Supplements symptoms and conditions

I am taking omeprezole & blood pressure medication & am having muscle cramps in my legs & feet mostly, but even in my chest (Thought I was having a heart attack).I am experiencing severe fatigue & like one of the previous posts, I'm having difficulty even holding the steering wheel of my truck.It's difficult for me to stay awake ,especially if I relax for more than 5 minutes.I assumed it was the blood pressure meds, & stopped taking them recently to see if that would help.(It didn't) I'm going to stop all synthetic meds ASAP & hope for recovery.I've been taking these for 3 years & am experiencing many of the same symptoms as other posts,including swollen breasts (I'm a male)...THANK GOD FOR THIS SITE!!! I'll keep you posted on my progress. Best to all fellow sufferers.P.S: My doctor thinks I have more symptoms than "a 90 year old lady" (I'm 54)God Bless, & I'm praying for you all.

Been on coumadin for a year, horrible medication. Have aches all over, legs, shoulders, back, always tired, want to be off this med. Was taking alternative meds previously...nattokinase, bilberry which are blood thinners but are also SAFE. Then I had no leg pain, no muscle pain. I now take vitamin e and fish oil with the coumadin, no interaction since I've been using them for a long time and are more beneficial than the coumadin as far as I'm concerned. What I need is a naturopathic doctor, but they are hard to find, regular mds have no clue about supplements..all they want to do is increase your prescriptions. Doctors try to scare people telling them they'll have a stroke without coumadin, but have no solution on how to prevent stroke, etc. without drugs.

I'm a 70 year old woman, I have taken this drug for 3 1/2 yrs. I was prescribed Spironolactone 25mg for high blood pressure of 140/80. After researching the side effects I chose to stop taking this drug 2 days ago. First off, it's a potassium sparing diuretic and one isn't supposed to eat foods high in potassium, like fruits and vegetables a contradiction to what is needed for both high cholesterol and high blood pressure, does this makes sense no it doesn't. Also I was taking a potassium supplement, maybe I'm lucky to still be alive?
I don't think Dr.'s read about side effects or what one isn't supposed to eat or take along with the drugs they prescribe. They only look at what the drug is supposed to do, then prescribe it to thousands of patients their, victims. This is probably why they're considered, "Practicing Physicians!"
This drug is known to cancer. This drug is known to cause muscle pains. This drug has caused me to go Bald on the top of my head. This drug plays with ones hormonal balance, it can help make someone grow hair, or lose it. This drug should not be prescribed for simple high blood pressure, it is a very dangerous drug!
I have huge rashes on my ankle and now my hands, they say it's eczema or drug induced atopic dermatitis.
Please do yourself a favor and research the many side effects and cancer causing of this drug. If you're taking simply to lower your blood pressure find a safer drug and try to stop taking this one particular diuretic and use supplements and foods to lower it if you can.
I'm taking this and Lipitor which I stopped one week ago and this one two days ago thank God, I thought I was going to be a cripple for the rest of me life from the toxic side effects, all drug induced.

Are there any meds that are safe? I was taking 10mg norvasc. I started taking 20/25 mg lisinopril. I was doing ok on the norvasc but the added lisinopril has almost killed me. They had cut my norvasc down to 5 mg then to 2.5 mg when I started the lisinopril. 4 days ago I stopped the lisinopril and added back 2.5 mg norvasc. Back to 5 mg. The side effects seem to be letting up. Now im wondering is all of my meds are killing me. I can't live without them. My BP sores. Im so scared of what I should do. Im afraid of all my meds.

I've been on Advair for 12 years.I'm 27 years old and fed up with all this medications that doctors prescribe.We are so brainwashed into thinking that we misbehave if we don't see a doctor.Let me tell you what: The majority of the doctors, only know to prescribe medication.They get bonuses from the pharma industries every time they prescribe their "new discovered"medicine.
Advair is supposed to be preventive, what you don't know it's for how long.Exactly!!!.....'cause it's not meant to cure Asthma, it's meant to keep you hooked for the rest of your life.
My worse symptom is a very fast heart beating.I'm a martial artist and every time i exert a fast burst of energy(while i'm sparring for example), my heart goes into pumped up mode.It beats very, very fast and i have to stop because it hurts.Sometimes i keep going no matter what and feel like i'm exercising for two people.When i stop, i breath very deeply for 5 minutes and all of a sudden it stops and beats regularly.
It's not fun, and one more thing: I'm from Argentina and my mom sends me the medicine from there cause it's way cheaper, sometimes i run out(i procrastinate sometimes), i'm left off with no medicine for a few days and boy.....I'm a wreck.The time you stop you go right back to where you started.I've been researching about an alternative to this "S***".I'm afraid 'cause i don't want to feel discomfort with my lungs anymore, but i strongly believe that there should be a natural alternative to all this laboratory drugs and i'm on a mission to find it.

