Magnesium symptoms and conditions

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,

UPDATE - Day 11 post removal

Still have not bled.
Still having vertigo migraines.
Still have numbness in R foot.
Still moody/irritable.
Still bloated and GAINING water weight.
Still crying (though not as much).
Still have NO energy.
Still having severe memory issues and BRAIN FOG!!!

NEW ACNE ON ARMS!!! :-(

Taking B12, B6, magnesium, multivitamin.

I'm upset/disappointed. I thought taking it out would make me feel better right away and gradually get better and better. So far I'm the only one on here who didn't bleed right away and start feeling good. Maybe more of the progestin got into my system and it will take a bit longer for it to leave?

NEED ENCOURAGEMENT!

I have low blood pressure, when i take the supplement Calcium with Magnesium it makes me drowsy, perhaps it lowers my blood pressure too much.

My daughter has this vaccine and was severely ill. Migraines, hair falling out, pneumonia, dehydration, you name it ... She was super healthy before this vaccine. You need to detox to feel better. Western medicine cannot help much - unless they understand the eastern side of medicine as well - trust me - I'm in a yahoo group Lets Talk About Gardasil.

You need to go gluten-free/sugar-free/casein(dairy)-free, drink bottled or distilled water and introduce extra vitamins. (B12, D3, magnesium, folic acid, and a liver boost, which you can find at a vitamin shop). There is lots of information at the yahoo group - so please join so you can get healthy. Gardasil is a GMO (genetically made) which has problems all its own - but you need to get the metals out of your body which are in this vaccine and in many foods you eat - start reading labels! No high fructose corn syrup and lots of rest. Please check out the chat group - and please file a VAERS report - that is URGENTLY needed to get this vaccine off the market.

im a twenty four year old student on paxil since i was fourteen.
coming off this medication is nearly impossible, i have tried at least ten times. The reason i have decided to come off it for good is because of memory loss. I can spend up to one hundred hours studying for a test and still only get about seventy percent.
Another reason i have decided to come off paxil is tooth decay. I now have a cavity in every single tooth and have lost three teeth due to paxil.
A common side effect of paxil is dry mouth. With out salivia in your mouth, it becomes difficult for your mouth to wash away bacteria, leaving you with tooth decay.
Im coming off slow, cutting up pieces of paxil to take each night, about two milligrams less per night. Ive been all the way up to sixty milligrams and im now down to twenty and hopefully will be free and clear within a few months. This is not a medication you can come off by cold turkey. you must cut it down very slowly

ok well update all my blood work is normal wow im healthy, too bad i feel like crap 3weeks after taking levaquin i couldn't walk for 7 days with pain , in hips, joints , and back . i have a cool burning in my legs. i will think twice before i take a prescribe medicine. im trying the natural way taking hot salt baths , drinking lots of water, eating lots of veggies, olive oil my multi vitimin made me sick . but i will try again i read vitamin c and bs and magnesium will help . sitting in the sun for a little bit helps too . this has been and unreal experience, i hope no permanent damage has been done. best advice to give is keep moving , don't give up , do your own research to help your self . my doctor didn't have a clue, pray to the great physician

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 am a male 45 years and used simivastin another statin for three and a half years. Over this time i had severe muscle pain at time then about 4 months ago the muscle pain in my legs came on with a vengeance. It started in both thighs then calfs got very tight sore ankles feet and eventually got in to my arms. A deep achey sort of a pain and an irritability that casesa feeling like a toxin in my inside elbows that makes me want to stretch all the time. I feel very weak compared to my former self. I tried many things to alleviate the pain but nothing really took the pain away or even decreased it much. sometimes i would lay and groan in agony. I especially noticed that draghts and weather changes made me feel worse????. I stopped taking the simivastin 6 weeks ago. I have not had a lot of improvement but must admit thet i have been trying to push my self over this and probably done more damage. My ck levels are normal but my liver enzyme is increased a little. I started also to take q10 and L- carnitine along with magnesium. I might be improving a little each day but nothing definite. I saw a rheumatologist who has no diagnosis and isn't to committal on whether the statin is to blame. He put me on celebrex which has finally given me some relief. Can anyone relate to the worsening of symptoms with cooler changes in weather? and is there anything else i could do to hasten recovery? Thank you to all contributors on this board although it is the first time i have contributed this board has been a scores of help to me.

