B12 symptoms and conditions

Ok, caseybo if I were you I would have my bloods checked. It's not a joke since Yasmine may cause a vit B deficiency. Sounds like vit B12 or B6, actually. Get yourself checked up. You can top up your vit b6 easy by introducing some vit. suplements and meaty and eggy diet but b12 as being stored in a liver has to be injected if lacked.I have just come off Yasmine because I had a descreased sex drive up to the point there was no purpose to take a pill.Also bad skin and getting erraticly moody. I have been off for just over a week now after being on for 8 mths. Blime!I soo bloated, have PMS-like symptoms including aching ovaries, back pain, mussle pain, tiredness, overall fatigue and the strangest one: tingling sensation all over my upper body, like something is creeping on me.anybody experienced that?Cannot wait to get back to my old normal. I only hope I won't put any wt on!I do not have an apettite at all as for now.Also want my boobs to get back smaller as DD seems to be to heavy.

I have been on topamax for about 7 months now for migraines && im about to get off of it. Im 18 years old and "trying" to do college but ive had so many side-effects its crazy. I cant go to the bathroom w/out taking laxatives cuz i just cant go ne more i literally have to take something everyday or i will be stopped up for a week or more. Ive been depressed and my anxiety has gotten worse.I take 150 and they want to put me up to 175 but i refuse because ive heard of people losing their hair taking it especially when they have a b12 deficiccency...which i have. I have horrible mood swings i can be happy one minute then sad or mad the next and i never used to be like this. Ive now started getting my migraines back so im stumped on what to do. I cant word things right....i was trying to say i didn't like something and instead it came up "im not to high"... yea so its deff a crazy drug but it can work for others and not. Not for me!

I've finally had the mirena removed - about 2 months ago. I'd had a very light period around the time that it was removed, but none since. My body aches a little, still, but it's more tolerable that it had been before. Initially i could NOT stop urinating! i lost easily 3 lbs of nothing but water weight in the first couple of weeks. As excited as i was about that, it's a bit at a standstill now, losing the weight, but overall, my tolerance has grown, my sex drive has returned and mood swings have drastically been more controllable. I enjoy playing with my daughters again, and i've been able to get a lot more around the house cleaned. I feel about 70% better now and i'll take that any day over what i had been feeling. I do still get melancholy every now and then but not as severely.
in the past 2 week i've started taking vitamins - w/ a little extra b12 and calcium w/ D - to try and help my body balance out. that definitely makes a difference in how i feel through the day.
1 thing i can't get over is the constant thirsty feeling and almost a copper taste that lingers in my mouth, but i can only assume that after retaining water my body is re-adjusting to the intake/release ratio. good thing i like water and tea :) over all - i love having the mirena! ----- REMOVED!

I too have had a great deal of hair loss, deep depression and sadness.
I can't seem to remember anything, feeling very loopy...
I have just stopped taking the xl 300mg after reading all of the posts today!!! I'm going to try all natural ( B12, fish oil, st.johns wort) after being
on meds for over 13 years. the hair loss was the, well ... hair that broke the camels back. I hope it grows back.

I want to ask a question. My mom takes Lipitor and just started Vit b . is there side effects to be expected? She just started a new bottle of Lipitor and is exper. dizziness. is this a side effect of one or the other?

I was prescribed Loestrin for mood swings and depression during perimenopause. After reading these messages, I decided NOT to try it. I was intrigued by the mention of B12. I've had 2 people suggest I eat more protein. So I put 2 and 2 together, knowing that red meat has lots of B12.......
I started eating red meat and feel 100% better!!!!!!!!!
I had not eaten red meat in years.
Try it!
Try more protein and try B12/red meat.

