Good doctor symptoms and conditions

My eighty year old wife wa given ten Avelox tabs and told to take them one each day for her lung infection.
She has taken them five days along with a cough syrup which contains codeine.
The result is that she has been sleeping about eighteen out of every twenty=four hours.
After finding this site, I stopped her from taking ant more of them.

My dad is 73 years old and has been in the hospital, rehab, nursing care, back to hospital, currently back in rehab since August 3, 2008. He was on Flomax which he was taken off of the first week in August after arriving to the hospital with low blood pressure and leg weakness to the point of being unable to walk. He had been taking it for years so doctors did not think Flomax the cause. However, once they ret'd him on Flomax he was unable to hold his head up when sitting in wheel chair (drooling) and very unresponsive. He also vomited and just stared at it, unable to respond to try to clean himself up. They took him off Flomax with some improvement. (He could hold his head up and respond.) His weakness declined to the point that he can no longer pee/poop without a diaper, can't swallow, can't speak (due to weakened vocal chords), and has no energy. He has a feeding tube. To date, they have not been able to pin point what dad's problem is. I noticed that on October 10, 2008, they returned him to Flomax. He again is sitting in wheelchair with head hanging down. No energy to do rehab. I have requested they take him off Flomax and LEAVE him off. I don't trust this drug. I think his long-term use of this drug could be what's killing my him.

Hello . . . why do we continue to take medications that cause us such physical and mental anguish . . . we hope for a life . . . I am one of those who takes a cocktail containing . . . Lithium, Lamictal, Cymbalta, Sequel, Topamax and other medications for high blood pressure, low thyroid and osteoporosis . . . down four medications . . . because I have a good doctor . . . it is impossible to distinguish which one or the synergism of the medications . . . which do what . . . what I want to say . . . there are more medications now . . . more doctors . . . change doctors . . . change medications . . . you might not feel great . . . but you will feel better about taking control . . . it has happened to me . . . M.

October I received my mirena in 2006, if I had known then what I know
1st now I would never have gotten it. My husband and I share 3
2008 beautiful children, 2 being twins, since the risk of having another
8.30am set of twins was high, and his refusal of a vasectomy, my
doctor assured me this was the best thing for me. During the
2 years that my mirena was in I gained 20 kilos and continued
to gain blowing me up to 130 kilos. I have always been chubby
but no efforts to lose weight would work. I suffered depression
and the same doctor started me on medication for that,
still saying nothing about my mirena as the possible cause for
my problems. I was suffering excessive sweating, and not the
nice smelling kind, terrible tiredness and fatigue, aches and
pains, pelvic pain and complete loss of periods. It was only
when I went to my doctor a few months ago and demanded
that the mirena be removed, that I have started to improve. No
more sweats, I am still on my depression medication and am in
the process of weening off it. I have started to lose some weight
but unfortunately have now been blessed with liver disease. If
it's not one thing it's another. I have been researching to see if
mirena has contributed to my liver problem as I did not have it
before the mirena was inserted ????????? My experience has
not been a happy one, but losing trust in who I thought was a
good doctor really sucks. Don't take what they say as truth!!!!
Now I have to convince my husband to have a vasectomy and
so far he is proving quite difficult!!!!!

I have now tapered to 10mg prednisone every other day and will end 75mg Cytoxan Aug 19th. Just went to the Dr. and she said protein is back in urine (bad) but also rising in blood. (good) I can continue to taper prednisone but will have to have another 24 hr urine speciman to determine wether I have to go on cyclosporine. Was originally diagnosed with Minimal Change Disease, but now she thinks it could be another kidney disease. Has anyone had successful tapering with the addition of cyclosporine? Does the urine protein ever get higher? What about side effects of cyclosporine.

