Seven months symptoms and conditions

I am 39 years old and work for an interventional cardiology medical device company in Tokyo, and so know the importance of controling one's cholesterol, keeping the LDL's low and the HDL's high. About two years ago, my doctor put me on 10 mg of Lipitor. Several months later I herniated a disc in my neck between C6&C7. From that point onward, I attributed all of my neck and back pain, and newly acquired total body muscle and joint pain, to the herniated disc, it made the most sense. Over the last seven months, I have really worked on my diet and began to exercise more (even though quite painful) and was able to lower my cholesterol. This resulted in my doctor lowering my Lipitor prescription from 10 mg to 5 mg. I noticed a slight alleviation of the pain I felt in my hip joints and calves. About two weeks ago I took myself off Lipitor completely and found further improvements in my total body muscle and joint pain. It's still there but greatly imporved. In retrospect, I now believe the Lipitor may have been the culprit (or at least a contributing factor) to my herniated disc due to muscle degeneration in the neck, and all of the subsequent muscle pain, especially in my hips and calves. I fully understand I am not going to die from calf-pain, but may from heart disease. However, I have found my quality of life has improved tremendously over the last few weeks. Less irritability, better sleep, less pain, clearer head. I feel like I have lost two years of my life on Lipitor via personal suffering and lack of ability to do much of anything with my wife and two young daughters. We all need to take charge of our own health and therefore I encourage anyone who feels completely different after taking Lipitor to engage your physician, and make sure its the right option for you. If damage has been done to my musculature I hope I can reverse it. It is evident to me that some serious clinical studies should be done to investigate Lipitor's effect on muscle degredation and hope others will consider carefully whether or not do go on this drug. If you do, monitor yourself closely.

I've taken prinzide for about seven months and have suffered dizziness, severe heartburn/acid indigestion, confusion, irregular heartbeat, numbness/tingling in my extremities, a general feeling of malaise, and tachycardia. The dizziness and heartburn were irritating; the tachycardia was downright scary.

I would wake up from a dead sleep and my blood pressure would be around 117/60 and my heart rate would be 105 bpm! I've been off Prinzide for five days and my heart rate is in the 70-80 bpm range -- still not great, but much better.

I have been on Lupron for almost four years for my endo. I have yet to get my period but have to say that while on the shot I had hot flashes, severe mood swings, and night sweats. All of the symptoms came in cycles and for the most part I felt great. I actually lost weight, and the best part, never got my period (duh). My sex drive fluctuated and I did experience vaginal dryness. I just want to get my period, it's freaking me out that I haven't gotten it over a month after I was supposed to take it last.

What a rotten drug. The past seven months have been hell for me. I am 42 years of age and put on this crap last November. I have suffered from bad headaches, leg cramps, Insomnia, Plantar Fasciitis, mood swings and the list goes on. After seeing this site and all your responses I believe the best thing to do is get of the crap. I will write in 2 weeks to give an update.
cheers from Down Under

My pubic hairs have changed color at the lower half. I have always been blond to lightish color. They have changed to a purple black ink color since having the coil fitted seven months ago. I mostly bleed rather than not bleed too. Have continual headaches with nausea.

I've been taking Loestrin 24 for seven months now, and it worked like a charm - my periods haven't exactly decreased in time, just in heaviness (my periods weren't really heavy to begin with). No side effects, no spotting, nothing.

But this might be something to watch out for:

This past Saturday I was too lazy to take my pill in the morning, and I stayed over at a friend's and didn't take my pill Sunday either. Saturday I ate a bunch of junk food (pizza, brownies, etc.) and I bloated... which made sense. So I just tried to drink water. The next day I began cramping... which was unusual. I would be just finishing the second row of pills and I can't say I've knowingly ovulated since I've been taking these pills. I come home and to my horror, I was spotting... which has NEVER happened before. And as the day went on the cramping hurt more (not overbearingly but there was a noticeable change) and I noticed the blood smelled HORRIBLE, like a mix between a rotting animal and vomit. And today I'm still spotting.

To make a long story short, I now have an appointment with my gyno. I don't know if it means anything, but don't be like me and purposely not take your pill... you're supposed to take a pill a day for a reason. ):

Hello ladies, I've had Mirena for seven months now. I too was told side effect were minimal and that my hormones would be altered from minimally to nothing at all. First couple months cramps were horrible during my period (not so bad now). During ovulation my ovaries hurt like never before and from ovulation to 1st day of my period I have a foul smelling discharge.
As someone who has been treated for depression in the past, I thought the depression and the weight gain was all "me" again. Not to mention the ACNE! I do admit to getting the occasional zit in the past, since Mirena my acne has worsened. Now, I also get acne in my neck and along my hair line.
It's comforting to hear that it hasn't all been in my head and discomforting the Mirena continues to advertise their product without giving recognition to all the true side-effects that all us women are experiencing.
First thing Monday morning, I am making an appointment to have removed!

