Dilemma symptoms and conditions

I had Mirena inserted Oct 3, 2008 six weeks after having my first child. I too really wish i had done my homework. My side effects were little things and i really wasn't sure if i wanted to have it removed since it does work and i enjoyed not having a period. But in the end i decided that the fatigue, hair-loss, acne, headaches, inability to lose my pregnancy weight and last but not least, my mood swings were all hindering my daily life more than i realized. i feel ugly due to the acne, thinning of my hair, and because im stuck at 170 lbs and i'm only 5 ft tall. i didn't want to go out in public. I was so so tired all the time for no reason. i feel more tired than i did being 6 months pregnant in the military working 15 hour days with only one 10 minute break an hour to sit with anemia. it just isnt fair to my daughter that i can't give her the attention she deserves. So, March 2nd i finally got it removed. The removal didn't hurt. My period came immediately. It's only been three days and my acne is about 60% clearer. Unfortunately the headaches continue. I still feel tired, but it hasn't been as severe. I really can't wait to get back to feeling like my old self. It's been so long. Now my dilemma is what to do about preventing pregnancy. I've never used any bc besides condoms but my husband and I don't really enjoy sex with them but i'm afraid after this experience to use any other kind of hormonal bc. Any suggestions???

My experience with Lisinopril is similar to many others here. Mine is further complicated by the combination of drugs I am taking.
Due to my BPH I was taking Proscar and Doxazosin (4mg), the Doxazosin helping with hypertension as well (140/90). My doctor decided to add 5mg of Lisinopril to augment and help lower the blood pressure some more. He also liked the overall helpful aspects of the Lisinopril on the cardiological system. After about a week and a half on this regimine I was having dizzy spells and light headedness.....disconcerting when driving. I also had the infamous dry hacking cough noted my almost everyone. I stopped taking the Lisinopril and things went back to normal.
On my next visit to the doctor, he wanted me back on the Lisinopril but trying 2.5mg doses. That seemed to be OK for awhile. I have now added Flomax to my regimine and noticed the same dizziness problem. So I am staggering my pill taking which seems to be helping somewhat.
However, after three weeks on this program, I am having severe dry hacking cough episodes, 5-10 times per day. Also have to be careful when I stand up due to dizziness. Additionally, I am having sporadic insomnia problems that are out of the ordinary for me. Also, runny nose, sneezing and a tightening feeling in the chest and abdomen.....Almost like a mild flu. The tightening feeling is more like a caffeine overdose high...ergo the insomnia.
I attribute the hacking cough to the Lisinopril. The insomnia could be the same or possibly the Flomax. I'm not sure about the tightness. I plan to stop the Flomax next week when I go back to the Urologist and will stop the Lisopril at the same time and see what happens.
I would be interested in any input readers may have on my dilemma.

I've been taking Fosamax once a week for about 4 months. During that time what began-before taking Fosamax-as mild pain in my lower back-has gotten progressively worse. This is the only negative possible symptom I’ve experienced, but of late it has increased and spread to my hips. I decided to stop taking it today, and see if it makes any difference. If it does, I will post another reply here with details.

I think all reading these personal accounts should consider this: obviously many medical professionals see far more benefit than loss in the majority of users. My osteoporosis was only diagnosed via a bone scan 6 months ago. -2.5 The increased pain and worsening conditions in my back might in fact be much worse if I hadn’t started taking the Fosamax. One must beware of apophenia setting in with self diagnosis.

Most posting here already had serious medical needs to have Fosamax prescribed in the first place, given a small percentage of diagnostic errors. Most of the conditions I’ve seen described vary greatly, and without a serious study are purely antidotal. I suspect there are legitimate adverse reactions, but for now the percentage and severity remains a big unknown. There seem to be some activists here, so get a campaign going for publicly funded analysis of the now considerable amount of data on file.

If my back gets better, I’ll still be unsure as it might have been a delayed benefit from the drug. Likely I will take Fosamax again either way. If it doesn’t improve in several months I’ll assume F-max wasn’t the cause and begin taking it again. If it gets better, I will take F-max again to see if the problems return when I do. If they don’t I’ll keep taking it. If they do, that will red-line my ‘coincidence meter’ and I’ll never touch the stuff again.

I hope some will find my approach to our common dilemma helpful. We all have to be our own advocates within the modern health care cabal. I worry about the old adage that when we do so, we have a fool for a client. Feel free to criticize my reasoning, and thanks to all the others that took the time to share your experience. It helped me make my decision, and I’ll share the results in about 6 months.