Please help me. I have had the Mirena for a little over a year now and I have been miserable ever since. I just yesterday one of my very frequent depressive states. I has become so bad that I often think about hurting myself. I am very petite, 4'11 to be exact and I have never weighed anything over 115lbs. I just recently went to the doctor and I weigh 147lbs. I have always eaten healthy and I couldn't explain my weight gain. It has become so depressing I refuse to take pictures and I no longer want to look in the mirror. I have horrible headaches and my periods are longer. I am now going through a divorce and I don't have a job or health insurance. I really need to take the Mirena off but I don't know what to do!! Every day that passes by I keep getting more and more depressed. I am afraid for myself...help me

Headache, nasty huge clot filled period lasted for 6 weeks straite, heart problems with left ventricle - abnormal t wave - invertion - dizziness, shortness of breath, craving water, spilling b12 and vit d, inability to concentrate.... to an other wise health 37 fit female! Oh, and 3 months later, I have a spoon sized dimple on my right arm at the site of injection! I WAS NOT WARNED OF ANY OF THIS CRAP, NOR WAS I GIVEN THE PAMPHLET ABOUT POSSIBLE SIDE EFFECTS! I AM PISSED THAT SOMEONE SCREWED WITH MY HEALTH AND LIFE! I AM A SINGLE MOM WITH THREE SMALL KIDS!

Ok...now I am really angry. I posted in early June. I am 7-8 weeks out from stopping the drug (only took for 2 weeks) and, while I feel better in the am, I continue to have "attacks" mostly at the end of the day after work or when going to sleep. I have minimal dry mouth/cough (keep drinking water/peeing constantly but ok because I am eating foods to dump water which is why doc wanted me on this poison to begin with). The feeling woozy and nausea has subsided. I continue to have racing heart (happens when about to fall asleep and causes anxiety/insomnia), sharp pains all over the chest and in left arm (constantly think I am having a heart attack/stroke), tingling/burning in hands/feet, and to top it off shooting warm burning pain (very annoying) up and down legs (this is new). My doc told me to get off all my supplements (because he knows nothing about them and thinks they are complicating the picture...now I think he is ignorant). I restarted my CoQ10 which is protective for the heart and the racing has stopped so far (been a few days). In my research, most of the symptoms fall under "peripheral neuropathy" which can be caused by toxicity from drugs. Natural treatments suggest making the body more alkaline and detoxing the organs by eating nutritious foods (organic when you can), exercise, drinking lots of water (with lemon and cucumber slices which make the body alkaline and purify the organs) and taking alpha lipoic acid. To treat the neuropathy make sure you are getting enough vitamin C, E, and B complex with B6, B12 and folate/folic acid (I take B100 caps). Please research these before taking anything and make sure its right for you. I used to say check with your doc but, in my experience, most don't know about natural treatments. I will post again in a week to let you guys know how its going. Best of luck to all.

For those of you taking this drug and want to get off, please know it takes 3-4 weeks (longer in others depending on your metabolism) to be "totally" out of your system. Don't think you'll feel better in a few days. Give it a least 6 weeks to show significant change in your symptoms. I know, my husband took this and was having mental sluggishness, depression, confusion which led to many other tests. He has been off the drug now since Sept 08 and off the anti-depressant too. Guess what...no depression has returned since being of this drug. He's back to an aspirin a day, what he took before this nightmare began. Anybody taking this drug should stop immediately. It's the drug from hell!

I am 47 year old female with 5 days of headache and high diastolic bp. Doctor prescribed lisinopril. It made me want to sit for hours without moving. I was sleepy but could not sleep, cloudy thinking, anxious, thought I was going to die, had pangs all over my body and in extremities, racing heart with difficulty catching breath, etc to all the above symptoms. I stopped it after two weeks. I had bronchitis for four weeks. Then I developed dizziness/nausea and burning in the hands and feet. After researching that, I took a B12 and that tingling symptom cleared in a few hours. I don't know if the drug changes the metabolism in your system. I still am fatigued, occasionally have racing heart, and problems with sleep. Don't know how long it may linger in the system. Can't seem to find an answer. It has been 2 months since I took it and 6 weeks since being off it. By the way, my BP is now typically 117/82 with loss of 15 pounds. I prefer to treat naturally. Look up Taurine, CoQ10 and Hawthorne and see which may be best for you.

