Mgs 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 have been taking Lamictal 150 mgs for about 2 years to prevent Basilar migraines. This medicine saved my life. I was having these scary migraines where I would have stroke like symptoms (loss of speech, vision and confusion) two or three times a week. My Dr. started me on a very low dose and stopped titrating me up when I hit a therapeutic level . I have night sweats, some nightmares and some anxiety at times but I'm willing to get over it because I don't have the migraines.

A brief note about "Adderall": this is the trade name of an amphetamines product. It consists of four different amphetamines, such as amphetamine sulfate and amphetamine lactate. However, the "sulfate" and the "lactate" parts are NOT important. The only thing that is important is AMPHETAMINE, regardless of which form. 100% of the effects of Adderall are because of its content of amphetamine, NOT the specific forms of the amphetamine (called, chemically, "salts"). You can get the same effects from generic amphetamine (typically dextroamphetamine sulfate) as from Adderall. The company that makes it claims that Adderall works quicker and lasts longer, but this is mostly bullshit. It is really not significant, and in fact plain old generic dextroamphetamine is generally considered superior to the other forms, including the forms in Adderall. (See the en.wikipedia.org writeup on Adderall for details.)

Incidentally, the Adderall company, facing patent expiration on Adderall and thus more generic competition, is now heavily pushing its new "Vyvanse" -- another amphetamine product with very dubious if any advantages, and indeed probably MORE side effects than Adderall or other amphetamines, and, of course, a much higher price. More pharmaceutical company bullshit! Don't buy it.

Anyway, to return to the main point: Adderall or generic amphetamine makes no difference, except this one big one: The PRICE! Adderall is ridiculously expensive -- typically $1-4 per pill, sometimes even more. This is a total ripoff, since amphetamine is a CHEAP old drug, and the actual cost of 10 or 20 or 30 mgs of it (as in one typical tablet) is negligible, well under a penny. In other words, they ought to sell for, say, $10 or $15 per hundred -- enough to cover the cost of the drug itself (perhaps 10 cents or so) plus all the costs of tableting, bottling, distribution and so forth, with room for the pharmacy's markup. The idea of paying $100 or $200 or even $400 for a dime worth of a cheap old drug is outrageous -- but it happens. It is the greed of the pharmaceutical company combined with the greed of the individual pharmacist that causes this. Pharmacies vary a great deal in pricing, but the producing company also grossly overcharges.

Bottom line: INSIST ON THE GENERIC. Even if insurance covers it and you only have a $5 co-pay. Why? Because the health care system of the U.S. is driving the country bankrupt, and super-high drug costs is one of the reasons. This is one way you can make a contribution, however small, to solving the problem of a medical-academic-industrial-pharmaceutical complex that costs the U.S. well over $2 trillion per year (far larger than the military-industrial complex, and far more per capita than any other developed country). Part of the problem is prescriptions that cost $300 for 50-cents worth of a drug. Be part of the solution.

End of rant. Be well!

I've been on prednisone for nearly 3 years continuously for Ulcerative Colitis. I've been on 60 mgs for quite a while but I am now down to 4 mgs. Once I went below 10 mgs. I started experiencing severe itching on my entire scalp and then upper back, ears and collar bone. I went to a dermatologist but she can't see any reason for the itching. Has anyone else had this side effect while tapering? It's making me crazy!

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!!

