B vitamins symptoms and conditions

I have been taking the generic equivalent of Wellbutrin for nearly a year. A few months ago I noticed my hair is thinning on top, in front. It has steadily become worse. I finally did a search on Wellbutrin, hair loss and found this site. I will start weaning myself off it now! Losing my hair will make me more depressed than I was to begin with. Can anyone tell me, does the hair grow back? How long does it take?

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 on doxycycline for three months for chronic prostatitis. I had similar bad side effects start last week, nausia, pain in the stomach, weakness in the legs, exhaustion, dizziness, etc... But no depression "yet". I have been off the doxycycline for four days and still having bad symptoms. I read your posts --- Thank you! I have read that doxycyline depletes the body of B vitamins. Many of the symptoms described by many of the posts are similar to depletion of B vitamins. Have any of you been tested for B vitamin depletion?

I was on doxycycline for three months for chronic prostatitis. I had similar bad side effects start last week, nausea, pain in the stomach, weakness in the legs, exhaustion, dizziness, etc... But no depression "yet". I have been off the doxycycline for four days and still having symptoms. I read your posts --- Thank you! I have read that doxycyline depletes the body of B vitamins at ****** Many of the symptoms described by many of the posts are similar to depletion of B vitamins. Have any of you been tested for B vitamin depletion?

I was prescribed Doxycycline for chronic prostatitis. I took 100mg. twice per day for 3 months. The doctor told me that he puts men on antibiotics (Bactrim and Ciprofloxacin) for 6 months and longer. I had been on both of those drugs in the past and had depression after taking ciprofloxacin for thirty days. I have not had depression from the doxycyline "yet" but did experience insomnia and minor dizziness off and on for a month before the serious effects hit me. During the course of treatment several times I felt unusual tiredness for a day or two but it would go away and I would feel strong again. One week before I stopped taking the doxycycline the bad effects started. Lower back ache, humming in the head, loud ringing in the ears, mild mental confusion, forgetful, headache, dizziness, lack of appetite, nausea, minor tingling in the upper lip feet and hands, sore anus, minor pain in the throat, unusual tiredness, scratchy eyes (like sand in them), redness of skin, pale hands and feet, joint and muscle pain, tight muscles in legs, bloating, abdominal pain, and blurred vision. I have been off the doxycycline for four days and still have many of the symptoms. I read at ****** that doxycycline depletes the body of B vitamins. The week I stopped taking a multivitamin / mineral pill the symptoms started. I was very cautious about taking the vit. pill four hours after taking the doxycycline throughout the course. I plan to get a blood test to confirm the B vitamin content. I took a vit. pill today and it has helped reduce the insomnia and color of the feet and hands. My question to you all is how long dose it take the body to repair the damage? Thank you for all your posts they give hope of recovery.

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.

I was diagnosed with Rheumatoid arthritis at the end of 2007 and have been on prednisone since then. I started on about 105mg a week and am currently trying to reduce it but it is really hard as the moment the dosage goes down I lose all mobility and cannot even get out of bed. I am only 23 years old and really feeling the disease to the extent that I cannot even cope with my life. The prednisone has really taken its toll on me and the side effects are crazy! I just want to go back to my old self as I am finding it sooo hard to get through a single day. My side effects include:

Insomnia, tooth sensitivity, depression, anxiety, mood swings, moon face (my face is so swollen that I cant stand looking in the mirror anymore, dizziness, temper, feelings of uselessness, nightmares, night sweats, water retention, and to top it all off the arthritis is getting worse and I am in constant pain. Is there anything anyone can suggest then please help me!

what happens if you stop after second dose.. Im so scared right now!!

I have been on doxy for seven days- I have gained five pounds in those seven days- I have a constant headache and am tired. after reading the other postings I am convinced that this drug causes or ENHANCES depression..has anyone else experienced the weight gain or am I going insane????

I had a lot of the negative side effects listed above by others including depression, fatigue, trouble concentrating, aching body, restless nights, irritability, my arms and legs falling asleep and so on. Then I found out that i had a vitamin b deficiency - a lot of these symptoms are also symptoms of vitamin b deficiency. Yaz along with other oral contraceptives interferes with the bodies ability to absorb vitamin B. Taking vitamin B supplements a few times a day has helped me. They are water soluble so you do not have to worry about overdosing- if you take more than your body needs you will just pee out whatever is extra.