Three and a half years ago i suffered a heart attack, i had three stents put in and was put on Aspirin 75mg, Cardicor, 1.25mg, Tritace 5mg and Lipitor 80mg. I was fairly fit at the time, didn't drink or smoke and ate properly.

But now i'm suffering, i've been to the hospital and my GP, but are told there is nothing wrong, my hear tis good. So why am i suffering with light headedness, pains through my body, back, neck, chest, stomach. So much so i thought i had gall stones or kidney stones. My right knee can't be touched, it is so sore. Chest heaviness, eyesight getting worse, slurred speech, depression i could go on.

I've said this to my doctor, he just brushes it off and says i'm on them for life, ....apparently standard treatment for anyone who's had a heart attack. I walk 5 miles a day, eat 5 or more fruit and veg, don't smoke or drink, do all what i'm meant to. My cholesterol is really low, but so is the HDL too. I was never recommended CoQ10 or a vitamin B complex.

It was my mother who told me to research the side effects of all the meds i'm on. I agree, we all want to live a long and healthy life, but at what cost. I am now of the opinion that doctor's are so use to thinking they are near god like, they have forgotten that we are individuals, that we know our own bodies. I'm sick of the fact that the large pharmaceutical companies send out there sales reps to doctor's surgeries and that is what is deciding what the patients end up taking and not the patient's problem.

DOCTOR'S WAKE UP TREAT THE CAUSE NOT THE SYMPTOMS!!!!!!!

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

My daughter has been ill for the past two years. Please check out other postings by me on this site. Chelation Therapy will help - Gluten-free, Sugar-free. NO CORN SYRUP (alum. in it). Start eating fruits and fruit juices and greens. If the greens upset you stomach too much, back off until you have been gluten-free for a longer period. Take these vitamins and drink only distilled/bottled water. B6, B12, Omega 3, Folic Acid,
Magnesium, Calcium. These should start you on the way to recovery. If you see a doctor, please ask them to check niacin levels because I believe that there is a link with a niacin impairment issue. Please check more at ****** if you want additional information and also file a VAERS report immediately so they will get this vaccine off the market! I am not a medical person but have done tons of research. Please pass the word to EVERYONE you know!

54 years old male on zocor (simvastatin) 40mg for 4 years, two years ago I start with problems in my shoulders (feel horrible) arms, hands and legs. Pain, numbness, cramp, tingling, muscle spams and weakness, my body is very weak.
I visited several doctors and pain management, therapy, medicine, nerve conduction test, MRI, CTscan, nerve block, carpal tunnel surgery, injection in my cervical and toracic spine I don't feel relief doctors doesn't knows the statin fault.
I found this page and I have been off zocor for 4 weeks and not relief yet.
Does any one know how long it takes zocor to get completely out of my system?

I am so glad to know it is not just me! I've been on the pill since I was 16. Loestrin for almost two years now. I went on it originally to lessen the length of time I had my period. Each time I had spotting, I've been told it's normal and that it's just my body getting used to it. I found that if I took the pill an hour later then I took it the previous day that I'd start spotting. I felt like I was spotting ALL of the time! or like I was getting my period twice a month at least. I was told that it’s just my body and hormones adjusting.

Over this past summer I actually set timers on my phone and blackberry to take it at 11am every day out of fear of taking it 15 minutes late and starting spotting again. In October I skipped the brown pill week due to a vacation. I thought it was ok to do this. I started to feel depressed, tired all the time, like I was getting sick, I was anxious about my relationships, edgy and completely over emotional- I attributed that to stress at work and maybe just PMS, or again my hormones just adjusting. In November out of fear of getting my period when I shouldn't have it due to the time change, I actually switched the times of my alarms and started taking the pill at 10am. In December after finishing that pack, I actually switched it to noon with the start of my next pack. Then mid-month I started having a lot of spotting.. for over a week before I actually got my period. Again, I figured this was due to my switching times. Since then I haven't changed the times I take it, and I'm not due until Jan 26th and yet I started spotting again this weekend- and still am.