I suddenly had high blood pressure. I was put on a heart monitor for 21 days because I was experiencing frequent palpitations. I was given 25 mg Metoprolol ER the genic for Toprol XL on June 6, 2008. I had the usual symptoms extreme fatigue, headache, constipation,swelling, weight gain for the first month. I am 59 yrs. old.
The second month I started to have horrible nightmares, and headaches that would not go away. On Aug.12 while driving home I started to hear voices, had blurred vision and hallucinations. I was driving fast and screaming to make the voices stop.. I ended up in a parking lot. I was crying and for a minute I had a bit of reality. I called the cardiologist office and told the nurse what was going on. She said to immediately stop the meds because I was having a rare serious side effect. I sat crying for awhile and was able to call a friend to pick me up. I stayed at home for 4 days. The entire time my hands shook and my headache was horrible. It was one week before I was able to function properly.
I called my pharmacist and she told me that this drug affects the central nervous system. 2 % of 100,000 people have this side effect. I told her that it was not written on my paper with the prescription. She said that because it is so rare they do not have put it on. She printed out the side effects for me from her web site. A site that is only accessible to pharmacists or Dr.'s. My Dr. wants me to try Cardizeim now and I do not want to because I am afraid. I told him that the BP was down to normal but he still wanted to because of the palpitations. I was given the option of the Cardiziem or seeing and Electrical Man at the Cardiology office. As of yet I have not taken the Cardiziem. This is the first time I have read this web site and I hope that this information may help someone. I finally feel good again except for the rapid heart beat and glad to be alive.

I am a 53yr old female, I started with bronchitis in Feb 2008, after two er visits, and treatment with antibiotics/ cough meds/ decongestants, etc. thought I was finally over it after 2/3 weeks, then all of a sudden I would start up with the same tight, non productive cough, twice accompanied by strep throut also, these symptoms started to return almost monthly, without warning. The last episode I had in July I was put on prevacid for acid reflux, (the first dosage of that gave me a slight improvement of symptoms of the cough, then the following week prednisone was added with almost instant improvement, Wow finally, each day better that the last, then as I started to taper off a bit of increase in congestion, nothing that a child's dose of mucinex didn't help. Then almost a month to the day after thinking that I was finally better, I started all over again, up for almost 36 hours straight from coughing, started back on steroids, antibiotics, etc. But this time is tougher, The initial steroids helped right away, but there is a lot more mucous with this episode, My Doctor set me up for a PFT (pulmonary function test) and pending results plan to followup with a Pulmonary specialist, but as I've been tapering off the prednisone again the symptoms have increased, almost back to the beginning of the episode, with more coughing than not. Nervous about the last day of my steroids, my doctor put me on the Advair Diskus, my results of my pft should be in tomorrow, I took my first dose this morning, (quite nervous about it because I have several medication allergies and reactions) Now for my dilemma, my dose went well, I almost thought I felt a little something good, I know it's supposed to take awhile to help, but I felt positive about it and looked forward to my next dose in 12hrs. A little later in the day I started feeling funny, kind of spacey, fuzzy headed. Is it possible that this feeling is from the Advair? I've read the side affects and a lot of feedback from Advair users, and nothing matches what I;m feeling. Is there anyone out there that has felt like this? Please help, I'm almost due for my next dose and don't know what to do.
PMB in CT.

My eight year old daughter was recently diagnosed with precocious puberty. This is devastating to my family...She was on singulair fo asthma for almost 4 years...Noone in the med profession will comment on how this happened but the internet is filled with other parents dealing with the ame dilemma. I am so furious right now.

I got the Mirena in Jan 2008. My periods were lasting 2 weeks long (light) every 2 weeks. I had EXTREME fatigue and actually had to go in to take a pregnancy test because my last period came late and I had ALL the effects of pregnancy (had 1 in 2006). I had nausea so bad I actually had to miss work because I felt the urge to be sick, but I couldn't get sick. I had it removed on July 7th, 2008 and felt a difference as soon as I left my doctors office, but now I'm faced with another dilemma. I may be pregnant again! My period never came after I had it removed and have the feeling of being pregnant. My doctor finally told me that my body thought it was pregnant and is going through the motions. I have to wait 2 weeks before I will know if I am or not! I NEVER SHOULD HAVE GOTTEN THE MIRENA AND DO NOT RECOMMEND ANYONE ELSE DOES EITHER! I have a hard time remembering to take a pill everyday, but that is much better than the side effects of this thing. I agree with a previous posting, IT IS EVIL!!!!