I had my second Lupron shot this last mid October that lasts, supposedly, 3 months. So I will be 5 months in this mid December and I have to say I was one of the people who was fine with Lupron...up until now. I had and have all of the typical side effects of hot flashes, headaches, memory loss, mental fog, etc. Then I had my first ever migraine a week ago that knocked me on my butt for 2 days. My memory loss and depression are by far, by far, the worst side effect I have experienced. At this point I am concerned my memory problems and mind fog will not go back to normal, which has already adversely affected by daily life. I was one of the people who spoke positive of this injection even after reading all the horror stories but now I am beginning to wonder if they were right on some levels. When reading all the different experiences I would get confused and wouldn't know what to believe. I am not saying I would change things, the jury is still out as to whether the benefits will outweigh the difficulties, but my personal experience and symptoms have been getting worse just in the last few weeks, so that would be between month 4 and 5 on it. I could lead a pretty normal life up until recently and I'm a pretty tough person, I clean houses for a living and work hard with a packed schedule so I am not just stating little symptoms I experience but ones that actually have affected my daily life. Just being honest so you know what to possibly expect, depending on your body's reaction. That is a point to keep in mind, everyone's body reacts differently but if the majority of people are saying the SAME side effects, makes you wonder if there is a consistent pattern.

One thing I will tell you that has helped me is B vitamins regularly in your system and staying as active as possible. Write things down to remind you for the memory issues, don't over-commit to things because of the mental affects-it hits you hard when you can't follow through, and try to watch your sugar intake, which messes with your emotions. Hope this is helpful.
I would love to know from someone who has the same symptoms (which looks like almost everyone who is on it) and who is now off of Lupron for at least a few months, if the symptoms of memory loss and mind fog go away. Is my memory permanently damaged?

okay ladies, I'm not sure what you all are experiencing since I'm not a doctor. But I will tell you that a huge amount of your symptoms can either be age related or post baby related. I have four children ages 15, 6, 5, 3.
The beginning stages of the Mirena granted are not pretty and can last for months. I was having a terrible time with my periods and was out of commission for the first three days of every cycle each month. I have had my Mirena for almost 2 years now and am going on 41. I had to wait it out for about 6 months before seeing any huge improvements. I will tell you this, over eating and NOT eating a healthy diet of fruits and veggies will aggravate bloating and mood swings. You could have these with or without the IUD. I never lost my hair unless I was 3-6 months post partum.
A diet rich in potato chips, bread, meats and cheesy pizza will show on your hair skin and nails. The typical American diet will leave even your special guy moody. As we age the expectation is that we will always feel 18 and I have had to come to grips with how my body ages and how I take care of it. A new baby whether it is your 1st or 4th will cause unwanted fatigue. I still struggle with fatigue because not everyone sleeps thru the night including my hubby so my sleep gets disrupted a lot. There are several things you can do to help your Mirena work for you and not scare you. I NEVER lose my sex drive unless I fail to exercise even a little each week and have fought back with a super charged diet. I'm not perfect at it but boy does it ever help. Sugar has a HUGE impact on your hormones and fatigue level. Limit it. Got to bed as early as you can and avoid late night TV. Don't give your precious zzz's to some silly show that won't help you be a better person any way. Get moving and add a little (or a lot) of weight training to your days- your sex drive will soar and your body will thank you. Pray for wisdom. God will help. Sometimes he uses fatigue to slow me down and focus on what is really important. Granted not everyone can handle an IUD. But if you try a little self care and be patient you might find that it works for you. I had heavy bleeding and at my age the doc said I got it just in time because from 40-50 I could expect more of the same. I am grateful for it because I felt like I was dying every time I had a period. A little fatigue is worth the benefits. Keep in mind that even your little ones get tired. They need naps and they are kids. We need rest in the afternoons too. It's okay to stay off the phone and rest a little if you can. My energy drainers are TV, negative people, talking on the phone too much, eating too much especially when I'm not really hungry, the wrong foods when I do eat, and not getting sleep or exercise. Start small and see if over time it doesn't make a big difference before you throw in the towel. Blessings to all and especially the new mommies.

