Vitamins symptoms and conditions

Just to give an update, ive been off Yasmin now for a month, and am starting to feel normal again, I am not as paranoid and jumpy. I used to feel like my blood was boiling at the smallest things! I was on Yasmin for about 4 years, came off it for a few months and then went back on it, it was only when I went back on it after the few months that I knew something wasn't right and came back off it again!

I have just had my first real period so am relieved it didn't take a few months, like some of the other women on this site. One of the things I noticed the last time I came off Yasmin is that my skin became bad, but I have been forcing myself to drink plenty of water the last month so fingers crossed the spots stay at bay. I have also started to take vitamins.

I have a lot more energy lately too, but am just glad that I am not half as paranoid and jumpy as I was, I think my poor BF is glad too, although I don’t want to speak to soon as I am highly strung as it is :-)

My son is on the 15mg patch. He is developing OCD type behaviors-right now it is an obsession with his fingernails-always picking at them, getting dirt out from underneath them, even when there is none. We have tried adderall and this. I think I am going to try something natural. Any suggestions? He also won't eat or drink all day so we need to go a different route.

I am a loving mother of a 5 1/2 year old boy. He has been on Singulair for over 3 years. In this past 3 years my son has suffered in an unspeakable amount. He came down with Rota Virus and was hospitalized at 2. He then came in contact with Pneumonia in the hospital while he was there. They automatically put him on Singulair, Zyrtec, Prednisone, and antibiotics to treat the pneumonia. Since that day, my son has gone though more tests than I have in my entire life. He has had asthma, sinusitis, leg cramping ( to the point he cannot walk for 2 years), IBS, Acid reflux,(they gave him laxatives for a year that made things worse and addicted to them also), stomach pain, constipation and diarrhea back and forth. He also got Erythema Mulitforme TWICE, while on this drug. All of which the doctors said could NOT be caused by Singulair. He has had several Upper GI's and CT scans. Along with Barium enemas, several hundreds of blood tests, and many many pokes and prodded that were not necessary. All since he has been on Singulair. He now has frequent bathroom trips, depression, confusion, and anger outbursts. He also has to go to the restroom every 5 minutes. He has had genital swelling, and many other aches and pains. None of which his "doctor" ever said could be a result of Singulair. I am 100% sure it was!!!! He currently has anxiety and emotional sporadic issues causing problems in school The teachers and counselors say that it is so strange because there is no TRIGGER and the outbursts are completely inconsistent. His preschool teacher and director are sure he has ADHD. Well, we had him tested and he does not have any part of it. He has no learning disability what-so-ever. So that brought me back to square one. He is in a positive loving enviroment. How could he be depressed and want to hurt everyone around him? He cannot sit still. He cries and says he is 'stupid" and "can't think" like the other boys. He has nightmares and cannot sleep alone. He is scared of everyone and everything. So, as I sit here crying, I realized that this has all been a reaction of his "medicine" Singulair. He never should have gone through all of those painful tests, only to prove they couldn't find anything. So many treatments and sound full advice speeches from his doctors. How could they be so naive and selfish in the life of my son?

When I called my pediatrician of 5 years, she told me that " parents that have children with behavioral problems will LOOK for something to blame their problems on." She also said "drug companies only put side effects on their labels to PROTECT the drug companies. (as she laughed at me) They are not always valid". Then she said "if you take you child off of Singulair you will be playing Russian Roulette in his life." Then she said that all children around 5 or 6 go though this emotional time in their lives." She told me that if I take my child off of Singulair that she would no longer be a part of his health regimen for his asthma. She told me to see a Pulmonologist for further treatment.
Who is paying who? This is my son's life???????? I decided to go with my mother-gut instinct and get him off of this medicine. No matter what. He has been a different person since. He is currently going though a lot of side effects and withdrawals (leg pain, insomnia, hic-ups, emotional distress) but every day is getting better. How can the drug companies say that this is a "wonder drug?" There are more reported side effected patients then clinical studied patients! How can a "medication" that stimulates the brain not be connected to other problems? This "medication" interferes with the bio synthesis and action of LTs and has been marketed as NOVEL medication against asthma and allergic rhinitis. Who the hell is playing God here??? The pocket books of Merck or our over PAID "doctors?" Who pays the price? Our children? Or us. Thank god I found this before it was too late. I would not be able to withstand the pain of losing my son due to their lack of scientific evidence. They are lucky I am one of the smart ones. I will not settle for less than Justice for the drug companies and their paid "doctors?" You all end up in the same place. HELL

There are 18 million people on this drug. Most of them are children. Please save a life if not your own child's life. Thank You

Ive been taking berocca for almost a year now. but not really taking it straight like once in a day for a year, but there was also a time that i skip for a month.

