day when she drove home, she started crying she was so mad about the traffic. Yes, she has always had a little road rage, but this was ridiculous.
By June, not only could she not be in crowds, like at a restaurant, but now she is having full blown panic attacks and IBS. We called the OBGYN and they said, “Yasmin won’t cause this, go see your primary doctor”. I knew that the only thing that had changed with her was taking the YASMINE. I knew it had something to do with all of this so I “Googled Yasmin” and this website (http://www.medications.com/se/yasmin) was the first one I looked at. All of her symptoms matched everyone else’s! I am so glad we found this website, it explained everything and I had her to stop Yasmin immediately.
So we went to the primary doctor, explained about the Yasmin and how we thought it was the culprit of everything. Of course this doctor also says, “Yasmin won’t cause that”. We told him to look it up on the internet and see how there are over 3000 complaints on this drug, more than any of the other drugs on the market.
Besides the emotional problems she starting having, her pulse and blood pressure was sky high, so he puts her on medicine for that, and puts her on an anxiety medicine and sends her to a psychiatrist. She is very thirsty all the time, and develops IBS. She can’t eat without having pains in her stomach. So, now we’ve have gone from having just irregular periods, to all of the above, plus a psychiatrist.
The psychiatrist doubles her medicine (and puts her Pamine for the IBS) because the panic attacks are gone, but she still is having a lot of nervousness, anxiety, can’t sleep at night, crazy thoughts, worrying all the time, etc. A month later he changes her medicine again, to Effexor. The first 2 weeks, she does okay, but the packet doubles the strength after 2 weeks. It takes 4 weeks for it to take full effect. Right after she doubles this medicine, it is like her senses are on hyper-mode. She can taste everything that is in her food (chili powder, seasonings, etc…), taste the metal in water, and she can hear someone’s phone vibrating, in another room.
Then she goes back to college at the end of August 2007, and it’s horrible. The Effexor is having bad, bad side effects. We called the psychiatrist that she was using at home and he doubled the dose. That was the worse thing they could’ve done. The side effects were worse than ever. I had her to immediately go to a psychiatrist on campus. She told him the whole story and he believed her! Needless to say we switched doctors. He then lowered her dose back down to ½ a dose and hopefully can slowly get her off of all this medicine.
The newest thing she has developed is being hypoglycemic. The campus psychiatrist sent her to a campus medical doctor and he told her that they would get to the bottom of this. He tested her for everything under the sun. Low blood sugar is the only thing they found. But, she hasn’t taken the Yasmin since May. No telling what the results would have came back like if it was done at the time she was taking Yasmin.
Thank goodness she has counselors and doctors there at the campus that believes that Yasmin can cause all of these problems, and are working with her. From what I have read from the people that have used this medicine, although most doctors do not agree, Yasmin takes like 6 months to get out of your system. I think I am going to believe the testimonials of the people who take this medicine, over a doctor who prescribes it.
If everyone goes to the media, their doctors, the FDA, congressmen, and make them aware of these horrible effects, surely we can get this drug off of the market! Does anyone know a class action lawyer that would pursue this? For my child to have to go through all of this is ridiculous, not to mention costly. What do we know of the long term effects this drug will have if it is doing all of this when you first start taking it?
If you have the same concerns as me about this drug, and would be interested in looking into a class action lawsuit, please email: ****** I would be interested to see how many would want to pursue this.

I have been on Yaz for a few weeks. The side effects are awful. I am 31 and haven't been on BCP's since 1999. I sat down with my NP to explore different options for dealing with my terrible periods and she thought Yaz was the answer.
Well I have averaged about 4 hours of sleep a night since starting it. Because Yaz is like a diuertic I am up peeing all night as well.I feel anxious and panicky. Normally I am very laid back but feel like I am going nuts.The thing that drives me the most crazy is having restless legs while lying in bed. Time to get my potassium checked? I will be stopping this med as nothing should make you feel this bad. Not worth it.As a nurse I would never tell my patients to take this. I feel like an idiot for starting a pill that 1000's of women on the internet are complaining about.Of course you would never see the positive comments. But this pill sucks!

I was prescribed levothyroxine by my nurse practitioner for a "slightly" underactive thyroid. I have experienced at times, headaches (feeling like the top of my head is going to blow off); stomach problems, cramping, loose stools; anxiety, sleeplessness, fatigue and a lowered libido. I am prescribed .50 mcg, but I took that dose for 2 months and then lowered my daily dose, myself to .25 mcg. I felt better, but still tired. I didn't tell my NP that I lowered my dose. After a month or so, I upped it again, just because I still felt tired. I have been on the full dose, once again, for a month. I still have some of the previous symptoms, but am due for a blood test this month to see where my levels are at. If they are close to being correct, I am going to ask her to lower my dose or stop it all together and try exercising more. I don't know that this is a horrible drug, but I am sure that it is not something to mess around with, if you don't absolutely need to be taking it.

I have been on Yasmin for three days. I switched to it from Lo/Ovral because i tend to have low sex drive on most pills and my NP thought maybe because Yasmin's progestin was so different that it might help. Well, not yet. But I will tell you this: I feel like crap, no matter how much water I drink, I am dehydrated. I pee all the time. I have headaches, and all I want to do is sleep. Which is not good because the MCAT is in 11 days and I need to be on top of my game right now.

This pill was my last option, next step is an IUD. I can't take this anymore.