Taking nicomide while taking Celexa and a b-complex for hair and nails. I read somewhere that nicotinamide may have anxiolytic effect. Not sure if this combination of vit B3 along with the other B vitamins and an SSRI is causing the SSRI to be less or more effective, but have experienced I think a tranquilizing effect, more noticeable at night. But at the same time I feel some depression and anxiety so I wonder if the Celexa concentration is being decreased secondary to the vitamins. I will stop taking all B vitamins for a few days and see how I feel. My work environment lately has been more stressful, too, so it's hard to say what exactly is going on. But will stop all B vits and see how I feel.

I can't believe this is prescribed for women in order to HELP them! I took it for a few days only, it was a very scary experience. My periods were irregular and my Gyn said this would help. I started the pill and by the next day I was having HORRIFIC cramps, not even double doses of Ibuprofen would touch them. I felt dizzy, nauseaus, and I started feeling depressed within a few days. I went to bed one day with the cramps and I actually felt suicidal, didn't want to get out of bed or speak to anyone. I just laid there and cried and cried!!!

Well, I know myself enough to know that this was not any way to treat myself so I stopped taking them immediately. Within 2 days I was back to normal. I told the Gyn but she shrugged it off, said I should have stayed on the pills as I would have evened out. How does she know??!!??!! I'd like her to take them and then say that.

I started taking some good supplements, Black Cohosh was one, along with B vitamins, E, Calcium/Magnesium, and I felt pretty good within a month or so. My periods evened out too!

Take care of yourselves ladies, you know your bodies better than doctors!
:-)

My 17 yr old daughter received her first Gardasil on April 17,08 with only pain at the injection site on June 16th 08 she received the 2nd within days she started complaining of severe headaches and eye pain so I scheduled a routine eye exam thinking that her glasses may need to be updated. After her exam her optomatrist called me intot he room telling me that she had severe swelling of her optic nerve and scheduled her for an MRI before we could get that done she went to the ER for severe pain in the eye and headaches there they did the MRI and it was normal no tumors or anything that would cause such headaches. On July 3 she called me from work asking to be picked up because the pain was so bad she could not function at all she was weak, dizzy and overall just not feeling good. I took her to the ER again where they performed a spinal tap and tons of bloodwork and admitted her for pain control on July 5th she had a 2nd spinal tap and every day more bloodwork was performed so far ALL tests ran have come back normal. She was in the hospital 5 days. She seen her ophthalmologist a week after being released and we talked to her about the Gardasil and she felt there was enough "coincidence" to have my daughters pediatrician file a adverse reaction form. That has been done and my daughter has learned to live with the pain since nothing seems to help it anymore. Also the last 6 weeks she has had bad insomnia and nose bleeds.

I am sure that all kinds of people told Kate Miller that Concernedcitizen was a cuckoo or a Merck competitor. I haven't been employed by a pharma company in many years. Everybody ever employed by a pharma company higher than a certain level (practically the mailroom) knows this stuff and what to look for.

I think that I am about ready to say my opinion on how montelukast works and why these problems develop. It will just be my opinion. I need to try to find actual proof but I may forego that and just say it soon.

I don't think that anyone can predict a time frame for getting over an adverse drug reaction. Below is my opinion but I see a lot of evidence that it is basically shared by other people maybe not exactly as I state it.

Adverse drug reactions deplete many essential nutrients from our systems. Inflammatory response is very stressful on the body. It is sometimes a very big effort to work on the diet to put back what has been taken away. It can take a long time.

Quinolines particularly deplete B-vitamins, folic acid (B-9), calcium/magnesium/zinc and omega-3 fatty acid. Sometimes the blood-lab work shows elevated homocysteine which proves that the body has suffered inflammation. Cardiologists now use homocysteine levels to show whether someone is at risk for heart disease due to inflammation. Deficiencies of B-6, B-9, and B-12 are known to cause elevated homocysteine.

Here is the pharmaceutical company ZINGER. Now companies such as Merck and Pfizer are going to offer niacin products to lower cholesterol. Well, yeh, duh !. All of these drug reactions are causing depleted B vitamins which elevate cholesterol. Then after they have tried to kill us by depleting our B - vitamins, they want to sell us another pill to give the B vitamins back to us. How many people out there are on some kind of a pill with side effects that cause inflammation? What a business? It is win, win, win.

