Calcium symptoms and conditions

I have been on Levoxyl 0.112MG for about 18 years. I do have some of the symptoms described by others, hair loss, hot flashes, etc. , but I think the alternative to this is a lot worse. If I do not take it for long periods of time, it gets to the point where I am freezing cold and the bags that develop under my eyes are embarrassing. I think the problem with most of you that are having very bad side effects is the dosage. If the amount is off just a little bit you can feel like you were just run over by a truck. I went through this many years ago. I would suggest continuing to change the dosage until you get it right. I wish I did not have to take it but it is absolutely necessary in my case.

Was prescribed HCTZ and started taking it off and on in early August. Pain in the butt cutting the pills in half. Started to feel weird feeling in my left ear and cheek and then numbness spreading up my face, forehead and scalp.(I did have a few beers the weekend before this happened) Took myself to ER. MRI, CT, full blood work, thyroid check, EKG, heart and lung xray. ALL PERFECTLY NORMAL. Of course I was diagnosed with possible MS, Belle's Palsy, and was told I might just be wired weird.

Went to primary the following day for follow up and was told that my blood pressure may have been the cause of the episode. Prescribed Lisinopril and started taking it immediately 10/12.5. Started feeling good pretty quick, but noticed a few crazy dreams and almost like I was falling.

Missed a few doses and and had a few beers over the labor day weekend. Started meds on Monday but started feeling pins and needles coming back in different parts of my body. Continued to take meds and then went camping. Had a few beers around the fire. Woke up next morning with slight case of Vertigo. Continued with meds through the weekend and have felt dizzy, dumb, tired, my eyes don't move correctly, my left arm has felt numb and swollen, my left cheek tingles and I feel so swollen in my gland area under my ears. Knee pain too.

I didn't take a dose today, and I feel 100% better. Still tingly and numb in spots, but better. A little anxious and my heart feels like it's beating really deep and fast. BP is 154/82 after going down quite a bit on the drug.

Anyone else had trouble with the alcohol? Any similar symptoms? This site has calmed me down as I've always been a worrier/hypocondriac type. any response or idea would be really appreciated. Thanks everyone...good luck!

I have SEVERE leg pain, behind the knee, kneecap and just above my ankle, Also my hip. This is concentrated on my right side although I do have occasional pain on the left side. My primary care doctor said it was arthritis. When I told my GYN Dr. about this, her head snapped around very quickly. She said to stop the Fosamax and start on vitamin D, calcium and vitamin E. It has been 2 weeks, and the pain is still severe. I'd like to know when it will stop. Does anyone know?

I just read many postings here regarding lisinopril/hctz and the sexual problems it had caused you. I'm a 26 year old male, just married, and am having major problems with my sex drive and erections as well. I've been to several andrologists and they all concluded that 'everything is fine' and that i shouldn't be having the problems i'm having (based on many blood tests of course). I actually used to have a very high sex drive and no problems at all with erections, but i started losing my sex drive slowly but surely a year ago when i started taking lisinopril/hctz. Few months later, my erection started getting weaker and weaker as well. Now, i almost have no sex life. I quit lisinopril/hctz just 3 weeks ago, and i THINK i'm experiencing better morning erections, but still my sex drive is abnormally low. Sometimes my wife gets offended. I may get an erection during foreplay, but the erection is usually short lived, since i have no sex drive in the first place. Could anyone please share with me their experience with quitting this poison, and please let me know if you recovered your sex drive/life. Many thanks,

