12 months symptoms and conditions

I had the Mirena inserted about two months after my second baby. I was not feeling any post-partum depression at that time, but my life was VERY hectic. I had never had a depressive episode before. After about four months of having the Mirena, I basically had a "nervous breakdown": deep depression and an inability to function in my regular life activities. Like I said, my life was very hectic at this point, but I want to point out that I had been heavily stressed out before in my life, with no depression. Anyway, my GP insisted on taking it out ASAP; she had heard that some women get depressed on Mirena (when they never had that type of problem before...). I went on Wellbutrin (still on it!), and am doing a lot better 12 months later. However, I'm still fighting the depression, and I have some anxiety, too. I'd say that if a woman has an experience like mine, the smart thing to do is have the Mirena taken out. You can always have it put back in later, if you want.

Shame on me... I had read similar reviews when I was prescribed NuvaRing a year ago, and thought "Side effects vary among women", but the general consensus seems to be that WE are the majority, not the "occasional" exception.

I have been experiencing many of the same disastrous effects of the Ring for the past 12 months I have been on it. Depression, ZERO SEX DRIVE, headaches, intense mood swings that lead to physical aggression, frequent (nearly daily) uncontrollable crying, anxiety, more vaginal discharge, pain after sex (on the rare occasion that it DOES happen) and overall a poor outlook on life. It's ruining my relationship with a wonderful man, who (bless his heart) is nearly at the end of his rope dealing with me and all the tribulations listed above.

To those of you who thought you were crazy, BEFORE you blame yourself, consider that the Ring may be a contributing factor.

Wow, i cannot believe what i'm reading. I have been taking Simvastatin for almost three years. My Doctor never mentioned any side effects. It has gotten bad enough for me to seek information on the internet. What medicine cause all my symptoms; Tingling in the hand and feet, weakness of muscles, dropping things, dizziness, memory problems, sore muscles, sinus problems sore knees, arms, shoulders, stomach,numbness, sensitivity to light. I'm sure glad i have found this web site. I think i am going to take myself off of it for a week and see if things improve. Drug companies must be making a killing on this medicine since they refuse to warn potential patients.

I took Cipro for a UTI and from the first pill I took I felt like I was going to die. My head hurt so bad that I thought it was going to explode. I thought maybe it was just fighting the infection so I kept taking it. The more I took the more I felt sick my tendons in my legs hurt so bad and my neck and shoulders hurt like nothing I ever felt before. On day three I phoned the pharmacist and he told me that side effects from cipro never happen and that if I was really concerned go to the doctor and get a new antibiotic which I did. I was so mad when I went online and read the side effects of this terrible drug.
I stopped taking the Cipro and felt much better within a day but it took weeks for my muscles to feel better.
I will never take this drug again nor will I let my kids. I tell everyone I know to ask for a different antibiotic if given this one.

Hi a little over a year ago i received a kenalog injection for allergies and have been having a lot of the same side effects you all have been having. I have a very large indentation on my butt. I have an appointment with a plastic surgeon to see about have the indentation fixed just out of worry that it will keep getting bigger because it has over the last 12 months. I have also had problems with my period. I have went from having extreme bleeding to 2 periods a month to now bleeding for 3 weeks at a time. I have also lost a ton of weight and am down to 115 pounds even though I eat all day long. A drug of this kind should not be on the market!!!! ON THE PACKAGE INSERT FOR THIS DRUG NONE OF THESE SIDE EFFECTS ARE LISTED. Somebody should be held liable. If any of you have any information on a class action lawsuit please let me know. Surgery to fix this is very expense not to mention just looking at it in the mirror and knowing that it could have been prevented if someone would have informed me that it could have possible happened.