Well I'm not sure if it's a side effect or not yet, still trying to research it. I had the mirena put in on Friday the 23rd and on Monday when i went work and went to go do my morning pumping session i got hardly NOTHING, i went from just the Thursday before getting 18 ozs to Monday barely getting 10 ozs. It says that it's not suppose to interfere with nursing but i have no other explanation for it. I already take supplements to increase milk supply so theres nothing else i can really do besides have it taken out and hope that, that was it. anyone else have this side effect? please let me know!

Hey Guys,
I'm new to all this but just wanted to share my story with everyone so I feel like i'm not so alone! I'm 23 and was diagnosed with SLE 3 years ago.
It started in my joints and then moved to my kidney's real fast. I now have stage 4 nephritis, finished 6months of cyclophosphamide in Feb and have been on no less than 40-20mg of pred for about 2years. Just when things were starting to look better it has stared in my blood so they are trying to up my dose again. It has thinned my bones so I am on special meds for that now too.
I know taking the pred is something I need to do to live but it comes at a really high price. I don't even look like the same person I used too because of the moon face. I know it's shallow but at 23 it is almost as bad as having to live with this disease. I now have really low self esteem and get anxious all the time, which is affecting my job. As much as I want to come off I also worry that I would have to stop work again as the pred is what keeps me going. All I want to do is get off it though! Anyone know any alternatives? Also, just wondering if you guys are still drinking alcohol while taking pred?
Thanks for listening guys!

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 have been taking prednisone for three years and I love it! It has helped me out with breathing problems and arthritis pain. I take a small does every day. And when I am without it I have trouble breathing and have painful arthritis pain. This drug has done wonders for me.

Hello,
How long do side effects last after completing steroid treatment? I've been off of pred for 4 months for crohn's first time. I was on 40/30/20/10 for a 6 week period. When I got to 30 my legs went into extreme pain. They felt like they were on fire, burning knees. Went to several doctors. One said steroid withdrawal, one said inflammation of nerves from Crohn's. Neurologist put me on neurontin to get off of the pain meds. I am still in excruciating pain and wondering if it really is steroid withdrawal. I can barely walk at times with extreme sharp pains, like someone is stabbing me in the legs. Can't stand for long periods of time and pain pills barely touch the pain. During steroid treatment, they gave me 3 rounds of Dilaudid in the ER and I was still crying, and I don't cry. Has anybody ever had this effect this long after being off the drug??

I am 24 and have suffered from severe to moderate acne my entire life. I have tried every cure out there and nothing has worked. I went on prednisone for an skin allergic reaction about 2 weeks ago. I started out with 50mg on the first day, and 40 mg the next, 30 the next day, and so on. I took it for a week. By the second day of taking prednisone, my acne was 100% cleared up and has been gone since. Now that I am off the medication, my acne is coming back. The only side effect from this drug was insomnia and CLEARING of acne. Does anyone have any idea why I had such a weird reaction to this drug?

Now it makes sense why doctors were so eager to prescribe Lipitor. Pfizer has been hit with a 2.3 billion penalty for illegal marketing promotions of 13 drugs that includes LIPITOR. They were awarding doctors free golf, massages, and resort junkets for "pushing" Lipitor, Viagra, Zoloft and 9 other drugs.

I have been reading all of your Simvastatin experiences with high interest and would like to share my adventures with all of you as well. My story began seven years ago when I was relatively healthy and enjoying life. My doctor prescribed Lipitor for my elevated cholesterol and two months later I found myself in the emergency room after having a severe bout with vertigo for the first time in my life. I have since spent the last seven years fighting this debilitating illness which continues to haunt me after having seen every top neurologist in my area and having taken every neurological test available. It would be as difficult to convince me that I was not somehow "poisoned" by Lipitor as it was for me to convince my doctor.

I was eventually prescribed Simvastatin 40MG and seemed to stabilize for a few years even though my dizziness problems persisted. Suddenly I began experiencing bouts of upset stomach and severe lower abdominal pain. I allowed my doctor to order basically every nasty test known to man in an effort to discover the cause of this new problem, but all have come up negative so far. Eventually I began to experience total exhaustion in the middle of my work day, not to mention the back, neck, and muscle pain that has been described so vividly in this forum. Basically, I have become a 53 year old man who feels much older, has absolutely no energy, and rarely has a day when I can honestly say I feel alive and well.

