Blood tests symptoms and conditions

Since I've gotten my Mirena Implant I've been diagnosed with 2 different STD's and an infection which after the blood tests came back negative! So far I have taken meds for HPV, Herpes, and a UTI. Each time I go in for my pap smear and check up to make sure the IUD is still in place I inform the doctors (have visited 6: 3 for the first pap, 3 for the second opinion) that one of the biggest side effects of the implant is abnormal pap smears, even hand them the same pamphlet that the inserting doctor gave me when I first got it (which clearly states abnormal pap smears as a side effect) however I still end up with some horrible disease/infection!

So far, in the one year I have had this thing in me, I have taken 20 different meds for these STD's that I NEVER HAD!!!! These meds have made me horribly sick and the UTI meds almost killed me.

Also, like many women on here, I have bad hair loss, headaches, horrible back pains, and crippling stomach pains. Constantly attempting to get my doctor to give me an ultra sound to make sure that the impant didnt tear me but she refuses! Go to the hospital to ask them for the same and they refuse also "Thats not likely with the implant."

This is my one year check up coming up, I want this thing out! If they do not take it out I'm threatening with a lawsuit. This is NOT a life saving device and they should have NO say in whether or not this stays in!

I am a 22 year old, healthy female and received my fist two shots last September. By November, I began to notice my hair falling out, which became more excessive in December, prompting me to receive blood tests for thyroid problems, nutritional imbalances, etc. Everything came back negative and I self diagnosed the problem to be a hormonal imbalance caused by my birth control (which was hard to believe being that I had been on it for two years with no hair loss). I stopped the pill the end of January and my hair loss coincidentally stopped as well. I received my third shot in April, and sure enough the same devastating hair loss began two months later, which is classic with drug induced alopecia (hair loss). I am CONVINCED that Guardasil has caused this devastating reaction that has caused me to loose half my head of hair. It is October and I am still experiencing significant hair loss. This vaccine has caused me nearly a year of emotional turmoil over my thinning hair.

Same story different person! I had my Mirena placed February 08. Three months later, I could not lose weight no matter how hard I tried. I have major hair loss, anxiety,sore muscles and joints, and extreme fatigue. Oh yeah, I forgot the memory loss and brain fog. I have been to my Drs. and have had thyroid, lupus, and other blood tests. All negative, therefore I am starting to point the finger at the Mirena! It's coming out Monday! Just can't live like this anymore!

hi there i have been on simvastatin about a year now and have felt so ill since taking them i am now due to have several blood test to see what they can find " as i suffer with nausea, pains in my legs and body /and terrible depression and i cant remember me feeling like this before i started taking these tablets i really don't feel like me no more / and i can easily sit down and cry because off feeling like i do / now i have been told to take double dose because my cholesterol is higher / i have spoke to others of these tablets and they have had same reaction so i have decided on my own thoughts to stop i will tell my doctor.and i am hoping i will get back to my old self i will try and keep my cholesterol in control and i think its well worth a try than to have all these side affects B.

Well where to start. It started one Weds morning at work. Suddenly came over all dizzy and light headed and felt really really sick. Went home and started with a temperature. Parents say I was pretty spaced out for several days and didn’t really want to talk to anyone. It’s like I was there but I wasn’t. Went to doctor a couple of times and they diagnosed a virus. Problems with sleeping started. Ended up at the hospital out of hours as I was shaking, felt sick, thought I was going to pass out. Nothing found so sent back home. Saw doc again and was referred to a doctor at the hospital who had an interest in viruses. Saw doc and loads of blood was taken for testing. Went back after a couple of weeks and blood tests where clear. By that point I was feeling a bit better so they thought it was post viral fatigue. Went back to work part time and worked myself up to full time. Then it started again. Had to be fetched from work. Colleagues said it was more like I was having a panic attack. Broke down completely. Couldn’t stop crying and was in a right state. Went to docs and was diagnosed with depression and still post viral fatigue. My main symptoms have been, panic attacks, anxiety, faintness, dizziness, nausea, general feeling of unwell, blocked ears, palpitations. There are probably more but I can’t think of them at the minute (Oh yeah, brain fogginess as well !) More blood tests were done and that’s when they said my hormones were a bit low but they didn’t think it was anything to worry about. That’s when I started researching Low hormones and started to come across the problems with Yasmin. I cannot tell you what a relief it’s been. I honestly thought I was going mad and that there was nothing wrong with me and it was all in my head. I sat looking that the screen going ‘that’s me !’ Have stopped taking them straight away. Will see how we get on. Doctor didn’t know anything about the problems and has said he will be interested to know how I get on. I cannot believe they didn’t know. Main thing is I know now and can start getting better.

