Poison symptoms and conditions

Dizziness, back ache, severe hip and shoulder pain, transient global amnesia, after discontinued taking of Lipitor, speech problems, loss of words.

I just stopped taking Yasmin after 2 weeks. I was previously taking Yaz, with no major side effects other than an increase in mood swings. The Yasmin has felt like poison! I had severe abdominal pain, nausea, fatigue, chest pain and a general feeling of being sick. Since I have stopped taking it I am starting to feel better but I feel like my body is still trying to recover. Do not take this pill, please try something else.

It took me forever to get this poison out of my system. Took 11 months to figure out what was causing my skin to look grey, itching head to toe, female infection, horrible stomach pain and more.....for some reason doctors are denying these side effects. I was put on it for slightly elevated blood pressure. Like everyone else you want to trust your doctor but you have to be your own advocate. If you think something is not right then do something about it and don't rely on another human being with a medical degree to let you know when you can quit taking poison.

I finally stopped taking Topamax because of the side effects. But the worst was getting kidney stones from it. I only drink water and drink a lot, but I still got stones. The first time I was in so much pain that I could barely stand it. The second time, I had the pain and with it a kidney stone that was too big to pass. I could barely urinate. Had to have emergency lithotripsy to remove it. The doctor did a CT scan recently and it showed I still have many stones in both kidneys. I can't take another one of these attacks because they are so painful. My neurologist gave me a natural remedy for migraines called Petadolex. This stuff works! It has made my headaches much less severe when I have them which is not very often and my daily low level headaches are gone. This stuff is made in Germany and can be found in most health food stores and pharmacies. It also cost a lot less than Topamax.

When the generic Topamax (topiramate) came out, my insurance company wouldn't cover the real Topamax and it was costing me $400 a month if I wanted it over the generic. The generic was the worst drug I have ever taken. It is NOT the same as Topamax. I got so ill off of it that I had to get back on Topamax. I am finally off of Topamax completely after decreasing the dosage over many weeks. I was on 200 mg a day. I had all the side effects too like tingling hands, cognitive impairment and depression along with some others. This drug is poison and I am so angry the manufacturer didn't state all the possible side effects when they knew damn well it had them. There is a class action lawsuit against this manufacturer for not disclosing some of the horrible side effects.

Hello everyone! I am a 28 yr old male, and I have now been taking this drug for about 1 1/2 yrs. What is so overwhelming to me is that I have been having some of these side effects, but it never occurred to me that they may have been caused by this medication. My side effects are not major, but they do really affect my self esteem and I think have some what depressed me a bit.

None of us have direct physical evidence that this medication is the cause, but I don't think this is a big coincidence. Below are what I believe may be side effects of this medicine:

Unlike before I now feel:

-Anxiety (im always nerves, and was blaming debt for it)
-Decrease in sexual drive (also blaming my financial problems)
-Joints popping all the time (blaming my gaut)
-Bigger forehead because of minor loss of hair (blaming age)
-Problem falling asleep (blaming financial problems)

and again im always scared, even if everything is ok (ive been holding together because on the other hand, since i was born, I have always been a very strong minded person). This is really depressing because two years ago, nothing would be scare me, I mean nothing, I was afraid of nothing. No matter what time it was, or what situation I found myself in, my buddy down south would be ready for action, now when im going to have sex, im all worried hoping that it works!, (dont get me wrong, it works like 90% of the time) but before it would work 200% of the time, i mean i was turned on by a damn broom, and now its not the same. This really *ux!

I have been blaming everything on my financial ruin that I am currently in, but am having second thoughts on what is causing all of this. This site has really opened my eyes and given me a whole new theory and even hope.

I once asked my doctor that if I went home and got on a diet, exercised and did all that was necessary, would he consider taking me off the pill or lowering my dosage and he immediately said NO. I mean he almost didn't even let me finish asking. He told me that If i wanted to go in a pine box to stop taking it. So he scared the crap out of so I have not stopped taking it. I can afford to go to different doctors because i don't have insurance or money to pay for the visit. I wonder if this doctors has advised me based on his financial convenience. I mean is it possible that a doctor may lie? I never thought doctors would lie. Im afraid of just getting off the pill, im afraid that all the doctors are going to tell me not to get off of it. my bp is usually about 130/85 some times up to 140/90.