I got all those problems but the higher the dosage the more attacks i had.Another neurologist think that i just have pseudoseizures-paranoia attacks.Anyways the doctor screwed me up,he gave me 5 years ago something different and my seizures started daily than switched me to lamictal.I must say that sometimes i have or HAD electricity in my left hand all the time and once a women touched me and got stunned lol.anyways lamictal is bad,i didn't have any side effects like loosing hair but i did have A LOT of head hecks.I must share something with you,when i read epilepsy.com it seems that my seizures called myclonics in the end they are not but they similar in effects.Myclonics its seizures that happens only in the morning.Heres the catch for me,i figured out that if i won't close my eyes the first hour after i got up and went to the sun outside than i didn't have seizures.Its not a real solution so i decided to raise the lamictal from 175 which was ok for me to 200-250 like the good doctor said,just made me worse.Now i started dropping it by 25 mill each week and i must say i feel better only a little tired after 5 years that my body got used to it.Anyway if any of you have myclonics than don't close your eyes.BTW i have AURA-feeling before the seizure but luckily for me after a second if i open my eyes nothing will happen although i don't always take notice of it.In midway it would happen if i seat in front of computer and will lose attention if someone will call me or whatever but its a mill-sec seizure,barely noticible if at all and i never get "disconnected" from reality!!!
the ONLY thing which is bad for me is that except that im sick now my blood pressure is huge-140/82 and pulse 106 which is being like that for couple of days but i will get trough that.Since i lowered my dosage my midway seizures stopped,now im on 100.

P.S=Check yourself with the neurologist with a different one preheps.IF you can describe the whole seizure it means you don't dispatch from earth which mean it might be psydo seizures which are psychotic and not epileptic,the most important thing is that if someone takes lamictal or any anti apileptic drug even tho he doesn't have real seizures the medicine can do this.I got screwed and now i try to get over it,the doctor trowed me on woods with tablets after having a first seizure WHICH IS WRONG because you sepused to get tablets only after 3 attacks and after describing seizures and doing eeg tests to make sure that you DO have the problem.

Anyways remember what i said about the closing eyes in the morning part,if you close your eyes and feel weird keep them open at least those that have them after they wake up,that was a solution for me and it can help you to...MY doctor said everyone like me but i think he is laying,the other neurologist said my doctor was wrong probably about the seizures,i think i have both but i do know that believing and saying that you don't have anything WILL help you and lower your seizures,after speaking with the doctor i actually started to believe i don't have anything and walla i have almost NADA,today i had zero!!!! :D

OF course don't lower dosage without first consulting with someone expert,but since i know i can control basically every seizure i have and i know what to do to avoid it i let my self start dropping dozes!!!

GOOD LUCK my friends believe in yourself and if you want some personal info leave your msn i will add you and try to answer you the best i could,i was researching my self trying to figure out the core of the problem for 5 years but after 6 months knocking my head in the pipe when i washed my face i learned what i should avoid to minimize the chance!!!Try that

I've booen on 100 mmg of toprol for over ten years. Have all the side effects including tinnitus and impotence. Last week for chest pain spent the night at the er , three blood tests, three ekgs, a stellar stress test and echo. All normal and still the sense of doom and the pain under the breastbone... This has been ruining my life. I'm furious after reading all this testimonies . Olease someone give me advise. ******

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 was prescribed Zyrtec a few years ago for allergies. I also have MPV and need to take Atenolol, I will need to take Atenolol for the rest of my life. My cardiologist recommended I stop taking Zyrtec because it can give you an irregular heart beat. When I tried to stop it I got very bad withdrawal symptoms, chills,heart racing, insomnia, itchy skin. I thought I was going crazy, so I took one Zyrtec as soon as I took it 15 min later the symptoms stopped. The next night I decided to try and cut the pill in half and only take 5 mg, that was ok for 3 day's then the symptoms returned. I had to take the other half of the Zyrtec and then the symptoms went away.
I can not believe that I have to find a way to wean off Zyrtec. I am very annoyed that they do not list on the label that their could be withdrawal symptoms after taking Zyrtec for a while. I am not giving up I am going to continue and try to wean myself off the Zyrtec, hopefully I won't have a heart attack in my attempt to get off this drug. If anyone has a successful way to wean off Zyrtec please post it. Thanks and I hope this helped someone who was thinking of taking this drug. STAY AWAY FROM IT..

I have come to the conclusion that our pediatricians, allergists and various other doctors, have been brainwashed by the drug reps,possibly even bribed. My friend took her son off of Singulair almost a month ago when I told her about all of this. He already suffers from a learning disability, but she feels that his ability has improved along with his disposition and complaints of various aches and pains. She took him for his usual appointment at his allergist and told him what she had done and why and he literally YELLED at her, calling her a fool and demanded that she put him back on it. She stood her ground and refused and now is under the impression that her son will be dismissed as a patient from that practice. That won't be a problem. From what I read and what I hear, a lot of doctors are dismissing the whole deal. They can't be bothered with finding out for themselves, what the truth really is. No, they might miss out on the "perks" from the drug reps, like free samples of the deadly drug, or free pens, or a chance at a vacation in the Bahamas, and the list goes on. The drug reps are a hazard. They lack education on the drugs that they are "dealing", and if they HAVE been educated and are still promoting it,
they are no better than the crack dealers in the alley.