Despite having a brush with the big C last year (I finished chemotherapy in January) I have been very fit and healthy during my 61 years! A few weeks ago I started having palpitations, hence a visit to the doctor revealed high blood pressure and cholesterol reading of 9.9!!! Shock, horror. He informed me that it was genetic and prescribed Simvastatin 400mg and Bendroflumethiazide 2.5 mg daily.
Not being satisfied with the enclosed leaflets I have looked up more info. on the net. Should I have done this!!! After reading some of the posting on the site I am feeling a bit apprehensive. Last night I had a terrible night couldn't sleep for the pains in my legs and a bit nausea this morning.
But I need to be sensible, I really don't have any choice but to take these drugs just hoping that I won't have to stay on them for the rest of my life and I don't get any of the side effects that some of you have suffered. I also wonder if the chemotherapy could have caused by raised cholesterol?
Hope to keep you posted and would welcome any comments!

Has anyone had worse symptoms with the NR than with the pill? I was experiencing terrible migraines two days a month, right before my period started. I was also finding that my period was getting lighter and lighter as the months went by. I've been on some form of the pill for about 15 years off and on, this time for about 3 years straight. A doctor told me the NuvaRing might help with the headache...so I switched to it. the headaches are no better, I gained 11 lbs in two months and I have NO sex drive at ALL. I also get hardly any period at all. Anyone else having that problem? I got worried that I was entering early menopause, but they did a pelvic ultrasound and blood tests that were normal.

I am a loving mother of a 5 1/2 year old boy. He has been on Singulair for over 3 years. In this past 3 years my son has suffered in an unspeakable amount. He came down with Rota Virus and was hospitalized at 2. He then came in contact with Pneumonia in the hospital while he was there. They automatically put him on Singulair, Zyrtec, Prednisone, and antibiotics to treat the pneumonia. Since that day, my son has gone though more tests than I have in my entire life. He has had asthma, sinusitis, leg cramping ( to the point he cannot walk for 2 years), IBS, Acid reflux,(they gave him laxatives for a year that made things worse and addicted to them also), stomach pain, constipation and diarrhea back and forth. He also got Erythema Mulitforme TWICE, while on this drug. All of which the doctors said could NOT be caused by Singulair. He has had several Upper GI's and CT scans. Along with Barium enemas, several hundreds of blood tests, and many many pokes and prodded that were not necessary. All since he has been on Singulair. He now has frequent bathroom trips, depression, confusion, and anger outbursts. He also has to go to the restroom every 5 minutes. He has had genital swelling, and many other aches and pains. None of which his "doctor" ever said could be a result of Singulair. I am 100% sure it was!!!! He currently has anxiety and emotional sporadic issues causing problems in school The teachers and counselors say that it is so strange because there is no TRIGGER and the outbursts are completely inconsistent. His preschool teacher and director are sure he has ADHD. Well, we had him tested and he does not have any part of it. He has no learning disability what-so-ever. So that brought me back to square one. He is in a positive loving enviroment. How could he be depressed and want to hurt everyone around him? He cannot sit still. He cries and says he is 'stupid" and "can't think" like the other boys. He has nightmares and cannot sleep alone. He is scared of everyone and everything. So, as I sit here crying, I realized that this has all been a reaction of his "medicine" Singulair. He never should have gone through all of those painful tests, only to prove they couldn't find anything. So many treatments and sound full advice speeches from his doctors. How could they be so naive and selfish in the life of my son?