I would appreciate peoples thoughts on what I should do?

Thanks everyone that takes part in this blog! it is really helpful for people like me that have no money to get advice.

Hope everyone makes the right decision!

Regards!

I took Zocor for 25 days when I suddenly had such pain at night in my upper arms that I couldn't raise my arms up at all. It's been 2 full weeks since I stopped taking Zocor, and every single night around 7 I develop severe pain somewhere in my body, usually in my hands, knees or feet. It's in a different place almost every night. Tonight it's in my left hand across the whole top of my hand, below the wrist. Can Zocor cause this kind of pain so long after stopping taking it? And I only took it for 25 days! Please help - this really hurts and I hope it will improve.

I have been taking 20mg Lisinopril for six days for 140/100 BP reduction. Muscle cramps, muscle pain, dizziness, ringing in the ears (which I already had, but this medication has made it MUCH worse),some heart palpitations...generally scary and, on balance, I am going to find some other solution. Frankly, this is like taking a slow acting poison.

I went on this POISON Yasmin for a year then went off after I gained weight. I proceeded to lose so much weight after I went off that I lost 40 pounds by doing nothing different over the course of three months. I got so skinny people became concerned but there wasn't anything medically wrong with me. However, I also didn't have my period for over a year after quitting Yasmin. I went to the gyno concerned but after a Progesterone test (which I failed) he suggested I just try going back on again with Yaz this time. I had my periods again of course but not on my own. They were hormonally controlled. After two months, I started craving food and getting anxious and stuffing my face as a way to cope with the mood swings and stress. This is was so not like me. Then I started to get horrible bloating and constipation. I had to use laxatives regularly to have any movement. After gaining 30 pounds and suffering in severe with the constipation, I decided it had to be the pill so I went off again. No surprise, I haven't had a period for 6 months since I've been off and while the crazy mood swings have gone away, I'm still having really bad GI problems. I have a sharp pain in my lower left bowel and I'm chronically constipated. After seeing doctors and running blood test which all ended up normal they still don't know what's wrong even though I tell them it's because of this pill. My gyno thinks I'm crazy, my GP thinks I'm crazy, and now I have a GI who thinks I'm crazy. IT'S BECAUSE OF YASMIN/YAZ!! This is POISON. Do NOT take this or give it to you kids. I'm just praying I can heal the pain and the constipation soon because I'm starting to limp and all the doctors have told me to do is eat a different diet. I've been eating cooked fruits and veggies for almost a month now because that's the only thing I can eat without severe pain. And I'm a 24 year old healthy girl who exercises every day. I am beyond amazed this crippling drug is still on the market place.

My whole life 120/70. Two months ago 160/103 wtf. I am on my second month of lisinopril. I am pretty sure it has caused me to be absent minded and grouchy. I was never these before. Worse yet for me is that I am a life long runner. I live to exercise so that I can enjoy the more fun things in life. beer wine and good food. ( I am 47 years old) I ran my first marathon 26.2 miles in January. I now have trouble running three miles with out getting fatigued, dizzy and winded. This sucks!!! any advice would be appreciated.

i ave a friend who has just had a bad case of the flu which has turned into pneumonia. her doctor out her on levaquin! i almost had a heart attack, called her and begged her to stop it. i sent her a bunch of info about it. why not put her on augment, something with less chance of adverse effects.
now i find she had a stroke over the weekend and is in the hospital! has anyone heard of anything like this on levaquin?

In addition to all I mentioned in my posting before, I am now having burning skin feeling and my shirt can't touch my skin sometimes without it burning, hurting.

Has anyone heard if this drug leaves your system or not???

