New zealand symptoms and conditions

In 2007 I was diagnosed with HBP and enlarged prostate at the same time. I was working and had medical coverage with my PCP at Nova Southeastern University. The doctors there are very good. They put me on Terazosin for both. I quickly developed severe rash, hives, swollen face, neck, throat, etc and had to go to emergency. They took me off Terazosin and gave me Flomax for the prostate and Lisinopril for the BP. The Flomax works fine-noside effects that I can tell except decreased semen production. I am a 58 year old male. But I quickly developed a cough and the took me off Losinopril right away and put me on Diovan, which worked great with no discernible side effects. Then I lost my job and had to go to the VA for my medical in January of 2009. Because my medical history included my emergency visit for a severe anaphylactic reaction to Terazosin, they allowed me to stay on Flomax. But I had no such record for the cough caused by Lisinopril. So they insisted that Diovan was too expensive and I had to try Lisinopril. Despite my complaining about the previous experience they insisted. I was given a little pink pill which did cause me to develop a minor cough. But being a good soldier, I decided to live with it. Then in August I noticed that my refill no longer had a pink pill but a larger yellow pill. And that was when the problems started. I first felt like food particles were stuck in my throat and nothing could get them out. That feeling would eventually disappear on its own only to later return. I visited the emergency room several times with severe flu like symptoms, including a severe cough. I also discovered a yellow film covering the back of my throat. And my tongue had a thick yellow coating on it that went all the way to the back. In some places this had strands that extended above the back of my tongue for about a half inch. In addition there were bumps on the top of the back of my tongue. This stuff could not be scraped off. The emergency doctors would examine my mouth and throat, tell me nothing was wrong and refuse to take a throat culture. They scheduled an appointment with ear, nose and throat and then canceled it. Eventually they scheduled a CT scan, which showed nothing abnormal. Finally my PCP examined me and said I had a severe allergic reaction to Lisinopril. So a week ago she took me off Lisinopril and put me on Amlodipine. I'm actively researching the side effects of that and will get off if I see anything I don't like. But my goal now is to find natural substances to treat both the enlarged prostate and the HBP. The yellow coating on my throat is beginning to disappear. Still no difference with the yellow coating on my throat. I believe I have seen slight improvement in the cough, but not nearly enough for my liking. I worry whether I will ever be able to get rid of it. I do have more energy now. Any idea how long it will take to get rid of this cough?

I am 17 years old and i got the three vaccinations of the Gardasil and ever since than i have experienced a lot of pain in my lower stomach area all the time like i have cramps. I have lower back pain all the time. Migraines run in the family and i usto to get them once in a while and now i get them at least four times a month. I dont know if this has anything to do with it... but im in pain all the time and, my mom wont talk to me because she thinks im lying and i dont know what to do.

Not a new, but seemingly common side effect, i just recently noted could be from Lipitor.......all over achey dead weight feeling, difficult to motivate and move without great fatigue an achiness....totally out of character & even herbal energy, once helpful was completely non effective. Also have arthritis and a knee replacement...knee ok but rest of body next to completely seized up, including hands, hip, sacro iliac, foot, and extreme neck stiffness and pain. Being a retired nurse i should have noted side effects, but attributed to another BP pill which was stopped... Of course absolutely no change and now tripping to chiropractor and acupuncture hoping to get this body going again, especially with much needed walking, post knee replacement. Also i had gained wt, maybe 10-15lbs in 6 months, but when lipitor ws recently doubled, i gained even more in a 3 wk period, and my midrift is cellulite lumpy looking, unlike ever b4, with my normally preferred very active lifestyle, that is now difficult with probs occurring. The chiropractor alerted me to the potential Lipitor side effects, but i know my cardiologist would not agree with this theory.....so afraid to mention, unless there is some conclusive test to be done. Otherwise they say everybody always wants to complain or blame probs on meds, if nothing else suits the situation. I have discontinued the Lipitor, just for 2 days so far and pray i will feel back to myself asap. Now of course i am torn with the lack of prevention of atherochlorosis and future bypass surgery as in father's family.... Feel like damned if i do and damned if i don't.....so definitely empathize with most. Thanks for commoradery and hoping i am not just becoming a cuckoo hypochondriac.

i recently took glucosamine chondroitin 1500mg a day
for 3 days and on the 4th day i woke up with
itchy red bumps all over
I attributed it to the glucosamine/chondroitin that i took
On the simivastin bottle it says to avoid herbal remedies

I am hoping these bumps will subside, they are very itchy.