Since July 12, 2009 (Saturday) my life has been altered by a cure for a UTI that caused me to be taken by ambulance to the E.R. with a 105.6 fever. The horrible feeling of waking up shaking from the fever and not being able to stop it was scary. That was quickly followed by an ambulance ride to the local E.R. It was explained to me that the cause of my fever was a UTI that became a kidney infection. The E.R. doctor prescribed Levaquin 500 mgs for 10 days and Lori-tab for the ache very typical of a kidney infection. I am a 42yo woman who owns a motorcycle, swims, dances with a group and loves to wear beautiful heels. My life has changed since that night in the E.R. July 14 (Tuesday) , I was in my doctor's office complaining about bad headaches and feeling achy. I asked if this should be a concern since headaches were part of the warning label. The response was to remain on the antibiotic since the benefit far outweighed the side effects. The rest of the week was full of aches, pains, swelling, and a cloudy mental state. By Friday, the 17th of July I was laying in bed after noticing I no longer had ankles and I hurt all over. Thinking maybe this would pass I rested for an hour and my partner came to check on me. My jaw was tight and felt like it was locking down, every part of my body, every joint was hurting including my head. I called my doctor's office and asked if this was an allergic reaction and should I go to the hospital. The on-call said she was at the E.R. and maybe I should come in to be seen although it would be a long wait time because they were busy. I was seen, they talked about finishing with Cipro and then decided they would give me Bactrim. I asked how long I could expect to feel the effect of the Levaquin, the answer was 3 to 4 days. Since then, I have been in and out of the E.R. with acute and chronic pain. Walking has become almost impossible on some days. All of a sudden I have a back and hip problem. I am getting lumbar epidurals now and have sold the motorcycle. Oh, Dr. Higgins said, "Levaquin is a great drug". This was a E.R. doctor that was angry that I asked if this seemed to be an on-going issue from taking Levaquin. I am desperate to be pain free for even one 24 hour period. A storm of depression and clouds have set in...the thunder is my pain....

THis website has been a tremendous help for me. Two days after I was prescribed 500 mgs of Bactrim twice daily, I started feeling really odd. First the achiness, then my left leg began to swell. I am not taking the meds anymore, but am now so fatigued, and sore, I feel as though I have had the flu for a week. I honestly do believe that it also has a negative effect on the liver. Just from the almost constant ache , I have on my right side. I just want to sleep all the time. I have not taken the meds for two days, and yet, the effects remain. Beware of this nasty medication. I don't know why the FDA allows its distribution!!

I just came off Geodon 48 hours ago, I took 20 mgs at night for mood disorder which was caused by PMDD. I am not on a micro pill so thought I should go off Geodon to see if the hormone replacement is really working. I feel horrible and cried non stop yesterday, hope this passes soon.

I was placed on Topamax, off label, for suspected bipolar illness (now disproven). My cognition, word finding abilities, memory has been so adversely affected that I am now on disability. I had 5 kidney stones due to the development of Renal Tubular Acidosis, nearing renal failure (a side effect doctors don't warn patients about). This in turn led to osteomalacia, softening of the bones, only discovered after I broke all three major bones in my leg and snapped off my foot stepping off the lowest seat of a bleecher. I've suffered tingling in arms, hands, legs & feet (nerve damage), lesions in the brain, muscle spasms, heat & cold intolerance, insomnia etc... Although I lost weight, I gained it back (then some) as soon as I reduced the dosage of 800 mgs. Upon stopping the drug to save my kidneys, thus my life, my kidney function returned to almost normal within a few months, although there is residual damage. All other side affects remain two years later. Losing weight is not worth dying! Beware of this drug being used off label! I would never trust this drug!

Hello everyone. I too am experiencing the same problems described here from Lisinopril. On January 1st of this year, ( 2009 ) I was taken to the hospital emergency room and admitted into the hospital under the assumption that I was having congestive heart failure. After a barrage of tests it was determined that I have diabetes and I was already taking hydrochlorothiazide ( 50 mgs ) for water retention. I was prescribed Lisinopril ( 10 mgs ) and told to cut my hydrochlorothiazide in half. Everything was fine for about a month and then it started...
I had noticed on the bottle of Lisinopril that the one side effect in some patients was a dry cough but disregarded it since it didn't seem to be affecting me. After being on Lisinopril for a month, I began having this awful dusty feeling in my throat. It actually feels like someone has a bellows filled with dust which they've placed in my mouth and released a spray of dust which caused me to have this feeling of needing to cough almost to the point of choking. I don't have this cough all day long. It only happens intermittently throughout the day. Sometimes when I am standing or sitting but mostly when I am laying down in bed. I've also noticed that it seems to have somewhat of a consistent schedule. Perhaps this is due to the fact that I would take the pill every morning around the same time. However, I've stopped taking it about a week and a half ago and still seem to have somewhat of a pattern of when the coughs occur. Strange.
Another thing I noticed is that I've seemed to have an excessive amount of saliva which would also cause me to choke at times. Have any of you experienced excessive saliva with this medication?
I've been trying to lose weight without success and I'm wondering if Lisinopril has something to do with that as well. After reading all of these comments on this forum, I am wondering if doctors as well as The American Medical Association should take a closer look as to whether the side effects of this medication out weigh the benefits and/or what this medicine is supposed to be helping the patient with. So far I see no positive effects from this medication.