I have had a merina in for 12 months to reduce heavy periods as tehre was no change I went back to the doctors to have it removed only to find it had been out of position, so had another one inserted and some blood tests as i was feeling unwell, depressed,weight gain,itching eyes, feeling cold, insomnia,heart palpitations,headaches the tests showed i had hyperthyroidism yet i had more symptoms of hypothyroidism i feel this was caused by mirena but the doctors deny it yet looking into different sites the above symptoms are very common so i don't know if i feel unwell due to the merina of the thyroid will be going to the specialist this week hopefully to find out has anyone else had hyperthyroidism diagnosed while on mirena

Hi all,

I had my mirena out on September 11th, so almost a month ago! I persevered with it for almost three years but I had a hideous time with it: insertion was the worst pain ever; it felt like I had constant period pain; my periods never got any lighter but got longer - in fact for the past 12 months I had two periods a month. I had two scans to check it was in position, which is was (which is something to be thankful for)

I got forgetful, I was so tired which is unheard of, I had night sweats - convinced myself that at 31 I was having an early menopause! And the weight gain, wow. I have been swimming almost every day since Jan and not a single bit of weight loss, despite a very healthy diet.

Having it taken out was pretty uneventful. Ten seconds and it had gone. The bloating seemed to go within a few days, I wasn't tired, this could be psychological but I just knew I felt better!

In just over three weeks I lost 10lbs. Now of course this could be due to more exercise I have been doing, due to having more energy, but considering how much I was doing from January with no effect, it makes you think.

I know three or four friends who have it and LOVE it, guess I am one of the unlucky ones. The doc did ask (who was fine about taking it out) 'would you like another one?' No thank you!

Moderately high cholesterol and BP 150/90. Was put on Lipitor 20mg and after a week felt more fatigued than usual but nothing much more than this. Had stress test and angiogram which showed 60-70% block in one artery as well as arrhythmia. Cardiologist bumped Lipitor up to 80 mg which I took for 2 weeks. But by then I was suffering most of the effects described in these postings: aches and pains, giddiness, nausea, extreme weakness and fatigue. I took myself off Lipitor and even after one day my head started to clear aches started to diminish, though urine still a reddish color suggesting a lot more flushing out required. And, best of all, the arrhythmia reduced from moderate/severe to mild (which it always used to be before taking Lipitor). This drug is not for me. I'd rather take my chances without it and rely on strict diet, weight loss, etc. It is surprising that the possible side effects are so understated in the manufacturer's descriptions.

I have been taking Lyrica for about 4 months (200mg total taken over 2 intervals per day) and have been having a terrible time with insomnia: I fall asleep but only sleep for 3-4 hours, then I either don't sleep, barely doze, or sleep extremely lightly with many awakenings for the rest of the night. I came online to research whether insomnia was a possible side-effect of Lyrica, but the information I am finding suggests the drug is used to *treat* insomnia... I am not certain my insomnia is linked to Lyrica, but in case there are more people out there experiencing similar problems and it's an as-yet undocumented side-effect, I thought I should add my two-cents-worth to mathews1965's comment. (No nausea; definite depression, although it's a bit of a chicken and egg thing considering the prolonged lack of sleep.)

Hi there - can anyone tell me of any suicides or attempted suicides by people taking this drug. We have just had this happen to a family member and the anxiety/depression symptoms mentioned by many seem to fit his symptoms. He was on Doxy for over 12 months as anti malaria medication

He went from a very capable fit man to a complete wreck.

After being on Lipitor for over 5 years, I was told to stop cold turkey by my doctor after my routine blood test. Within 10 days I got blood clots and a pulmonary embolism. I had been on an aspirin a day for over 10 years, I drank cranberry juice often and always ate green leafy veggies. I never had any blood clots before coming off the Lipitor and I am convinced that it caused them. It has been a struggle with the pains in my legs ever since. Has anyone had the same or have heard of someone with the same side effect? ******

Yasmin is a steroid so when coming off it you can suffer all the same symptoms as someone stopping a steroid drug... and by the way, when people are taken off steroids it's done in a controlled way - they cut down on them very slowly by reducing the dosage. It's a real shock to the body to just stop a steroid. This could explain why a lot of us feel so terrible when we stop taking it. I know I had a real increase in severity of symptoms followed by months and months of exhaustion and fatigue.