Please, is the anyone who knows of a way to treat the dibilating muscle/joint pain experienced as a result of taking the antibiotic, levaquin?

I'm 57, female and have been taking Lisinopril since July. The cough appeared quickly, then the fatigue. Now I am experiencing the joint pain mainly in my fingers, shoulders, knees and toes. Occasionally I get shortness of breath and the fluttery heart palpitations . My blood pressure is way down though and I've been feeling more light headedness lately. I'm going for a follow up with the doctor and will discuss these symptoms with him and see what he says. My dosage is 12.5mg.

33yr Male, fairly fit. South Africa.
(very cautious on any drugs or illness - thanks for the internet for research)
About 5 weeks ago I developed severe sinusitus (headaches, dry nasal paths burning like hell, irritating eyes, sore throat...) Doctor prescribed the usual Augmentin SD. this cleared the nose, pain, throat. On the last day of the course, my chest started burning, together with coughing. Diagnosis was bronchitis (not pneumonia). so the doc prescribed Avelox for 5 days.
The pharmacist took great care in explaining all the side effects to me, and warned me to rest enough, drink lost of water (as with many medicine), don't take multi-vitamins or supplements with iron, zinc, magnesium, and most important that for 6 weeks not to do any exercise, not even walking too much, as your muscle tendons can be damaged. (I even stopped working in the garden, or lifting heavy boxes)

Taking the advice, I got better, and up to today (2 weeks since last pill), I haven't had any side effects as mentioned here. I will continue to check for any in the next few weeks.

When I was first put on this we started at the lowest level and worked up from there, after having labs every 6 weeks for the first few months. I did feel better and had a little more energy, but I had to pee all the time and it smelled god awful, went to my GYN she said it came back fine.....then a G/F who had thyroid cancer told me she takes Armour (a natural ,made from pig liver)...OMG what a difference, I can take less meds, it is cheaper and my urine no longer smells.My energy level is back too!! Armour has T3 and T4 and Synthroid does not. I suggest to those not happy with Synthroid to try Armour thyroid, again it takes about 6-8 weeks to notice but what a great change, and better for your kidneys (which is how synthroid is excreted)

I have been having a terrible itching on left side gland,i do think its from that Lisinopril plus feel agony on right side of stomach rib cage,am getting off of this stuff now after i read these messages before i crack up with more pains else where.om toplax and potassium and water pills so thank that's enough for now,,love to get rid of it all,

Hi guys. I am so glad I found this site. I am 29 and I have been on Yasmin for four years. In the last few months I have toned up and shed a few pounds and all of a sudden last week I got home and felt a tightening in my legs that I had never felt before. Then a tingling in my left arm and I had trouble swallowing and breathing. I am a very healthy person so I freaked out and went to the ER for the first time in my life. After the blood work, EKG, MRI and stress test they told me I was normal, except for low potassium levels and mentioned that I should go to a neurologist. I also thought I must be allergic to something but all the foods I had been eating were the same as before. Well it happened again tonight so I went online because there was no way I was going to spend more money in the ER to have them tell me it was nothing. After reading all the comments on this page I realized it is amazing how many other symptoms that I didn't realize also correlated to the pill. My hair has been falling out at the root like never before and I just recently developed troubles with eating tomato based foods. I haven't been sleeping good lately either and I started crying uncontrollably for no reason. Well I am throwing away my Yasmin and I can't believe that the doctors in the ER aren't mentioning the side effects of this birth control.

I am 39 years old. I have been taking Lisinopril for nine months now, for my High BP. For the first 7 months I had not really had any annoying side-effects other than a mild dry cough. But for about the last 2 months I am having a really odd sensation in my heart. It seems like a flutter and it goes across my upper chest area and into my throat. At times they are mild and other times, during a lot of moving around, I have more aggressive sensations. One night while in bed. My wife got her stethoscope out, (she has a medical background) and listened to my heart. She told me not to tell her when I get the sensation, but to let her try and determine when I have the feeling. this nailed it as soon as I had one. She said that it seems that my heart if pumping too quickly. Meaning that I may have a Premature Ventricular Contraction. This has really scared me. I am scheduled to see my Doctor tomorrow. In my last visit which was about 3 weeks ago, I had brought this up to him. He didn't really try to hear my heart on his own. He just listened to what me and wife were explaining about the sensation. I had hurt my leg about the same time this started happening, and I was taking large amounts of Ibuprofen. So he partly chalked up to Ibuprofen and maybe a drug interaction and stated that I lay off the Ibu and see if they go away in 2 weeks. And if not, he wants to do a Holter Monitor on me to see what may be happening. Well they haven't stopped! I am thinking maybe I should ask for a different BP med. I still want to do the Holter to make sure, but I think it may be time for a change. I have only heard of this fluttering feeling happening to one other person. Has anyone else out there had this same scary sensation? if so please let me know what you have done or have found out. Thank you!