When I called my pediatrician of 5 years, she told me that " parents that have children with behavioral problems will LOOK for something to blame their problems on." She also said "drug companies only put side effects on their labels to PROTECT the drug companies. (as she laughed at me) They are not always valid". Then she said "if you take you child off of Singulair you will be playing Russian Roulette in his life." Then she said that all children around 5 or 6 go though this emotional time in their lives." She told me that if I take my child off of Singulair that she would no longer be a part of his health regimen for his asthma. She told me to see a Pulmonologist for further treatment.
Who is paying who? This is my son's life???????? I decided to go with my mother-gut instinct and get him off of this medicine. No matter what. He has been a different person since. He is currently going though a lot of side effects and withdrawals (leg pain, insomnia, hic-ups, emotional distress) but every day is getting better. How can the drug companies say that this is a "wonder drug?" There are more reported side effected patients then clinical studied patients! How can a "medication" that stimulates the brain not be connected to other problems? This "medication" interferes with the bio synthesis and action of LTs and has been marketed as NOVEL medication against asthma and allergic rhinitis. Who the hell is playing God here??? The pocket books of Merck or our over PAID "doctors?" Who pays the price? Our children? Or us. Thank god I found this before it was too late. I would not be able to withstand the pain of losing my son due to their lack of scientific evidence. They are lucky I am one of the smart ones. I will not settle for less than Justice for the drug companies and their paid "doctors?" You all end up in the same place. HELL

There are 18 million people on this drug. Most of them are children. Please save a life if not your own child's life. Thank You

My 12 year old son started on Singulair 10 days ago. Yesterday, he threw up blood twice, so I took him to urgent care. He said it felt like someone was shoving knives into his stomach. He had blood tests and a CAT scan -- the connective tissue in his abdomen was inflamed and his lymph nodes are slightly enlarged. His white blood cell count is up slightly -- just above normal -- and his liver enzymes are elevated, which the doctor said is common with a viral infection. He has also had migraine-type headaches twice in the last week. HOWEVER: my 16 year old son has been on Singulair for four years, and it has been a lifesaver. He has had some hand tremors, which could also be aggravated by the decongestant he also takes, but no other side effects.

I have had a "Lupus" like and "MS" like nervous/arthritic pain since I took Levaquin, have been through lots of tests, Lumbar Punctures, and blood tests, and MRI. Interesting....

Anyone Else?? Trying to figure out what is causing the following.
Bruising like feeling at the sides of my pelvic bones...Tail bone pain when sitting...Low back ache. Started 20mg Simvastatin Feb 2008.
Michele

I had mine inserted the first week of July. Yes, it was freaking uncomfortable getting it done and I had cramping the rest of the day, but my OB warned me of that and I made the decision to go ahead. I'm not in a position to complain about it now.
I bled/spot for 2-3 weeks after insertion. Only heavy enough to require a tampon for the first week, but I had it inserted when I was supposed to be starting my period anyway. Again my OB suggested this and warned me about the possibility of bleeding for up to 6 months. Again my decision to go forward!
Since then I have had cramping once a month like I'm going to start my period and never do. Within the last few weeks I've started getting the acne and an oily scalp. It's all over my back and not poppable. I'm hoping it will eventually subside when my body gets used to the new hormone level I'm giving it. If you think about it, it's the same thing in puberty (ie change in hormones) that kicks off the acne so it doesn't surprise me that this is a side effect. If it doesn't subside I'll make a decision then whether or not to have it out.
I have not had any of the other side effects. In fact I had terrible headaches and neck pain before I got this and those have gotten much better.