I have to say that I have had the total opposite experience with Mirena. After several weeks of research and careful deliberation, I chose to have it inserted. The live journal website "iud divas" provided so much information, and mainly showed me that all women have different experiences. Sure the insertion was painful, but it was also brief. I took the rest of the day off work as a precaution. I was a little nauseous for a while and had some cramping and spotting. It has been over 3 weeks since my insertion, and I have nothing but positive things to say about Mirena. I feel great and it's wonderful not having to take a pill every day. Instead of cautioning about the dire consequences of using Mirena, I would advise women to bear in mind that every woman's body is different. I would also advise looking at the iud divas live journal so you can see that there are many many women who have had positive experiences with both Mirena and Paraguard.

I am so glad that I found this site and to see that there are other women out there who are having problems with the Mirena. I thought it was just all in my mind! I had the Mirena inserted in February 2008. Started having problems with high BP when pregnant with first baby and when I went back on pill after his birth BP wasn't doing any better. After having my second child, I contemplated about Mirena vs. having tubes tied. My OB said the Mirena was the perfect thing for me and was pretty much like tubal ligation, but without the surgery. I had no problems when Mirena was inserted..just bleeding (seemed like forever for me to stop bleeding) and the normal dizziness. For the first three months, I never knew when my period was going to be, but I just kept remembering what my OB said "your periods will be like nothing after the first three months." My periods did get a little better...however not the "light" or spotting periods. After the first three months, I started noticing that my hair was starting to fall out more but thought it was part of postpartum. I started feeling really tired, skin started to break out, felt depressed, my mind was racing, couldn't sleep, had problems remembering things (simple things), migraines got worse and more frequent than what they used to be before, moody, agitated, had chest pains, nausea in the morning (at one point I thought I was pregnant again!), stomach pains, diarrhea/constipation, kept having vaginal discharge (like when you are pregnant), came down with bacterial vaginosis, UTI's were somewhat common,no sexual desire and my BP was out of control. Seven months after having Mirena inserted, I started having sharp pains near right ovary. I had problems with cysts in right ovary before and had them removed so when the pains started, I had a hunch that most likely it was another cyst. My OB closed her practice so when I went to new OB for annual pap, I mentioned all the things I was experiencing including suspicion of cyst. I told her I had been experiencing all symtoms since Mirena was put in. She told me that she has never heard of the Mirena to cause symptoms like these. Told me that perhaps I was still having effects of postpartum and that my body was trying to get "back to normal" and get used to Mirena. Had all these blood test done and everything came back normal. I did have a cyst on right ovary and was told that it should go away within 2 months. Just had a follow-up ultrasound today (2 months later) and cyst is still there along with other cysts on right AND NOW left ovary. Most of the time, I am in a lot of pain especially on the right side. I was told to just take Motrin for the pain, but that nor heat packs work at all. I am really considering to have the Mirena taken out. I REALLY believe that the Mirena is the cause of my cysts. Is there anyone out there who have gotten cysts while with the Mirena? And has anyone experienced having no problems with cysts after the Mirena was taken out? Since finding out that I have multiple cysts on both sides and knowing that my doctor will probably tell me they will eventually go away on their own (first one is less than 2cm and others are smaller), I don't know if it is even worth keeping the Mirena in. I hate having all these symptoms...I just want to be "normal" again. BUT, IT IS VERY COMFORTING TO KNOW THAT THERE ARE OTHERS WHO ARE OR HAVE EXPERIENCED THE SAME. Now I can tell myself that it is not all in my mind and I am not going crazy!

I've recently had a staph infection on my right knee, and my regular dr. was closed so I decided to go to a nurse practitioner. She decided to give me samples of Avelox and actually had me take one of them in the office. Little did I know I was about to experience hell on earth!! After taking the first dose, I began to get extremely dizzy and disoriented but I slept well the first night. I thought I just felt bad from the staph infection and figured I would take another dose of the Avelox. Big mistake!!!! After that second dose I started having uncontrollable anxiety, depression, extreme confusion, and even became paranoid that I had some type of serious illness. I couldn't eat or function well at all and I have 3 small children to care for. When I tried to sleep I felt like I was passing out rather than falling asleep. I saw weird images in front of my eyes and jumped out of bed at 2:30 am panic-stricken. I found this site and saw what so many others have been through and was convinced it was the Avelox. But I've been off of it for 2 days and I still feel out of it, unable to think clearly, and have an odd detached feeling. I'm hoping this is not permanent damage. I just want to feel like my old self again! And I agree with so many others- Avelox should be taken off the market!! It is a horrible drug!!!!!