I got the Mirena after my 2nd child in April 2007 at the age of 25. It was very painful and I can handle pain I had just done completely natural child birth to a 9 pound baby. I bleed for the first three months. With really bad cramps!!
However until seeing this website I never realized that all these things that have been happening to me are probably from the Mirena. The last 6 months I have been having anxiety attacks, dizziness, headaches, mood swing, acne, and I have been so tired I thought I was pregnant, now after today I believe it is from the Mirena. I am going to call my doctor and have it removed!!!

I'm back.. I posted back in June when I've had my Mirena for a few weeks... I go to my GYN on july 29 for my check up.
I can actually be one in a million to say I'm very happy I had this IUD inserted. I have never been able to take the pills. I tried the shot once and had a period for 6 months straight... and that was only ONE injection....
The first couple of weeks I did feel like I had a yeast infection... it burned when I pee'd... It hurt to shower... I started to get frustrated..
I didi wait it out.... I told myself that I would tough it out until my check up appointment and IF I didn't feel better I woudll discuss removal ASAP !!!
but I'm fine ... I did cramp for a couple days after insertion. That is now gone .... I was moody for a few days ..... moodiness is gone.... I still get tired but I notice that is getting back to normal also....
I FOR ONE AM GLAD I HAD MIUD INSERTED !!!!
I say good luck to the rest of you...

I wish I had found this site before taking my first dose of Femcon. I had been on Loestrin, and then Loestrin 24 for years. The only side effect was a severe migraine 10 out of 12 months of the year. All of my friends that take BC recommended YAZ-what a nightmare!!! I bled every other week and was miserable.

Went back to the doctor, who prescribed Femcon. Until I read this site, I thought I was losing my mind. In three weeks, I've put on about 5 lbs. that i can't explain-no change in eating or exercise. Although a bigger chest is nice, tight jeans and pants and severe bloating are awful. I can't wait to be done with the pack-any recommendations for low dose pills without these awful side effects?????

Aged 39, been on SIMVASTATIN 40mg for 6 days after spending 12 months trying to reduce my cholesterol through diet and seeing it rise to 8. Have been experiencing discomfort and flatulence since 12 hours after taking the first tablet. Have put it down to getting used to the drug, but found this website and wondered... Also been taking Ramipril for BP for a year. I am fit & exercise regularly (I'm used to muscles randomly aching)and although I drink virtually every day I don't smoke. Should I just wait and see?

Hello all Yasmin Survivors.
I stopped taking Yasmin in July 2005 and three years on I am still re-building my life! I feel this pill and its side-effect stole some of my best years, I am 33.
My main side effects were extreme anxiety, agoraphobia, pounding heart, panic attacks, fear of doing anything (even going 10 minutes away from my own home). I was on it for 12 months and the side-effects started very gradually at about 5-6 months, I barely noticed them creeping up on me. It took me another 6 months of taking it to start to question whether Yasmin could be causing the extreme change in my personality. I think if I hadn't stopped I'd have had a major breakdown. I had lots of weird physical symptoms too including, bloating, passing urine all the time, leg cramps, dizziness, hair loss.
Anyway, all the extreme anxiety and stress caused by Yasmin left me with exhausted adrenal glands - which I'm now trying to re-build. Anyone feeling fatigue, nervousness, anxiety, inability to handle stress in the same way as you used to, PMS several months after stopping Yasmin should look into Adrenal Fatigue as a possible cause of their symptoms. It's hard to treat and can take a long time to recover - but there are lots of things you can do to help your body re-build. Visit ******(doctor Andrew W. website on Adrenal Fatigue) as a start to find out more about the condition and how to find out whether you are suffering from it.
It would be good to hear from more people re-building their lives after the impact of taking Yasmin on this site. Also, is anyone out there trying to put together a class action?
Sarah

I have been taking LIPITOR for about 1.5 years and have been feeling the cotton head but thought it was allergies. for about 8 months or so I have been feeling pain on the left side of my chest and upper back by the shoulder plates. I've told my doctor and had several tests done incl. MRI, C-scan, etc. Once I even had to go to the emergency room thinking I was having a heart attack. But the doc. said the EKG was normal and that it might be muscular. I have not read that anyone else is having the chest symptoms. This is very scary to me. Lately I feel my neck getting stiff and I am also constantly tired and keep waking up at night and have a hard time going back to sleep. I don't seem to have the arm or leg pains that most people here seem to be suffering from but am now convinced it's LIPITOR since it is the only prescription medicine I am taking. I would appreciate hearing from someone who has had the same symptoms I've described above. I stopped taking Lipitor about 4 days ago and do feel already less tired but the upper body pain is still present.