Our son started taking Singulair when he was 2 for severe allergic rhinitis and cough variant asthma (in addition to Zyrtec, which didn’t control all of his symptoms). He is 5 now. For the last three years, he has been an increasingly violent, difficult, defiant, argumentative, volatile child who has intense mood swings--one minute he’s laughing uncontrollably, the next he’s weeping over nothing. His doctor and therapist recommended that we see a psychiatrist to have him evaluated for bipolar disorder, which used to be unknown in children. Because he has such chronic sleep problems, the doctor also suggested we take him off Singulair (and increase his Zyrtec dose) to see if it improved his sleep issues. Within a week, he was sleeping much better and was a calmer, happier, gentler boy. He suddenly could take “no” for an answer without flipping out and trying to hurt me. We thought that we were just in an unusual, calm window that would shift either to mania or intense sadness or both, any minute. We also thought that his behavior change might be due to sleeping better. We were enjoying the rare reprieve. Over the last weekend, his springtime allergies really flared up. We gave him Singulair on Monday and by noon, he was completely out of control. I had to strap him into his car seat at one point to keep him from hurting either me or himself. It finally occurred to me that Singulair might be causing his “bipolar” disorder. Of course, we stopped the Singulair. After two days he was a new boy. Yesterday, I Googled “Singulair bipolar children” and got a few hits. I am stunned to read how similar other families’ experiences have been to ours and I feel sick that we gave this drug to our child for three years.

Wow. I can't even express how blown away I am by all of this.My son is 7 and has been on singulair since he was 2. He was moved to the 5 mg last year in March. The only difference between my son and all of your stories is that when he was in kindergarten we discovered a rather large arachnoid cyst in his brain that had to be drained. It was easy to blame some if not all of his behavioral problems on the location of the cyst. It is in the left temperol lobe. Having something in that region of the brain can cause behavior problems. His cyst was also big enough to push on his pituitary gland making him think he needed to use the bathroom all the time. He had a slight case of diabetes insipidus. During all of this he was complaining of headaches, fatigue, leg pain, the boy could not walk from one end of the mall to the other, he would melt down at the slightest provocation and turn into an angry little monster at around diner time. We attributed it to low sodium levels messing with his head, but his blood work never reflected someone who was THAT bad. After his surgery he had some normal depression, but in March, four months after, he became a different person. He was full of rage and anger and almost got kicked out of school. He broke things at home and lashed out at people, he said awful things. He was put on Tegretol, (that made him very sick) and Wellbutrin. Since he couldn't tolerate the tegretol they switched him to abilify. He still takes this. The one time we tried to take him off he went completely nuts again. Same kind of aggressive behavior, lashing out, no self control, crying all the time, very moody, saying things like "nobody loves me." My son is the sweetest person you will ever know. Before all of this, he would melt your heart with his kind words. Now he has been diagnosed with ADD, Aspergers, and has all of one friend at school. I go every day to eat lunch with him so he doesn't have to sit alone. I completely understand that my son will continue to have problems once this medicine is out of his system, because he does have other issues, but this morning the first thing he said to me was, "Mom it's weird, I don't know why but I feel so happy."
He has been off the Singulair for 6 days now. I called his allergist and he was VERY interested in all of this and wants to meet with me. He has always been so heartbroken by how my son has struggled. Don't think all doctors are bad. This one isn't. He is going to help me report all of this. He is really upset too. Of course he is older, been around for ever. I don't know. He cares about his patients. His receptionist said she thought they would be getting a ton of calls about this and I was the only one. Hang in there everyone. Alone we are quite together we are LOUD.