I started feeling much better very quickly after being off Lipitor now 7 months. However, the symptoms I had using the RX has cause significant problems. I fell so many times with my weak joints and muscles, that I had severe problems. I now need to have knee replacement surgery after falling so many times injuring my knees and weakened muscles to support myself. I am getting cortisone shots in that knee, as well as physical therapy. My MRI shows a torn meniscus, stretch PCL very thin, cartlidge loss and debris, still swollen with csyt after all these months. With no meds, and lack of being able to exercise, I now have hig-chol back. On and on it goes.... a real catch 22. Take care of yourself, watch out for symptoms. I ignored sx's thinking it was stress but after reading adverse reactions, it fit me to the T.
My original posting re: Lipitor is Forestseaski on Jan. 2, 2009

C.

I have been on Lipitor for almost 5 years. I started with a low dose of 10mg for 3 years but my cholesterol did not come down significantly enough so the dose was increased to 20mgs two years ago. I have noticed my hair thinning almost immediately after being put on Lipitor but when the dose was increased the hair started falling out where now it is noticeable, at the front along the hairline, on top and at temples. It has become another problem, at this point, like having high cholesterol. It seems to be happening now at an accelerated rate and my scalp is visible from my hairline 3 inches back. Styling is now impossible without coming the hair all the way forward from the crown, what's left of it. I had no idea hair loss was a symptom of Lipitor until I thought about when it started and the fact I take no other medications. There is no history of this type of hair loss in my family. The Lipitor brought my cholesterol level down to preferred levels but if I stay on it much longer I will be bald on the top and sides of my head. I'm worried it won't grow back.

been taking 20 mg for several months, stopped it for about a month, and started back taking it at night for 1 month now. It seems that every time I bump my hand or arm it turns into a bad looking blister, someone asked me tonight if I had poison oak, which I don't. I have had blood tests and everything is normal. It really looks bad.

my mom has been on simvastatin
40 mg for 3 months & she has had
back pain leg pain & know kidney
failure she is a diabetic but never had any problems before but taking tthis medication it has ruined her life plus she gets lots of night mares & night sweats she
feels & looks like she is drunk
but she has never drank in her life

I am a male, 61. and have a history of switching around cholesterol meds, most recently because of cost due to my high number of medical conditions and large number of medications for, but not limited to: CAD. CHF, diabetes, hypertension, renal impairment, and herniated disks. I have barely been on zocor a month and have experienced extreme weakness, pain in neck, shoulder, hands, legs & feet. Because I have both cervical & lumbar herniations, I was somewhat uncertain until I began reading these posts. I took myself off zocor yesterday and emailed my doctor's nurse. It also occurred to me that after any length of sitting, my legs hurt upon standing while i was on Lipitor, but don't really recall other symptoms. Sometimes, when you have a number of health issues, you come to believe this is "as good as it gets," but now I believe differently, otherwise why bother with the meds at all.

I have been taking 40mg lipitor for over 9 years now.

I have had back issues since an injury to one disc (L4?), and had microdiscectomy in 2001? Took about two years to actually get close to normal.

The last few years, I have had multiple issues with shoulder pain, wrist pain, elbow pain, lower back pain, Upper rump muscle pain , and now both hips are killing me (the shoulder, upper rump muscles and hips are by far the worst). And I am now so weak in my lower back muscles, that it feels like I will (and do) pull out my back.