Hi I am 31, have been put on prednisone for a pinched nerve in my shoulder blade. Iv taken two pills of 10 mil. For two days. one pill a day for two days. I'm stopping now. I feel so tired weak and unable to exercise. My chest is so heavy and heart flutters. I'm a smoker so it seems worse after a cigarette. I also have a few glasses of wine a day. I'm so frightened at these feelings. My tummy is now bigger in just that short of time. I really wish I knew all this first. Can any one tell me how long before I'm normal from the short usage. Please this really sucks and very scary. Also the smoking and alcohol how does it effect this? Please

I have p. neurapathy in my feet and legs and it "may" be happening to my hands. I say "may" for I'm thinking it's ANOTHER side effect from Lyrica (150mgs, twice daily). In aprox. 8 months I've gained about 50 pounds which has cracked bones in both my feet! My fingers hurt and are so swollen it's very difficult to play the guitar, something I've been doing for almost 30 years. I'm also take Tylenol 325 2X daily. AM / PM.
These are the same doctors on the Pain Management clinic I attend who also prescribe 80 mgs. of methadone. Okay, the pain only lasts an hour every morning but all these side effects are making me lethargic from all the extra weight. I'm 240, up from 190 - big difference! I've got to find another way! All contacts welcome. ******

I'm 15 years old and i've been taking prednisone for a few months, and from what i've read i'm on a really high dose. i was diagnosed with rheumatoid arthritis and another autoimmune disorder concerning my muscles at the same time. my doctor told me prednisone was my only choice; it was either that or i would lose the ability to walk. he told me there'd be side effects, but i had no idea it'd turn out like this or i would have fought harder for another course of action. i started out on 30mg twice a day, and since then was weaned down to 20mg twice a day and now i'm down to 30mg once a day. i've been looking up a bunch of information trying to figure out if there's a way to lessen the side effects or any hope at all that they will get better. apparently there isn't much. after reading a bunch of these stories i gotta say i'm not feeling great about this. i totally understand everything everyone is going through. i'm sure you can imagine what it's like being smack in the middle of high school with a huge puffy face, acne so bad on my face, chest, back, neck, and shoulders that wearing a bra could put me in tears, and mood swings so bad i've lost friends over it. everyone knows how brutal high school can be, where appearance and attitude are everything. and i try to tell my doctor about it and he literally looks at me like i'm a whiny teenager and says "you're just going to have to deal with it." and people like my mom and my closest friends don't get it either. nobody understands how beyond frustrating it is. i'll get into the worst moods and not have a reason for it, but i'll stay angry for hours or burst into tears over someone looking at me the wrong way. it'll get to the point where i have to isolate myself from other people because the abrubt mood changes get so bad. as bad as i hate to admit it, the pain from the arthritis is gone now and supposedly my muscles are doing better too. developing arthritis caused me to have to quit cheerleading, something i've loved doing for 6 years, because the pain got to the point where i couldn't get my arms above my head or bend my knees. however, i'd almost rather deal with the horrible joint pain than deal with the side effects of prednisone. if your doctor gives you and alternative method, take it. i've always been confident in the way i look and really outgoing and happy and now i sometimes catch myself thinking about suicide. that's shocking to me because i've got so much going for me, but this medicine makes me miserable. and when i complain about it, anyone i'm talking to just looks at me like i'm being a cry baby. my mom does too, she'll say things like "you just have to do this. i know it's not what you want but to be honest i'm sick of hearing you bitch about it."
i feel a little better knowing other people feel the same way - like nobody gets whats going on with them. the prednisone does give me days of really great euphoria and days when i feel like i could run a marathon, but waking up in the morning to the acne and huge face puts me to tears every day. i have to pee all the time, usually getting up at 2 or 3 am. i don't sleep well anymore and i do sweat all the time. which also sucks being a teenage girl. i'm always hungry, and when i eat i never feel full so i don't know when to stop. my neck and face have put on so much weight that when people see me in the halls or out and about they ask me what happened. mind you these are people i don't talk to, just ones i know from classes or whatever. and it's pretty bad when teenage boys i've never really talked to ask what happened to your face. kind of a blow to the ego, or whatever is left of it at this point.
i'd like to know if, as my dosage gets lowered, the side effects will diminish and when i'm off the prednisone completely if they will disappear altogether. any help there?
or if there is any way to help the acne or puffy face