I am not a doctor and I can't honestly prove that Simvastatin is the cause of all of my problems. However, I do have common sense and after reading all of your thoughtful comments on the subject I would be foolish to at least not suspect that the drug may possibly be making me less healthy and not more healthy. Thank you all for opening my mind to this possibility and I certainly plan on discussing this with my doctor very soon, who may no longer by my doctor should he continue to insist that I take this nasty drug.

Like many of the others who have posted to this site, I have been dealing with what I thought was IBS for the past 3 years or so. I'm healthy and mid-30s and couldn't figure out what was causing it. Colonoscopy and other tests showed that all was normal. I don't drink caffeine, coffee or alcohol. Healthy as can be. Finally discovered it was a dairy intolerance. Coming off dairy solved the diarrhea issue but really limited my diet. Shortly after I discovered Lactaid Fast Act supplements and started to take them at meals when I had dairy.

For the first three weeks, the pills worked great. I loved them. I could eat like normal again without diarrhea. But after that time, I started to feel a sharp pain in my stomach when I take them...like someone slugged me in the stomach. It always comes within 5 minutes of taking a pill. Since then, it has gotten worse. Gas, bloating, and a constant pain (gnawing feeling) in my stomach that nearly has me doubled up. I've never had an ulcer, but from what I've read, that's what it feels like. I decided to stop using the pills.

I just discovered this site and was amazed to see that others have had the same. I should have checked for side effects before I took it! I've not had the vomiting that many of the others have had, but I won't be taking it any longer and risking that!

Hoping there is some alternative solution out there. Hard to imagine the rest of my life without cheese or dairy in anything (bread, dressing, etc.).

I have been prescribed a 20 day course of flagyI. I was prescribed this med for a uterine staph infection caused by an iud...as you can imagine I was ready for any antibiotic that would bring relief. I tried a few antib's (Cipro, Macrobid, Doxycyline) before flagyl while the drs waited for the culture to return from the lab...flagyl brought immediate ( 24 hours) help with the staph but causes metal mouth, a woozy feeling and a strange aching in my feet. In my situation the side effects are worth it...Also the severity of the side effects have been temporary, as the bacteria die off the toxins they leave behind will leave your system and ease the side effects. It is important to replenish your natural bacteria while taking antib with probiotics in yogurt and supplements this helps me with the yeast problems also taking Caprylic Acid and coconut oil have kept yeast under control. Stopping your antib treatment before the course is through can cause a relapse in your symptoms worse than the original illness and can cause antib resistant bacteria...MRSA (bad stuff!!!) I hope this helps you.

I am experiencing severe hair loss - I was on Wellbutrin XL for a year and a half with no side effects, then changed doctors and we prescribed the generic, bupropion. That is when my marked hair loss began. I then switched to Lexapro, but felt like a zombie, and so went back to the bupropion hoping that it was a vitamin deficiency that was causing my hair loss and not the med. But, with all sorts of supplements, my hair continues to thin - I used to have thick, healthy shiny hair, and now cannot bear to touch my head because it is so upsetting to have lost so much hair.
Has anyone else experienced NOT losing hair on the brand name Wellbutrin, then switching to the generic and losing hair? I don't want to give up the med because it has worked so well for my depression, but I don't want to loose my hair either. HELP!!
Thanks!

OMG...I want to thank everyone for their comments, as I thought I was just crazy, I have not been able to walk more than 25 steps in three years because of this stupid Lisinopril. I could honestly just cry. Three years have been just taken. My daughter was 8 and now she is 11. We have not been able to go to the mall one time because mommy's muscle pain and weakness is so bad and it is just embarrassing to try to walk around a mall or the airport. I am only 39 there is no reason my primary Dr. should not have caught this. I have been referred for and had multiple MRI's, cortisone injections, nerve testing and nerve blocks, taken Tramadol until I can not take it anymore. Thank you all of you. Thank you. God Bless you, in Jesus name, Amen.

Wavy feeling of anxiety in my head (like I used to get from codeine). Fuzzy feeling in big toes. Dry, choking cough when I lay down at night. Now, I am morbidly obese and have bad acid reflux. If I don't take Prilosec every day, I cough. I also have sinus/allergy problems. So I take Claritin-D. And for health benefits, I take baby aspirin. So I'm wondering if it is the combination or if I am getting ready to have a stroke. It's my own fault for being so overweight, but it is frustrating. I also have swollen ankles and legs. And lately I feel like I have to pee too frequently and that I'm not quite able to finish. This worries me because I was feeling like this before I found out I needed surgery to remove an ovary due to a very large cyst. I wonder if I am getting another one.