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.

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.

Here is my update:
I last took Lisinopril on July 7th 2008. .I am slowly recovering with the help of a good diet, exercise and supplements.Lisinopril strips the body of Zinc and Zinc supports the immune system. I am taking zinc,magnesium and co-enzyme q10. This c0-enzyme is wonderful! It takes about two months to actually feel the results but for the first time in 5 years I have energy.

I also take vitamin c. I try to exercise at least 5 days a week.My blood pressure is slowly coming down naturally.I will not take those pills. I will take my chances.
I think I have permanent right shoulder damage,although if I take Glucosamine, it does feel better.I still also have major stomach problems such as pain, indigestion and rib pain.

I was diagnosed with adult allergic asthma one year ago at 38 years old. I started having problems breathing ONLY AT NIGHT on occasion and palpitations. Had a physical and ekg, totally normal. Went to allergist and they said I have alot of allergies and diagnosed me with the asthma. Funny thing, weeks before I biked 20 miles, hiked 12 miles, canoed 3 miles, played golf in a 3 day span and no problems. Since they told me this and started me on advair 250/50 I haven't been able to jog more than 2 miles or bike more than 8 to 10. Its very strange indeed, I have gotten more paranoid feelings when just get a little out of breath, and sometimes cant keep still in a car or sitting down. I cut back on sugar, sodium and started exercising a little every day, only 15 minutes and felt better. But came down with a cold recently and back to square one. I am trying to take the advair only ONCE a day instead of twice and almost feel withdrawal symptoms like shakiness, paranoia, irritability. I do have higher blood pressure than I should. Does anyone have any idea about this? I am really confused! Thanks... J

I find some of these posts interesting because it seems as if some folks either do not completely read the dosing instructions that come with all medications when they are picked up from a pharmacy or given by a doctor, or they just choose to ignore them. I have been on Doxy for six months for the treatment of Lyme and Rocky Mountain Spotted Fever. It's been no picnic at times but I feel 100 times better than before I started it. When I started taking Doxy, I too didn't pay much attention to the dosing instructions and I learned the hard way with some uncomfortable side-effects. Here are a few recommendations from someone who has been taking this drug long-term. 1. You must eat! Eat a small snack (banana, crackers, fruit) before you take the drug. Do not take it with something that you know upsets your stomach, also do not take it with dairy or any supplements containing magnesium or iron. 2. After taking the drug, eat another small snack, same as in #1. Avoid any of the supplements or dairy listed above for at least two hours. 3. Imperative!!! Take a good probiotic regularly (30-50 billion cfu). Antibiotics are designed to kill stuff in your body. They do not distinguish between bad and good however. You need the probiotic to replace the good bacteria in your digestive tract, otherwise your body will not digest properly. I was constipated for quite some time before I figured this one out. 4. I saw a few other folks mention this one. Do not lay down immediately following taking the drug. Again, I learned the hard way, I had severe GERD for a time as well. 5. Avoid long-term sun exposure. This was the latest. My skin has always had some natural pigmentation in it for a white guy and I have not burned too easily. On the Doxy though, I found out that I burn extremely fast. I guess I will be under an umbrella at the beach in a few weeks. 6. Don't panic! This drug was made to fight infections/disease. Be prepared for some side-effects, but also don't be afraid to see your doctor if they are just unbearable. All people do not respond to medications in the same manner. What works for you or me might not work for someone else. I hope this information helps someone out there. I know it is incredibly frustrating when you are taking something to cure an illness and more things go wrong.

