Multivitamin symptoms and conditions

I've had the mirena out now for close to 3 months. At first I was losing a lot of water weight - I had gained well over 20 pounds in 6 weeks after having it inserted. Unfortunately, I have plateaued in my weight loss, it's always easier to gain weight than to lose it, right? I still have numbness in my hands, to the point where I am quite clumsy, and I have spells of fatigue and dry-mouth. Before removal I had suffered from the anger and depression towards myself and others, and though it has improved significantly, I still have days where I feel like I could snap just because the 2 year is talking too much. I have found that a multivitamin in the morning gives me a little more boost through the day, and Motrin helps with some of the aches and pains. I'm not quite back to 100%, but I'm getting there. The hardest part for me to come to terms with is how poorly I've treated my boyfriend and our children because of the side effects. Even after 2 or 3 months without it I do suffer some of the side effects, but each day I can feel it starting to get better. I've even woken up a few mornings with feeling in my hands, instead of the tingling "sleep" sensation. All of this from 6 weeks of an IUD... Ugh.

All of the symptoms I suffered were made in previous posts including:
Nausea, severe cramping, severe mood swings, minor hair-loss, increased back pain - especially in lower and middle back, souring/reduction in breast milk, severe weight gain, fatigue, mental fog, vision changes, dry mouth, loss of libido, aggression towards others and myself, severe depression (thoughts of hurting myself), shortness of breath, hives and many more I'm probably not even aware of hahaha. Good luck ladies, this one is a doozy - and remember to report ALL symptoms related to Mirena to the FDA.

I'm a 65 year old type 2 diabetic with low-functioning thyroid. I was put on lisinopril over a year ago to prevent kidney problems. I have been on 10 mg tablets. Even before I was diagnosed with diabetes I had low blood pressure so that was not a problem.

My main side effects are hair loss, coughing, insomnia and leg cramps, joint pain. I think the lisinopril is pulling nutrients from my body. I told my family doctor about the side effects I had found but he seemed more concerned about the possibility of kidney problems than any of the side effects. I know my hair loss is not age related as both of my parents had full heads of hair when they died and my mother was also a type 2 diabetic.

My blood sugar is under control, tests usually 85-90 twice a day, last A1c was 5.5 which is quite good. I take Byetta and metformin twice a day, levothyroxine, enablex. I recently started taking magnesium as it was besides calcium plus D, a multivitamin all ordered by the doctor. I also take crestor. Feels like all I do is take pills!

My weight is 166 but I'm short, 4' 10", so still heavier than I should be for my height. I try to get exercise but have degenerative arthritis in lower spine. Funny that I developed bursitis in my right hip recently, I just thought the arthritis was spreading. Now I'm not so sure it might not be due to the lisinopril also. I stopped using it yesterday so we'll see how long it takes my body to recover from this drug.

Does anyone have any experience with how long it takes to stop coughing or for the hair to regrow after quitting lisinopril?

I was diagnosed with pneumonia on July 6 and prescribed Levaquin 500 mg for 10 days. I took my last pill tonight and could not understand the pain in my right hip, red eyes which I suspect comes from the insomnia I have been experiencing since July 10. I am still having difficulty sleeping and tonight I feel extremely tire with discomfort in the back and shoulders. I wish I had read these comments earlier, I would have discontinue using this drug. I have not experience any depression, but lack of appetite, stomach pain and upset stomach. I have had intermittent diarrhea. How long will it take for this drug to get out of my system.

Wow, thank you all for your postings. I just wished I had found this before I had Mirena put in. I had it placed in Feb 2009, it's been exactly 5 months. I have been extremely tired and agitated. I didn't really associate this with the Mirena until reading the other posts. My hair comes out by the handful (with root attached), I never have solid stools, I have gained about 10 pounds even though I have been trying to lose weight through a diet and exercise program. All the weight is in my stomach and people keep asking me if I'm pregnant. I started to wonder if I could be seeing as I was crying all the time, extremely moody, and that I look at least 4 or 5 months pregnant. All pregnancy tests have come back negative. I got this put in the day before my fiance and I got engaged ( not knowing at the time) and last week we were about to call of the wedding because of my emotional state and constant conflicts. I have to wonder how much of this is caused by the Mirena. I have already made an appointment to talk to my doctor after reading what all these other women have been through. It's just so tough because with any type of birth control their are side effects so I don't want to make it out to be like this is the worst thing ever, it may be exactly what someone is looking for, but just be informed that there are some side effects because I like a lot of other women on this post was lead to believe that there were no side effects or very little side effects.

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 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.