I got Mirena in April 2009. After 2 weeks I started noticing I was getting hives. At first it was not that bad but the hives got worse and worse. I reacted allergic to my supplements and started to react to food. Even though I was on a strict diet to avoid anything that could possibly cause any reaction the hives were getting worse. I had Mirena taken out yesterday. My doctor thinks I had an allergic reaction to Mirena. I still have the hives. I have lost lost of weight and life is pretty hard when you have hives non stop! I hope it get better.......

Has anyone had problems with their eyes on this medication, my have been going blurry and then I get a terrible headache.

Does anyone have any thoughts on after stopping the nuvaring. I was only on it for 2 months but the extreme moods and depression made me stop and never look back. Its been 6 months since I stopped, I have not used any birth control since. My hair started falling out when I was on it, but it never stopped and is now getting worse. I am not feeling well and seem to have all the symptoms of hypothyroidism, I just had a blood test today and am waiting on the results. I am 25 yrs old and otherwise healthy besides this. I feel like all my symptoms, physical and emotional started with the nuvaring, I am wondering if anyone else has developed hypothyroidism after being on and stopping the nuvaring???

I took Zocor for 9 months after I had a heart attack. After about 8 months I began having sever muscle spasm in my legs. I had a couple of episodes where when walking I couldn't pick up my feet and thought I was having a stroke and had to sit down and rest before walking on. I had to do this several times to get where I was going. I told my cardiologist and he had me stop the Zocor. The spasms stopped but I never regained the strength in my legs. Today I have had to put ramps in at home cannot climb steps. The ramp is difficult because of the incline but it is better than crawling up my steps to get in the house. I can only walk about 50 steps before my legs give out on me. I cannot walk on uneven ground without holding on to something or someone. I have now had 2 back surgeries because I have been told over and over it is my back with no relief for the legs. This last surgery my left foot drags and my big toe hangs down and I cannot pull it up. Now I fall a lot because of that and have to wear an AFO to keep my foot and toe up so it doesn't drag and trip me. The back doctor thinks it another pinched nerve and wants to open back up again. I am so tired of them trying to convenience me it is my back when I know it was the Zocor and the damage apparently is irreversible but no one wants to agree with me. I am sick of it and just wish they would say yes it was the Zocor and get you a scooter and live the best you can. I know I am headed for that road I use a walker and cane when I don't have someone with me to hold on to. Because I am so unstable on my legs.

I have been on prednisone since I was two years old (I am now sixteen) because I have Autoimmune Hepatitis IIa. I would like to point out that there is still a life worth living being on prednisone, maybe I say this because I do not know life without it, but at least we're alive! Last year I had a flare up of the AIH and had to 6x my dose of prednisone. It sent me into a spiraling depression of constant sleep, crying, hopelessness etc....but I made it through. Just PLEASE keep hope that things would get better, because I know what it's like being on the dreaded drug better than most.

Less than 2 months after taking Lipitor I have been experiencing intense weakness of the legs, especially the hip area. A normally avid walker, last week really woke me up when I was unable to walk over 40 feet without having to stop from sheer leg exhaustion. I'd have to actually lean on my partner until I could manage to shuffle again- a shuffling gait is what I had to resort to just to make it back to the car.
This is bullshit because even though I've had some angina symptoms, right up until I went to the hospital I was able to hike; was still relatively strong.
So today I have spent hours researching side effects and have seen on this site alone many mentions of intense leg weakness and pain with Lipitor.
This, along with simultaneously educating myself on the truth about high cholesterol has convinced me to gradually cease taking this medication.

Instead I will replace with sufficient quantities of VitC, buckwheat combined with gingko, and of course I can never stop with the garlic because it is delicious.

I have been using the NuvaRing for about 6 months now. I thought it would be a blessing because I would not have to take a pill everyday. I am 23 years old. Have a fantastic serious boyfriend. and NO sex drive. I have always been a happy person, so this behavior has been obvious to not only me, but others. I have been considering going to see a therapist because i just can't seem to get out of this "funk". And thanks to all of the posts, I now think I have a legit answer to my behavior. Besides having little, to no, sex drive.. I have been having waves of depression, headaches, moodiness, feeling anxious, fatigue, weight gain, (looks like someone put an air pump in my face, ugh.) and plain weird thoughts. I really just feel out of my body, just not with it at all. I have tried diet changes, regular exercise, etc. Basically, trying to fix my depressed feelings/anxiety without having to see a doctor or get on another medication. Does anyone know how long it takes to get the NR out of your system. Just ready to get back to normal!!!