In September of 2007 my then 13 year old daughter was put on Singular for mild asthma. At the time she was a straight A student, vice president of our school and a popular girl who's guidance counselor described as "the glue of her grade" because she was so well liked. In November she told me that she was struggling with advanced Latin and Science. She asked to drop down to on grade Latin so we did. In December her science teacher notified us that she had a C average. She told me that she thought she had ADD/ADHD and she couldn't keep up. At the same time she was having a lot of problems with friends at school and we just attributed it to being 14. 3 weeks ago we discovered that she is significantly behind in English and it was then that she told me that she is been having horrific night mares. She said that they usually involve someone killing her or her killing herself. She said that they were so graphic that she couldn't repeat it out loud. She also said that she would feel waves of anxiety that would come over her at school and she would act "witchy" to the kids in her class for no real reason. She said that sometimes when she is trying to do her homework she will read the same passage for 2 hours and still have no idea what it's about. She also said that the suicidal thoughts from her sleep happened during they day and that she had thoughts of her harming herself. Fortunately her pulminologist told us that this may be caused by singular and we immediately took her off of it which was 2 weeks ago. She has only had 1 "bad dream" not even a nightmare since. She had one anxiety attack 3 days after she was off it and she describes her moods as the "cloud lifting....slowly". Now, we have to pick up the pieces. Her grades have suffered, her friendships have suffered and most of all her self esteem is very low. I'm grateful that we found out the cause but I feel as if my daughter lost a year of her life and I worry that because Merck won't admit there are side effects we can't find out how long it remains in their system. Is anyone else concerned about the long term affect and has anyone pursued a class action suit to try to get this drug tested properly?

I've been on Yaz for about 2 years and I really like it. I am taking it for PCOS (so I don't have a choice to NOT be on BC) and so far, I have not experienced any of the problems other people have had. I did notice a decrease in sex drive, but I'm fairly certain this is due to my under-active thyroid.

At any rate, my doctor said that Yaz, like other BC methods, can deplete B vitamins from your system which can contribute to loss of sex drive. He suggested I start taking a High-Potency B vitamin (they come in standard doses) as well as DHL or DCL or something, I can't remember, 2-3x a week. I have seen my sex drive return, although it still isn't what it used to be.

Good luck to all of you with the other symptoms. I am shocked at the problems it has been causing and I'm horrified for each and every one of you. If you are like me and only have a few mild problems, talk to your doctor about some vitamins!

This is by far the worst pill I have ever taken. Before Yaz I was on Nordette, Ortho Tri cyclen and Alesse. I saw the commercials and got sucked into trying this pill. All I can say is proceed with caution. I ended up taking this pill for the unhappiness 8 months of my entire life. I had problems with other pills causing weight gain (Nordette, Ortho Tri cyclen) or acne (Alesse). However, those symptoms are mild compared to what Yaz inflicted on me.

I have always been described as happy go lucky and Yaz gave me extreme moodiness, panic attacks about my future and life, and major depression. I did have the best skin of my life and lost about 5 lbs but I was an emotional MESS! I would cry at the drop of a hat and find fault in everyone and everything. This symptom didn't start right away but each month I was on Yaz got worse. My friends coined my "alter ego" "she devil." I almost felt possessed at times on this pill. I finally realized it was the pill and not life causing these problems when 3 of my girlfriends had the same problems and got off and the problems went away.

Prior to having this experience I thought people tried to blame too much on the pill but my experience showed me just how much these can mess with your body. I switched back to Alesse 5 days ago and it's like I am a different person--even my skeptical boyfriend noticed the change. As for the acne, I am going to go to a dermatologist to address that. I will be happy to have a few zits as opposed to being a crazy woman.

Proceed with caution on this pill and watch your moods carefully. Just because you've been on it for a few months doesn't mean you're safe. The majority of my emotional disorder started about 5 months in. I do have some girlfriends that like this but most have found it to bring out "she devil".