I am a 49 year old male and took a 14 day course of Cipro for a UTI. By day four the souls of my feet were very sore, especially first thing in the morning but no other side effects. Mentioned sore feet to Dr after 7 days of Cipro but he did not believe it was from Cipro and had me complete the course. After 14 day course of Cipro feet were now so painful that I could barely walk on them especially after resting or getting out of bed. Also burning sensation on skin of feet and hands and some minor tremor. Saw a specialist and he immediately confirmed Cipro as the culprit and advised never to take that drug family again. Have since done the whole web search thing and discovered the whole saga of these drugs. Other symptoms have also appeared, some pain in middle of back, sharp pain in middle of back of both knees, hot and cold flushes, pain in left bicep, fingers that are very susceptible to joint injury and feelings of weakness and anxiety. Has been over three weeks now since I stopped Cipro and condition shows no improvement, may even be slightly worse. About to try a shotgun approach with treatment as there appears little documented evidence of anything conclusive on line. Starting course of anti-inflams (Voltaren) and these have already reduced the pain in my feet. Also magnesium and calcium supplements (theory goes that it may mop up any remaining Cipro and there is plenty of reports from sufferers saying that symptoms continue to appear for some months after stopping Cipro), Vitamin B6 (can apparently help with some types of nerve pain and tingling) and Fish Oil (omega 3's can help reduce inflammation). Not very scientific I know and can't be sure that all these are compatible with each other but am a bit desperate at this stage. Bracing myself for a three to six month recovery (just based on experience of many others). At this stage I am just hoping that damage is not irreversible as this appears to be a real risk. As everyone here will agree it is amazing how this situation is being allowed to continue. I could have stopped my Cipro on day two or three if I had been made fully aware of the risks and what to look out for. I am no expert by any means on this but from what I can gather Cipro and its relatives do nerve damage by the very way they work. It appears that anyone taking these drugs will inflict some nerve damage but for many it will not manifest to a degree that is a problem or at least a noticeable problem. So in some ways we are all sufferers, just to varying degrees. Another point mentioned often is that the symptoms may not appear for some months after the Cipro is stopped and therefore is not always associated with the drug. Also some say there is an accumulative affect with using the drug a second or third time. Symptoms may appear only after multiple use or symptoms may get much worse and more likely irreversible with multiple use. It's all scary reading. At this stage I am just hoping I can make a full recovery. Do damaged nerves repair themselves, does the Cipro eventually leech out of our systems .... I don't know. I will post in this forum again in a few months or sooner if I make a recovery.

I have been on Yasmin for 3 years and everything seemed to be going okay,skin was great,moods were good and all was going to plan..until 6 weeks ago. I decided to go off the pill to give my body a break,during this time i was extremely moody and caused my boyfriend and i to have huge arguments all the time. So i decided to go back on it for the sake of our 6 year relationship.So i was off for a month then went back on it. Within 2 weeks of going back on it i started to feel anxious over the smallest things and had several uncontrollable panic attacks at very inconvenient times. At first i thought i was just run down but it started to happen everyday,on the tram,in social situations and finally even at home.Over nothing worth stressing about! As my heart would race i thought id go to the doctor and was put on a 24 holter ecg monitor to see if we could 'catch' the palpitations so it could be treated with medication. Nothing showed up,my levels were great and he couldn't give me an answer. I just happened to search Yasmin on the internet and found this website..and thank god i did!!I have been loosing my mind! I feel as tough i am loosing my spirit and becoming something that i am not.i can't do anything without being worried itl happen again,making me a nervous wreck. As soon as i read this website i went straight off it and have been off it for 3 weeks and i has not been fun! The first week i felt a little better,but the last two weeks have been hell! I feel weak,shakey,paranoid,over-stimulated,cold and clammy and wake up everyday feeling depressed and nauseous.I feel like screaming.I can't do anything i used to,i was a mad high level basketballer,went out to dance every weekend and loved life generally.I went to a natropath and got put on magnesium and a mixture of herbs to help the nervous system and they seem to be doing nothing.I seriously need some help and have no idea what to do,i can't keep putting up with this,its just not me...someone please tell me that i gets better???I feel like an addict coming off heroin!

Hi all. I'm posting again after being off Advair for about a week. I've noticed a dramatic change in my emotional health. The anxiety that I've been suffering from for the last three months while on Advair has now entirely vanished. I feel like my old self again, and friends and family have also noted the difference. I won't ever take this medication again-- I'd rather deal with my asthma in a preventive way.

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".