After you read a representative sampling of this website's testimonials, you certainly ask yourself inter alia: Can this be true? Did thousands of people inject an antibiotic from the fluoroquinolone family, which crippled them for longer or for shorter? Most of us, I suspect, never really get beyond the initial litmus test: Did this medicine poison me or save me? (The answer depends, of course, upon the age, gender, medical condition, and most importantly, the DNA make-up of the individual patient. For hundreds of thousands of patients this antibiotic is a boon. For thousands of other misfortunes this antibiotic is a disaster.) But there is another important question here.

Who gains from self-revelation? To be sure individual sufferers gain certain emotional catharsis from posting their adverse drug reactions (ADRs) to levaquin. E-postings are one-way anonymous tracks that form ruts on a well-traveled trail of tears. Unless these postings are hoaxes written by mischievious gnomes, then they consitute prima facie evidence for a causal link between levaquin injection and sundry crippling ADRs.

Curiously, this e-forum cannot be used as a tool for organizing thousands of potential litigants who might coalesce under a class action lawsuit. Yes, we can analyze each other's anonymous revelations to see if they muster our respective sense of the "ring-of-truth" re: levaquin toxicity, and we may contact each other one-on-one, but no-one can harness this intoxicating communication's technology to reach simultaneously all respondents en masse as a bloc.

So, who wins? The emotionally unburdened e-poster who learns belatedly that s/he is not alone and that prescription medicine likely caused more pain than the underlying malady for which s/he is being treated? Or big pharma that continues to manufacture and market a medication that poses downside risk to many consumers who unwittingly incur more damage than therapeutic value?

Indeed, who wins in a forum where consumers anonymously reveal their symptoms and unconfirmed suspicions? The answer is big pharma wins. Pharmaceutical companies data-mine our postings to estimate the frequency and bredth of ADRs about which consumers complain. House statisticians estimate the ratio of active complainants : silent complainants, i.e., the ratio of complaints who show up on this website to the far heftier percentage of complainants who never post on this website because either they are technology-challenged or they are incurious. House actuarians proceed to estimate how much operating profits their employers must set aside to cover losses in out-of-court settlements or in awards made to plaintiffs in class action lawsuits.

I think this is how the game is played in a behavioral sink where billions are made in a deregulated marketplace that allows predators and prey to interact anonymously. Sorry to be such a downer, but I fathom only the desperate plight of tens of thousands of levaquin consumers for whom no monetary award ever will compensate them adequately for their suffering, and the hundreds of millions of dollars at stake in court awards if consumers ever brought to bear their aggregate numbers and draw a bead on their big pharma tormenters.

I think it a true horror and shame that pharmaceutical companies have not devised a test which determines in advance which patient safely may consume levaquin and which patient's DNA places him or her at risk. I suspect the genome technology is available, but would dig too deeply into big pharm's bottom line. The economics of "parachutes-for-everyone" is infeasible. We are all guinea pigs in a B-grade movie featuring Russian roulette, billion-dollar pay-offs, and an FDA that pretends not to know.

This is further to what I has posted here below on the 16th of October.(you may look at it for symptoms). My dad passed away last night. The doctors had administered steroids to him saying it is the only solution to healing him out of this in order to save his eyesight.I am crying to myself now remembering how he suffered those last 10 days of his life due to this drug. He had never experienced anything more horrible in suffering like this during his life. His death report says, cause of death: Steven Johnson's Syndrome.