After reading these blogs I'm starting to wonder if EVERYTHING I've been experiencing is due to these pills. I had read an article last week that stated the low dose birth control pills cause a decrease in Vitamin B6, Folic Acid, B12, Magnesium. A Vitamin B6 depletion can inhibit the production of serotonin, which increases a woman's risk of becoming depressed. A magnesium deficiency is associated with insomnia, anxiety and depression. Since reading that article I've been taking a multi vitamin- Woman’s One a day brand, and have felt 200% better emotionally. The article also links taking pills and having an increased risk in cervical cancer and/ or dysplasia cells- Which I’ve had the cells, and had them removed about 6 years ago. I’m also wondering if my levels of Progesterone are low, and that’s why I’ve been spotting so much. These pills contain progestins, which block the action of natural progesterone. Low levels of progesterone are what make you start your period every month.

My appointment with my Dr. isn't until next month, but I will be sure to bring up that article and this blog and get my pills changed. I seriously can’t take this anymore.

Hi, I've never posted on one of these sites but here goes... Lamictal does indeed affect some vital nutrients. They are biotin, b12, b6, L-carnitine, folic acid, calcium, vitamin A, vitamin D, and vitamin K. My hair started falling out in clumps. I had my levels checked and I was VERY low on biotin, and L-carnitine. I was also low on zinc. I dropped my dosage from 150 to 100 to 75 to 50. With doctors approval. I started taking centrum silver and skin, hair, and nail vitamins and my hair stopped falling out and is starting to regrow. I am now back up to the 125 level and feeling better. I also started taking L-carnitine and that has helped as well although it had nothing to do with my hair loss. As to the other side effects...I have headaches, and neck stiffness, and sex headaches at the 100 plus level. And a buzzing/ vibrating in my right ear. For the migraines I take Advil. DO NOT TAKE TYLENOL WITH LAMICTAL. It lowers the level of lamictal in your system. I only take Excedrin when I must. I know this is long. I hope it helps. Even with all the side effects I still will take lamictal. It has made a huge difference for me. ( I also have occasional nausea and dizziness.) Hope this helps.

Like many patients, I started out on a low dose of Lamictal. Eventually, I was taking 300 mg. This seemed fine for awhile. Then, I started feeling a bit down, so the doctor increased the dose to 400 mg. Increased dosage does not necessarily mean improvement in mood (bipolar). I began to experience a good number of the adverse side effects reported here, including excessive fatigue, gastrointestinal disturbances, cotton mouth and very bad taste in my mouth, muscle tension (particularly in my legs), forgetfulness and confusion, and sinus and chest congestion. At one point in time, I even had difficulty articulating words.

Though I did not suffer from rash, I have been up in the middle of the night with itching all over my body. I had a few episodes of mouth sores and one pimple on my chin. Many of these have improved since the doctor brought me back to 300 mg. However, they have not entirely disappeared. I continue to suffer from the excessive fatigue many of you have reported here.

I recently had a blood test and learned I have very low levels of Vitamin D and Vitamin B-12. I do not know if there is any relationship between long-term use of Lamical and these test results. However, I do know that low levels of Vitamin D can cause fatigue.

Though I am willing to follow through with further blood tests, I am beginning to understand why some people are tempted to discontinue their medications. I am so tired of being so tired and sleeping so much. When I finally get up, I am still tired and drag through the day.