I have seen NO many doctors I can't even name them all. I have had operations, multiple injections (cortisone) taken pain meds, etc. Nothing has helped and in the last year and a half, I have gotten steadily worse. To the point where I can't really do much of any activity. Sleeping at night is painful. Can't lie on left shoulder, and can't lie on either hip for more than a few minutes. If I fall asleep on my side, the pain wakes me up. When I try to walk, 80% of the time, I end up with a pain in my upper right rump (sacroiliac area), that I MUST sit down to get the intense pain to go away, which it does. But comes right back when I walk again.

I have had x-rays, MRIs etc, and never reveals all that much. Disc issues, yes. NOt much else.

Recently, I have begun to get a nasty clicking (catching) on my left jaw (joint?). Not really painful, but something definitely wrong. My dentist sent me to his Chiro. I went and liked him right away. I had gone to another chiro for years and I believe in them. But this one is the best I have seen.

Anyway, one of the FIRST things he suggested, was that it was POSSIBLE that the Lipitor is causing all of my problems. Put me on COQ10, and doing multiple adjustments and treatments. I will be seeing my regular doctor 5/26, and my chiro wants me to see if he will take me off lipitor and put me on Niaspan instead.

I guess my question is: Can Lipitor be fine with me for so long, and then in such a short period of time, turn me into a compete wreck from the pain and wasting away of my body/muscles? I've told doctors for over a year now that there is SOME connection as to all these issues and pain. One Doctor, of course, gave me the "you are getting old" bull. Yes, I am 56 yrs old. But I understand the process of getting old, vs the complete failing of ones body.

Also, IF it is the Lipitor, can it possible all go away? Or should I expect some damage forever?

One more thing, the last ortho I went to the other day for a second opinion, wants me to do a EMG, to see if there is muscle damage. I was not planning on doing it, but wonder now, should I? He was not doing it because of lipitor, as he never even talked about that to me. I had shoulder operation and have not had the results I feel I should have had.

hi
I was on a stain for 1 1/2 years on a 80 mg didn't effect me at all, me and the doctor decide to bring me down to an 40mg my chol was at 119 now
on the 40mg for 3 weeks and all hell breaks lose.my joints and mucluse and my feet just hurt,i was walking like an old 100 year man,I took myself off now 8 days much better maybe at feel 80/90 percent better,lease im walking better joints still hurt a little,still cant sleep used to sleep like a rock now its like 2 maybe 3 hours a night and wicked night sweats,lets hope I sleep better in a few
im so glad I found this site,THANK YOU EVERYONE for letting read your letters

I have stopped taking Lipitor after 3 yrs. I was told I had a mini-stroke because of my slurred speech 6 mo. ago. Since then I have had a battery of tests and my neurologist told me "I don't think you had a stroke." I saw the words "Motor Neuron Disease" (I looked it on the web because I never heard of it before) on the script for my EMG. I blame it all on Lipitor and the wasting of the nerves and the muscles. I sound as if I am drunk. No one can understand me . I am taking speech therapy but it doesn't seem to help.

After many months on Zocor, I began to experience sore knees, stiff legs and sore lower back. All at once, in about a one week period, I could no longer walk. My leg muscles were completely gone. I have been for xrays, MRI and more. I am convinced it is the zocor and have quit taking it, however after almost a month without, I still cannot walk without support. My upper body is fine..Right leg better than left leg, left leg almost useless. No more statins for this 71 year old and used to be VERY active male. I hope I can get it all back.

Has anyone experienced heart palpitations from taking Zocor? I've been on it for 6 months and about a month ago started having palpitations that are becoming more frequent, like daily at this point. Went off Zocor yesterday just in case that is the problem. Has anyone else had this symptom?

Hi . I am a 69yr old male. My doctor has recently increased my Lipitor from 20 to 40mg. My cholesterol reading was 3.6 which he considered to high after a quad bypass. I am suffering painful cramps down the front of both lower legs as well as cramps down the back of my lower right leg. I plan to revert to 20mg to see if the cramps stop. I am not sure if I should stop completely.

