Vytorin symptoms and conditions

I have been on simvastatin for 2 yrs . The past six months have had foot pain my doctor described as neuroma.By the time I started physical therapy the pain was in my arch + tendons. I went to physical therapy for two months, the therapist became concerned when improvement peaked. Still have burning nerve pain. I think its time for natural supplements . I hear "red Rice Yeast" is effective.
S. M.

Been reading everyone's postings and now I'm scared. I currently am on Vytorin 10/80 and today the doctor added Welchol. I just had and ACL replacement surgery 4 weeks ago and my leg aches anyhow. I can't remember a time I have not had back pain, and I have arthritis in my joints and neuropathy in my feet. Any yeahs or nahs out there for you experienced ones? Is it worth taking, do you assume all my current pains will only get worse?????

I have been taking Crestor since early September 08. Prior to that I was on Vytorin for quite awhile. I now have right sided parthesia and my face tingles constantly on the right side. I have had MRIs MRAs not to mention blood tests that say my kidneys are spilling calcium. No one seems to have a clue what is going on. My feet and legs hurt so bad if I sit for too long I can't hardly walk. My uncle passed away from ALS and now I'm really scared that all of these statins are killing me slowly. I wonder if I quite taking this drug will I have a heart attack. I really just don't know what to do.

After just two days on three WelChol a day, I have flu symptom. I'm going to stop the pills and see if it clears up just as quickly. If it was the WelChol, I'll just live with high cholesterol (273). WelChol will be the third strike after trying Vytorin and Lovastatin and having issues with all of them.

Began taking 500mg of niaspan after 81 mil of Bayer 30 minutes prior (at 11:00 in the am) about 3 weeks ago. Recommended at this time since I do enjoy my 2 glasses of red wine at night. I then take 10mg of Lipitor before bed. Side effects have been swollen lips that keep peeling, after many OTC lip balms, racing heart and unbelievable insomnia. Only had flushing the first day before nurse, not doctor, told me about aspirin. I don't know whether my allergic reaction is the Niaspan or the Lipitor. I also had mild nausea and foot cramps at night. The nausea has subsided but not my lip problem.

For one year prior to taking these drugs, I was on 10/40 of Vytorin but since all the negative results of that drug, my doctor has taken all his patients off of it.

On Vytorin for the first time 10/80 for 8 weeks -cholesterol numbers are fine now. My liver count was slightly high and my doctor said that was fine. I took myself off. This is the 3rd day without and I am less tired each day and I am feeling like myself again.

* Completely sunburned after 30 minutes in the sun
* Have to get up at least once a night to urinate (never had before)
* Extreme pain in my feet when I first get up in the morning. (Goes away in 30 seconds) If I feel it when I get up to urinate, I won't feel it later when I normally get up
* Decreased sex drive
* Cholesterol decrease from 310 to 147

Afraid these side effects are just the beginning

Yes, I have been taking Vytorin 10/40 for about 10 months, and it did reduce my cholesterol and triglycerides to 'normal', however, I slowly developed (initially) some 3 months back, problems in my left solder, diagnosed eventually as 'rotator cuff' ligament damage, however, it came on slowly and progressively worsened. I had not done anything strenuous to develop such a condition. It became so bad that I was basically redd to using my right arm. On top of this, the muscles in my lower arms became sore and felt strained even lifting a glass of water was painful. My Doctor was informed of increasing on-going muscle problems, did an emzine muscle test, which turned out to be 'clear'. And I also lost my sexual drive gradually.
I went off taking Vytorin a week ago on my own gut feeling, and my arm muscles and left shoulder have improved. I am also hoping no permanent damage. I am moving to a much higher exercise regime to 'burn' cholesterol and reduce triglycerides, and in the mean time look for 'natural' solutions as well.
I am not impressed with the medical responses I got, along with miss-diagnosed muscle / tendon supposed 'rotator cuff' serious problem that developed in my left shoulder, which I suspect may never be the same functionally. I recommend looking at other alternatives and natural remedies, this is my course of action. MM

Boy, after reading all the negative testimonials on Lipitor, I will throw mine in the garbage. That is what they are meant for. I have severe headache, and muscle pain, and foggy head, and I have only been on the crap for 2 months. I believe a lot of people's health is being ruined, and a lot of deaths are happening as well because of Lipitor and other statins. Mark my word, one day this drug will be withdrawn from the market, and the poor Pharmacutial companies will be in huge trouble.. They have the world convinced that we all need statins to bring cholesterol down.. The era when my parents lived , and lived long lives, and on farms, with butter, bacon, lots of fats, and never heard the word STATIN. I think every one that is writing to this forum and complaining about LIPITOR, should make a phone call to PYzier and tell them your side effects, that is the only way anything positive will come from this forum.. thank you for listening... I have called Pyzier and told them as well.