If none of the other postings tell you to get off of this drug, I certainly hope this one will. I began taking 5 mgs. of Lisinopril after visiting my Physician due to back pain. I have been a runner my whole life and went in because I had pulled my back out. I was very nervous; hence the high blood pressure….I was told by the nurse that I probably had white-coat-hypertension. Anyway, after being scared out of my mind, by this Doctor, I agreed to go on this drug, even though, at 50, I had never taken any other kind of drug in my life….HATE DRUGS! I began having heart palpitations after the first day on this drug, and one month after taking this poison, I began experiencing severe itching on my head, neck, and top of my back. I had just visited my salon and thought it was due to hair dye, which I had never had allergy to before. The itching increased and then I started getting severe cramping of my legs. I called my Dr. and was told to purchase organic shampoo/conditioner/soap, and that the leg cramps were probably Restless Leg Syndrome. He told me it was DEFINITELY NOT from the meds. He told me to let him know if the cramping got worse as there was something else that he could prescribe for it. This itching went on gradually for about 5 months. I purchased ever kind of organic shampoos, etc. with no relief, and the cramping of my legs became unbearable. Then, in April of this year, every thing starting to happen. I began itching all over my body and when I itched, it left big red welts wherever my nails hit. After about a week of this, I began breaking out in hives here and there. Went in to the Dr. and told him that I thought this medicine was doing this. This Dr. assured me again, that this would not be the cause of this and told me to take Benadryl and come back the next day so that he could see if I was any better. The Benadryl helped immensely and upon the next Dr. visit, he told me that I had come down with some sort of allergy and it was NOT due to the medicine. Went home and itched my body raw for the next week. Now the hives had turned into huge welts with water in them and my body began swelling with each new day! I stopped this poison on my own and was told to come back in to the Dr. immediately. I was put on Prednisone and told to take massive doses of Benadryl and this idiot Dr. still insisted that it was not from the Lisinopril….my ankles, arms, etc. now were almost double in size and the itching was unbearable. The seven day pack of Prednisone didn’t do a thing. I will say, though that after three days off this poison, my leg cramping subsided and my heart palpations did as well. I decided to take this in my own hands and went to see another Doctor. The Doctor I had been seeing, I found out, owned the Center where he practiced, and I believe he kept having me come back just to make more money. By now, my entire body had huge sores and pits and scales on my skin….I felt like a leper. I went to a Holistic Dr. and told him my story and he could not stop apologizing for the agony that I had been doing through. He told me this was ridiculous. His nurse asked me if I had ever heard of Johnson Steven’s Syndrome, and told me that she thought I had it. I was immediately sent to a Dermatologist and given steroid shots….which did nothing. My skin was pealing off each and ever day in flakes and I itched so bad I wished I were dead. I underwent skin biopsy’s and blood tests which came back showing that I was overwhelming reacting to some sort of allergy. This Dermatologist, who was excellent and didn’t even charge me due to his concern for what I had been through, sent me to an allergist. My small stature body had now increased 25 lbs due to water retention and sores covering my whole body. I can not put into words the agony I was in. Upon the visit to the Allergist, he recognized immediately what I had. He said he saw this type of thing, (not this bad, however), often due to the Lisinopril. Why didn’t that other QUACK Doctor stop this from the beginning…I believe it all comes down to money! Anyway, after almost 6 months of the hives, sores, etc., I am finally seeing a bit of improvement. My legs and back and back of my arms are permanently scarred…they are poke-a-dotted due to the huge hives and massive sores, and I still itch all night long if I don’t take my Benadryl. Who knows what the Benadryl will have done to me in the long run. Please, please look into this medicine and all other medicines that you take. There are holistic, natural methods of getting your ailments under control. Through my experience, I have encountered the most money-hungry, unprofessional Doctor in the world, but I have also experienced the most considerate well-intentioned Doctors. Please do your homework, and find a Doctor that has your best interest in his sight. Through this ordeal the only thing that sustained me was prayer. I have always been somewhat superficial about my looks, weight, etc. and this truly was an eye-opener. It’s amazing what these medicines can do to you, and don’t you wonder if the Pharmaceutical Companies don’t know all of this and could care less due to their hunger for money?!!!! It’s gotten to be a sad world. God Bless!!