I am a 65-year-old female. I was given Lipitor 10mg in Feb 07, which I appeared to tolerate, with the effect of reducing my high familial cholesterol. Because of a genetic enzyme problem, I am careful about my diet; having been a vegetarian for decades. I don’t smoke, and rarely have wine. By May that year my GP increased the dose to 20mg., but days later I was sent to A + E with cardiac concerns. The hospital adamant it had nothing to do with Lipitor.

By mid 2008 I told my GP of dizzy spells, and loss of balance, also swallowing difficulties, but after liver function tests I was reassured it couldn’t possibly be Lipitor.

Early October 08, saw me in hospital with a ‘stroke’, although the CAT scan and MRI were puzzling. I was sent home with no help or guidance after the Consultant insisted Lipitor was not a problem, and I should not reduce it, as it was already a very low dose. Unable to walk to the end of my street, my calf muscles feeling as though I’d run a marathon, and experiencing cardiac stress. Severe neck and shoulder pains, and confusion with words. Frequent muscle spasms in my feet, legs and hands, etc. etc. No energy for anything, and so difficult coping - living alone. End of Dec. a friend from out of town visited, and was alarmed, as she’d researched a web site for her brother, who was using a walking frame. I was astounded at the reports from users of Lipitor, so many suffering in the same way. Although my GP had arranged more laboratory tests for me, I was not prepared to wait.

On 6th January 2009, (almost 2 years later) I reduced my dosage to 10mg., and within days was experiencing improvement in many areas. By 17th January, I reduced to 5mg., (maybe a little hasty) and by 24th stopped it. By 28th my GP could see for himself, the considerable improvement generally, with a lower blood pressure reading.

By then, I could complete half, of what used to be my regular walking regime. To date, I am able to cover more than that, and hope I will eventually be able to cover the full distance. I’m hoping there will be no lasting damage, but am so thankful that my friend found this website. Its scary to think I had no quality of life, and doubt I would have survived more Lipitor. So I’m taking my chances with high cholesterol, and a near normal life.

M.

New Zealand

Been on Zocor for two years went from 20mg to 40mg and since being on the 40mg I have increased leg & foot cramps so severe @ night that I have trouble getting out of bed, the foot locks up. Even getting up after sitting is a problem, sometimes my feet and legs go numb and I even fell a few times. I get very tired during mid day. The newest problem is my sight, I have notice that there is a blurriness that I don't know if it ever clear up, after telling my doctor this she said it was the arthritis and to take arthritis nonasprin and to stop the zocor for about a week, I am going to stop period.

I am 71 years old, I have been taking 80mg of ZOCOR ( Simvastatin ) for the past 16 years. five months ago I started to hurt in my lower back, hips,Knees,thighs, for two months then it traveled to my shoulders, wrist, hands, fingers. the Dr. gave me a round of prednisone (one shot and 11 pills) the pain stopped and everything was wonderful for two weeks,the Dr. stated that I had avused my body in the years gone by now the pain has started back in my shoulders, wrist, hands the pain is very strong,and my legs are starting to get weak again, I am taking Naproxen 500 mg two times a day and also taking Hydrocodne10mg every four hours also have Oxycodone 10mg to take every four to six hours, I have mentioned the results that I have read about the Statins in this forum but the doctor, does not act like it has any significance. does anyone have any suggestions??? if so please let me know, this pain is killing me, if you have any info. please email me at. ******

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.

I have posted here before. I have been off the lipitor for almost a week, now. I am still feeling dizzy and wobbly. Does anyone know how much longer I should have this side effect? Also I was reading that elevated cholesterol levels and MI's and strokes can be caused by elevated homocysteine levels.Anyone been tested for this in your blood?

I'm a 47 male and took Crestor for a year. I experienced muscle tremors, constant fatigue and muscle soreness. Not just a little sore but as if someone had hit me so hard as to leave a muscle bruise in both arms. One night my left arm and leg began to tremor and it was as if they were too heavy to move.

What I noticed was that all of my little aches and pains became severe aches.

I experienced blistering on my hands, a common side-effect of your liver rejecting the medication but my doctor didn't pickup on the symptom. Instead, he gave me a steroid-based topical cream that actually eliminated the blisters but they would return within weeks.