I was put on Toprol XL 6.5 yrs ago. My heart rate had soared to 130+ and b.p. was elevated. So my family doctor put me on Toprol XL 100 mgs. From day one I felt exhausted. He told me that would soon clear up and not to worry, we needed to be more concerned with my heart rate and b.p. I listened and was a good patient. After a year of total exhaustion and having to quit my job I asked to be taken off Toprol. He said it was the only medication that would control my heart rate and b.p. together. He agreed to reduce it to 75 mgs. After a few months I went back and said it was still too much! My b.p. was better as was my heart rate so he lowered it to 50 mgs. Things got a little better at least I could get out of bed by 10:00! Fed up I lowered it to 25 mgs. and tracked my b.p. Finally I told my doctor and he said as long as my b.p.was better 25 mgs.was ok. By this time though I was having other symptoms, body aches, joint pain, mind fog. He attributed it to arthritis and put me on Vioxx. 2 pills later I stopped due to chest pains. The symptoms I had experienced over the past 2 yrs continued so I sought a new physician. Once again he said Toprol XL was the only medication I could take for tachycardia and high b.p. My b.p. was again elevated so my meds were increased to 50 mgs. he wanted to go 100mgs., I said NO!
In 2004 I was diagnosed with Fibromyalgia, the pain had become so bad now it was debilitating. I had all the full blown symptoms of Fibro, extreme exhaustion, body aches, joint pain, mind fog, depression etc etc. So I sought treatment for Fibromyalgia for 3 yrs. Not so successfully I might add.
I should note that I had none of these symptoms before Toprol XL.

During a recent Gynecology visit my b.p. was extremely high. I told her my story about Toprol. She said point blank, They are NOT listening to you. I think all the side effects you have been having are due to the Toprol XL.She sent me to a Cardiologist. God bless her!!
After many tests he immediately took me off Toprol. He put me on another medication instead. I am having withdrawal side effects from Toprol, shakiness, shortness of breath, heart rate acceleration and mind fogginess. But, anything is better than another day on Toprol. He told me what I was experiencing was normal withdrawing from Toprol. He also assured me there were many other alternatives to Toprol and if the new medication doesn't work there are other options.
I think Toprol XL is the next drug that should be banned!! I pray everyday my life will return to what it was before Toprol XL and that I will not have any lasting side effects from this horrible drug.

I was on toprol-xl for almost 8 years without many problems. i also take isosorbide mononitrate.A few months back I was switched to the generic version (metoprolol succinate er by sandoz) now i have many problems.First I have to say I am disabled with severe COPD. Although I do not feel depressed I have a lot of symptoms of depression. Remember I had no symptoms what so ever until switched by Walgreen's or HMO or Doctor to the generic version. Not sure what to do I have a doctor that does not truly listen,plus he did not want me on toprol xl to begin with. Even though it was good for me. Good luck people!

My sister died of a heart attack after being on lisinopril for a month and a half.. She had no known heart problems..

She passed away in 5 am. The evening before she told me that she was going to stop taking lisinopril because of the side affects.

I miss her so much.

Are you aware about short and long term side effects of this Devil's drug??? Of course, everybody reacts differently while take or withdraw. But there are high number of people who react terribly bad!!! Doctors do not want to recognize and discuss this. They just keep silent... Do you know exactly how Prednisone works??? Nobody knows this for sure, even doctors!!! From my personal experience, and despite gradual withdrawal, I developed extremely high blood pressure, weakness, panic attacks, depression! Practically it ruined my normal life! Doctors have no clue how to deal with its devastating side effects. Steroids are not selective. When you take a steroid, the drug infiltrates the nucleus of every single one OF YOUR CELLS AND STARTS MONKEYING AROUND WITH GENES IT FINDS THERE!!! It probably plays with hundreds of genes. And just a small number of these genes control the pain and inflammation associated with inflammatory diseases, so steroids turn many of these genes off which is good thing. However, because steroids are not selective, they also regulate the genes that control kidney, liver, BRAIN, and HEART function - which is not good thing!!! It is likely that steroid treatment plays with other genes, too, including those we do not know about a lot right now...So, Prednisone pervades the entire body, which increases the likelihood of short-term side effects and long-term DAMAGE. My advice is: THINK TWICE BEFORE TAKING PREDNISONE!!!

Hi everyone, I have been on Loestrin fe for 8 months and I am 45 years old - taking the pill again after a four year absence. I have found that all of the posted side effects are true - but are greatly minimized by taking the pill EXACTLY at the same time every day.... if you are off by even a half hour you WILL have breakthrough bleeding - sometimes with clots and with drawl-like headaches... my gyn says no way - but I actually tested my own theory this month - much to my regret - I am right... I am ready to quit as I am at the end of my rope. Fortunately for me my blood count has come back into the normal range after the last two years of horrific bleeding every 11-26 days without a break.