Hello: I am so sorry that all of us are suffering since taking this pill. My experience with Yasmin was brutal and 3 years later I know am told that I have developed b12 deficiency or a very serious, but treatable condition called pernicious anemia. I never had it before then pill. I took Yasmin for only 5 months and felt sick the whole time. Headaches, strange moods, even a popping sound in my head some times, bizarre symptoms. I called my OBGYN and told he I was stopping. She said the pill did not cause this, but if I felt it was related to stop. AND IT WAS! She now admits to feeling bad for this. She did not mean it. Doctors only know what they read from the literature of a drug. I stopped taking it and was in the hospital within three days. I was in shock. Night sweats, tingling skin, no energy, stomach problems of every kind. Severe pain in my left ovary, suicidal depression and on and on. The worst part is that I began to get sicker and sicker. 3 years later of still being sick. The only thing that has helped my system is acupuncture and a serious diet change to aid my system, I find out that I have a serious b12 deficiency, which I never had. They call it an autoimmune disease which impedes you from processing b12 and all this starts in the tummy! I lost a baby during this time while pregnant, now we know it was this! The Yasmin pill has been pulled off the social medicine of some European countries due to such severe side effects. Their is a girl on this blog getting names together to start a class action suit. I am in. No one can get me my three years of suffering back, or my lost baby or my lost work. I am a professional flamenco dancer and let me tell you it is not easy to perform with a serious b12 deficiency which affects nerve endings, heart tissue and neurology! And the cure for this is b12 injections for life! If you want me to forward your name to the girl with the attorney you can write me at:****** Well I am going to keep trying to be well. I am young and have a whole life ahead of me.

Hello all!
I am so happy I found this site and so is my husband. I'm 44 and was suffering with all that "pre pre menopausal" period. I had my tubes tied when I was 30. After an ultrasound showed very small section of overlie left. My doctor decided to put me on birth control pills (I'm a smoker) on once a day everyday cycle. My menses stopped and some things got better and some worse. After a year, my doctor then felt this iud would help everything. He found out yesterday that this morning he was taking this thing out of me or else. (9 hard months)
I had my iud removed this morning, so I'm only 2 hours out.

Sept 2007 I scheduled for insertion. Since my doctor told me it was 5 minutes in the office, I went on my lunch hour. I never made it back to work. This was on a Friday, so I had the rest of the weekend to rest. This 5 minute insertion hurt more than dilation pain in child birth. I actually cried out! The "measuring" portion felt like my dr poked a hole in me. Sharp hot pain. Then the device, when he said it would "cramp" for a bit, but it actually felt like he was trying to shove it into my left tube or wall but a too small place with painful pressure and a hard pinch. I asked if it had sharp edges. It felt hot, like a hot pin. After I cried out, he said ok ok it's in, Thats it.
I had tears in my eyes it was that painful. I was totally not prepared for there to be this much pain. My doctor told me that I might be a little crampy but that would be it. What I actually felt was so much burning stomach pain where it was hanging on to me with what felt like claw like hands. I could not stand totally straight up or I would get a fast, sharp, hard pain in the left side on my stomach where all the pain I felt at insertion. This lasted everyday for 2 months then happened less and less until now a few times a month. Mostly when I over do it by stretching, exercise and vigorous sex. I always have to slouch a bit or I get those pains now.

I get cramps on and off and it would usually follow a cycle, but I was not mensing at all. Only spotted a few times. The other side effects were making me crazy and my family worried and upset. Mood swings are horrible. They can be quick and fast abnd very dark, mad and angry. I would never have acted this way before insertion.