Hi - just to say firstly, I have my mirena in for almost a year and a half and am hoping to have it out next week, before I kill someone!! So I am in no way 'pro' mirena.
just wanted to comment on your hair loss posts- after my first daughter, this happened to me too, without mirena. I actually had bald patches and was super paranoid. My hairdresser told me that this is very common in the few months after giving birth - the hormones are trying to rebalace and this unfortunately is a side effect. My doctor confirmed that it was not alopaecia as I was self-diagnosing. I used to cry in the shower seeing all my hair in the drain - but now, 3 years, another daughter and mirena later, my hair is beautifully healthy again.
But on the other mirena symptoms I have. My poor husband has not had any affection in the bedroom for almost 2 months now, which is scary as we enjoyed a healthy 4-5 times a week sex life until a few months ago. My first year with Mirena was fantastic, I recommended it to friends, but the past 3-4 months have been hell. Who is this psychotic person that has taken over me???? My husband is almost afraid to talk to me some days, because I go from sweet and cheerful to a screaming, raving lunatic in seconds, without warning. The weight gain has been huge - about 45lbs in 16 months and then the days where I don't feel depressed, I look in the mirror and it makes me depressed with the huge gut I now have. I've always been a curvy lady, but I never had a big stomach and it seems that all of this 45lbs is just sitting around my tummy.
Now I have to decided to have it out, and I'm left with the dilemma of birth control. My 2 daughters are 18 months apart, the oldest just turned 3, so I don't want another baby just now. However I would like another one in the future. Pills don't work for me - I took them religiously and got pregnant with both my daughters whilst on the pill. Do I choose condoms? Would I actually stop a spontaneous moment of passion to go to the drawer to get one, lol? I'm kinda not really sure what to do. All I know is that I need to get this out next week, and pray that I find another form of birth control. But in saying that, another baby in the house couldn't be as bad as what this thing is doing to my mental health.
I'll post again after I have this out

I've been using it for 5 months. i go through a bottle in a week and a half and every time i try to get off my nose gets so congested it hurts and makes it hard to breathe. if anyone has any tips on how to get off let me know

I was diagnosed with strep throat about 1 week ago and at first the doctors tried to kill me! They had prescribed amoxicillin--I am allergic to anything with "cillin" in it, and before heading home, I caught the mistake. The doctor apologized profusely, and then prescribed me erythromycin. Upon taking this drug, my face became swollen, and my eyes were itchy and red and my throat stung and my ears burned like fire! I returned to the doctor's office, and he was like, "oh, well, you're allergic to this, too! I'll give you some Bactrim. It helps for UTI's". I don't have an UTI, but I was desperate for anything to stop the burning pain. After taking Bactrim(sulfamethoxazole trimethoprim) for two days, my throat felt much better and the ear pain was gone, but I had a horrible rash on my chest, arms, back, and face. My eyes became itchy and puffy, and after day six of the treatment, I stopped taking my medicine. I couldn't take the rash or the itchy eyes anymore. Something strange happened: I felt just great! My skin had cleared, and no more itchy, puffy eyes! Now, two days later, I wake up to another sore throat AND itchy, puffy eyes. I do not have insurance, and any treatment I receive comes straight from out my own pocket. Could this stuff be silently killing me? Please someone help me with this strange dilemma