Does anyone here ever had any tingling issues? I had total thyroidectomy in Feb. 2009. Felt good the first month or two and have gone down from there! Some days are good, some are bad. Never know from day to day how Im going to feel! I started out for about a month and a 1/2 on 125 levothyroxin.....then my doc lowered it to 100.......as of July 14th, Im now taking .88. The tingling Im getting is all over my body, different places, here and there. Ive had some heart rate issues for a couple of months now too and finally had my regular doc send to me see a heart doctor.
Thought maybe the tingling could be from low calcium.....it was normal, CBC was normal, ECHO was normal.....waiting on the holter test results right now. The heart doc gave me a prescription for Toprol. I told him I wasn't going to take it cuz sometimes my heart feels like its barely beating and Im afraid it will make it worse. Im glad I didn't get it! Ive read of too many side effects.
Palpitations, kinda fast heart beat with pounding.....sometimes it feels likes its barely beating! Most of this occurs when first laying down......every now and then while sitting, etc. I do not exercise.....and should but just don't find the time. I switched jobs around the time I found out I had several nodes on each side of my thyroid. I was getting tired a lot and just thought i worked too much. I went from a physical job to a sit down, 12 hour, graveyard shift. Since the surgery, Ive felt it more. Im tired of feeling like crap all the time......I was already going thru some perimenopause stuff before all of this! Before I ever found out about my thyroid, I did have real light pounding of heart when laying down and tingling every blue moon, but very mild as well.
Now with no thyroid.......and medicines with all the side effects......IM GOING NUTS!!! Right now the moodiness and tingling are whats bothering me the most. Some days Im really tired, others Im ok. My body gets hot off and on, no fever. The past 3 days my calves, feet, and ankles have started to swell........never before! Plus I get some throbs and pains in my legs and arms and under my arms here and there. I probably need a new doc and I change of medicine......but Im afraid.
For one, Ive decided to go back to a physical job........and hopefully it wont screw with my heart rate even more. Ive read up on tingling........Im guessing maybe its from all the damn stress since my calcium was normal. Does anyone here have any suggestions?????

I love It! I have been experiencing low back pain when standing for over a year. I could hardly walk when I crawled out of the bed in the mornings. I was diagnosed with one point away from osteoporosis. The supportive tissue between my discs was deteriorating. I was given Evista to drive the calcium into the bone along with Limbrel 500 mg twice a day for the arthritic pain. My nails have become stronger which to me indicates my muscular structure must be getting stronger. I took Naproxen and Arthrotec previously to Limbrel and experienced severe stomach distress. I am 65 and I see a daily improvement from my previous condition. I have never experienced fever or chills. I am almost totally pain free and look forward to the future continuing to take Limbrel!

started this 7 days ago for a prostate infection... I thought i've been going crazy this week until i saw this post..im having a horrible reaction to this stuff..although it does seem to help my prostate...it leaves the rest of me in bad shape. First off ive been getting lightheaded like every other day to the point as i think im have a panic attack but heart isn't racing...I've gotten diarrhea 3-5 times a day i go now...i had a bagel the other day for breakfast..it was the hardest thing to eat as i felt sick to my stomach and knew i had to eat something so forced it in..today i had a banana and some grapes and 15 minutes later was throwing it all up. I just called my doctor and asked for a change in antibiotics as this thing has lead me to believe there was something wrong with me although my doctor seems to think these side effects don't generally happen...i come here and see they happen EXACTLY how i have been feeling and just hope this doesn't last much longer in my system!

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 wish I had read all these comments before I took my first dose. I feel like CRAP! I have not been able to sleep, my back aches, I feel like I am coming down with the flu. It is not worth it, as far as I can see. I will research taking extra calcium, etc - I am really into healthy diet, etc. and should have known better than to put some foreign government drug in my body.
Shame on the FDA for still pushing this drug!!!!!!!!!!!!!!
I knew I didn't trust government agencies.

I have been taking Doxycycline Hyclate 100 mg for about a year. Two pr day. I have had on occasions pain that is similar to heart pain. I now know that it is NOT heart. My Question: Do any of you take this tablet with food? With milk? On a Full stomach? On an empty stomach? The manufacturer gives NO directions on these questions! How do Pharmacists and Doctors arrive at their directions?? I take WITH food at breakfast and dinner. I stay away from dairy, calcium, iron etc for two hours before and after taking the Doxycycline Hyclate. The medicine is accomplishing what it is intended to do.

Hello I am clinically depressed. They doctors said I was "severely depressed." I haven't done these post ever so I apologize if I can't make my side effects clear and easy to understand.

Well to the point I am taking Lamactil and Wellbutrin for over a year now. The side effects I have are acne, laziness, always tired. But the side effect I hate the most is really perverted thoughts. Every waking moment I am always thinking about sex of some sort. I can't enjoy a movie because I am always thinking of sex with the person I am with, be female or male. I am straight but I just can't shake thoughts and hate it to no end. PLEASE let me know if anyone is experiencing these side effects.

