Diseases symptoms and conditions

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.

Just had to comment on these side effects I'm reading about Lipitor and other Statin drugs. I don't take anything and I never will after finding this site. Guess what, I have had high cholesterol since I was in my early 20's. When I say high... it ranged from 240 - 260...remember when 250 was OK? Well folks, it's 30 years later, my cholesterol is just about the same range, and Oh My GOD...I'm still here without any drugs.!!! They lowered the range so they could pass out the pills!!! Greed, greed, greed. Do you wonder why our Healthcare system is out of control? Well, when you keep feeding people medications that are presenting the side effects they do, making them sicker, they just keep testing and testing and testing for other things. Let's do blood work, MRI's, CAT Scans, Spect Scans, Pet Scans...Scan away...and guess what...all comes back OK...hmmmm why not look at the drugs you're prescribing. We need to see "all the side effects" listed. Not just some. They're misdiagnosing, Alzheimers, Fibromyalgia, MS, Lupus, Dementia, Arthritis, and on and on when it's been the drugs causing the diseases!
Ween off everything and anything you can...take your chances...when God wants you, he's going to come and get you no matter what you're doing...right or wrong!

I have had asthma since i was 10. I am 44 years old now. I have never in my life been on prednisone this long (since Feb 2009). It is now July 11,2009. I was admitted to the hospital for IV steriods (prednisone) because for the first time in my life the general 10 course with the pills wasn't working. so there i was on 165mg of pred every 6hrs. After eight days in the hospital i was released and was to take 40mg for five days and decrease by 5mg until done. I didn't do to well and had severe exhaustion where i couldn't even walk 2 steps the next day. so I went to my pulmonary dr. who said he noticed a severe anxiety side affect in me from the drug and said i needed to get off it as soon as possible, he had me drop my dose every day by 5mg. TO FAST! I had breathing problems again, started over going slower, got down to 10mg and had to jump to 40mg again! side effects for me are severe anxiety (which i have to take ativan for) and especially massive painful foot cramps. My hands will cramp to while trying to write, but the foot cramps and the feeling of being wired are the worst. I am still trying to wean off....sometimes i wonder if i will ever finally be off this stuff. I just want to cry sometimes. It feels like being pregnant and going thru post partum at the same time

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

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.

Im sorry for all of you ladies who have had issues with the Mirena but I love mine. I had it put in 1/09 7 weeks PP with my 3rd Daughter. I never had any cramping or bleeding with the exceptional spotting for the first 3 days and my sex drive is better than ever knowing I have less of a chance of getting pregnant than when I was taking the pill. No headaches or dizziness either. After reading all of your comments, I asked my doctor about all of those side effects when I had to go back a month later to check and make sure mine was in place. She said that they are possible side effect because every woman's body is different and some peoples bodies react differently as with any method of BC. There is still many women out there like me who have no side effects and Mirena is god-sent. I do apologize to all of you and hope you do end up finding something that is right for you.

<3 K.

I have been on Lipitor for five weeks. I can't believe how awful I feel. I ache all over. I my arms and elbows are sore; I have had pins and needles in my hands; charley horse like spasms in my calves (mostly at night); sharp knife like pains in my upper thighs; even my teeth hurt. I am a 46 year old female – I can’t believe this. I have made an appointment with my doctor as I have to get off this drug. I have experienced some blurred vision and hearing impairment too. If I hadn’t of found this website – I truly would have thought I was a bit crazy….
I have never had any symptoms like this before and never thought of myself as an old lady - but that is what I feel like. It is unbelievable.
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My 13yr old niece has always been a healthy, active and straight A student. Then on 11/5/08 during a routine physical, she received her 1st dose of Gardasil. On 11/28/08 she started to complain that she felt weak and had a headache. Since it was 2 days after Thanksgiving we thought that she was tired from all the holiday activities. On 11/29/08 she had a headache and stayed in bed all day. She got up that afternoon & had 2 seizures. She was rushed to the ER.
As of today, March 8, 2009 she is still in the hospital in Intensive Care Unit. She has been in critical condition since. Within 2 days after her seizure, she lost the ability to eat,speak,walk and communicate in anyway. She is completely unresponsive. She is on the ventilator, she is basically in a coma. We do know she has an viral infection with a shadow on the left side of her brain. All of the testing that has been done all show negative for any illness or diseases.
We are still unsure if she will come out of this. This has been completely devastating to our family.
We have no answers from doctors. Even though we know in our hearts that this was a side effects from Gardasil. I don't know if they will ever fully admit it.
We are left to watch and wait. That is what the doctors tell us daily..