I am going to go off next month - and I may have RESET MY SYSTEM so to speak - if no I will take a hysterectomy please... straight up with a tummy tuck to match!!!!!!!!!!!! Please email me if you ever want to discuss - I am a nurse anesthetist and have a great deal of sympathy for all of you out there. I am not sure if this drug is a bad one - but I think it is so low dose that timing must be precise for it to work properly. I have stayed on it only to reduce the bleeding (perimenopausal/estrogen dominant I am sure) twice a month periods that last 7-8 days. It has worked for me in that regard - but the first 7 months were plagued by horrific (and I mean really bad) right sided headaches that scared me. I had relief from NSaids (Motrin) so I almost overdosed on that stuff. Not good. My next strategy is to do saliva testing for cyclic hormones OFF the pill to see what kind of hormonal swings I really am having - and to adapt a more natural approach - possible progesterone cream to alleviate the misery of it all....
Much Love, Ellen M

I have been reading all the entries for this website and thought I would pass along some useful information. I have been on Levoxyl for 8 years now and have had lots of the symptoms that all these people have had. I then had an appointment with a great Endo doctor at the *** and discovered some interesting things. There is a number "range" they put all people into when checking your TSH levels, only problem is each person is different and even though the doctor may say your in the range, it may not by the right dosage for you. Unfortunately the only way to determine the correct range for you is to experiment with the dosages and it takes 3 months or more for your body to adjust. Also, thyroid hormones are accumulated in the body and depending how active you are is how you may feel. The hormone pill you take today will not be used by your body for up to 10 days, so if you feel good for a few days at rest, then exercise the next day you may feel drained. It will take a few days for your body to replenish the stockpile of hormones to feel "normal" again. A working thyroid makes hormones as needed, yours now does not so this is why so many people feel fatigued, or racing heart beat if they don't get enough exercise. I also had leg and muscle pain. The medication depletes your body of Calcium and B complex especially B12. My leg and muscle pain have disappeared. I still get headaches, but much less with the B12, and some days I still feel tired but I say again, your body cant regulate its needed thyroid hormone and a synthetic pill is only a substitute.. You will always have some side effects. Hope these tips help someone.

Been on Toprol XL for 4 years. I am 64 with SVT and mitral valve prolapse. I was started at 50mg daily and got relief but when breakthrough SVT started the dose went up to 50mg in the AM and 25mg in the evening. I still have breakthroughs but can wait them out. I did notice that my SVT or palpitations seemed to be triggered with an imminent BM. I have been diagnosed with fibromyalgia but coincidentally....it started with severe muscle pain when I started taking Toprol XL. I wasn't told that this could be a side effect.HMMMM When my insurance was discontinued (retirement) I started taking the generic due to cost. I haven't noticed any difference between the two. I also noticed that after a SVT episode I have a increase in urination....Toprol or SVT? I also noticed that I am very aware of an increase in a feeling doom. I have had ekgs etc and my heart is in good shape otherwise.

Struggling with a sinus infection that threatened to bore into my brain, resulting, ultimately, in seizures and death, I've been taking Levaquin now for three days. I'm experiencing anxiety and sleeplessness, however, it's not from the medication. It's from all the hyperbole on the internet.

Look, I understand that many have had adverse reactions to this medication. One dose of penicillin can kill you without warning. At anytime. No warning. I suspect that few of those labellings Levaquin "poison" would ever bother to consider that - or anything else. All wrapped up in your misery, you spout off with rhetoric that is really better left to lawyers and politicians.

If you were uninformed of the possible side-effects of this medication, blame your doctor. I see that the last post here is dated November 2007, and the bottom of this first page takes us to October 2006. Perhaps one could take a bit of responsibility for oneself and do some research on one's own before popping a pill handed out by a disinterested physician. This information is out there - and yes, your doctor could have seen it, too. But he didn't bother, did he? Neither did you.

So, yes, with my first dose, and despite the impact drill driving through my eye-socket, I waited for the seizures, swelling and signs of imminent demise. Nothing. Sorry. Oh, my sinuses feel better, I don't have a brain infection, and so I won't die frothing at the mouth on my living room floor.

I'm sorry you feel bad - and if you hadn't run off at the mouth calling what may be one of the last effective antibiotics "poison", I might mean that with some sincerity. Oh, and lest you forget, antibiotics are poison by definition - the idea being that they affect/poison/kill the source more than they do the host.