I was on the pill for 15 years before getting mirena and I had much worse side effects with that (extreme moodiness, loss of sexual desire, bad cramps, long periods, etc). I tried multiple brands of pills and never found one I was 100% happy with. But I dealt with it because I made the decision to go on B/C.
I'll take the acne over those any day! (not to mention I got pregnant on the pill!!!)

I understand that these side effects suck, but you act like it's the company's fault. They specifically list the common side effects and the majority of the ones you're complaining about are listed in plain site Taken directly from their website:
Menstrual changes
Lower abdominal pain (cramps)
Acne or other skin problems
Back pain
Breast tenderness
Headache
Mood changes
Nausea
Ovarian cysts have been diagnosed in about 12% of Mirena® users. In most cases, the enlarged follicles disappeared spontaneously during two to three months of observation.

Did you think that's just for show? Did you ever stop to consider (before getting the product) you might actually get those side effects and what you would do if you did? It is your body... YOU are the only one responsible for what goes inside it. No one held you down and forced you to do this. Mirena didn't hide anything from you or trick you into it. Take some responsibility for your actions! Quit blaming others. This is a great example of what is wrong with our society today!

Take responsibility! Do your research! Make your own decisions and deal with the consequences of them without blaming others!

If you look at the mirena website it gives you the FDA number to call to report side effects. If you're having major ones call the FDA and report it so that more than just people that stumble upon this forum know about it!

I began taking Yasmin in July 2006. I had been on bcp for about 10 years at the time, mostly due to bad cramps and pms symptoms. Yasmin worked out well, but there was just one side effect, I would become extremely emotional right before my period. In October 2007 I went for my yearly check-up and mentioned this to my doctor. He switched me to Apri (Desogen) saying that this would be a better pill for that side effect. I began taking it that next month. Right away I had feelings of nausea and breast tenderness. Even though I felt like this I gave Apri a chance. In January 2008 I couldn't take feeling like this anymore and stopped taking it. In February I noticed my hair began falling out. I hadn't gotten a period this month either. I went to the doctor in March and she ran many blood tests. My estrogen came back extremely low (at a level of a menopausal woman). Instead of exploring any other options as to what to do, the doctor put me right back onto Yasmin, since now I went two months without a period. I figured that I would have to learn to live with a little moodiness before my period that Yasmin gave me. The doctor also made me believe that this would put an end to my hair loss...Nothing could have been further from the truth!!! I went back on Yasmin in March 2008 and what a HUGE difference than from the first time I was on it. Not only was I emotional now ALL the time, but I physically felt much worse. I had constant breast tenderness, acne (which even as an adolescent I never had), oily skin, and my hair was constantly falling out. Emotionally I was a wreck! I was constantly crying and very depressed! I began going from doctor to doctor, which is unlike me. I hate doctors and would only go for a serious illness. Now I was hoping that one of these doctors could give me an answer. But 6 months later and NO ANSWERS. The only thing that a few doctors said was that Yasmin was good for those with hair loss. So after reading many of the entries on this website and after much soul-searching...I am going off birth control for good!!! I have lost well over half of my hair, have practically pushed everyone that means anything to me away, and have personally hated myself! I have literally lost the past 6 months of my life! It is now time to see what my body is capable of on its own. I'm done putting this poison into my body and would tell anyone else to do the same. I always knew that there were side effects associated with any kind of medicine, but I could not have ever imagined that all of these side effects could have and would have happened to me. I felt like I had to write this after reading all of the other entries. Many of those entries gave me the courage to quit and I would be happy if this could help or inform even just 1 person! I would appreciate if there were anyone out there that had a similar experience to either post it or reply. Thank you.