Im a recreational biker and there was a month that i took berocca 2 week straight and i take it during night time before i sleep so ill be pump up for the ride in the morning.

After the two week straight this is where the symptoms took place i am having a manageable pain on my lower right rib (the part where my last rib ends), my wife told me its the liver part on that area of the body. I was thinking its just a muscle pain on one of my bike rides.

but i stopped taking it not because of the pain but its because i run out of stock. I already forgot about the pain but after a month i bought the vitamins again i drank one tablet and hit the road, while on my bike i felt the pain on my lower right rib again. but this time it made me think its not a muscle pain at all because its been 3 weeks i stopped biking. Just today when i want to just bike around the city.

I haven't gone to the doctor yet/

Three years ago, my Doctor said he wanted my cholesterol lowered. He prescribed Lipitor 10 m every other day.. Last year Cat Scan revealed a clogged minor artery so doctor increased to 20m PER day.. Test results proved Cholesterol down to " perfect" said the doctors BUT the rest of me was falling apart.. Severe muscle cramps in both legs, fatigue, muscles all over had no strength, weakness, nausea, headaches etc.. My cousin who is a doctor had been taking Lipitor herself but stopped because of the above symptoms.. Both my Cardiologist and internist have told me to stop taking Lipitor for a period of time to see if these symptoms dissipate.. After three days I already feel better. I have begun to eat 100% healthy: taking vitamins: vitamin C, Omega 3,6,9. lecithin & exercise, etc. And praying a lot..

Im so happy I found this site, as I too thought I was alone in this. I really beg someone to tell me, oce they came off the pill, how long did it take for them to recover? and for their first period to come? I was on the pill for less than a year, and came off it in Feb 08. It's now Sept 08 and still have not had a single period since. My weight has been fluctuating ridiculously, and the mood swings have made me lose SO many friends its unbelievable. i don't have energy to do anything, ive it a total depression. Im begging someone to just tell me how long after they stopped did everything feel back to normal? im worrying as its been 6 months for me and still nothing!!

I have been experiencing the following side effects after taking Januvia for the last year. Night sweats, nightmares, GA (which is fatty tumors on my left forearm I have about 40 of them), arthritic type pain in my left shoulder and left hip that radiates down the arm and leg. eczema on both hands SEVERE. I have quit taking the blood pressure medicine (used only as precautionary) cholesterol meds, and prozac for a week now and am very sternly watching my diet!!! and exercise regularly, I have yet to quit my diabetic medicine but will quit one at a time to figure out which is causing my side effects. I believe the drug companies are making a killing off all these drugs that make me feel like crap. I am taking more herbs, vitamins and like I said eating HEALTHY. I won't even use splenda or sweet and low, Have been using Stevia if I use any sweeteners at all.

Am 47 y/o male have been taking 10mg since June 30, 2008. Over last couple of weeks have had bouts of severe leg pain, not cramps but just achy. Also have lower back pain especially in morning when waking. Problem is i have chronic back pain so hard to distinguish between the two but it just feels different. Also bouts of fatigue. Called my doctor and was told that the aches in legs not a problem because the side effect is cramping not soreness. I don't buy that.

Hello Everyone,

I am 33, male, I have been doing sport actively for at least 10 years (swimming and running) and I have been leading a health-conscious diet. I have a hereditary high-cholesterol condition, a type which appears in adulthood (so they say). Since 2004 my blood tests have showed roughly the following results: HDL 1.1, CHL 6.2, LDL 4.1, TRI 4.38 (mmol/L).
I have been taking Zocor 40mg for about less than a month and recently I have been experiencing cramps in my left lower arm, fatigue, itching (this morning for example I was woken by the cramp in my left arm, not nice). I have just read all your posts and have decided to abort my Zocor treatment at once. I have bought Q10 capsules and vitamins and started to drink 4 liters (herb tea) a day. I hope the pain will soon abate because now I have a totally dysfunctional left arm (I can't grasp because of the pain).