I get depressed on and off, mostly on, in most often 3 week cycles. Crazy super anxiety over the smallest thing. I have gained weight, feel totally fed up with my appearance. I feel suspicious of everything (my husband keeps saying I'm paranoid about everything and everyone, I didn't see that of course). My mind constantly races and have found myself confused, or forgetful. The worse moment when I was filling out a form and couldn't remember how to write my last name and spell it. I could see it but not write it down, I was unable to spell it out loud for too long not to really scare me into thinking what the heck was going on. I have had almost every side effect everyone has posted except the acne. I see more pimples now and ones sort of under the skin, but not often enough to see a dr about and nausea I haven't a problem with yet.
I will list the rest but there are more if I think about it I have. Now I want to see how long it takes for them to go away.

, Headaches and/or migraines everyday, constant stomach and vagina issues including: aches, full feeling, and sharp shooting hot pains, terrible moods that can come on instantly, feeling depressed, angry and mean, weight gain, fast graying hair, some hair loss, bloated breast that feel real full all the time, breast tenderness and sharp sudden pains, numbness at times in arms and hands, chest pain, anxiety, paranoia, racing thought, some slurred speech on occasion, confusion, memory loss, leg pains and aches, low libido, painful sex, painful orgasm.

I hope someone steps in and has this product taken off the market!

I took Lipitor for 2 years with all the pain in my shoulder, hand and arm as well as fuzzy memory. I had a friend over for Lunch an have no memory of anything that happened including his arriving and leaving on his Harley and we all know how loud they are. I ended up in the hospital with all kins of tests including an MRI all of which I have no memory of to this date. My hospital bills are still coming in as well as all the Doctors that saw me. I just received my Divorce and then this happened , I was out of work for a week , the Doctors thought I had had a heart attack, stroke or aneurysm.I also had all the foot pain making it impossible to stand up , leg cramps, sleeplessness, sheer exhaustion, depression, headache and nausea. The Doctor at the Hospital took me off of the Lipitor and said to take a 325mg. aspirin daily . This happened on March 23, 2008 . I am felling better but I still pain in my shoulder , neck , stomach , and feet and legs but is nothing like it was. Here I am left with a few thousand dollars of Doctor and Hospital bills. Why can`t something be done about all of this we are all going thru? I called the FDA to report it and got no where. Did I really expect anything to happen ! I hope someone gets something done for us . I would be one of the first to sign up to take Lipitor off the market and get what is due us.

Found this on a web site listed at the end.
Very scary!!! COQ10 is a must when taking any statin drugs your body needs it for your
muscles. Other statin drugs may be better.

Numerous adverse side effect reports have implicated Lipitor as a possible cause for severe neuromuscular degeneration. Some people who have been using Lipitor for two years or more report symptoms similar to multiple sclerosis or ALS - Lou Gehrig's Disease - in which they are losing neuromuscular control of their bodies.

For instance, in an article entitled "Life After Lipitor" that appeared in the newspaper Tahoe World on January 27, 2004, Tahoe City (California) resident Doug Peterson began having serious neuromuscular problems after taking Lipitor for two years. He began losing muscular coordination and slurring words when he spoke. Then he lost balance, followed by loss of fine motor skills - he had difficulty writing. He went from doctor to doctor, trying to figure out what could be happening. Finally one doctor suggested that he stop taking Lipitor, and the downward health spiral stopped and his health is now slowly improving.

These adverse effects have begun appearing in peer-reviewed medical journals, and numerous people have reported similar symptoms at public adverse effect reporting websites such as medications.com. People have reported "trouble swallowing, trouble talking and enunciating words, feeling fatigued all the time, neck aches," "motor neuropathy which mimics ALS," "Blinding headaches, nausea, vertigo, disorientation, memory loss, extremely dry eyes, pain and stiffness in my neck and calf muscles, abominal pain," and "Muscle pain, weakness, spasms, buzzing in right leg. Can't hold arms or head up in vertical position for 2 minutes without extreme pain and weakness."

