Magic pill symptoms and conditions

Hi
I am in the UK - where any knowledge of side effects related to Yasmin appear to be non-existent. I was prescribed this to treat my endo after having problems with another pill (constant bleeding and mood swings).
Initially it was like a magic pill - immediately improving the mood swings and stopping the constant bleeding. Then after about 4 days I felt so nauseous I wanted to go home from work - this lasted a few days.
A week and half into my first pack, I suffered continuous asthma attacks - with no obvious cause, this developed in hours to spontaneous vomiting along with a hacking cough.nI was prescribed antibiotics for "infections". The symptoms continued until it was unbearable and I was put on anti-vomiting tablets. and changed onto a different antibiotic.
A week later back at the doctors surgery I had a series of tests - awaiting results as I type, as I have very dark urine, stools that are not "normal" (clay or yellow), pain in my stomach, pins and needles, continue to vomit if don't take the anti vomiting tablets. Have now stopped taking Yasmin and await results...
HOw long does everyone appear to improve after stopping taking Yasmin? Also does this sound like I may have a case of hyperkalemia? (I am awaiting results).
Many thank

I decided to do some research and stumbled across all of you!
Well is started Yasmin about a week ago and...i stopped eating, im nauseous,tender boobs, my period as stopped but the after bits are still coming. I am in such a bad mood! i want everyone to stay away from me!!
All my friends have been on Yasmin and they praise this magic pill! I wasnt sure if it was the pill - but now i am.

Thanks for the posts!

This is an update about my son who took Levaquin 16 months ago when he was 16 years old (he is now 17). My son was given Levaquin September, 2007, to prevent an infection after minor sinus surgery. His symptoms were severe muscle weakness (he would get exhausted walking from the parking lot to a store and back, severe joint pain (in thumbs, wrists, elbows, knees, and ankles), dizziness (he felt like the room was moving away from him and would lose balance), and headaches (a severe pressure in the back of his head that was constant and then shooting pains in his head that would come and go for no reason). He then developed IBS a few months after taking Levaquin. He was an athlete at the time and in very good shape. Prior to Levaquin, he was rarely sick and headaches were equally as rare. He was a junior at the time and as a result of the Levaquin, missed most of his junior year. He kept up through home instruction and maintained 2 honors classes, but had to drop his AP class.

In the first 4 months, his muscle weakness, dizziness, and joint pain (except for his knees) went away. As a parent, it is very painful to have your son hold his head in his hands and ask you to make the pain go away…but you can’t. It took 9 months for his 24x7 headaches to go away. His IBS recently went away after giving him enteric coated peppermint pills twice a day. All that is left now is his knees hurt when he plays sports, so he can't. The knee issue is pretty minor compared to where he used to be.

Here are some things we learned: 1) We tried giving him magnesium, potassium, selenium, calcium, and B-complex after the Levaquin...but it didn't make him better; 2) We took him to over 20 doctors; most couldn't believe it was Levaquin, but some did; 3) Ortho-McNeill will admit that Levaquin can cause these symptoms (I called them); 4) There is no magic pill, once you have ingested Levaquin and develop symptoms, you can only treat the symptoms; 5) Numerous tests of all types over several months never came up positive for any disease or illness; 6) Filing a Medwatch report with the FDA is important since every report helps; 7) Levaquin is not FDA approved for anyone under the age of 18, but is still allowed to be prescribed; 8) Doctors get most of their information on drugs from the pharmaceutical representatives, so BEWARE and do your own research before taking medication; 9) Most drugs have side effects, but beware of the ones that have long lasting effects like the fluoroquinolone family; 10) Never ever lose hope or the belief that one day you will be better. The power of faith does wonders for your health.

I don't know if this post will help anyone. People are affected by this drug differently and recover at various rates. Most people do recover and you need to believe you are one of them. Fortunately for my son, it looks like he is okay now, but it has been an extremely long, difficult road. Keep your faith as my son did, and I'll pray that you all recover. If you haven’t taken this drug yet, then don’t. If you are taking it, then stop. If you have already taken it and have developed symptoms, then be strong and keep the faith.

This pill %&*^%&$ sucks!!!!!!!!!! I thought this would be it! The magic pill.... the one.... needless to say.... NOT SO !!!!!!!! I have been on my period for 2 weeks now!!! This is ridiculous! I got on line only to see if I could find someone having this same problem. That would definitely be a yes!!! I will not be taking this pill any longer... I am not waiting around to see "WHAT HAPPENS" or "IF THE BLEEDING STOPS".... I'M DONE!!!!