OMG!! This is insane, I thought I was going crazy, I started YAZ about 2 weeks ago, I usually try to maintain healthy and workout a lot, but in 2 weeks i gained like 10 lbs out of nowhere!!! I am freaking out! I completely lost sex drive and as well as other said completely dry, nothing can make me wet, I also notice that I started getting a really heavy discharge everyday, Oh and depression (mood swings, snap at everything I feel like I don't want to live anymore, I don't care for my job as I used to or school...I feel helpless) I stopped YAZ 2 days ago and so far i haven't notice any change...I am still very moody and SSSOOOO tired, I can sleep all day and all night with no problem and when I do try to get up is like a magnet that's keeping me in bed, its awful!!! When does it get better???? Anybody knows??? I am falling apart!!! HELP PLEASE!!!

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!

I have been having muscular pain and ringing in my ears since I have been taking Benefiber with Calcium in powder form. Has not helped with the constipation either.

had a moderate to severe reaction to levaquin 2 years ago.. we know the symptoms.. Here is what i did to help.
1) Eat only ORGANIC They spray meat that isn't organic with floxins, do NOT eat processed foods, fast foods, start cooking at home and eating RAW You wont believe how much better you will feel when you go organic. Vegetarian and Vegan even better. ALKALIZE get your PH to 7.5. Acidity is the worst when you are sick like this
2) Hulda Clark cleanses...Dental Kidney, Liver , Parasite , Bowel ( *******)
3) Keep moving
4) i used some stuff called waiora its amazing
5) sun, swim in ocean if you can and walk an hour a day 5) be positive 6) JUICES buy a juicer and drink a beet, cucumber, lemon , ( ORGANIC!!!!!) with one tablespoon of organic olive oil, drink every day
7) fish oil, calcium and magnesium , a good pure multivitamin ( crainuls on *****)
8)Don't be obsessed with whats wrong, get into what feels better.

I have crohns and was on a very high dose of prednisone from Jan. - Sept./08 (having a operation to take part of my colon out in Jun/08) and now I am suffering such joint pain in my back shoulders and both arms that I am taking ibuprofen (approx. 8- 10 a day). My general doctor said to me "somethings can't be fixed" and I said to him well I did get my crohns under control, surely there is something I can take to block this pain. I take Calcium with Magnesium, Vitamin D and an anti-inflammatory, Mesalamine, prescribed by my internal specialist. I have not been well for over a year, finally get crohns under control and enjure such pain in my shoulders and arms - it makes me cry sometimes because the pain is so great. I finally realized, maybe this is the after effect of prednisone. Anyone have any ideas if I might be correct. I am going to internal specialist March 12/09 so I am going to ask him if he can help me as my regular doctor seems to brush my pain off. Thank you, D.

There may be no way to get Levaquin out of one's body except time. But I wanted to at least try to speed it up. I don't know if it will work for me or others, only time will tell. There is genetics involved since each of us has a unique tolerance for Levaquin. But here is what I am doing:

1. 8 glasses of water daily with fresh-squeezed lemon juice.
2. Lots of fiber - a tblsp of wheat bran 3 times a day with more water.
3. Plain yogurt with live active cultures 5 times a day.
4. A hot bath with epsom salts once a day.
5. Magnesium, Calcium and Iron, a couple of times a day.
6. Vitamins B and C a few times a day.
7. Body Cleanse and Liver Cleanse from the drug store, as directed.

I took 7 Levaquin pills and stopped 10 days ago. Some symptoms have improved. Notably, my appetite is better, the bloated stomach is gone and food moves through normally, anxiety spells are gone, the brain fog is still there but maybe a slightly better each day.

I will be watching my body for any signs of tendon pain in the 12 - 18 months ahead. No pain so far, but Levaquin is capable of doing damage with the pain not felt until later. I will ease back into exercising very slowly over the coming months.

I will be posting updates periodically over the next couple of years. I am a 50 year-old man.

Good luck to all and God bless.