my doctor just put me on something called methotrexate or something like that to help wean me off the prednisone, and does anyone know what those side effects will do? or if they'll affect the prednisone side effects?
i'm constantly obsessing over gaining weight and what my skin looks like and what i eat and how heavy my face feels and the occasional pressure in my eyes to the point where i just want to be put out of my misery.
and after reading other people's stories i really don't understand why this drug is still given out as freely as it is. but maybe all doctors are like mine, they just don't get it.
best of luck to anyone who's on prednisone, my heart goes out to you; i'm right there with you
sorry this became like a book it wasn't meant to be this long

Adderall has worked wonders for me. I was prescribed about a year and a half ago to 10mgs twice a day. When I first started using it, I thought it was great, but like others I hated the side effects. Through trial and error, I have found ways to mostly cut out the side effects. To avoid stomach aches, I never take it on an empty stomach. I always eat a good meal before I take it. I do eat slightly less than before I was prescribed, but I take a good multivitamin to make up for that. I only lost a little bit of weight, just less than 10 pounds. Another way to get rid of the stomach aches is to take a few puffs of some you know what. I rarely get headaches from adderall, but when I do I just take a few ibuprofen and its gone right away. Before I was prescribed, I had tried 20, 30, and 40 mgs of adderall and that was hell. Coming down made me want to kill myself. I feel bad that have severe enough ADD or ADHD to require that much. Overall, I think you have to look at individuals instead of just saying adderall in general is a terrible and addictive drug. Before I was prescribed, I didn't think I had the motivation or will power to make it through school. A year and a half later, my gpa has raised dramatically (2.2 to a 3.0) and I'm in the process of finding what grad schools I want to apply to.

I have put on weight I am 104kgs.I am picking up bacterial infections.I have a persistent cough and feel somewhat deflated.I also suffer from mild schizophrenia as well as my O.C.D.I take 375 mgs of Effexor and 10mgs of
Olanzapine or Zyprexa.I have had bouts of depression since the age of 25.I am now 39.I would dearly like my medication to be reduced as I'm finding it hard to be happy and content.Any advice?

Responding to a couple of posts: Low energy and leg cramps are signs of low iron, you might be anemic, ask your doctor to have your iron checked at your next blood test. Also, ask about taking a multi-vitamin, all of the literature about Warfarin mentions not taking vitamins but it’s more about consistency. I’ve been taking a multi-vitamin daily - with my doctor’s permission - and I’ve had very consistent PT’s and INR’s. I’ve been on 7.5 mgs of Warfarin daily for six months and am holding steady. It is very important to take it every day if you do take a vitamin, it’s important to be consistent.

And about the socks, they are called compression stockings and can be prescribed by your doctor, or some are also available at drug stores, ask a pharmacist at the store.

And also about headaches, it helps me if I stay hydrated. When I don’t drink enough water I tend to get headaches.

I’m back to exercising at my pre-pulmonary embolism rate, it took me six months to get there, and I started slow, but my body has gradually responded. I’m 52 and was pretty healthy before I got sick. Just keep at it, you’ll see results (and feel better too!).