I was on the Yasmin pill for 5 months and suffered severe health problems for 3 years. It almost took my life. I actually heard popping sounds in my head when I first went off of it and on it. My symptoms were digestive, head aches, numb limbs, weakness, tired, severe menstrual bleeding, clots, depression, instability, low immune system, heart palpitation etc. In short I was very sick all of a sudden for no other reason than taking this pill If this has happened to you I advise the following which saved me. You need to do the following. Find a doctor that will take you seriously and understand that your problems started with this pill. My OBGYN resisted it for a long time until I was so sick it scared her. Seek an endocrinologist and neurologist if needed. Make sure your blood work checks the following: Any issues with blood clotting including protein c antigen. Mine was low which left me at risk of a blood clot after this pill. Also the pill can lower and this one more than others your b12 levels in your blood which is very dangerous. Research b12 deficiency and see it the pill did this to you. B12 levels should be no lower than 500. Also have your vitamin D levels checked in your blood. This pill depletes b12, vitamin D, causes clotting, affects the liver and so on. It took me 3 years to fully heal. Once I was on b12 shots, Vitamin D daily and had other blood deficiencies corrected after being on this pill I began to get better, but that took 3 years and I was so sick at one point I could hardly do anything and my heart so affected I almost had a heart attack. My blood pressure was uncontrollable. I am currently involved in a class action suit. You can be a part of it too. Good luck with your health first. I can say I am finally on my way back to health fully. Some have not been so lucky after taking this pill, but it took me personally 3 years to get back to the healthy woman I was before this pill. In the process I also lost a pregnancy due to the severe health problems. Don't lelt anyone tell you it is not this pill. If you know it is, no one knows your body better than you!

I'm 14 years old and I've been taking ocells for the past six or seven months, and I haven't experienced any of the symptoms or side effects of this pill. My period is three to five days long, and I'm very light, I've only gained about five or ten pounds, and my heart rate and blood pressure are normal. It does say on the side effects may make you lose or gain weight, like I said, I've only gained a few pounds, which I could easily lose.

i am so happy i have found this site! ive had the mirena coil removed just the other day (Thursday 16th oct) im now hoping that all the symptoms ive been suffering will fade away. i had my coil inserted a year ago last October. since having it inserted i have experienced headache, light periods that last around ten days which seem like forever every two weeks, with spotting in between which i was was told seven months after insertion by the doctor it would calm down and be less frequent but did that happen? NO! slowly but surely around two and a half month ago i started experiencing achey back pains where no matter how hard you try and get comfortable its impossible till it subsides, mild abdominal pain, pain in my neck and shoulder blades, chest pains, breast pain, shortness of breath, tearful, and paranoia thinking that theres something terribly wrong and im going to die and constant moaning about my ailments which im sure my poor boyfriend is secretly tired of! i just thought to myself hopefully putting two add two together that it may be the mirena coil thats making me feel so unwell. i have bled since having it taken out but i think thats the norm. so two days on im looking at this site that i found and its given me hope to know im mot the only one thats suffered with these awful side effect. im still going to get a check up to rule anything els out but im quite sure that its the coil that has done this to me. my advice to anyone would be don't have it fitted or get it taken out! good luck.

I have been on Yaz for eight months and absolutely loved it at first...about three months ago, my boyfriend and i broke up and i had a full blown period when i wasn't supposed to.....I just figured it was from stress. But for the last 5 weeks, I have had two full blown periods that lasted four days each and spotting every week to the point that I have to wear a tampon just so i don't ruin any more underwear...ive heard this could be from stress or weird hormone levels, but its just weird that i did so well on it for the first seven months and now this???? whats going on??