I was on Yasmin from November 2005 to February 2007. I didn't have a period until June 2007, and have only had 4 periods since then (and one was medically induced). I have been to a gynecologist and an endocrinologist. I have had a battery of blood tests done and all have come back normal. I have some more coming up.
Before going on Yasmin, my periods were relatively normal. I didn't have a "set your watch by it" kind of period, but I did have a period every single month (just different times during the month). While on Yasmin, I can't name specific side effects that I noticed. Looking back, breast tenderness increased (and continues), increased propensity to headaches and fatigue, and weight gain were all present. It is going off of it that has really messed up my system. My doctor originally thought I had PCOS, but blood tests have come back normal. I was even convinced, because since going off Yasmin, I have developed some of the classic symptoms. I am at a loss as to why my cycle has not returned to normal.
I am so frustrated, and while it is nice not to have periods, I want to know that I am okay. I am wondering if my being on Yasmin is still haunting me.
Has anyone else had difficulties for such an extended period after coming off of Yasmin?

I've been on simvastatins for about 2 years after TIAs. I'm 56. I had two small Strokes about year ago despite being on simvastatins. Had brain scan which showed two small areas of scarring and carotid artery scan- arteries fine. Started experiencing dizziness last year and GP diagnosed vertigo and gave me seasickness pills which didn't do much good. Since then I've experienced headaches which last for weeks, increasing fatigue (now struggle to get out of bed in morning) muscle pain which is getting really bad and sore feet (?). Increasing memory loss, confusion, lack of concentration, eye problems (when I first wake in morning my vision is blurred for ab out 30 minutes or so. I've been worried i mmay be developing Alzheimers. I've also piled on weight and the texture of my hair has changed - it has become very soft and silky and become thinner - normally my hair is very thick. Also I've had two perms in last 6 months which won't hold curl - been having perms for years and never had this problem. I've had several blood tests including for under-active thyroid and they have all been clear. I've been really worried about all these problems and did some research and came up with this site. I am beginning to think my problems stemm from taking 40mg Simvastatins so am going to stop them and book appointment with GP. Any comments/advice would be appreciated.

I was a competitive runner with a number of sub 3 hour marathons under my belt before I was prescribed statins for elevated cholesterol 2 years ago. The first go round was 40mg zocor but muscle soreness and loss of strength started within 2 months. Switched to NIASPAN but couldn't tolerate it. The last 7 months have been on 10mg of Lipitor and now have intense pain in my legs, soreness in my wrist and thumb and swollen feet. I can still run but much less than before and much slower. I regularly go to the gym but have seen a steady decrease in the amount of weight I am able to lift. I have a blood test in a couple of days and will be looking for myalgia again. I have discontinued the statin and don't plan to start again. I was healthier before the DR decided to "help" me with my cholesterol problem.

I'm a 38 y/o woman. For 7 yrs I knew my cholesterol has been high. I refused to take cholesterol medication and decided to diet and exercise but that didn't work. I've had 2 children in the past 3 yrs. In May of this year I started having chest pains and palpitations. I had blood tests done. I was given Inderal and also prescribed Zocor 20mg for my cholesterol. It was 243 with and LDL of 178. I took Zocor for a week. I felt so awful. I was weak, I lost my appetite. I was constantly tired. I couldn't even carry my 10 month old son, yet alone care for him. I informed my physician and she changed it to Lipitor 20mg. I thought I was doing fine. I checked my levels again after a month. My cholesterol was 113 and LDL 58. I trusted the doctor knew what she was doing. At the same time I also was taking Omega 3's. I asked my doc to lower the dosage to 10mg. From the time I was taking Zocor and the start of Lipitor. I was feeling tingling and numbness in my arms, hands, fingers, toes, feet and legs. I also was having muscle pain. I asked my doctor about that. She mentioned because of my heart palpitations, it could be symptoms of anxiety and panic. I had feeling of pins and needles throughout my body, not knowing when it would occur. I had muscle pain in my arms and legs and neck pain. I went online to see the side effects of Lipitor and came across this website. I decided to do an experiment. I stopped taking Lipitor 9 days ago. I was on statins for almost 4 months. I don't have the feeling of tingling and numbness, but I still have pins and needles and muscle pain. I have to say, I feel so much better. I hope to get better. I 'd really like to know, how long does the medication stay in your system? What are the effects of getting off it so suddenly. I'd love to feel myself again.