How could Lipitor potentially cause this kind of harm to so many different parts of the body? Lipitor is a "statin" drug which inhibits the production of cholesterol in order to lower LDL cholesterol counts. By limiting the production of cholesterol, Lipitor may be indirectly causing membrane degeneration in neural and muscle tissue.

The problem is this: cholesterol is essential in your body for many functions. It forms part of what is called the cell membrane - the outer layer of every cell in your body. It helps transport and pack the major components of the cell membrane, called "phospholipids," that are made from essential fatty acids (EFAs). Without sufficient cholesterol we would die, because our tissues are constantly being repaired and replaced with new cells.

Our body produces several thousand milligrams of cholesterol per day to carry out these essential functions, and each day the excess of cholesterol is supposed to be naturally recycled. If your body doesn't have enough new cholesterol each day, you cannot repair and replace your cell membranes and they will eventually degenerate.

The continual recycling of cholesterol happens naturally when you have sufficient ascorbate, another name for vitamin C. Excess cholesterol is naturally converted to bile acid and then excreted. But if you don't consume enough vitamin C (about 2000-3000 milligrams per day for an adult), cholesterol builds up in your bloodstream. It is here that doctors make a critical error: instead of telling you to take more vitamin C, they prescribe Lipitor.
If Lipitor and other similar statin drugs are in fact indirectly causing neural and muscular degeneration, this is a very serious matter indeed.

There are twenty million people in the U.S. on Lipitor alone, and probably millions more on other statin drugs (Zocor, Pravachol, Mevacor, Altocor, Lescol, Crestor, etc.). Are they all going to become victims of cell membrane degeneration and nervous system problems? There are few long-term studies that bear out the safety of these drugs, and side effects such as "muscle pain or weakness" are just classified as a reason for some to stop the medication rather than an indication of something very wrong with the drug.

What is most horrifying about this problem is that cholesterol balance can be achieved without drugs, simply and safely by taking 2000-3000 milligrams of vitamin C per day for an adult. Unfortunately, vitamin C was misclassified as a micronutrient in the 1930s and 1940s, rather than an essential nutrient involved in dozens of body processes. Our health authorities recommend that we take only 60 milligrams per day, barely enough to prevent scurvy.

It is my hope that people on Lipitor and other statins learn that they do not need to take these potentially harmful drugs.

For more information about the connection between vitamin C and the prevention of cardiovascular disease, see the article Natural Therapy for Cardiovascular Disease, or visit the research website of Dr. M.
******

I am 30 years old and have been put on Depo Lupron after a laproscopy to help with endometriosis. I am 2 months into a 6 month course (one shot every 3 months) of Depo Lupron and my life has drastically changed. I started feeling life altering hot flashes and night sweats two days after the first shot and nearly drown myself in sweat 24 hours a day. I experienced a little postpardum depression after giving birth 6 years ago but have found myself sunk into a sinking hole of depression and anger like I've never felt before. I bawl at McDonald's commercials and become enraged if the dishwasher isn't loaded properly! I am ecstatic one minute and severely depressed the next. I have even had thought of suicide since being on this shot. I am normally a very outgoing, athletic, cheerful, happy person - but since taking this shot, I have become a stanger in my own head. I tell my family all the time that I need to "go stick my head in the freezer" to cool off because of the horrific hot flashes. I have to carry a handheld fan with me 24 hours a day and sleep with ice packs to keep cool. Since the shot started 2 months ago, I have lost all sexual drive, am thoroughly exhausted by 9am and find myself crying at my desk at work by late afternoon because I am so tired. My family thinks I am going crazy and I've never fought more with my husband. My daughter has gone to grandma's for awhile because I'm just so tired and irritable that I feel like an awful mother. Migraines have also come full circle since the onset of the shot as well as blurred vision and shaky hands. I'm a little achy throughout the as well. I know that everyone responds to medication differently, but I'm finding a lot of people with the same side effects as myself and have to wonder why the doctors don't warn patients about these types of problems before prescribing medications such as Depo Lupron. I don't think I'll be going back for the second shot. Could it get any worse?