I am a male of 67 years old. I took Lipitor for a year, and after a few months of taking it, I felt muscle pains in my arms and shoulders, as well as my back. I felt weak and could hardly put my socks on by myself. I told my family doctor that I thought the problem was caused by LIpitor. He said it couldn't be possible, but he couldn't figure out what was wrong, so he sent me to a rheumatologist, who gave me an initial diagnosis of polymyalgia rheumatica. I went back for a checkup, and although the sed rate was normal, the C-reactive protein was elevated. He felt his diagnosis was an accurate one. He prescribed prednisone for me. I had some doubts about it, since I am diabetic, and was concerned about the elevated blood sugar it might cause. Well, it did elevate my blood sugar, and I weaned myself off it within three months. My blood sugar went back to normal, and while the prednisone helped the symptoms of muscle pain and aches, after I stopped it, the pain returned with a vengeance.

About a year passed after discontinuing the prednisone, and I felt worse and worse. Any time I engaged in physical activity, such as yard work, I was almost incapacitated for two or three days. I felt weaker and weaker, and by now, my activity is about ten per cent of what it was three or four years ago. I am unable to do anything physical without paying a heavy price.

I would tell the doctor that I felt the problem was caused by the Lipitor. He would dismiss my comments, saying that the pain should have gone away after discontinuing Lipitor. He sent me back to the rheumatologist with results of recent blood tests. Both the sed rate and C-reactive protein were normal. The rheumatologist touched my back and other areas, which caused me to jump. He said it might be fibromyalgia. I told him again that I thought it was caused by the Lipitor. He said the same thing my GP had said: if it had been the Lipitor, the pain would have gone away when I stopped taking it. I know the Lipitor caused the pain, because I tried red yeast rice for a couple months. The pain increased to almost unbearable, so I discontinued the red yeast rice. If I were not susceptible to the pain from the Lipitor, would the red yeast rice have increased the pain?

So here I am with a fuzzy diagnosis from the rheumatologist, and no clue from my family doctor (that he will verbalize, at any rate). My life has gone steadily downhill. I used to be a strong, active person, but now I can do very little, and my strength is a shadow of what it formerly was. What can I do?

I have had progressive muscle weakness, pain in my joints with swelling of the knees, ankles and hips. My doctor said it is not related to the antibiotic and to continue taking it. The symptoms are so disabling I can barely make it to the bathroom alone and I have had to miss work. I also told him the inside of my throat felt swollen, and my tongue is turning white. It just isn't a pleasant drug to be on.

Got Mirena less than 2 weeks ago and have had horrible heartburn and bloating almost daily since. Also increased acne - but that was expected - the heartburn was not - is this normal???? And will it go away after my body adjusts?

I have been on Yasmin for 4 months,but had to switch to Loestrin. While on Yasmin my periods were very regular and timely directly down to the day. This month i took loestrin each day on time, and used back up methods. There was only one "slip up" and even it would make it almost impossible for me to be pregnant. i've taken 4 pregnancy test and each reads negative CLEARLY .However im almost a week late for my period according to the loestrin pill pack , and i'm beginning to get nervous because i'm still waiting on my period! Can switching brands of bc cause you to miss a period, anyone experienced this?

I took Fosamax 70 mg once weekly for seven months before getting off due to intolerable side effects beginning after four months. The worst problems were vertigo and dizziness, which came on suddenly. I woke up one morning and when I tried to get out of bed, I felt like I was falling. I had to call my husband to assist me to the bathroom. Although these symptoms became less severe, I never regained my equilibrium while on Fosamax and was unable to exercise on the floor due to vertigo when I lay flat. I also experienced heart palpitations,extreme coldness, and general malaise about two hours after taking my weekly dose. I now wonder if I was having atrial fibrillation, another serious side effect of Fosamax. I am so glad I got off it!

I gave my body a month to clear out the drug and then I began taking strontium citrate 680 mg once daily. I feel well again and began a blog to relate my progress at http://strontiumforbones.blogspot.com/. Please visit and comment.

Bonelady

I am 52 years old and switched to Singulair last Fall for severe allergies. I have taken all others on the market and have exhausted the list. Since starting Singulair I have had chronic ear infections, the first since I was 11 years old. Have also had a mild cardiac arrhythmia accelerate to a severe state, for no apparent reason, and cannot get under control with the usually curative medications. All cardiac testing proves negative, other than crazy ECG's showing nearly every beat to be premature and weak. Has anyone heard of this side effect?

I was initially very excited to start the NuvaRing. I had been on BC for about two years before and wanted something that was a little easy to take care of, and since you only have to change it once a month, I thought the NuvaRing was for me.

I was probably on the Ring for about seven months. I enjoyed the ease of care, but I completely loss my entire sex drive! This was extremely detrimental to my long term relationship with my partner. Luckily, he understood it was not him but the BC, but it still caused a strain on our entire relationship.