I experienced lapses in my memory and I started to forget words. I would forget the names of things and I found myself substituting the word 'thingy' when I could remember what something was called (like a phone).

I visited the hospital 4 times and my doctor countless time. Each time my doctor treated the current symptom and not the person as a whole.

It became too much to bare when I started having chest pains that felt like something was crushing my chest. At this point I started to do some research and found forums like this one.

During my time of the worse pain, I felt like I was actually dying. I started to get my effects in order and finalized my estate.

I stopped my Crestor about a year ago, after about 3-6 months my muscles began to feel better. After a year, I am finally starting to feel like my old self again (not that I was all that well before).

Statin affect people differently, but there is NO DOUBT that these drugs can have adverse effects on people. Listen to the commercial for Lipitor, "contact your doctor if you have muscle fatigue or weakness"......

I took Lipitor for about 6 months. Right after I began taking it, my legs, especially my right leg began hurting. I got off the drug at 6 months because my legs hurt so badly I could not sleep at night. I just had X-rays of my right knee done, and I have almost no cartridge left on my right knee cap. I now may have to have knee replacement therapy. My doctor that put me on the lipitor said that it was not the lipitor that caused. I think it is very odd the pain began when I started the drug.

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

I got my Mirena fitted 5 weeks ago. After the 1st week I could feel myself starting to become really low, my head began to get ‘foggy’, total lack of motivation and the headache from hell. This peeked at 3 weeks when I became very depressed, snappy, anxious, extreme tiredness, tearful, severe headache and an inability to concentrate – my brain felt it had no depth to focus or absorb anything. I also felt I was standing on the outside, looking in! I had a similar but far milder reaction to the POP so recognized the symptoms immediately.
I went back to the doctor and tearfully explained how I was feeling and how I was convinced it was a reaction to the Mirena. She totally dismissed this and said she felt there was a lot more to it than that and started talking about PN depression. She also said that in the 16 years of fitting the Mirena she had never experienced anyone with these symptoms. I assured her I was not suffering from PND, but in my ‘fragile state’ wasn’t capable of arguing my point and began to wonder if she was actually right, so what a relief to discover this web-site! I also found a great document issued by the New Zealand Medicine and Medical Device Authority, a Government Agency (http://www.medsafe.govt.nz/Consumers/cmi/m/Mirena.htm ) acknowledging that all the side effects I was experiencing were all common occurrences in between 1 and 10 in every 100 patients – it also acknowledges virtually all the other symptoms everyone else is listing and states that ‘These side effects are more common during the first months after insertion’- so why wasn’t my doctor prepared to accept these symptoms when they are officially recognized in other countries? Are the drug company bonuses more important than patient health?

Anyway, 5 weeks on and my mood has lifted, deep down I still feel low, but my normal self is sitting on top of it. I still want to snap at the kids, but I can control the urge to do so! My head is still foggy and I still feel detached from everything, the headache is still there and I still can’t concentrate / absorb anything! My fingers, knees and wrists now get really stiff / sore and the back of my neck aches when I wake every morning. Fortunately, I haven’t had any cramping or much spotting.

I am due to get it checked in 1 weeks time, but have decided to get it out and hopefully get it replaced with a non-hormone coil. Heavy periods seem great compared with how I’m feeling right now!.
I can’t wait to get back to my old self!.

Hi I started taking Lipitor when I was about 41 and gradually noticed a big toe becoming numb. Then later another toe became numb. I had just started swimming about this time with fins and thought at first it may have been caused by them. But then I stopped swimming and the numbness continued. I visited a Neurologist a couple of years ago who tested for everything and found some peripheral nerve damage to the feet. I said the only thing I could think of was Lipitor. He said here was no conclusive evidence it causes this but explained how nerves are made of Lipids and lipitor limits the production of lipids. I stopped taking it but later my GP said I need to go on something for my cholesterol. He put me on Crestor. I took a Lipitor the other week and my toes tingled that night. So I am convinced it is Lipitor. I am not sure how to reverse the damage though.