So let's stop the hyperbole, and simply say you had a bad reaction to this medication. Not everyone does. Your option might have been to skip the doctor and the meds altogether, and see how you'd fare. But that would leave the responsibility, and the blame, all on you, then, wouldn't it? Far better to spread it around some.

I have tried 4, soon to be 5 birth controls. I have just (finally) been diagnosed with endometriosis. My favorite thus far is Orthotricyclen cycle. BUT my sister is on Yasmin and I have been on it a year without much complaint. I would say it has less side effects than most, though doesn't seem to stop the bleeding. I have some form of my period three weeks a month on this! I will say it didn't decrease my sex drive BUT what good is it when you always have your period. My sister is having really good luck with it, little to no side effects, and neither of us gained any weight from it. I think its important to note to the readers of this site that every pill hits everyone different, unfortunately its trial and error and a good doctor that can see what works for your body. Just keep that in mine, at least I try to as I start a another new pill.

Ok. This is crazy. My doctor is a VERY good doctor, and has denied my charges against the Mirena. I had not looked into the reported side effects when I complained to my doctor. I have had my Mirena since 2004. No problems at all until about 3 months ago. (maybe longer than that adding the mood swings, loss of libido since the birth of our last son, vaginal irritation, dryness, yeast infections that I never had before the IUD, breast tenderness, joint pain, recent bleeding that lasted a month) I began having heart palpataions so severe that I thought I was having panic attacks. Like a heavy weight being laid upon my chest, too small of an area for my heart to be able to properly beat, loss of breath, loss of sleep (causing me to take tylenol pm to be able to rest). I went to the doctor, and was concerned about the symptoms. She was alarmed, she has known me over 5 years, and I have been in her office only a handful of times. She ran an ekg, did chest x-rays, and found nothing. She sent me on to the cardiologist to have blood work and an echo. They found nothing. I asked her about the possibility of the Mirena being the problem. She thought it was doubtful, but wants to look at it during an exam anyway. My hubby and I are considering having it removed. We can't figure out what other problem there would be. Please email me if anyone has had symptoms similar! I am VERY concerned.

I have been on Toprol xl 200mg for over 3.5 years now. due to high blood pressure problems. and Hmo Doctors who refuse to change meds. typical of hmo systems. I dont like this medication and have been fighting with Doctors to get off it.( no luck) as yet! I have tryed myself a few times doing it slow at small dose, however I have withdraw symptoms! and im forced to go back to the medication again. I think most Doctors fear this problem so they try and pass the buck to a hmo cardiologist, who only tells you, I dont do that - go back to your primary Doctor? its like running in circles !
bad part I have every know side effect from this medication, Doc gave me 4omg of Diovan to counter act the toprol effects.. ahhh! that didnt help.. make them worse..and caused more effects ! blurred vision -chest pains
short term memory loss, Hair loss, and thinning real bad.. I have counted over 56 side effects for just toprol xl alone.. and another 31 for Diovan
plus the fact Diovan was recalled one time before.. and then changed and re-released again.. I feel like the walking dead - Im so tired all the time..
and boy! if your out in the heat.. 85deg F. or more.. watchout people.. you can pass out cold ! from this crap - its got some real bad effects when it gets hot outside. stay in doors and out of the heat ! unless you have to work like me.. I guess one day I will find a good Doctor who will help me
for now, Hmo systems stink ! but im stuck with one till October.. then its bye bye for Hmo's for me.. there has to be a better way to go !
Toprol xl is not the ansure or cure ! by the way I get palpitations off and on from diovan or toprol xl .. its very strange... hate this medication

Hello, my doctor has me on Toprol xl 50mg and just a week ago lowered it to 25mg. Since then i have had mild dizzy spells and just feeling of uneasyness. Please let me know if this is normal and if anyone out there has experienced this when they had Toprol xl lowered by DR.
Thanks

i've been on synthroid for 9 years. started at some low dose and gradually went up to112 mg. get extreme itching all day everyday if i don't take allegra for that.not a rash just itching. that doesn't bother me as much as the fatique. every joint in my body aches all the time. sure there are better days but fo rthe most part it's bad. tried physical therapy and chiripratic care but no avail. they ended my sessions. my legs get sooo weak and my feet burn lower back really aches. sometimes muscle cramps. i'm very negative towards my loving family and it hurts me to do so. can't seem to keep upbeat. soo tired all the time.
is it the syntroid? i used to be very energenic and a doer. now i have spurts of activity in the morning , but then i just can't get motivated. help me any suggestions?