I have had I terrible live changing experience with Nuvaring. I experienced the a loss in sex drive and vaginal pains during intercourse. I was on the ring for over two years, and have been off it for almost a year now. I went off because my husband and I wanted to try to get pregnant. I knew that the drug can stay in your system for a while after it is removed, but nearly a year is impossible. I also know I wasn't infertile before the ring because I had been pregnant before. So I shouldn't be infertile now. I have seen numerous doctors and they can't find any thing wrong with me. I have never had any diseases and my husband hasn't either. We have always been completely monogamous healthy people. There is not outside reason we shouldn't be pregnant. I am going to a fertility specialist next week and I am very hopeful that I can still have children. I don't know for sure if my problems are from the ring, but it seems too likely. I highly suggest that anyone contemplating using the ring look for something else, and if you are on it get off as soon as possible. It's so much easier just to not have to deal with the problems.

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 am 34 years old. I am a pharmacy tech. I have asthma and allergies. I have taken singulair pretty much every day since it came out on the market. I've had asthma since i was about 10 years old. I took theophylline as a kid. Steriods on and off especially during times when my allergies are bad. I still use Advair during the fall and spring. Every drug has a side effect. However breathing is pretty good damn thing. Do I have days when I feel low? Yeah. Do I sometimes have nightmares? Yup. Are "natural" products the answer. Not always. The fish oil that some of the posters are touting can also cause GI problems. Some of the natural products contain herbs and other plant derivatives that can be harmful for a child that suffers from allergies. Not proactively treating asthma can be deadly. Some of the parents are suggesting steriods as the answer - those can cause weight gain, growth suppression and can lead to a worsening of asthma.

Singulair has never made me feel like I've wanted to kill myself. I was more depressed and angry as kid when my asthma did not allow me to partipate in normal childhood things. I was sad and hated life when I couldn't keep up with friends at recces because I was having trouble breathing. You have to outweigh the costs with the benefits. I am more irritable when I have asthma flareup then I am on a normal day. For me, I choose to breathe. And singulair has been helping me for almost a decade.

I'm not saying the medication isn't causing these symptoms but maybe there is an underlying cause to your child's depression.

Any drug has a side effect. But without medical research and the medications that come with them - people would still be dying of simple diseases and we wouldn't have vaccinations. As a society, as a whole, we are a culture that looks to someone else to fix things and then blames the people who try to fix it. We need to stop being the "hot McDonald's coffee'" society.

Today is Christmas day 2008. And a Merry Christmas to me ha!!!!!!!! I was given a prescription for the drug Levaquin on the 19th of December for a suspicion of pneumonia. The x rays done at the hospital found no evidence of pneumonia but my doctor wanted me to take it anyway because since I have asthma and my lungs sounded so bad I was told that I was at risk for developing any secondary infection that was out there. My husband filled the prescription on the 20th which was Saturday, took the first one of a seven day supply 500 mg tablets. About 4 hours after taking just one pill was awakened by severe and agonizing pain in both of my feet and my knees that I was writhing in pain. Since I have nerve damage in my feet anyhow I know what the pain that I normally experience feels like and instantly knew that this was not normal for me. When I thought that I finally might be able to walk I hobbled into the kitchen and dug the list of side affects out of the garbage (stupid me had not read them first.) I discovered that it was one of the side affects. Called the on call doctor in the morning since it was on the weekend and he stopped it immediately and put me on something else. I only took that one pill and since Saturday night every night I wake up in agonizing knee pain and I have never had pains in my knees before. The pain is so bad that I feel like I am ready to go on a morphine drip, or cut my legs off above the knees. Six days now from one pill, how much longer can this go on? I really feel bad for the people that contined to trust their doctors and continued with the full course of the medication and I realize that what I am experiencing is minor compared to what others are going through. This drug should come with a handout that says: Take this drug at a risk to your health!!!!!! Last night the pain lasted all night and I cried all night. Have to get through this day am entertaining for the holiday and have had no sleep. Actually getting afraid to go to sleep at this point.............D.