Adderall has worked wonders for me. I was prescribed about a year and a half ago to 10mgs twice a day. When I first started using it, I thought it was great, but like others I hated the side effects. Through trial and error, I have found ways to mostly cut out the side effects. To avoid stomach aches, I never take it on an empty stomach. I always eat a good meal before I take it. I do eat slightly less than before I was prescribed, but I take a good multivitamin to make up for that. I only lost a little bit of weight, just less than 10 pounds. Another way to get rid of the stomach aches is to take a few puffs of some you know what. I rarely get headaches from adderall, but when I do I just take a few ibuprofen and its gone right away. Before I was prescribed, I had tried 20, 30, and 40 mgs of adderall and that was hell. Coming down made me want to kill myself. I feel bad that have severe enough ADD or ADHD to require that much. Overall, I think you have to look at individuals instead of just saying adderall in general is a terrible and addictive drug. Before I was prescribed, I didn't think I had the motivation or will power to make it through school. A year and a half later, my gpa has raised dramatically (2.2 to a 3.0) and I'm in the process of finding what grad schools I want to apply to.

I am 23 and never used to experience heartburn until I had my gallbladder removed last June. So at my Dad's recommendation, I bought the generic brand of Prilosec which was Omeprazole from Target. I was using it as the pamphlet instructed, (1) 20MG tablet for (14) days. Today is my 10th day and the only side effect that I believe I am experiencing is vivid nightmares. I have been taking birth control pills and a multivitamin for a long time now and because I just started with the Omeprazole, that is the only explanation I can come up with. That is how I found this site because I was trying to see if it was a common side effect. I have only experienced the nightmares for the past three nights however, I dream several different scenarios within a night. The last time I experienced consecutive nightmares was about 2-3 years ago when I was taking Lexapro for anxiety in which I had them for six months straight! As for the frequent heartburn -- it has disappeared but now I am afraid of continuing it in the future because of the massive list of complaints from other users. Just when I thought my problem was solved...you're damned if you do and damned if you don't!

J. T.

I am generally classed as an active, happy and positive person, loving life.... but the last 4 months have been a blinking nightmare....
It seems we all pretty much have the same symptoms, horrid shoulder pain, muscle soreness, spasms, feet and generally feeling like "what the??" is where we are all at..horrid thoughts of MS? Motor Neurons, Parkinsons, etc. all sorts of possible sinister problems.
I too have stopped taking Lipitor only a week ago (and I only started back in October 2008 after "arguing with my doctor for many years not wanting to take it...and i didn't even know about the horror side effects, i just thought it was totally unnatural to strip the body of something almost totally,).. within 2 months I started showing signs of chronic neck C5/6/7 and left shoulder. Maybe I had injured myself once before and suffered pinched nerves, but the pain eventually went, but this is not normal or should I say usual...... I have constant buzzing of left thumb/forefinger and hand and my right leg. NEVER NEVER have I suffered from this type of symptom before in my entire 50 years... Even some days when the spasms are at their worst I get an itchy nose and tingling lips. The scariest symptom of a white flash in my left eye convinced me...So fed up with it and after stumbling on all the negative comments and side effects with this drug I made to decision to take control of my own life. It is too uncanny....As I said, it's only a week now free of Lipitor, I have increased my Vitamin C intake and making sure I take a Mega Multivitamin daily too. There is some interesting reading in various websites of Vitamin C vs Statins...

BUT it would really be nice to read any comments of people who have recovered from these rotten symptoms and what sort of time frame it took to get over them. Is there a light at the end of the tunnel for us all. Some indication of Recovery period is probably our greatest "want to know"... and also...when will i be able to enjoy cycling again. Thank you to everyone for the input and may our strength be returned, not only physically but spiritually as well. :-)

i had the mirena inserted after my third child, may 2006. the hairloss started right away, but i did not contribute to mirena.the first year was great. everything the doctors and pamphlets said it would be. no periods, birth control thats inserted and you forget about it.my mom always said if it sounds to good to be true, it probably is! after the first year, symptoms were so gradual. the depression,moodiness,low libido,weight gain, muscel and joint pain,and the hair loss. it never stopped. my hair was always really thick and much longer. now with every trim, it gets shorter and thinner and thinner and shorter. i had it removed 3 weeks ago. im not hearing a lot about regrowth with the hair.im hoping women are having their hair grow back and too busy being happy about it to get on their computers.anyone having regrowth of their hair, please update. how long did it take to have a normal period again?

I am 37, and developed a DVT in my left calf possibly due to birth control pills. I was tested for Factor 5 Leiden and since I was positive that may have been a contributing factor as well. Waking up in the middle of the night and first thing in the morning with excruciating pain was a daily occurrence and finally after 2 weeks of Lovenox injections and warfarin the pain subsided. I still experience post thrombotic pain in the back of my leg three months after starting the medication. My INRs are inconsistent and my doctor keeps changing my dosage. I have been avoiding all food that that can interact with the meds, it is extremely irritating. I have been doing an hour of low impact exercise daily and am looking forward to when I can finally go jogging and increase my cardio workouts. I can't wait till I can finally be off the medication it affects everything I do.