I am a 38 year old female, not overweight but hbp runs on my dad's side of the family unfortunately! I was prescribed Diovan by my doctor who had a list of my allergies. So, i went to get it at walgreens and luckily they have my allergies also because this drug is a sulfa drug and I am highly allergic and they caught it before i took any. You would think my doctor would have done a better job as I could have gotten really sick. YOU NEED TO BE YOUR OWN ADVOCATE WITH THESE DRUGS DOCTORS ARE PRESCRIBING, YOUR LIFE DEPENDS ON IT! At that time my doctor then called in LISINOPRIL. I just got off of being on it for 10 months with horrible, horrible side effects.
If your doctor has prescribed LISINOPRIL for you, please look the drug up on this site before taking - WARNING! There are 1,800 entries from people who have/had debilitating symptoms. I have now chosen to be off of HBP meds for a while and monitor it 3 times a day and see if i still need to be on it. After what i have been through, i would rather run around the block 10 x's a night and change everything I eat and drink and lose weight before I would consider another pill!

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.

Was on Vytorin for 2 years & experienced no noticeable side effects during that time. It lowered my cholesterol to 179. Had a hysterectomy (complete) in Dec., 2007. In May, 2008, I began a sudden on-set of severe numbness in both hands (especially when lying down)--classic carpal tunnel symptoms and intense pain in all joints. When I move from a sitting position to stand up, I can hardly do it. This is what I thought I would feel like at maybe 80 years old--not 46 yrs. I thought maybe it was because I'm not taking hormone replacements, but my doctor said it could be the Vytorin & he took me off of it. I've been off for 2 months, but the symptoms are not improving. The carpal tunnel seems to have lightened up a bit, but the joint pain (especially hips) has not gotten any better. I wonder if it ever will????? Also experience fatigue, foot pain, & weak fingers.

I am a 45 yr old female and I have been on Vytorin for about 2 yrs or so for my cholesterol problems. Was on Lipitor before that and was getting leg pain so I stopped taking it. When blood work time came around it was still up so my doc put me on Vytorin. I have noticed that I feel like I'm dying. I have severe neck,back and arm pain, cold and hot attacks, can't sleep, chest pain,blurred vision, sudden stomach cramps, nausea, throat and ear aches, and bad stomach problems. I have had heart cath, ekgs,endoscopy, blood work and everything keeps coming back normal. Matter of fact, I went to the heart doc today and he put me on a 24 hour monitor and for low heart rate that has gradually gotten worse over the past few months.He even mentioned a pace maker. I don't even want to start about the depression and anxiety attacks that I have. They are AWFUL. But the more blogs that I have read, I think I know where the problem may lye. The Vytorin, so as of tonight I will NOT take another one..I just hope that there is no permanent damage done as far as my liver. I hope you all the best and I will let you know how I start to feel in the next few days...