I have been taking Zocor for 6 months. In the past 3 weeks I have developed intense tingling and burning in both legs from my feet to my knees. I also have a feeling of numbness in my right foot that at times is in the whole ball of my foot but will move to the side of the ball of my foot. I have been to the ER twice and all my neuro checks were normal even though my legs felt like they were on fire. I just this past week had a MRI of cervical and lumbar spine. My doctor is thing the symptoms may be related to the significant arthritis I have in my neck and may be due to nerve compression at one of the discs but I don't think so. I was worried about MS and Guillian Barre as these can be symptoms of those diseases as well but I didn't have any other symptoms of those diseases. At my last ER visit the doctor put me on Neurotin for the burning in my legs. I just happened to think to look on line for med interactions and side effects of the meds I am on and would have never expected that Zocor could be the culprit. I was astounded to find that the tingling and burning was more than likely due to the zocor. I stopped taking it about 4 days ago and am showing some improvement but I am still taking the neurotin. Does anyone know how long it takes Zocor to get completely out of your syste.? I also have nerve conduction studies scheduled.

Since my daughter second gardasil shot she has become tired all the time, she passed out on November 10 and was taken to the doctor. She orderd an EKG, chest xray and blood work. They called me that night and said she has an irregular slow heart beat ( which she has never had before). We went to a heart specialist the next day, he did an echo cardiogram and said things looked fine. If she passed out again, for me to call him and he sent us on our way. Tonight, while she was walking at work, it happend again. We went to E.R. and basically were told to follow up with her doctors on Monday. She is supposed to get the third shot in December, now i am afraid for her to get it. Im wondering if her suddenly getting the slow irregular heart beat, and passing out, irregular period, and headache is connected to the Gardasil. She is 17 and a senior in High School, she was planning on going to college, but now she is afraid to be alone, drive, or do anything that typical teenagers do.

My hair kept coming out by the handfuls. I've lost at least 8 inches since I started simvastatin! I mentioned this to the endocrinologist and he said he didn't know, but he prescribed it. I am furious, hair is a woman's crowning glory.

On October 11, 2008 my 14 year old daughter began to complain of being dizzy, headache, faintness, nausea, vomiting and stated that her heart hurt each time she took a breath. This warranted her being admitted and transferred to a specialized children's hospital. They discovered an inexplicable enzyme (troponin) surrounding her heart muscle which only appears when someone is having a heart attack. All of her echo cardiograms were normal as well as her other blood levels. She was tested for all of the typical high school diseases as well as lupus, etc. She remained in the hospital until Thursday and is now exhibiting an irregular heartbeat pattern. After visiting with her pediatrician since her release, it is extremal possible that this is a side effect of the Gardisil shots that she had this past November - February.

I recently lost my brother Marty to ALS. Marty asked me to tell everyone about his experience and I promised I would. Marty began taking statin drugs in his early 40's. He took them off and on at the suggestion of his PCP. It began with Lipitor and progressed to Crestor. In Dec of 06 tests revealed elevated muscle enzymes, he was also having pain in his left leg. His PCP called and told him to discontinue the Crestor, which he did. The pain continued and other symptoms began to materialize. Symptoms included muscle weakness, toe drop, fasciculations and continued pain in his leg. In June 07 after many tests he received the diagnosis of ALS. He passed away in August 08 at age 52. He believed as I do that statins caused this most horrible disease in him. He also believed that cholesterol is a symptom not the causal agent of heart disease. Now you must decide.

Why is it OK with the DR. if synthroid makes us gain weight?!!! I've been hyperthroid before and lost weight...why does the med make us GAIN weight...I've tried EVERYTHING....We must demand they do more research..something just isn't right..but what do they care as long as our blood work LOOKS right! We should have the same rights to meds that work as the rest of the population.

I am a 51 y/o white female that has been on Lipitor for 2 years. I am 5' 1" and when I had to go on it my cholesterol was 267 I weighed 112 lbs. I was shocked.... my doctor told me weight had nothing to do with cholesterol. She kept a close watch on me and my cholesterol came down...... and then my ex-husband of 17 years and I re-connected and got back together and I moved so I had to get another primary care physician. I took all my meds to her, she also kept a close watch on everything. At this time my cholesterol is down to 109 and I asked if I could stop taking it, as I take quite a lot of meds, due to different things and if I could stop anything it would be great, but she said it I stopped it, my cholesterol would go right back up. So since I am not experiencing any side effects I'm okay with continuing it.

I surely hate to hear what you all are experiencing with your Lipitor..... could your doc try another cholesterol medication?

The only one of my meds that is giving me any problem is TOPAMAX........ that we are using as a Migraine preventative! HORRORS!!! Today is pretty good day. But my cognitive abilities are in the trash... I say the wrong word when I mean something else...... I search my mind looking for a memory...... I am also on disability since 2002 because of the Migraines....... I have has them since 1978, but they got progressively worse over the years until I was sick more days per week, sometimes more than 7-10 days at the time, having to be in the hospital being rehydrated and on IV pain meds.......... and as awful as the TOPAMAX is.....it has been reduced the migraines to approx 2 per month and they do not last nearly as long.