I started taking Levaquin in December for a respiratory infection (500mg for 10 days). The only side effects I noticed while taking it was a terrible headache, insomnia and anxiety. I experienced that after the first dose. The next day I called my Dr. to tell him and he said he would prescribe Ativan and I should continue with my prescription. I wish I had listened to my common sense, but I listened to the doctor. I finished the prescription and felt somewhat better from the infection but after 10 days of being off the Levaquin, I started to get a burning pain in my left arm. At first I thought it was a blood clot or something. Two days later, the pain had spread to both arms. The pain was so intense I thought I was going to pass out. I had severe joint and muscle pain. I suspected it was the Levaquin when I found this and other websites where people have been describing their experiences. I made copies of a lot of information to take to the doctor. When I went the doctor I described my pain and tried to show him the information, but he didn't believe me. He said it was not caused by the Levaquin. Since then, the pain has spread to my knees. I have decided to find a new doctor since I refuse to waste my time on a doctor who doesn't even believe me. I called the FDA to file a med watch and they said they were going to send me paperwork..guess what..that was last week and I still haven't gotten paperwork. I believe that everyone is trying to keep this undercover! I am going to go to their website and download my own forms and file.
Two weeks ago I started taking a regimen of vitamins: Daily 3000 mg vitamin C, one B Complex, Milk Thistle, 1000 mg Calcium, 500 mg Magnesium, Potassium, and a Probiotic supplement. I don't know if these have helped me, but I do want to say that I feel better than I felt two weeks ago. I still have a lot of pain, but it's not as severe as it was. I'm hoping that it goes away soon. I am spreading the word among family and friends to NEVER take anything in the quinolinone family of antibiotics. I really don't believe that these side effects are as rare as they say. I just believe many people don't report because most don't connect the dots that their symptoms were caused by the antibiotic. My symptoms didn't start until almost two weeks after I completed the antibiotics. I was just lucky enough to have figured it out. The other symptoms I am having are muscle twitching, trouble focusing, insomnia, and cold hands/feet. I also just once had a ringing in my left ear that made me feel like I lost some of my hearing after it finished. I hope that's not the case. I will continue to pray for all of you.

Hey all. I suspect many of you would agree that one of the most infuriating aspects of this antibiotic nightmare is that seemingly, there aren't many {none that I've dealt with} doctors/nurses or pharmacists that will even acknowledge the potential {and VERY REAL} side effects of these drugs.

On 01/10/08 I was put on Cipro 500mg twice daily, two week supply, for epididymitis, which likely stemmed from a bacterial infection/urinary infection back in late Oct of 07. It's an infection that can require a lengthy dosage due to eliminate bacteria growth. I was also prescribed a painkiller along with it.

That night after dosing had horrible nausea/vomiting, and chalked it up to the painkiller ... which at that point it likely was. Within a few days the groin pain from the infection had subsided a great deal, and although felt a little 'odd' from the Cipro, nothing too noteworthy. At eight days into treatment, became nauseous around the clock with bizarre flu like symptoms. I called the doctor at the ER who had diagnosed me, and she switched me to Doxycilline {sp?}, which isn't a quinolone. After stopping the Cipro, nausea disappeared. However, within a week the pain of the infection returned, apparently due to the weaker antibiotic.

So I was re-checked on 01/24/08 and put on Levaquin, 250gm once daily. Within a day or so the pain subsided once again, but on the third day developed horrible diarrhea and pain in my left knee/leg. Stopped taking it immediately, and decided to research my dilemma online, where to my horror I've discovered all sorts of people from all walks of life experiencing debilitating side effects from this grouping of fluoroquinolone/quinolones antibiotics.

I'm now on Cephalexin, and the pharmacist I spoke with today assured me that it's not part of the quinolone grouping. He also suggested that I must be part of that small pool of the populace that has trouble with quinolone antibiotics ... one begins to wonder just how "small" this pool is given how the average person isn't likely to associate muscle/joint pain with the antibiotic they're ingesting.

How this POISON has lasted so long on the market without more exposure/media coverage speaks volumes about the state of corporate America, with nearly every social system compromised {usually at the expense of the corporation's victims} , with little or no help from the corporate owned mainline media, which serves as nothing but a megaphone platform for vested intertests to transmit "official" opinion to the unwary. So here I be with very painful knee, which I should add is already compromised due to a major tibial plateau fracture in 2001.

I'd love to know whose palms are being greased to keep this rat poison available ... hell, I even had to pay over our insurance co-pay fore the Levaquin, as it's apparently a "top shelf" drug.

Good luck everyone ... and it probably doesn't need to be said, but man, I know after this I will check and double check any and every antibiotic that may be perscribed to our daughter in the future!

I started taking Yasminelle (its dosage is much lower than Yasmin's) about 5-6 months ago; the side-effects I endured during the first two months keep coming back as soon as I start a new packet. Side effects such as nausea during the first week of taking the pills, continuous breast pain. These side effects are completely making me seem like a total freak when I am out- I am always complaining about how sick I feel and I also can't drink because as a result i feel queasy and I'd have to stop. Does any one else feel the same way on Yasminelle particularly? i have been searching online for discussions regarding Yasminelle but I have found none at all...anyone else on Yasminelle and do you consider it a good form of birth control?