I am a 52 year old female and my bad cholesterol is fine but my good cholesterol is low. I have been taking Lipitor now for a few years and have numb hands and feet to the elbows and knees. My feet are extremely sensitive, worse at night and now I'm getting sharp pains that feel like a bug just bit me. My tongue is also always numb and I do get migraines.I have insane stomach issues and food intolerance. I also take medication for high blood pressure, acid reflux, & thyroid. I have now been diagnosed with type 2 Diabetes but control that with diet so far. Until four years ago I had nothing wrong with me. I am slim and healthy. I had a lump in my thyroid which was removed and there was a trace of cancer. Then like dominos all the other conditions lined up. I have had MRIs and all the tests and doctors insist that I am not a severe enough diabetic to have neuropathy. I can hardly wear shoes now and it hurts when I wear runners while I walk and exercise. Does any of this sound familiar to anyone? I hate that my health has become so much a part of my daily life. Does anyone have neuropathy as a result of Lipitor and am I even taking the the right medication since I don't have high cholesterol?

I don't know if I can blame Zocor on my weak thighs--my doctor says that muscle weakness as a result of the drug should include all of my muscles. I've also developed an extremely itchy neck-also not sure if this is related. Weight keeps going up in spite of increased exercise and limiting daily caloric intake to below 1500 calories.

I am a generally active and fairly healthy 77 yr old who had been taking 10 mg of Lipitor for over 12 years with no obvious adverse effects. Recently I started having pain in my right leg, severe enough to wake me at night. This was followed by a significant weakness in both legs, and for a while, accompanied by a lightheartedness. The doctor had me take a series of lumbar and leg x-rays which didn't show much of significance. He wrote a prescription for physical therapy, which I did not follow.
I did internet research on my own which made me aware that Lipitor could be the cause, in spite of the fact that I had tolerating the drug for so many years. I told the Doctor of my suspicions and we agree to stop the Lipitor for at least 6 weeks to see. A few days later, all my symptoms were gone. So be cautious, adverse effects from Lipitor can occur anytime.

I have been on vytorin for about a year and a half now and I do experience some side effects. I get up at night at least 2 times to urinate. Now about a week ago I started getting double vision. I will be calling my doctor in the morning because it is getting worse. I stopped taking vytorin until I consult with my doctor. But I know I will not go back on vytorin any time soon. I just hope my double vision clears up. I can't even drive a car now. Vytorin is a poison that we are putting into our systems.

4 years ago i was given simvastatin 20mg for high cholesterol when i was diagnosed with type 2 diabetes....last year (November) i stopped taking it after someone commented after hearing me complain about aches and pains and asked if i was taking statins....i checked and found i could relate to several reported side effects...over the last 10 months my aches and pains had slowly disappeared and my cholesterol was recorded at 4.9 in July ....however 4 weeks ago i suffered an optic nerve stroke and my doctor immediately put me back on simvastatin at 40mg despite my complaints is there an alternative i can take as i don't want to risk loosing any more off my vision and as the aches and pains are returning ...i will reluctantly take it but carefully monitor myself....

My daughter just turned 19 years old yesterday. She is a Christian and has kept herself pure and plans to until marriage. She attends a Christian University. She had her last gardisil shot in May. Since this shot she has been complaining of severe fatigue, dizziness and has had no menstrual cycle. My first thoughts were concerns that this was caused by the gardisil shot.She just saw a doctor at her University last week. All the test run were negative and the doctor wants to further test for osteoporosis and place her on birth control pills to regulate her periods. She does not want this.The doctor did not perform a pap smere due to her being a virgin.I have contacted our local doctor and was informed that there was no way to tell if any of her symptoms could be side affects of the gardisil shots she received. My husband decided to investigate the side affects of gardisil and came upon this web-site. I am just wandering if this should be legally investigated and how could someone find out if there are legal ratifications for this problem. I am just praying that these are temporary symptoms and my daughter will recover and be able to have a children after marriage. Please pray with me and I will for each of you as well.

Loss of appetite and change in taste. I haven't eaten a meal since about 26th March 2009. I have a sweet, sickly taste and I can only eat cornflakes or crisps. Cups of tea don't taste like tea and I try and taste different foods each day but still can't eat anything other than cornflakes and crisps.

They have ruined my life and I have been told it could take 12/18 months so I have another 12 months to go. I don't think I can do it!!.

I would love to hear from people who have had this problem.