So sorry, I got waaay off topic, but I know that it is not the Lipitor that is giving me the side effects as it the last med I had to go on and I had no new side effects....... but that TOPAMAX is kicking my behind.

Through the past years I have been looking for information about the quinolone antibiotics, Levaquin, Cipro and others.

I have not taken this kind of medications myself but a close friend did and I am absolutely sure that`s why he suffered psychiatric symptoms as well as extreme sesitivity to light and also had cramps/convulsions.

It`s a terrible long story which also etails other medications for instance statins.

I am surprised at how similar quinolone and statin side effects seem to be.

A few minutes ago I found a new site which might be interesting:

Google for "Death by Levaquin" and you will probably find the site I am thinking about.

If I write down the exact address it will be replaced by *****.

O passed away at an old people`s home at the age of 74. I will never forget his suffering.

The best thing you can do for yourself and the people around you is to "educate" yourself on diseases/medications and how the pharmaceutical industry is run.

Here are two books on that issue: Overdosed America (John Abramson) and The Truth About The Drug Companies (Marcia Angell).

Don´t give up.

I just googled "Prilosec & weakness with sweating" and came up with this site. I have been on OTC Prilosec for at least 2 yrs. taking it off & on...mostly on (everyday). I have been getting more ill over the last 2 months than I have ever been! I am diagnosed with Firbomyalgia & CFS, so I keep blaming my worsening symptoms on those two diseases. My doctor has done so many tests & can't find any answers. I am so glad I found this site. My symptoms of severe weakness, & profuse sweating, with many heart palps, may be coming from the Prilosec. I am going off of it starting today to see if I get any relief. I will have to find something else for my acid reflux...no more medicine!! If anyone knows of a natural product or food to lessen the acid, I would love to hear!

I am a parent of a 14 year old son. He has been on many meds due to having migraines, adhd, seizures, and asthma. For 3 years his ADHD meds have been switched. Now Thanks to a friend she told me about singular side effects. OH MY GOD. it blows my mind reading this stuff. He has been on singular for 3 years and never once did I think all these problems were caused by that drug. Flipping out over the smallest things, arguing with us his parents, his friends, being mean to us and a real smartass, depression, and MAJOR attitude. Getting upset over nothing at all then crying for no reason What was his Dr. thinking? Needless to say, I took the singular while she was telling me this stuff about her own son, and threw them away, I will never allow my son to take that shit again. I hope in three days like all of you say, that my son will be that loving, caring, friendly person he use to be ! Singular free is how he will be!!

My son (9) was on advair off and on for a while for severe asthma. I noticed depression, anxiety, fatigue and fibromyalgia type pains all over his body. I had him checked for lupus and other diseases and all negative. He also developed a severe rash between his legs causing much pain and discomfort as he had to walk like a bull-legged horse-riding cowboy. Showering often never helped. I assume he has candidis yeast infection(systemic). He was finally put on Prozac and I took him off Advair against my doctors advice. i took him off slowly and your body may need to make it's own steriods and not go into shock. He takes as much albuterol as needed to get him better and then i give him prednisone for 3 days when things become an emergency. tTe prednisone leads my son to anger and suicide but it goes away after he finishes his course, but it saves his life. He is now 13 and much happier and his face and body has thinned out by half. I will never give my son Advair again.

I Take loads of medications & have always tolerated all side effects but Lipitor has floored me. I have only been on it for a month but have ceased last night after waking up vomiting. I spent a day where I had so little energy I hardly moved & was almost suicidally depressed. I have no sex drive, such an itchy scalp that my colleagues were worried I had fleas !. No appetite, flu like symptoms & muscular aches that were unbearable. I still feel woozy headed but can feel some normality returning, my doctor will not be happy as I have scarily high cholesterol that needed urgent treatment, but I am afraid that I have to find an alternative as my reactions to this drug actually made my life unlivable.

I am 22, I have Lupus and RA. I am on other meds too but I am more than positive that Prednisone has brought about my moon face and maybe my sleepless nights. I workout everyday and in the best shape I have been in my whole life but it sucks because I am only able to be this healthy because I am on all these meds including Prednisone. I probably would be using a walker. So basically its a choice of vanity(huge head) or good health.But I have asked my doctor to lower my doses. Was at 30mg, I am now at 20....hopefully I can get down to just 5mg and still be able to move my joints as freely as I do now