My 20 yr. old daughter was on Loestrin 24 Fe for almost a year with seemingly few side effects (except larger breasts). When her Rx ran out, the doc would not prescribe more until she had an exam. She ended up going off the pill for a couple of months, which was okay because there was no boyfriend or sexual contact during that time. She then got a prescription refill and went back on it. Within about 3 weeks she started experiencing random panic attacks including, headaches, nausea, rapid heart beat, sweaty hands and dizziness. At first she wrote it off as stress, but now they are happening ALL the time and are interfering with her life. She is a college student and is becoming paralyzed by the anxiety and the fear of a panic attack. She can't go to class, can't drive and is worried all the time. This is soooo unlike my happy-go-lucky daughter. She feels like she is going crazy. I talked to the GYN and she thought that the pill could definitely be enhancing these symptoms, but didn't feel they were the main cause. I now have a completely different opinion from her since reading all the posts on here describing the exact same symptoms while on this pill. My daughter has now stopped taking them (it's been about a week) and the doctor said it could take a couple of cycles for the drug to be completely out of her system. I'm praying that these symptoms go away after the hormones are flushed out....anyone have any experience with the anxiety going away after going off the pill??????

I'm a 26 year old female and I've been on Topamax since March 2007. It has completely gotten rid of the debilitating headaches I experienced 3-6 times a week. It also got rid of my anxiety. I got my life back, my antidepressant kicked in at the same time. I experienced all the usual side-effects, tingling hands and feet, forgetting words, memory problems, loss of appetite, but was COMPLETELY pain-free. I still am. However, I never remember anything now, forget whether or not I did something, paid my bills, etc, lose things constantly, and I have lost about 20 lbs. Not good. I look anorexic. I have bones sticking out. Eating is hard. I forget to eat and drink all day and food is just unappealing. I feel fuzzy and stupid and slow. Not sharp like I used to be. It has killed my confidence and self-esteem. But I was wondering if any women out there got yeast infections while they were on Topamax. I've had one monthly since I started it, and my doc said it's a rare side effect. Oh yeah, I've had mild hair loss and mild to moderate acne now. This drug, it is such a 50-50. Living with chronic pain, those headaches were awful. But doubting yourself is awful too. Anyone have similar experiences?

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.

I have been off Yasmin for almost 2 weeks and the panic attacks are gone!!! I feel much better. I decided not to use another form of birth control "with hormones" until my hormones are balanced! The only thing is I am having HORRIBLE headaches, the muscles in my legs and arms are still aching and my mood swings are still there. I hope this ends SOON!! Right now I am taking vitamin B complex to see if that helps any.

I'm so happy I found this site. I've been thinking I'm crazy or just getting old for the last 3 years while on Yasmin. I started taking it at age 29 and almost immediately after started having mood swings, extreme irritability and depression. I had previously been on Ortho Tri Cyclen and the Ortho Cyclen before Yasmin and was on them for MANY years and never had one side effect. I only switched in the first place because I like to have very very few periods and I run all my active pills together to forgo periods very often and I was having breakthrough on the Cyclen. Hence, the Yasmin trial.

I'm actually a doctor (which is why I CANNOT have frequent periods with all the accompanying issues), but I didn't even realize the possible connection between IBS and Yasmin. This needs to be studied and taken seriously. I never once had IBS symptoms until a few months after starting Yasmin. Now, 3 years later I have almost constatnt trouble, to the point everytime I eat I run for the bathroom, yet my weight has never been higher. I asked a GYN friend at work if they could be related and she said definitely no, but reading all of these "real life" examples, coupled with my own experience has made me think otherwise. Often, the symptoms will occur shortly after taking the pill, even when I haven't yet eaten breakfast. It's crazy!!

I'm going to switch either back to Ortho Cyclen or to something new ASAP and will report back. I'm both excited at the thought that my "IBS" might really be Yasmin related but also scared that it might not go away and therefore might really be IBS. I'll report back... It honestly never entered my mind that all of it could be the Yasmin. I had just moved, started a new job in a town I hate and I thought it was all stress related.

I've also had an interesting side effect no one has mentioned yet- my hair texture has dramatically changed. It isn't falling out, but has gone from VERY curly with a nice soft spiral curl pattern to very dry, straight and hard to manage. Nothing else has changed and now I'm wondering if it's not the DRSP. If pergnant women can have hair changes, why not women on the pill?? It's all hormones.

As always with a drug, there are always possible side effects. No one drug is perfect, and humans are so complex in their make up and they way they process drugs. Therefore, please don't judge your family docs or GYNs too harshly as not even the best doctor in the world can predict every side effect.