Well I have been on Lipitor 80mg for years (family history of high cholesterol) although no hearts attacks/strokes ever been attributed to the h/chol....without sounding like I'm a hypo I have 3 disk out in my lower back & years ago suffered intense back as a result...the pain which seems to be now all over is horrid ...I have been thinking that it was perhaps arthritis & old age (59yrs).....several months ago I mentioned it to doctor he said Lipitor could cause side effects but he'd keep an eye on it....well this morning after googling "Lipitor" iv'e made a decision & that is to get rid of this medication...everything I'm reading sounds just like what I have been experiencing...thanks for the input I think I have come to realize that it is the medication that is causing all my problems.

I took levaquin for 10 days and then cipro for 10 days after being misdiagnosed with bacterial pneumonia when I really had cocci mycidioidosus (valley fever) a creepy lung infection from a fungus that lives in the dirt here in Ca . Within a few days of stoping the antibiotics I experienced severe joint pain,dizziness,swollen neck ,hives,pain and tingling in my legs and feet,taste perversion,neck pain,hallucinations,nightmares,suicidal thoughts,dead skin,head ache,conjunctivitis. All of which I thought were valley fever related . A few weeks later I started noticing loss of vision and an inability to focus or concentrate on anything. I have ruptured 5 tendons and sometimes can't lift my right arm off the table.
I'ts been a year and 3 months and I still suffer from these side effects and about 3 months ago I started to notice some hearing loss and then ringing in my ears so load that it wakes me up!

This drug has ruined my life.I have lost 2 profitable businesses,a house a car .a commercial building, my credit score is 309 from 760 a year ago.All from a stupid antibiotic that should not be sold in the first place unless you are going to die if you don't take it.....personally I would rather be dead I think.

I think that we (the 1000's of people effected by this drug) should protest,march at ORTHO McNEIL's doorstep and perhaps the FDA....write a letter ,call or write to OPRA...do something ...It's not right that they get away with selling this crap.

Please email me ...I see 1000's of you on these sites...lets get busy!

******

Thanks for reading

Amazing! Like you, I've fallen into this trap. So healthy and in shape at 59, (more like in my 40's), working out every day, happy. Now, after 2 months on Simvastatin, 20mg every other day, my shoulders and neck muscles are so inflamed, swollen and there's more hurt in my upper body than ever in my life. For the past week, I've been having trouble even getting my clothes over my head! Also headaches have started which I've never had before. I thought it was the relatively wet summer we've had this year in Denver, and was believing the weather had brought me into full-blown arthritis. I am so disappointed in myself to have poisoned my body this way, especially after telling my trusted MD for the previous 3 years "no thanks" to a satin drug. Thank God for my chiropractor sat me down yesterday for a consultation for why I was so much in pain. When she found I'd gone on a satin, the light bulb was lit. I will never taking any satin again and will work to always be as drug free as I can be after this lesson. Thanks to those of you who give me hope that I may feel better very soon (yes, it's no way to live) and I pray for no permanent damage from this "Simvastatin".

I have been on LIPITOR for years 10mg. at least 8years my doctor told me as long as my blood tests were normal "I had nothing too worry about" through the years I had so many health problems,along with so many tests I thought this pain was normal.My pain was gradually getting worse I started to think this pain has to be because of my age.I'm 67yrs old. Last week I had an appointment with one of many Drs. I mentioned that I felt more pain than usual when I told him I was taking Lipitor he was concerned I was told this medication I should stop but it was up to me if I wanted too or not. I had an appointment with another doctor the same day to found out the results of all my blood tests. I was pleased that all my blood were within normal range but there was the blood test for muscle enzyme,CPK was mildly elevated. I was told that Lipitor could make that test elevated. I had another test that that day and was called and was told that that blood test was elevated a little more.I have been off Lipitor for one week now and never going back to taking Lipitor again. I'm so glad I found out about Lipitor and the damage it could do to your health. I'm also grateful for finding this sight by accident. I hope one day I will feel better also I'm not going back to the Dr. that started me on Lipitor and wanted me to stay on it!