I am only 42 years old and have been on zocor for the past 30 months. I've had mild tingling in my feet and achy joints along with slightly elevated liver enzymes and fatigue since then. Ever since my doctor increased the zocor to 80 mg per day ( because although my cholesterol level is normal, my triglycerides are still very high) , I feel like I am 100 years old! All my joints ache so bad and my feet and hands alternately tingle or feel very cold! I am also having trouble focusing when I look from something close up to something far away! I am also clumsier and more forgetful. Could these symptoms be caused by coenzyme-Q deficiency?

Hello Again,

This is my second post and was just wondering; How long has everyone been on doxycycline and how many mgs? How long have they been OFF it and has the depression/anxiety been better? PLEASE HELP!

Thank You

I am 37, and developed a DVT in my left calf possibly due to birth control pills. I was tested for Factor 5 Leiden and since I was positive that may have been a contributing factor as well. Waking up in the middle of the night and first thing in the morning with excruciating pain was a daily occurrence and finally after 2 weeks of Lovenox injections and warfarin the pain subsided. I still experience post thrombotic pain in the back of my leg three months after starting the medication. My INRs are inconsistent and my doctor keeps changing my dosage. I have been avoiding all food that that can interact with the meds, it is extremely irritating. I have been doing an hour of low impact exercise daily and am looking forward to when I can finally go jogging and increase my cardio workouts. I can't wait till I can finally be off the medication it affects everything I do.

I think it's really sad when everyone here has the same side effects without seeing this site ,thinking they are crazy and your doctor looking at you like you should be in a mental ward! I took lisinopril 10 mgs for about 8 months I was borderline high blood pressure ,ok I am over weight and did not eat as well as I should have ,but instead of my doc telling me to lose weight(and I know I needed to) and eat better she put me on the drug from hell! I had started walking and eating better since she put me on the drug,at first everything was great I was feeling better I started walking and started the dash diet ,which works great by the way.then all hell broke loose ,I started getting weak ,tired all of the time, my feet felt like they were on fire ,numbness in my hands and feet(felt like I was having a stroke)started taking the drug in may and by thanksgiving I was in the emergency room,I was supposed to work on thanksgiving (I am a bartender)and could not get out of bed,of course they found nothing,I went home an then a week before Christmas the heart palpitations started ,I was lying down watching t.v.and I started having them.still weak and then the palps started,I was scared I was having a heart attack,I went to see a heart doc. and he told me I need a holter monitor for 24 hours and an echo (did I mention I don't have insurance)so after three e.k.g's from different doc's my medical bills are sick and an emergency room visit you can imagine.well to let you all know you are not crazy we all have the same symptoms without seeing this site!My echo and holter monitor test both came back normal,my doctor took me off the meds my bp is 120 over 80 , and I am loosing weight with the dash diet ,and my palps are coming less and less,I don't know how long they will last but hopefully not long.good luck everyone and god bless

I was prescribed Topamax for back pain( experimental) 25 mgs for five days on the fifth day i increased to 50 mgs that evening i suffered a stroke.I spent the next several months hospitalized learning to walk again.One more side effect of the stroke i have been dizzy for five years.I know Topamax caused the stroke but I cant prove it.

I am a 31 year old male, in decent shape (play basketball, volleyball, workout at least 3 times a week) but I have a family history of high blood pressure and have had it myself as long as I've been tested. Went to cardiologist as a check up on my slightly enlarged heart, long story short, ended up on Metoprolol (25mg) beginning of 2008 and have been fine but no real help with bp. Then was put Lisinopril (5mg) a few months ago and my blood pressure was great at last checkup. However during that time I had a couple of weeks where I was very dizzy, that sort of feeling your brain is taking a second to keep up with your head as you get up, along with a fogginess and what seemed like sinus issues but I chalked it up to weaning off of a small dosage of Zoloft I had taken for over a year. I also developed "the cough" everyone refers to, but since it is winter in New England I chalked it up to dry heat, even though it was a choking cough unlike any I've ever had before. Also during that time I seemed to completely lose my sex drive, again figuring it was just something to do with the Zoloft or general anxiety. Then in the past week I started getting a constant headache, having really interrupted sleep, very foggy and out of it, tired, dehydrated, constipation, nausea, all things that I would normally associate with allergies or some kind of sinus/flu, but yet I couldn't really pinpoint anything that would be causing it.