I am just starting (hopefully) to come off the Medication Ride From Hell. I I am 61 and take estrogen, diovan, vytorin, boniva, and just started back taking Prozac (1/2 dose) after this fiasco. Two weeks ago today I started having pain in my face like I got hit by a MACK truck for 5 days, especially one tooth hurt if I touched it. Then on Tues, I went to dentist, took x-ray, no abscess. So figured sinus infection. Wed I go to have epidural shots in my back for 3 bulging discs. But I had a slight fever and suspected sinus infection, so they would not do an epidural, for fear of introducing bacteria into my spine which could result in paralysis. OH BOY So this doc gives me tramedol 50 mg for pain in 3 of my discs. Eventhough 2 ibuprophens work great, I can't take advil because of stomache issues. I am sensitive to meds, so a little goes a long way. So then back to my reg doc who gives me AVELOX . And now the nightmare begins......At 7:30 pm I took Avelox and 1/2 half of a tramadol (never took either one before). Around 9:00 pm took another 1/2 tramadol. Figured I was tolerating well. At 1:30 a.m. took a whole one. (RX is 1-2 3 times a day) A few hours later I wake up itching all over. By 5:30 a.m. the slightest move I make I am spinning and nauseous. Fall back to sleep, get up and am having vertigo and nausea. I think maybe a little sprite will settle my stomach. I immediately throw it up. My body feels paralyzed with muscle spasms, pain and extreme weakness. Also pain between my shoulder blades, heart palpitations, sense of panic, extreme heaviness in my limbs, headache and continued dizziness and nausea. Felt as if I had a slab of concrete on top of my chest, as if the muscles would not move to let me breath. Call my hubby home. He takes me to urgent care, they started an IV ad then because of "possible heart symptoms" they ambulance me to the hospital. At hospital, they gave me anti nausea meds in IV. The ride in ambulance was a big blurr. My first time in 61 years ever in an ambulance. They confirmed my sinus infection with a CAT scan which probably ruled out some other things too. I leave hospital around 5 pm and am feeling somewhat better, as all meds are now out of my body for about 15 hours. Fri, no Avelox...took a break. Sat, Sun took it and all the symptoms came back except for the vertigo and nausea which was caused by the tramedol. Skipped Monday, to test theory that it is the drug. Take it Tues, within 2 hours symptoms back with a vengeance and major panic attack out of no where, hearting pounding. I am at work so I manage to get through and when I get home I collapse in chair and can't move. Finally Wed I said thats it NO MORE AVELOX. Thurs, back to doc. She gave me Bactrim DS. I am still having some muscle weakness and fatigue. Woke up at 11:30 a.m. and took pill around 2:00, fell back to sleep around 4:30 pm with spasms in upper back and shoulders, causing weakness in my arms. I hope I can tolerate the Bactrim for the next 9 days and my side effects let up. The doctors and pharmacist look at you like your crazy when you tell them what happened. When I found this site I was so relieved when other people described the same symptoms as mine down to the smallest details. Thanks for being here.

every day my feet, legs up to knees, hands and up to mid forearm and face become tingly, numb and very weak to where I cannot get out of my chair or out of bed. Sweaty and chilled, headache, neck ache, thirst. I am on vytorin10/80. 63 yr old female. It sucks!

I'm 44 and have taken Vytorin for several months. Having a lot of the symptoms listed. Has anyone had a problem with the heart skipping beats? I took myself off the stuff yesterday and already I feel a lot better - not great yet but I'm hoping thats to come.

In Feb 2007 my primary doctor took blood tests and put me on a diet because I was 100 pounds overweight with fatigue symptoms. Blood Tests indicated I had diabetes (126 mg/dl) based on an FPG, and high cholesterol. The FGS was repeated and it dropped to 115 mg/dl. I have been on a low sugar low fat diet since Feb 2007.

In June 2007, I was put on Vytorin (Statin Drug) for Cholesterol. I also saw an Endocrinolist who determined I was a Predibetic and had also Reactive Hypoglycemia based on an OGTT, and determined my fatigue and neuropathy problem was not due to diabetes. She recommended a Rheumatoligist to me in September of 2007.

In late September of 2007. I saw a Rhematolgist for my sleep problems and fatique problems. I had severe muscle fatique (firing pains and numbness), chronic sleep disorder. breathing difficulty during day and when sleeping, difficulty swallowing, vision problems, fluctuations in FBS between hypoglycemia and hyperglycemia symptoms.

He determined after physical examination I had Fibremalagia since all test points on my body were sensitive to touch. He also had his lab do repeat and other blood tests (CPK, Aldolase, etc..), and prescribed a sleep study done by a specialist in my area. He took me off all Caffeine and Vytorin immediately (As I have been off it since that date). He prescibed Diclofenac for Inflamation, Citalopram 40mg for stress and anxiety attacks, Zolpidem 10 mg for Sleeping, and he requested I continue monitoring my blood gluecose twice a day.

After Leaving his office I made an Appointment with the Sleep Study Hospital to have the test done the following week. The study indicated I had Chronic Sleep Disorder where my breathing would stop anywhere from 30 seconds to two minutes during the night. The Sleep Order doctor also indicated that there was something else wrong with me out of his expertise.