I am going to write in a week's time about the de-Zocoring of my body. In the meantime, I wish a speedy recovery to everyone.

Peter

Honestly thank you for this website! I mentally feel better if not physically yet. I was prescribed 3 day/2 dose Bactrim for a UTI. I have NEVER had a reaction to antibiotics or any type of medicine. I can no longer say that.

That said...thought I was dying. My temperature was 102 for days, every muscle in my body felt so sore I felt like a car had hit me and then hit me again, ridiculous size headache, massive stomach pain, insomnia, thought I would faint every time I stood up, could barely walk, no appetite, etc. It was ridiculous and I thought I was going crazy because how can one medicine do all that?? I now have a whole new respect for antibiotics.

Since I was feeling so horrible by the 2nd day on it I went ahead and finished the last day. (hindsight probably stupid)

This is my first day off and all my muscles are still killing me, especially my neck, chest, stomach, back. Still feel weak and my temp. this morning was 101 and went down to 100 now.

And I don't know if it was the medicine or just being sick but I've been so 'out of it' today and just depressed. I can not WAIT for this medicine to be out of my system! And I will never use it again.

To add insult to injury I'm not sure if it cured the UTI all the way. Not running to the restroom but still have slight (non-painful) tingle down there.

I stumbled onto this site while trying to find a reason for these headaches I get sometimes for no" apparent" reason. Imagine my surprise to find your testimonies about your lives on warfarin sodium.At 38, I had surgery to repair a congenital defect of the aortic valve and had to have a hema-shield graph to repair an aneurysm of the aorta. That was in Oct.2002. Warfarin has been a part of my life since then. I was also put on anti-depressants because my family Dr. thought I was depressed since I repeatedly complained of not feeling well.(I took myself off the anti-depressants a couple of years ago.) Extreme fatigue , serious memory issues, thinning hair,dizzy spells and numerous other ailments continue to plague me.Add to that a large weight gain ...and, well, you get the picture. If anyone knows of an alternative to taking this "poison", PLEASE, PLEASE let me know. I just WANT MY LIFE BACK!!! I actually cried after reading this blog. As I explained to my husband, I suppose it was from the sheer relief of knowing I was not going insane!!!

I have been on Norvasc for some time,but was switched to the generic form a little more than a year ago. I have been very unhappy with the quality of the pill from Mylan Labs. It dissolves in my mouth, tastes horrible and sticks in my throat. Last month, I had it go down my trachea and was coughing it up for 2 days, which included alot of burning. I asked my doctor to prescribe the name brand but she refuses, stating state drug laws as her excuse. I know it really has to do with my insurance company's formulary and she just doesn't want to go to the trouble of getting it approved by them. I tried calling all the local pharmacies to see if another company's version was available ,but they all only carry Mylan's version. I take a lot of prescription drugs for several chronic health disorders, and several supplements and vitamins and can swallow a handfull of pills at one gulp, so I know this problem is not my pill-taking technique. I also started to experience swelling in my feet, ankles and hands about the time of the switch to generic, which I never correlated to the generic Norvasc until now. I told my doctor I will not take the generic from Mylan and am awaiting a call back from her as I sit writing this. I am having surgery in about a week and can not afford to be playing around with my meds, but this is important to me. No one should have to accept an inferior product. By the way, I'm writing to Mylan, too.