My son has been taking Singular for a few years for mild asthma and recently in the past few months all of the sudden he has been having a hard time falling asleep,anxiety at bedtime taking hours to get to sleep with me having to stay in the room. We took him to his pediatrician who ran blood tests and referred me to a sleep specialist who suggested he may have OCD or Anxiety. I just thought it was just something that would pass after 4 months it still has not passed. I am removing him from Singular TODAY. After all these visits with these doctors who knew he was on the medication and never said anything to me about possible side effects . I cant believe it took an article my husband saw in the paper for this to come to my attention.

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..

I have used the NuvaRing for about 3.5 years, starting after my 6 week check up when my daughter was born in 2004. In the beginning I felt like it decreased my sex drive but also that maybe post baby body that caused that too. For three years I had no problems. I had noticed breast tenderness throughout but other than that no side effects. About 8 months ago it began with a missed period, then two periods in one month. My OBGYN recommended 'resetting' my body by taking out the ring until my next cycle and starting it up again. I followed his directions but the next cycle came along with a bladder infection followed by a yeast infection. Over the next 4 months I either had one or the other, continually visiting my doctor I didn't make any connection to the two. Stomach pain, chronic fatigue and kidney pain also added to the list. My doctor prescribed a series of medications followed by blood tests and a referral to a specialist. Over the summer my husband asked that I stop using the ring because my sex drive had hit rock bottom. After a few weeks of taking out the ring, the burning sensation during urination has gone away. Stomach cramps and back pain has ceased and no infection to date. I am in my early thirties and after a week off the ring I realized what they mean by 30's sex drive. My husband and I are both happy with the changes. I visit my OBGYN again in a few weeks to revisit non-hormone options for BC

Let your body heal from child birth before you get Mirena, that is my opinion. I didn't get Mirena until my son was over a year old and i haven't had any crazy side effects, at first the bleeding and spotting for about a month and then my period stopped. i love it so far and reading some of these comments i realized the common theme in them is that many of the women have had problems got the Mirena right after having their child. i really think your body needs time to process all the hormone changes and get back to normal before you add birth control to the mix.

I'am only 26 but I have been a insulin dependent diabetic since the age of three. Being a diabetic for so long has made it difficult for my body to maintain normal cholesterol and triglceride levels. (I'am not overweight and I am very active) At 19 I was put on lipitor but it gave me severe stomach pains when I called the doctor they told me "it was just a side effect" and should subside. I wasn't on it for very long when I found out I was expecting and had to stop taking it anyway (can't take statins while your pregnant it can cause severe birth defects) Anyways, after I had my daughter they said my cholesterol was fine and they weren't going to put me back on anything. Yes! Until just recently my doctor discovered that my triglceride and cholesterol levels were so high he had the lab re-draw my blood tests! Odd because I feel perfectly fine. Because of the stomach pains years ago with Lipitor he put me on Simvisatin and Antara. Every since I have been on the Simvastatin my cholesterol levels are perfect but I am soo tired all the time. When ever I tell my doctor he says it's because I am a young mother of three and work full time. But this is a different kind of tired. I seriously could drink a five shot extra strength espresso and fall asleep this isn't normal. All my blood work is fine. It has to be a side effect.