Okay soo... I have said before that I liked it... well my mind might be changing. I had a bladder infection last month and after using antibiotics to get rid of it got a yeast infection which is not abnormal, when I use antibiotics I normally get a yeast infection. Well this month around the same time I got a slight yeast infection. I have also had breast tenderness the last week or so, I had a weird discharge on saturday but it only lasted one day and I was very emotional last week. So... here is my dilemma is this because of the ring or am I pregnant? (we did have sex while I was on antibiotics which does counter-act birth controll) I took a in home pregnancy test two weeks ago and it came up negative. But I had a friend who was on birth control and her in home tests came up negative when she was pregnant(with twins even). Can anyone help me out here, let me know what you guys think? Or have any of you had negative pregnancy tests on the ring and actually been pregnant? Or has anyone gotten pregnant on the ring? Just some questions I've been having. Thanks!

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

I've been taking Yasmin for almost 2 years now. I was first put on it after being diagnosed with PCOS (polycystic ovary syndrome). In the passed few months, I have found myself so tired, restless, having insomnia, anxiety, acute panick attacks, hives all over from the anxiety. I thought I was losing it. My only dilemma now is that if I do go off the BCP, I am at risk again for no periods, high blood pressure, weight gain, diabetes, cancer...alot of stuff. So, anyone else out there with PCOS who has had these symptoms, and gone of the BCP..what did you have to do in order to keep your horomones in balance?

I've been on Yasmin since Febuary 2006, and its now October '06.... so about 8 months now.

Now I'm tall, but I'm no amazon woman; a little over 5'8. I, like most other women (even though I've supposedly not stopped growing yet, which I have a rough time believing...) have one breast bigger than the other. Ok. No problem, right? Wronnng. I've never been small chested, I developed early and even before I began taking Yasmin I had a chest side of 38-40D.
Now after taking it for 8 months, I've noticed that, as I was told it probably would, increased my chest size. The thing is, it increased one a LOT and the other very little, if at all. I now have to wear a 38DD bra just for the ONE boob, so theres so much extra space in the cup with the smaller one. =| Then, its impossible to find clothes that make me not look like a... less than "nice" girl. I'm incredibly self conscious, I feel like its getting more and more noticeable. I've discussed with my mother having a breast-reduction surgery, which I've wanted for a long time and she is finally beginning to see how its a good idea too...
But my dilemma, is if I GET the surgery and continue taking the pill, will this just keep happening anyway? Like I get the reduction surgery, but then the one boob just starts to grow again, making the surgery wasted. Is this really worth STAYING on it? I'm thinking about it all the time, I want like. A boob-corset. An X-TREME bra, if you will, and not a minimizer. Those hurt, and it doesnt fix the problem of one being bigger than the other. I feel like I've tried everything.... :\

I started Celexa 2 days agao, and on 2nd day..My head felt very strange numbing pain from top to back of neck..plus a numbing of cheeks and lips..also strange heaviness-numbing in arms and knees...so I stopped taking it right away...afraid of having convulsions and ending up in the hospital with a cerebral-accident as what happened to me last year...I will have to find something else which will work for me to calm my panic attacks......what a dilemma...because these panic attacks absolutely make me stop functioning.....

You make me laugh Silke because you sound just like me. All day the only thing I do is google "weight gain-oral contracepitves and the like in search for an answer to my dilemma. Well the only thing I guess is to sit it out and wait to see what happens. A year seems like a mighty long time (that is another 7 months for me.....lol) but there's not much for me to do. I've exhausted all options. Posting here definitely helps, as is seeing that I'm not suffering alone.
It's just that I have already seen better days and I thought I'm heading towards recovery when I've been dealt a blow this past month. Oh well!
Take care Silke and everyone else.
Love & light.
Sherry

I've been on Zocor for two years 20 mg after having a heart attack. I've had muscle pains recently and I stopped taking it after consulting with my doctor. Now, I am on pravachol which is similar to Zocor but less side-effects on muscles iad to me. After reading these complains here I am on dilemma to carry on using this medicine or not! If anyone tell me another option exist? ******

SEVERE jaw/tooth pain, I drink something immediately after and assumed that was sufficient.
20 lbs weight gain in two months with diet and exercise. Was actually losing weight up until that point.
Restlessness
Arthritis type pain in hands, very painful and swollen, comparable to what I experienced with toxemia during late pregnancy.
Has helped my asthma tremendously. Terrible dilemma. I need to breathe but diabetes or a heart attack because of weight gain doesn't appeal to me either.