In early October 2007, my Rheumatologist contacted me by phone and requested me to leave work and come to his office that afternoon to discuss my blood work. I was scared since they would not discuss it over the phone. The doctor dislosed my blood results and was concerned with a CPK of 2600 (should be less than 155) and my Alolase was six times higher than normal. He suspected I either had Polymyositis (not cureable, but treatable) or Inter-myositis (not cureable or treatable). He said he did not want to start treating me with a medication for it until he knew exactly which one I had. He said the only way to find out was to do a muscle biopsy (about the size of a pencil) on one of my large muscles preferribly a Thigh muscle.

In mid October 2007, I was scheduled to see a general surgeon and a week later I had a minor operation to remove a pencil size piece of my left thigh muscle. It was analyzed by the Childrens Hospital in New Orleans who were experts in the muscular diseases.

In Late October 2007, I was diagnosed with severe myopathy caused by the Statin in the drug Vytorin.

I remain on the same medications, have my blood tested every three months, and the CPK last indicated a reading of 900 (still very high, but it dropped all most 2/3 of what it was six months ago. It can usually take a year or so for most folks my age to fully recover, some do not. I still have the same symptoms, but the firing pains have subsided. My vision had also drastically changed, so I saw an Opthomoligist after providing her all my past records. She indicated I did not have any Renal disfunction which is good.

All the doctors agreed I should continue the stress, sleep, and inflamation medication and none of them have any reported inter-related problems. I am also on an AUTO CPAP machine when I sleep because I have two kinds of Atnea that affects my breathing (muscular and brain related). My breathing patterns seem to change quite a bit and my pressures vary from 7 to 20 and more so on the high side.

BAD BAD BAD BAD BAD! I took this drug today and thought i was going to die from a heart attack. I began getting palpitations and then it progressed into a full blown panic attack. Thank god I had some Xanax to bring down the side effects. But now I just feel out of it and foggy. I almost called 911, it was that bad. I felt like I couldn't breathe, like there was something standing on my chest. I called my doctor right away who said they had no other samples, that Avelox was the only thing they are really getting right now. That seems really odd to me that a drug like this is on the market with so much negative press and yet its all our physicians have on hand for people like me with no insurance. PLEASE DONT TAKE THIS DRUG, it is terrible...

My son is 8 and has been on Singulair for 4+ years. When he was as young as 5 he said he should just throw himself off of our staircase and in first grade, age 7, he told a friend he wanted to kill himself with a knife or scissors. I have taken him to psychiatrists, psychologists, pediatricians and guidance counselors and none have linked it to Singulair. I spoke with our allergist and he said to take him off of it. He said their office was not notified when Merck changed the side effects last year. Obviously the fat cats at Merck are enjoying their big bucks with little regard for the people taking their drugs, look at the new evidence about Vytorin-it does not work yet they have made millions on it. They knew it did not work 2 years ago. I am so happy that I now know this drug is dangerous. We will stick with our Nasacort, Clarinex and allergy shots, which are helping tremendously. I am planning on getting off of Singulair for my asthma as well. It is not worth it. There are too many reliable drugs out there to waste my money on the suicide drug! I am on Asmanex and may add or change to symbicort. I am so sorry some have already committed suicide because of this drug.

55 yo male. I started Vytorin (20mg zocor) in Jan of 2007 until May of 2007. I lowered the dose to 10mg in March but am still suffering side effects (3/29/08) It did lower my cholesterol dramatically but at what price?
I began having tingling/burning in my feet and shins. Also, muscle pains in my calves and something like shin splints. I had been very active but have not fully recovered. B-12, methylcobalimin, has helped the tingling. I was taking as much as 10mg per day. Also, L-carnitine for the muscles, CoQ10, and Ribose. I do feel like I am gradually improving. The tingling is much less but my legs are weaker than before.

I think all of you folks with side affects are are blaming your ills on Lipitor rather than putting the blame where it belongs: on your own mental health. I am a 65 YO male and I have been on Lipitor for more than six years now. I have no side affects, I work out four days per week with cardio and weights and feel that Lipitor should be added to the public water supply. My total cholesterol has gone from the high two hundreds to under one-forty on a single daily dose of 10mg. All of you hypochondriacs get a grip.

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!

a lot of pain on the right side , back pain, nausea, gas, lots of stomach distress