If you are taking this medicine, STOP! I took this medicine for about three months. I started to feel like I had a congestion. I cough lightly at first then into a hard cough which progressed into a hacking. My wife thought I was critically ill. I was spitting up clear congestion at work into my garbage can. This stuff is bad, I found this site and stopped taking the medicine. It took 3 week for the cough to subside. It’s been about 4 months, and I would say I am only about 98 percent back to where I started . About every 3 weeks I out of the blue start to slightly hack. I know one thing this is not a good medicine. When I started my BP was 138/109. My doctor told me to try this. Because of this medicine I could not do my job and my doctor never told me it was the medicine. When I told him he told me he didn’t think it was the medicine and prescribe some cold medicine

After having the third shot I noticed my hair began falling out (July 2007). It is now over a year later and after having numerous blood tests, visiting a dermatologist and doing tons of research, I have concluded that gardasil must be causing this. My hair continues to fall out, I have bald areas around the crown of my head and my mood is very depressed by this. I also experienced soreness in my legs and joints but these are not constant. My periods also are out of whack. They can be between 28-50 days apart. I would not recommend anyone getting this vaccine. I wish my OBGYN had not sold me on it. I was 31 when I got it but she said age didn't matter, she said one day insurance companies would cover this vaccine for all women no matter what age they are. I paid $190.00 a shot and now I have a thin head of hair that may one day soon be bald if it doesn’t stop falling out. I think they should take this vaccine off the market. If anyone else has had severe hair loss, has it stopped falling out after a certain point?

unfreakinbelievable. every single drug ad I see on TV these days for new drugs claims that it will cure you of something. the only catch is: it will give you a million side-effects, half of which can be life threatening!!!

What kind of a job is the FDA doing that it lets these kinds of drugs enter the market and puts people with common problems like asthma in greater danger for developing extreme heart problems and psychological disorders???

I used Reactine. The very 1st tablet I used gave me a dream so vivid that I jumped out of bed - I was about 30% conscious and I still believed that I was in that dream. I dream that a Black Widow was in my bed right under my back and when I woke up I actually envisioned the Black Widow. Now consider that I live in Canada where BW's don't even exist. That's how powerful these drugs are and that's why you should stay away from them. I know this sounds crazy, but DON'T BELIEVE A THING YOUR DOCTOR TELLS YOU!!!!! Use common sense in common situations!!! Think for yourself and listen to your gut instinct or you will wind up dead before your time.

Here is a follow up- I have been off of the Lisinopril now for about 6 days. I am slowly feeling better and getting energy back. I still have some residual muscle burning, bouts of fatigue, bouts of depression. The shortness of breath is getting better also.
The irregular heartbeat is almost gone and the cough is now only occasional.
I have been taking vitamins such as vitamin c, multivitamin and drinking lots of water.
My memory and loss of words is getting better also.
I am forcing myself to exercise and lose weight. This med almost killed me.
I just pray that I don't have any permanent damage.
Also significant is the symptoms got worse when they were manufactured bu IVAX.

I'm 25, and I have never used bc. I was given this from my gyno. because my bf kept taking off his thingy. So the first day, the very first day my hair started to come out. I gave it two weeks, and threw it in the garbage. I had hair falling out everywhere, I had EVERY side effect listed. My vision was also screwed up. I didn't know what the hell was going on with me. My bf broke up with me, my moods were crazy, my boobs hurt, i had cramps, heavy bleeding, nausea, all i wanted to do was eat food, stomach pains, depression, anxiety, a headache, I was dizzy to the point were I just wanted to start crying, I even had the shits...This pill is a joke. I can deal with minor things like spotting, and I realize it takes 3 months for your body to adjust, but I couldn't even take it for 2 weeks. I did notice that if you take vitamins, the side effects were better.. but still my heart hurt so much I thought, holy crap, I'm going to have a mini-stroke at the age of 25. I am so thankful to god that I found this site and I could read other people's stories. I really think the idea of bc is wonderful, but until they make a pill that my body will accept- I'll stick with condoms, they have worked so far, I would even go on to say, I rather never have sex again then to go through the toll of this pill. This should have never been put on the market.