Hi,

Is there an antidote for Levaquin? I took it for 7 days and stopped 3 days ago. Is there anything recommended to reverse it and detoxify in order to limit the damage? I saw in the warnings sheet from the pharmacy that it should not be taken with Iron, Magnesium and Calcium. Maybe it's good to take all of those now to try to neutralize it.

It would be good to get the antidotes published here so that others who come along later can start removing it from their bodies it as soon as they find this web site.

Anyone with detox recommendations, please post them.

I was diagnosed with breast cancer in 2003, age 53. I had excellent medical care at NW Cancer Specialists, Dr. D. G., Portland, Oregon. I endured Chemo (8 treatments) I had a lumpectomy and 36 radiation treatments. I also took Arimidex from 2004 - 2009. My doctor suggested exercise would lessen the side-effects and he was right. I followed everything my doctor told me to do, it was very difficult at times, but we are talking about my life and the quality of my days, his suggestions worked. I began a regime of walking, up to 3+ miles a day, water aerobics 3 times a week and I joined Curves. I also took vitamins: Costco multiple vitamin, vitamin E & C, Calcium + D(Viactive), Melatonin (natural sleep aid), probiotics, and fish oil. I also drank up to 6 glasses of water a day. I am now "cancer free" and not taking any RX.

I am a 35 year old woman and my doctor put me on lisinopril 10 mg at first I had the cough that I see almost everyone gets,but I could deal with that then I started getting very tired all the time,I had started working out and was feeling better since I had been diagnosed with hbp,I ws following the dash diet ,it is said to be real good for hbp.I started taking lisinopril in may and by November I was a complete mess, My doctor never told me of any side effects so I read the little paper that the drug store give you on the side effects but it does not do this justice!I was so weak and tired I could not get out of bed,On thanksgiving I went to the hospital and told them I have no energy I feel sick all the time and dizzy,of course they sent me home thinking I was insane because I was crying ,I felt depressed all the time I did not know what was going on .About two weeks later very close to Christmas I started having palpitations at first I just thought it was stress from the holiday then they came more often ,I was so scared I went to my doc. told her I was have palpitations and she blamed it on my weight! ok now I am overweight but I have lost almost forty pounds and was walking four days a week ,then I said to her do you think it could be the lisinopril ,then she said something I will never forget she said well who put you on lisinopril? I was done then I said well you put me on the drug ,her face went white she said oh yes you should stop taking it I will give you a different one ,so I went home and took it for week and the palpitations kept getting worse so I went back to her and told her I was still having palpitations so then she gave me an e.k.g. and found nothing of course.I told her I was going to stop taking the meds all together and she then said she wanted to see me in two weeks ,In the meantime my boyfriend made an appointment for me to see a heart doc. ,he took another e.k.g.(did I mention I have no insurance)and said there was nothing he could do that I need an echo and a holter moniter for 24 hours to tell him whats going on .I had been off work for a month now so I had no money left so I started crying but my boyfriend paid for the tests to be done which cost a pretty penny .I am still waiting for the results of those tests yet but the more I think about it the more I wonder if I was having lisinopril panic attacks?I have stopped taking all blood pressure meds and my bp is most of the time 120/80 sometimes it is lower sometimes it is higher but I would rather not deal with the side effects of the drug until I really need them!

I have been taking Crestor since early September 08. Prior to that I was on Vytorin for quite awhile. I now have right sided parthesia and my face tingles constantly on the right side. I have had MRIs MRAs not to mention blood tests that say my kidneys are spilling calcium. No one seems to have a clue what is going on. My feet and legs hurt so bad if I sit for too long I can't hardly walk. My uncle passed away from ALS and now I'm really scared that all of these statins are killing me slowly. I wonder if I quite taking this drug will I have a heart attack. I really just don't know what to do.