Sometimes, I think I'd rather have a down day or two than take this medication. I should add, though, that my bipolar is not severe, and that I am only reporting how I feel. I'm certainly not recommending anyone discontinue medications for this or any other condition they may be suffering from. If I were to recommend anything, it would be to get a second opinion if one is concerned about his or her treatment.
If I were to make any suggestion to doctors, it would be this: more is not necessarily better. Send your patients for blood tests (mine were ordered by my M.D. and not by my psychiatrist). Increasing the dosage--at least of Lamictal--might result in a host of negative side effects. Your patients might then become disillusioned with their treatment and give up.

If anyone out there has suffered from B-12 and D deficiencies, let me know. I'll let you know what I find out.

And remember, most doctors are really trying to help us.

Hi, I have just started Lisinopril today, and wanted to search the internet on side effects. I was taking atenolol and felt I was on the right blood pressure med because it was working. Well I started getting tired after 4 years on atenolol, it started 1 month ago. I went to the Dr. and they did a ekg and told me they are surprised I am still walking/standing because my pulse was measured at 41 and that explained why I was so tired all the time. I am 49 years old and am going through menopause and deal with high blood pressure. Well the Dr. told me to stop the atenolol immediately. Then 2 days later I went to see th Dr. again and they switched my blood pressure over to linsinpril. I also take HCTZ a water pill and have been taking it for years. I hate to say it but I am developing the sore throat thing after 5 hours on the med and I am worried about that. I took my BP reading and it is better than ever 108/59 pulse 68. I guess I will get some honey lozengers for the sore throat. Not saying it is the lisinopril causing it but my body is very delicate and I watch my meds carefully so I know when something goes on in my body (meds) and I feel it right away that I have to wonder if it is going to be an ongoing problem for me. I will keep you updated on this as I really am hoping that the lisinopril helps and I can get my energy back. Have been taking the B12 and magnesium and vitamin D and Calcium. I also take vitamin B2 and B6 every other day. I had yeast infections constantly and the B2 has really helped me with that. I get night sweats and hot flashes and take soy pills for that and the herb sage every other day. I was taking low dose prempro about 6 months ago for 2 years and that made my hair fall out terribly, but also made it grow a lot too, it was a ongoing problem with the hair laying everywhere in sink on the floor etc. I stopped the Low dose prempro and the hair loss stopped, so if I lose hair from lisinopril I will be used to that, but hope it also will grow. I need to give this lisinopril a chance as I have little choice right now. My heart they said was pumping too slow, the pulse should be 60 or above not low like 41 so I will keep updated on how the lisinopril side effects are with my body.

hi i had the mirena fitted 4 weeks ago,not had any side effects since fitted but is it normal or not to smell a bit down below

I a 49 year old male. A little while ago I was diagnosed with Hypothyroidism. My TSH was at 43. I have been taken Synthroid for a little over 3 months. I started with 25mcg and was recently increased to 50mcg since my TSH was still at a high 15. I also thought it prudent, since I had gained a lot of weight over the last year and a half, to also diet and exercise a little. In the last 5 weeks I have lost 32 pounds. (I was about 80 pounds more than I liked). I have more energy, have not lost anymore hair than normal, and my hair is not brittle. I have episodes of Atrial Fibrillation since I was 30 and occasional "heart flips" ever since. Since taking the Synthroid I have not experienced these "flips" at all. I sleep well. My blood pressure was High in the past and was taking two meds for it. Since taking the Synthroid (I'm also guessing the weight loss, diet and exercise has also helped) I am down to one med and I now have a BP of 110/65 with a resting heart rate of 64. By the way..I am taking the generic form of Synthroid.