I just went to the Dr. for my second Lupron injection and to get some help with the side effects. Menopausal/emotional me, started crying!!! Gawd! I went in with my list of side effects from the last 3 months (and it was long!) and wondered what was worse, the pain of endometriosis or the life changing side effects of Lupron. My Dr. is wonderful and spent an hour with me; he decided to put me on Provera (progesterone or add-back therapy) for a week to see if the side effects improve. If they do, I get my second dose of Lupron in a week. If not, we stop it all and let my body slowly try to get back to normal (although I have never known what "normal" is since endometriosis) and see how the "therapy" worked. He is strongly encouraging me to follow through with the 6 month course as that is the recommended length of time for the best results. I'm 5'8" and have lost 10 lbs. in the last three months, I'm down to 107 lbs. He told me to try and eat more if I could (although my nausea is constant 24hrs. a day) and make sure to take a daily vitamin and calcium for bone loss. He said that he has never heard of blurred vision to be a side effect of Lupron, "But every woman is effected differently." I'm really hoping the Provera works - any kind of relief is better than this! I'm still having 3-4 hotflashes every hour with extreme exhaustion/fatigue, night sweats, daily migraine headaches, nausea 24hrs. a day, life changing mood swings, and shaky hands. He kept reminding me that this only 6 months out of my life - it's not forever ... forever feels like an awful long time when you can barely get out of bed!

Lately my wife has been experiencing of depression, lack of energy, muscle cramps, nausea, enlarged and soar breasts (nipples are hot also), headaches, insomnia, vaginal discomfort and sourness with and without physical contact, constipation, and other symptoms, which I cannot as a male, properly describe. Is this accumulation of symptoms normal or should we look in another direction for birth control (besides condoms)? A concerned husband, Kenny...

I have been on lisinopril on and off for over 2years or better.I started with 20 mg.then i cut that down to 10 mg. then to 5 mg, still feel bad,that includes 6 mg.hctz.many side effects,muscle weakness,neck pain,cramps in legs mainly,and just feeling like your about half sick all the time, have to force myself to move because of feeling tired and aching all over, if i work in my garden i have to sit and rest every 5 minutes because the muscles in my back start hurting and get weak,blurred vision, itching ,bad dreams,irritable( my poor wife) etc. Also take metoprolol 150mg. per day and have for a lot of years which also has side effects.Tried taking hypavera which is a natural herb mix after 2 days bp went up to 204/94 so stopped that fast so be careful on mixing certain vitamins and herbs with prescription drugs.

This is the first time I have actually looked up side effects to NuvaRing. I have been on it since March of 2006, so about 2.5 years. I never really noticed side effects, and I have been to the doctor more than once and told them about the same side effects that have been discussed here. They blamed it on lack of vitamins, lifestyle changes and other random facts of life. Maybe that is the cause of my problems, however, why would they all happen at once???

Until today, I was soooo happy with NuvaRing, and I still am. I am just more aware of why I feel the way I do....It is soo easy to use!! I would NEVER remember to take a pill everyday, I would not like the patch, and the shot wouldn't go with me very well either.

Seems as if every birth control has side effects...here are mine from NR

EXTREME fatigue..
I asked my doctor about this. It has been going on since January. I sleep for 13 hours a day and am still exhausted. I cannot get enough sleep. I am a 20 year old that used to lead a pretty active lifestyle, but it seems the last few months that I have slowed waaaaaaay down. It isn't like me. I usually stay busy

Weight gain
I can accurately say that I have not been as active as I was in the past...but in one year I have put on about 17 lbs, and no matter what I do, the scale keeps climbing....I joined a gym for about 4 months, and I didn't lose a single pound. Before, I was able to LOOK at a treadmill and get in shape, now I spend an hour a day on it, and it does nothing for me.

SEVERE Headaches...with sensitivity to light and sound
I have not had this bad of headaches. EVER. It usually starts in the back of my head and moves to only one side. My doctor told me to wean off the caffeine. I did and they are still there. I drink no caffeine daily and I still am getting these terrible headaches. I work at a casino, so sometimes it really interrupts my daily life, with the lights and sounds and everything.

I AM ALWAYS THIRSTY!!!!!

I have NO sex drive
My boyfriend and I used to have sex every single day when I just started the NR, but now I NEVER want to. I have to pretend that I want to have sex, just so his feelings are not hurt. Sometimes I even catch myself thinking "is it over yet??" That is SOOOO not like me. I was an animal the first few months I was on NR. Now I have no desire.

I feel as if I am just living the motions of life sometimes instead of participating in it. Like I am just here everyday, not always feeling what is going on around me. I am semi moody, but nothing out of the ordinary. Week 3 of the ring is ALWAYS emotional, but the week before my period has ALWAYS been like that. I find it very normal.