I am currently 58 years old and lead a very active, healthy lifestyle. I began taking 10mg of Zocor, along with 1000mg of niacin in the summer of 2004 to reduce cholesterol (251) and triglycerides (571). The therapy dramatically improved my blood tests, however, within 6 weeks, I began to experience minor chronic skin infections, both fungal and bacterial. They were easily controlled with topical over the counter type medications, but they were annoying. At no time was this new condition linked to the statin/niacin therapy by my doctor(s). The infections became progressively worse over the next 3 years, and evolved into chronic folliculitis in my scalp, neck, and face, cystic acne, and persistent fungal infections that were becoming more difficult to control. In addition, I began to get chronic eye infections. It was as if my immune system was becoming ineffective. I stopped taking niacin in December of 2007 and the symptoms immediately lessened. I stopped taking Zocor in March of 2008 and within 2 weeks, all the skin problems and eye infections completely ended. My health was restored completely and I am glad to have put that whole mess behind me! I have been taking Omega 3 supplements to control my cholesterol and triglycerides and have had results that equaled the Zocor and Niacin therapy, with cholesterol at 160, triglycerides at 91, and a favorable HDL/LDL ratio. My physician is skeptical, but I know that my body was not functioning correctly with the statin/niacin treatment. I have found anecdotal reports from others who seem to have experienced a change in their immune system, but no mention of this as a side effect by the medical establishment.

My 6 y/o daughter has been taking Singular for approx. 2 years. She began to have regular stomach pains shortly there after. She was sent to Children's hospital where they put her on a laxitive which made things worse. Then we began testing for food allergies only to find out that she tested positive for a 3 page list of foods. We eliminated those food and had her tested again. She was subsequently allergic to the foods we eliminated. She was recently down to rice, a few meats and some vegetables. Guess what, she is now allergic to those foods.

All this time she has been complaining of severe leg pain, eye pain, throat pain, numbness and tingling in her hands a feet, all of which come an go. I have reported this to all the doctors and specialists we have seen. She had undergone countless blood tests to rule out autoimmune disorders and all come up negative.

She began to develop severe anxiety and just had the blues most of the time. She would be crying and saying off the wall things like, "I don't think my fish is happy". She couldn't stand to be away from me and would stress out about even weather or not she would sit by me at a restaurant. I mentioned this to all of the doctors. They said to not make too much of it. One suggested she see a psychologist. NOT ONE DOCTOR EVER LOOKED AT THE SINGULAR.

Finally about 4 weeks ago my neighbor who is a scientist at a pharmaceutical company called me and told me about the "black box" warning that had just come out on Singular. I took both of my children off of it immediately. My daughter went through about a 10 day period where her anxiety got worse and then it was just gone. We are adding foods back into her diet and at this point she has not had any severe allergic reactions.

The last 2 years have been a complete nightmare for her and for us. I am a medical professional and I have had doctors treat me like a hypocondriac, hypersensitive, attention seeking mother. I feel so justified and saddened by the recent findings all at the same time. Most of all I am so grateful that we figured this out before things go even worse.

Please let me know if anyone else is suffering food related reactions as a side effect.

I had the mirena put in in june after my third child. I did feel a bit dizzy when it was first put in but did not cramp at all. I was still spoting then from giving birth, so it just continued for about 3 more weeks the stopped altogether. I have not had a period since, woooooooohooooooooooo!!!!!!!! I don't feel bad about that at all. I did have a day when I woke up cramping and thought I was going to start but never did. My doctors nurse told me everything I needed to know about the mirena long before i had it put in. I actually made the appointment to discuss it with her. Everyone should have been smart enough to ask questions before it was done, not the day it is. You cant think straight when someone is getting ready to put a device in you. I have to say I love my mirena and would not trade it for a pill, a shot, or any other birth control method. Ladies know your gyn very well before trusting them. I think most of you just think it is your doctors fault. It is not it is yours for not researching it more. And come on what women is not moody a day in her life, not many. How many headaches did you get before the mirena? How were your sinuses before mirena? Probably the same. Some womens health simply changes after having a baby. I also advise against you removing these mirenas yourselves. It is not smart, you could get a bad infection from not being in a sterile environment.