I started on Yasmin about 3 years ago and about 4-6 months on it- I started experiencing ringing in my ears. The ringing started with just 6 hours at a time maybe every other month- very minor in the beginning. Gradually the ringing would last longer and would occur more frequently. I saw an ENT Dr., hearing tests, MRI, you name it... There was nothing that came up and then I started doing some investigating in trying to make connections with the pill and the ringing. The pamphlet that it came with said that you could experience a deficiency in Vitamin B, B12.. whatever. So, I thought that I could start taking the B Vitamin and perhaps that would help.. I haven't gone off of it yet, because this pill has been amazing for me.. I don't have mood swings, heavy periods, bad cramps on it.. I love it compared to Ortho and the generic.. I felt like I was going insane on those! I think I just need to get off Yasmin altogether because of this ringing in my ear.. I really am trying to search for some answers!! If anyone has experienced ringing in their ears with Yasmin and never had it before- please email me... My doctors say that there is no connection and if everything else is great with the pill to stay on it; they say I have Meniere's Disease.. Also, I started getting a rash on the front of both of my calf's.. nothing to serious.. they say that it shouldn't appeared right away, instead of half a year later.. I'm at a loss.. like I said this pill has been great...

My mother was put on Prednisone 3 weeks ago because of severe muscle pain (15 mg at first and increased to 60 mg). After she starting taking it she began to have weakness in her muscles/joints and was unable to walk by the end of the week. She also had severe water retention and could not catch her breath. Most of all she was very weak all the time and could not seem to sleep at all. She wound up in the hospital and was classified with a type of Congestive Heart Failure due to the excessive dosage given by a pain doctor. She had to be admitted to a Rehabilitation Center where they have now cut her down to 10 mg a day and she is trying to take Physical Therapy to walk again. She is fighting with depression and overwhelming feelings of anxiety. She still cannot sleep and wonders if she will ever by back to normal again. Just a month ago she was living a normal life and because of the pain, was given this medication. I wonder if the benefits outweigh the horrible side effects she has experienced. After reading some of the responses above I see others are having similar side effects.
Any encouragement from someone with a positive long term outcome would be beneficial at this time to her. She feels very helpless in her situation.

I have been reading all the entries for this website and thought I would pass along some useful information. I have been on Levoxyl for 8 years now and have had lots of the symptoms that all these people have had. I then had an appointment with a great Endo doctor at the *** and discovered some interesting things. There is a number "range" they put all people into when checking your TSH levels, only problem is each person is different and even though the doctor may say your in the range, it may not by the right dosage for you. Unfortunately the only way to determine the correct range for you is to experiment with the dosages and it takes 3 months or more for your body to adjust. Also, thyroid hormones are accumulated in the body and depending how active you are is how you may feel. The hormone pill you take today will not be used by your body for up to 10 days, so if you feel good for a few days at rest, then exercise the next day you may feel drained. It will take a few days for your body to replenish the stockpile of hormones to feel "normal" again. A working thyroid makes hormones as needed, yours now does not so this is why so many people feel fatigued, or racing heart beat if they don't get enough exercise. I also had leg and muscle pain. The medication depletes your body of Calcium and B complex especially B12. My leg and muscle pain have disappeared. I still get headaches, but much less with the B12, and some days I still feel tired but I say again, your body cant regulate its needed thyroid hormone and a synthetic pill is only a substitute.. You will always have some side effects. Hope these tips help someone.

I have been taking Singular for over 5 years for mild asthma. My allergist has told me several times that taking it is "as safe as drinking city water". Last year I had trouble with palpitations and had the cardiac testing including the Holter monitor. All the tests were fine. I have had trouble sleeping for a couple of years--waking in the early hours and finding it nearly impossible to return to sleep. Additionally, for the past 6 months I have had an annoying tingle in my feet and lower legs. My PPO just set up an appointment for a Brachial index test to test my circulation. The tingling is worse after lots of walking. Most recently, people have said my skin looks yellowish! No, I am not gorging on carrots! Just the other day I came across an old sheet that came from the pharmacy when I filled a Singulair prescription. I noticed some "unusual" side effects with long term use--yellowing of skin, palpitations, tingling in extremities, sleeplessness! Yikes! I have stopped taking Singulair. So far, so good, no asthma problems. But this is very scary. Has anyone else had the tingling, the yellow skin? I've started taking B12 and B vitamins as I read that the tingling is from a B12 deprivation caused by the Singulair.