My periods are WONDERFUL. I used to have a full 7 day period from hell. Now they last only 3-4 days, and I can basically tell you when I am going to start to the hour. It is AMAZING.

All in all, I love NR still. I am not going to stop taking it yet. I am just glad I found this site so I know the reason behind all of these changes in me. I have never put two and two together....that NR was causing all of these things...but now I know it could be. Or maybe it isn't. Who knows, but as long as I keep an eye on symptoms, I think I will be okay...

If any of you have any questions I have been on NR for quite a while, so feel free to email me at ******

I am getting my MIUD removed next Firday after 5 years use. I assumed many side effects that I have had were due to my Fybromyalgia condition that I have had for 12 years. I have been treated appropriately by my Doctor. I also have degenerative disk in lower back that keeps me in constant pain. I have gained 20 lbs. over the 5 years and assumed that to be do to getting older, I am now 42.

I was going to have a new MIUD put in but I decided to give removal a possible shot at hopefully relieving me of some of these symptoms. I really have had no known issues with the MIUD and had regular light 5 day periods the entire 5 years.

I am anxious about what I have read and hope that there will be some positive post MIUD removal stories for myself and others. Meanwhile I will take my vitamins, exercise, and hope for the best.

Take causation when assuming that your symptoms may all be due to the MIUD as many symptoms copy other disorders. When in doubt take it out may apply here.

Just a quick tip... i've read several times that certain vitamins and drugs effect the pill such as tylenol and vitamin c... iv been spotting a ton and i take a large dose of womens multi vitamin each day. every time i stop taking vitamins, my spotting goes away. i don't know if this is directly related, but it might help some of you, because it has helped me. i am also only on my third pack.

I am 31 yrs. old and this is month 4 on the NuvaRing. I have been on several different types of BC over the years the side effects had been so severe I decided to give up on BC all together. When my doctor recommended NuvaRing I was leary, but I tried it anyway and was quite pleased until recently. I am not experiencing head aches, nausea, or irregular periods, but I am experiencing problems with my moods. Most of the time I am sad or I get agitated very quickly for no reason. I was shocked to read about some of you experiencing loss of energy. I thought I was going crazy. I don't seem to have any energy...I am tired all the time. I have been taking vitamins, but they don't seem to be boosting my energy any. I have gained weight in my stomach and seem to be gasy and bloated. My jeans are so tight...It is depressing! In a matter of 2 weeks my breasts have grown in size...I am sure I have gone from a 36 C to a D! What I am most concerned about is the blisters that appeared about 2 1/2 weeks ago on the exterior of my vagina. They are very painful and over the counter creams are not working. I am not sure if this is due to the NuvaRing. I have my anual checkup with my OBGYNE tomorrow. I plan on getting all of my questions and concerns addressed. My delima is do I stay on NuvaRing...I like that I don't have to worry about popping any pills and I don't get any major side effects. What should I do?

I gotta tell ya this is scary. I am a 30 yr old guy my wife is 27 we have four children.Our last one was born Mar. 2007 She has been on Yasmin 6months or so.She has never been regular on periods. Well a few weeks ago she started having massive headaches.As of June 31st her doctor said she has migraines. Well by July first her left eye went blurry by the 2nd she has lost vision in both eyes.She only sees light and is very cloudy and can see shadows. We made 3 trips to ER. They did Cat scan and it was neg. the doctor said she might have even had a mild stroke because her left cheek went numb. By the 2nd we were in ER again because of total vision loss. They did a lumbar punture and no Meningitus. cat scan again neg. blood work neg. except UTI sound familiar ladies??? By the 3rd we visited her doctor and she passed out and was rushed by EMT to Hosp. They did and MRI,MRA,had a eye Doctor called an ophthalmologist clear her of vision problems.She has talked to a neurologist. So here is a 27 yr old female with all the test's coming back normal but she can't see.They even had a psychiatrist talk to her because she is on Prozac because she has PCOS and had half her ovaries removed and almost died.They even suggested that she had conversion disorder(google it).Finally I decided to check side effects for all her meds. When I checked this one I almost jumped outta the chair.She has about 10 symptoms. But before I get too excited has anyone had vision loss for a period of time and did it come back once off of it?? I'm throwing these away