Then I finally started looking up things about the meds I was taking and came upon this site, and guess what? Everything and every way I was feeling was described in hundreds and hundreds of posts on this site. I don't think my side affects were quite as strong as some have experienced (for instance the cough is very infrequent, like twice a day) but I have only begun my journey with Lisinopril. So despite the warnings, I decided to stop taking it a few nights ago, and almost instantly I began feeling better the next day and since then.

I have since called my cardiologist and he has recommended I switch to Diovan, basically saying that based just on the cough symptom alone, he wants me off of Lisinopril as this is a known side affect. Now I am left debating whether or not I want to continue down this path of trying different combinations of pills to poison my body in order to lower my bp. It seems like others have noted marked differences between taking Diovan and Lisinopril, where the Diovan has been much more tolerable than Lisinopril (with a great decrease in any side-affects) but I'm 31 and although I know it will be very difficult to reduce my bp on my own (believe me, I've tried) maybe I'm too young to start with the "last resort" of these toxins. Just reading about the possibility that Lisinopril was robbing my body of zinc or other minerals, so that my immune system is greatly weakened, likely being the cause for most of the symptoms, is enough to ward me off of pills altogether. It's a sad statement on the state of health care in America when I am left to basically make such an important decision on my own, because I can't trust that my doctors aren't just working in the interest of the drug companies to boost their income. I don't want to have to choose between a silent killer and a horrible existence filled with "side-affects".

In the end, based on some of the reports on here, I think starting on 40mg of Diovan will be fine, but I will certainly be VERY wary of anything unusual and immediately find other options.

I am being treated for ulcertive colitis. I have been on prednisone since Sept of 08. I started out on 40 mg. In late Oct. my doctor started tapering me off 5mg per month. Each month following the tapering date, I would get sick. As I look back, all the signs of withdrawal were there. This Jan. I tapered once again, but the window was only 3 weeks. I hit rock bottom. If there was a symptom, I have it. Nausea, burning in my digestive tract, diarrhea every time I eat, muscle ache, numbness in my legs, swollen feet, sore bones and joints. ( The worst was in my feet. I ended up seeing a podiatrist. He thought plantar faciaitis until I told him about being on prednisone. The small bones in my foot were swelling, The muscles in my calf were buning they were so sore. That was last week. Today my other foot started. I can hardly walk. In addition to that, I am lightheaded, have elevated blood pressure, and fatigue. I also had some vision problems that sent me to the doctor. I went through a ton of testing which all were negative. It seems that pseudotumor is another symptom of withdrawal. I have a history of that. It would have been nice to know that. As I look back each month, I had different muscle and joint pain that lasted about a week. I was put on an acid reducer in Dec. to help my stomach, but in all of this time, I was not told that these all may be withdrawal symptoms. I have been off work for two weeks now in addition to the days I missed each month. My physician is now controlling the tapering procedure. They up the dose to 10 mg again. They plan on weaning me by 1mg doses. This has been a terrible experience for me. I have only been severely sick one other time in my life. This pain is awful. It is chronic. This drug may be beneficial, but it is like poison too. Anyone who takes this should really ask a lot of questions, and be careful..

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 am 38 years old and had my second child 7 months ago. My family history for heart disease is very poor and my cholesterol was 6.2 so my doctor prescribed 10 mgs of simvastatins in November. Before taking them I felt fine in myself, since taking them I have felt exhausted, not just tired, I have insomnia, very bad nightmares when I do manage to sleep. On top of this I have started to feel depressed and anxious, short of breath and my hair is falling out! I had myself convinced that i had post natal depression but decided to stop taking statins a few days ago, feeling slightly better. My doctor prescribed me an anti depressant today, should I take them? Does anyone know how long statins stay in our system?