My pain started within a few days of a switch from Fosamax to a generic form. I had been on the med for about ten months and hadn't had anything significant as far as side effects are concerned. First my shoulder blew up with very painful tendinitis and bursitis - doctors said it was likely a strain. Then I had jaw pain a few weeks later and that was supposed to be because of a crown I had done. The latest and worst has been my right hip and right leg to the knee - very sharp and burning pain - really made it impossible to walk. The doctors did not make the connection to fosamax and I think they probably still think I am crazy - but I KNOW that it where it is coming from. I am being treated for the pain with the usual stuff - it has been about two weeks. I think I have a long haul ahead before I feel really great again. The biggest problem with these drugs is that the side effects can present so long after you start the drug that most people don't make the connection. I figure people have been living with osteoporosis forever - so I will risk my osteopenie without any more of this toxic stuff. How many people are out there suffering without a notion that this is the cause - still taking that magic pill once a week?

I'm crying reading these posts. I thought there was something wrong with me. I'm 41 years old - and my family has a health history of "making" cholesterol. Both parents were on statins. My total cholesterol was 267 a few months ago - LDLs were 171 and my HDLs were 42. I started taking flaxseed meal every day - and within a few months, my cholesterol dropped to 193, my LDLs were 117 and my HDLs were the same.
My doctor's didn't think it was the flaxseed - they had prescribed Vytorin which I reluctantly took for about a week. They attributed my lowering numbers to the statin, not the flaxseed - so I followed their advice and started taking the Vytorin about 3 weeks ago......
Now I don't know if it's coincidence, but I have developed a severe left ear problem....and have taken 2 separate antibiotics, but to no avail. I have also developed a severe pain in my left shoulder, the back of my left arm and sometimes it shoots into my chest.
I suffer from anxiety attacks, so of course, to me, this is a heart attack, but since I've been tested so many times and I'm a healthy woman, I know that's not it. I thought I'd log onto google today and search out what could possibly be causing these troubles. I read these posts and I literally have been crying for about 15 minutes. My doctors have told me that Vytorin is almost a "magic" pill. They said if someone could tell you that you could take this pill and it would reduce your risk of heart attack and stroke by 50%, why wouldn't you take it? Given the history of your parents, it would be foolish to not.
I have also been given instructions to lose about 25 pounds (not bad), and I know that if I could just exercise, eat well and take my flaxseed as well as making sure I eat 2-3 meals of fish a week, then I have to be better, don 't you think?
Do you think statins are the only way to go? I'm so happy to know I'm not alone - I'm not going crazy - I'm not experiencing any heart attacks....my anxiety is ten-fold lately - I wake up after a full-night's sleep feeling exhausted. I have four wonderful children and a wonderful husband - I live for them - and I feel so sad and depressed lately.
Oh my gosh everyone - do you really think that the Vytorin would have such an incredible impact on all of our lives?????

Hello. I started taking lisinopril 20 mg about 1.5 months ago because of hbp and I also started taking toprol for rapid heart beat 1/2 a month before that. Although it did lower my hbp it made me feel lousy. I started getting anxiety all the time, aches in my body (stomach etc), nausea, dizziness, spaced out, and numbness in my hands. My father passed away about 2.5 months ago and so I figured that the anxiety was something normal given the circumstances. I thought that the other side effects were part of the anxiety. I felt as thought I was going to go crazy or die. I also started to become a hypocondriac thinking that if I had a pain in my stomach it might be stomach cancer etc. It was not until I found this site that I see that lisinopril and/or the toprol might be the thing that is causing me to feel lousy. I was always healthy and I never had anxiety. I understand that I shoud feel a little anxiety and sadness because of my father, but I don't feel a little anxiety, I get intense panic attacks. I feel as thought I can't get back to normal, I just feel as though I'm not myself. I want to stop this meds as soon as possible before I, too, get worse side effects. Please let me know if you all think that it is the medications or is this just part of the griving process. All I know is that I started taking this pills and all this started to happen.