i have been on aviane/alesse for about a year. i have noticed any side effects really. i took it because i have endometriosis which is heavy irregular, painful and emotional periods. the pharmacy keeps switching me back and forth from aviane to alesse which is suppose to be the generic brand. but lately i have noticed that alesse makes my cramps come back and i lose weight, while aviane makes me gain weight but feel better. i have noticed with both i get angry, but briefly, and its a million times better than when i would faint cuz of the pain, and take so much Tylenol that i wud hallucinate. i recommend anyone sick of trying so many brands of birth control pills, and sick of finding different side effects with each try Chaste- Berry (tree). its natural and amazing, but WARNING..it does increase fertility. but it has really helped. the brand i use is VITEX by lorna handerhaeghe. but if you really want to keep with birth control stay with the same one for least six months if your side effects are not bad. they do go away once your body adjusts. also some side effects may be because you are missing some vitamins that you need. ask to get tested at your doctor or naturalist. you would be surprised. for those that live in dark and dreary winter climates, most of us miss some vitamin D. a lot of us miss calcium which makes it possible to absorb vitamins. you can get your medical insurance to pay for chaste berry if you get a letter from your doctor.i wish you all luck!

This is an update about my son who took Levaquin 16 months ago when he was 16 years old (he is now 17). My son was given Levaquin September, 2007, to prevent an infection after minor sinus surgery. His symptoms were severe muscle weakness (he would get exhausted walking from the parking lot to a store and back, severe joint pain (in thumbs, wrists, elbows, knees, and ankles), dizziness (he felt like the room was moving away from him and would lose balance), and headaches (a severe pressure in the back of his head that was constant and then shooting pains in his head that would come and go for no reason). He then developed IBS a few months after taking Levaquin. He was an athlete at the time and in very good shape. Prior to Levaquin, he was rarely sick and headaches were equally as rare. He was a junior at the time and as a result of the Levaquin, missed most of his junior year. He kept up through home instruction and maintained 2 honors classes, but had to drop his AP class.

In the first 4 months, his muscle weakness, dizziness, and joint pain (except for his knees) went away. As a parent, it is very painful to have your son hold his head in his hands and ask you to make the pain go away…but you can’t. It took 9 months for his 24x7 headaches to go away. His IBS recently went away after giving him enteric coated peppermint pills twice a day. All that is left now is his knees hurt when he plays sports, so he can't. The knee issue is pretty minor compared to where he used to be.

Here are some things we learned: 1) We tried giving him magnesium, potassium, selenium, calcium, and B-complex after the Levaquin...but it didn't make him better; 2) We took him to over 20 doctors; most couldn't believe it was Levaquin, but some did; 3) Ortho-McNeill will admit that Levaquin can cause these symptoms (I called them); 4) There is no magic pill, once you have ingested Levaquin and develop symptoms, you can only treat the symptoms; 5) Numerous tests of all types over several months never came up positive for any disease or illness; 6) Filing a Medwatch report with the FDA is important since every report helps; 7) Levaquin is not FDA approved for anyone under the age of 18, but is still allowed to be prescribed; 8) Doctors get most of their information on drugs from the pharmaceutical representatives, so BEWARE and do your own research before taking medication; 9) Most drugs have side effects, but beware of the ones that have long lasting effects like the fluoroquinolone family; 10) Never ever lose hope or the belief that one day you will be better. The power of faith does wonders for your health.

I don't know if this post will help anyone. People are affected by this drug differently and recover at various rates. Most people do recover and you need to believe you are one of them. Fortunately for my son, it looks like he is okay now, but it has been an extremely long, difficult road. Keep your faith as my son did, and I'll pray that you all recover. If you haven’t taken this drug yet, then don’t. If you are taking it, then stop. If you have already taken it and have developed symptoms, then be strong and keep the faith.

I had horrible side effects (body aches, joint and muscle pain, headaches, hallucinations, insomnia, anxiety, heart palpitations, etc.). I did some research and I am currently trying to detox using calcium (tums or vitamins), magnesium (liquid antacids or vitamins), orange juice, apple juice, and grapefruit juice which all limit the absorption of the drug. A high protein and high fiber diet with no refined sugars is suppose to help. Drink plenty of water and add a B-Complex to help with Anemia (another side effect). Apparently, it takes three weeks to eliminate from your system. Good Luck and God Bless.

Is anyone experiencing confusion, trouble thinking, trouble concentrating, decreased cognitive function, mental sluggishness, trouble solving problems or situations which require logical thinking and sequencing, and memory loss? Would love to hear from anyone experiencing any these symptoms and if so, how long were you on the drug.
Thanks!