It was sometimes difficult to insert the Ring, sometimes taking about 10 minutes. The ring also fell out once while I was removing a tampon. I did not notice and had unprotected sex with my partner. Once I noticed, I took Plan B and everything was okay.

I had Mirena put in straight after the birth of my second child as recommended by my maternity hospital to have inserted 6 weeks postnatal and kept it in for seven months. At first I just had minor symptoms like spotting slight cramps and a little bit of vaginal discomfort due to the wires, and the only good thing was that my periods stopped eventually. As the months went on my health started to decline as the side effects crept up on me and I couldn't figure out what was wrong. I just thought it was because I have two small children and I was feeling worn out/burnt-out, it got to the point that I was struggling to do everyday tasks and look after my children. I am only 24 years old and I felt like I was a 50 year old grandmother!

I had the Mirena removed 3 days ago after reading this site and I feel so much better! This company must know that there are more side effects than they have listed, yet they still fail to list the serious and debilitating side effects their product is causing people. They were sending the maternity hospital I went to products with Mirena printed on to push their crappy product. The biggest worry I have about this thing is that I am breastfeeding and I had this stupid thing in for 7 months and some of it was coming through my breastmilk and I have noticed that my 9 month old baby girl had really bad clicking joints that have got better since the Mirena removal as have mine! (although not 100% back to normal yet) This company deserves to have their product removed from the market and someone to sue the pants off of schering. The product is completely unsafe!. If there are any long term side effects to myself or my daughter I WILL SUE THIS STUPID COMPANY AND THE DOCTOR AT THE MATERNITY HOSPITAL WHO PUSHED THIS PIECE OF JUNK TO ME. The warnings are completely inadequate - because I'm sure if all the possible side effects were listed next to no-one would have it put in. I feel that this thing is pushed on mothers so that you can't distinguish the side effects from hormonal changes that could possibly occur after the birth of a child to hide the fact their product is dangerous.

one year and seven months ago i was given a coarse of laviquin--750 mg--for seven days.after 5 days I was so sick i thought i would die and at times wanted to--I had severe depression, diarea, musle pain a weakness, ancles ,knees, back and shoulders hurt so bad that I had trouble getting out of bed. my heart was raceing at 120 beats per minute and blood pressure was very high. I also had a lot of pain in my butt muscles and could not sleep, then I got to where i could not breathe and had to go to the E R

now it has been over a year and a half and still have trouble walking because of pain in knees and ancles. shoulders are sore all the time and I can not sleep more then a couple of hours at a time. my butt hurts so bad that I can not sit in a recliner for over an hour with out extreame pain.. I changed doctors now tree times and none of them will consider that the laviguin was the cause. the last one did send me to a hospital for a rectal exam but they found no problem. now that I know what caused the problem, the depression is most replaced by anger. this drug should be recalled and the drug companys should be made to pay for our care. I am 67 years old and been in pain now all that time and think I will never be the same again. my advise would be---DON'T TAKE THIS POISON--AVOID AT ALL COSTS

YOUR FRIEND---ALP

I had a terrible experience with Mirena, I lasted seven months and I could not bear it any longer as the side effects were too great. I bled continuously for seven months give or take a few days here and there. I also had changes in my vaginal discharge whenever I wasn't bleeding. I became very self conscious and it greatly affected my sex life.Sex was painful at times too as I had unusual pains in my abdomen. My emotions were all over the place and I did start to worry that I had depression as I did not feel like myself at all. I am so relieved now that the Mirena is removed. I could not wait any longer for things to improve as my doctor assured me that they would. There was some trouble with having the Mirena removed as the string had gone up into my uterus. One doctor claimed that she could not do it and referred me to another who had no real trouble in getting out. I had a horrible experience with the Mirena as I did with Depovera. I cannot believe that some people have no trouble with these contraceptions, they are very lucky!

I am just about to burst in tears from reading all this information. Our daughter is 4 years old. She is been in Singulair (for her Allergies) since she was almost 10 months. It been quite a rollercoaster for us. We have been told she is ADHD (although can't be diagnose until 6), she has almost all the characteristics. hyperactive, mood swings vary between days, now leg pains, nightmares, etc. Two years ago our allergist took her off Singulair but our pediatrician didn't agree, so we went back.
It has been very painful because our daughter is such a bright girl; we don't want her to suffer, not to be accepted because she is acting like this. From reading all this information my husband and I decided to take her off Singualir. Hopefully we see some changes that can give us a sense of relief. Any words of wisdom?