I think what a lot of people are posting here are more side effects of thyroid conditions rather than side effects of thyroid medication. After my RAI treatment I started on a generic brand of levothyroxine. I even got my doctor to let me try Armour Thyroid since many people do well with it rather than Synthroid. Armour didn't work well for me, but it definitely is the only way to go for some people. After months of misery, things finally smoothed out. I was a royal pain in the butt to my doctor because I questioned everything. The biggest side effect for me going from hyper to hypo was edema. A clinical name for water retention. It wasn't so much the bloated feeling that bugged me. It was the pain in my hands and feet from the water retention. I have never, ever had a problem with carpal tunnel syptoms even though I have always used my hands a lot for work and I play the guitar. I had to add a small dose of dieuretic to control the edema and relieve the hand and feet pain. Sometimes it does flair up depending upon what I eat and how much I sweat, but that's what goes along with this type of illness. It's not just a magic pill that makes you feel "back to normal". You have to be demanding of your doctor to try other things to get you to feel right. You even have to pay attention to how you feel at different times of the year to figure out how to adjust what you take, eat, or do to feel better. I have noticed that with all things remaining constant, how I feel in terms of energy level and edema is related to the season. The body is weird that way. I still have side effects from the treatment from time to time, but I finally figured out what seems to work best for me. Maybe things could change over time, but I've learned that medicine just doesn't have a black and white treatment plan that works the same for everyone for thyroid related conditions. To sum it up, question everything your doctor tells you, demand to try things that you think would help you feel right, pay attention to what your body is telling you and adjust, and fire your doctor if they treat thyroid problems as black and white. Your doctor is not the one suffering from the condition, you are. It's your life and there's nothing wrong with being demanding about wanting to feel right.

Thank all of you for your candor. I too had been on anti-depressants for the past 3 years. I finally said enough is enough, each med had different side effects.I had lost interest in my "life" didn't want to exercise, work or really do much of anything...unless I "had to" & was becoming quite the actress going through the motions...this was NOT the ME I had known for 30+ YEARS & will not BE ME. I have the blurred vision, confusion, forgetfulness to name a few of the side effects. It has been 1 year since my divorce (reason I started it)... I no longer felt "situationally depressed" and assumed the unusual feelings I was experiencing was due to the drug and that I needed to get off of it to get my life back. So I stopped Effexor cold turkey.After two weeks & unusal side effects I got on line to see what other experienced. I too have experienced the vivid dreams / nightmares, where I literally felt as though I was "drugged". I have the cotton mouth, when tired "spaced out", mood swings, tiredness, night sweats, flu like symptoms, my appetite has increased, I had no sex drive on Effexor, 2 weeks off and it is coming back at least I'm thinking about it....I can identify with most of what I've read others have experienced on some level.

Bottom line...if I had it to do all over again. I would NOT take any anti-depressants, I suppose I was depressed divorcing & I should have been it is a major change in ones life. In hindsight I should have let my mind and body go through whatever the "natural process" was to be... because the experience going on, waiting to feel "normalcy" (which neve happened) and coming off has been awful. My point of view, there is no "magic" pill that is going to make us get up and go like the TV commercials portray. Life is difficult & I will survive without a "pill", I definately feel better over all getting the Effexor out of my system ...I'm hopeful the side effects will be short lived.

I have been reading about this now for three hours, and it has made me feel both better and worse. I have been on antidepressants for over 10 years; I think I have been on Effexor for around 4 or 5. It has all but banished my panic attacks; I haven't had one in months now, and those that I have had over the past few years have been endurable to say the least. What worries me is the changes in my personality that have taken place over the past decade. I have been thinking that what I have been experiencing is my depression getting worse and that I have been spiraling down into severe mental illness. It's frightening to say out loud that you think you are going crazy, and so I have managed to keep a tenuous hold on reality and ever onward I go. I mentioned my symptoms to my doctor almost 2 years ago, and her response was to increase my dosage to 112.5 a day. This only served to confirm my belief that my mental health was indeed declining. After reading these posts I want to weep with joy that I am not crazy, it is this magic pill that I take every day. I too have avoided going off Effexor because of the side effects; it seems that it would be easier to withdraw from a serious heroin jones with less suffering. My side effects while being on the medication have been: loss of interest in everything in life that ever interested me, weight gain with loss of appetite (go figure), loss of sex drive and almost an aversion to sex or intimacy, fatigue, confusion, and an emotional withdrawal from those around me. The few times I have tried to go off Effexor (or missed a few days due to forgetfulness or lack of interest in going to the pharmacy to pick them up), my symptoms have been: that weird feeling of your brain having to catch up to your eyes, that feeling of being shocked or zapped, a descent into depression equaling the speed of an Olympic bobsled run, a feeling of hopelessness, headache, cotton mouth, diarrhea, mood swings so severe and radical that I frighten myself, irritability to the point of wanting to chew off my own fingers, tears over everything and anything, and restlessness. Reading over this, I'm thinking that being depressed was not so bad after all. It's kind of sick to wish for simple depression; it reinforces my belief that this medication is bad. I see that in another post someone is asking if there is any rumble of a class-action lawsuit; I would also be interested in this information. Thank you for sharing what this medication has done to all of you, and I hope that my post helps someone else with similar experiences.