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 been on Loestrin 24 Fe for 2 years and it is the best BC for me! I am a newlywed and our sex life is great! Previously I had tried OrthoTriCyclen Lo and Yaz. Both did not work for me at all!!!! I felt awful with both, especially Yaz. On Loestrin 24 Fe I might have a very short period or sometimes I do not even have a period at all and it is amazing! My doctor said that is okay and normal. I love Loestrin! It has saved me a whole lot of pain that I used to go through once a month. I had the worst cramps and bleeding in the world. I would have to go to bed I was so sick and take tons of alieve and ibuprofen. Now I take nothing but my multivitamin in the mornings! I feel great. Actually I just went to Disney World and my period was due, but I felt great and didn't even have a period!!!!!!!!!!!! INCREDIBLE! Life has changed for the better. I hope you all can give it a try. I will forever be thanking my OBGYN!

I started using Yasmin 2 weeks ago & am having serious problems like heaviness in my chest, short breath, nausea, headache, acidity. At one point I felt as if I got an heart attack! My physician sent me for an ECG yesterday & I am worried about the results! I hope to recover from all these side effects soon because my work is getting affected due to discomfort.

I never thought that my depression could be linked with my BCP until someone recently suggested it to me. I am simply amazed at the frequency that others have posted symptoms similar to mine. After a traumatic event in 2002, I dealt with depression and took an anti-depressant for about two years, but gradually came off of it. In the spring of 2005 I began taking BC to regulate my menstrual cycle. That summer I was back on anti-depressants. I have coped just fine until recently. I got married 11 months ago and I did not know that some anti-depressants have sexual side effects. (we waited until we were married) My psychiatrist decided to switch me to Wellbutrin. I may as well be taking nothing. Horrible depression. I plan on switching back to my original anti-depressant, but I would like to know if anyone else has had a similar experience. I can't pinpoint if my depression is being caused by the Loestrin 24 Fe or an ineffective anti-depressant. Maybe it is both. Any ideas would be appreciated.
C

I have hypothyroid. Have been taking Synthroid for about a year, 0.075MG a day. Had my levels checked 3 times since on the meds and still have never gotten to normal, but a lot closer. I have gained 20 pounds that I can't get rid of, which for me, is crazy. I have never had a problem dropping weight, and for the past month or so, I have started losing my hair. Not just losing it, but the texture and everything has changed. No matter what I do it looks dry and flat, and even when I condition it and also use a leave in conditioner, it still knots up and tangles. I have NEVER had a problem with tangles. It's coming out in handfuls. Im not taking any other meds, so I imagine it has to be the Synthroid. My problem is..What else can I take? I mean, I have Hypothyroid, so I can,t just leave it untreated, But I have no wish to be fat and bald either. Please...anyone know of others meds without these side effects?

Same here. Pretty much like a zombie. Numbness and tingling in hands and feet. Spaced out. Stoned like in high school.

Hello I'm a 41 year old female, and I took Lipitor 20 mgs for 6 months about two years ago. When I called my doctor's office to complain about side effects they told me it couldn't be the Lipitor because I had been taking it for a month already, and would have had problems before that. I eventually took myself off of the drug 5 months later. Here are some of the side effects I experienced:
Itchy fingertips, increased blood pressure, 30lb weight gain, shaky hand writing, acne, poor driving skills, poor memory, hair loss, "frozen joints", IBS, incontinence, low grade fever, itchy feet, numb toes, numb hands, foggy brain, joint pain, muscle pain, foot pain, plantar pain, dizzy, jaw pain, back and neck pain, week ankles and wrists, nasal allergies, skin rashes, migraines, heartburn, Increase in Astham, heart palpitations, knee pain, difficulty standing up from sitting position, difficulty climbing stairs, water retention alternating in feet, hands, arms and legs, almost constant taste of bile in my mouth.
These are only the ones I can remember. Two years down the road everything but the muscle and joint pain and weakness is gone. even those have improved a lot. I stopped taking the Lipitor and lost all 30lbs I had gained on it, without dieting, in a months time. I still have two toes on each foot that are partially numb. I have trouble climbing stairs, and getting up from a sitting position. I can do both, but I move slowly while doing them. The pain in my muscles and joints drives me crazy, but I'm grateful that the rest of the symptoms have cleared up. My doctor never believed me about my symptoms, and neither does my new doctor really. Went to the emergency room for asthma that was not responding to my inhaler, and they were about to let me go home when I mentioned to the doctor that I had been on Lipitor. Suddenly a huge battery of tests were ordered including a CT scan and a stress test. When I asked the doctor why he said that they just wanted to be sure that it wasn't something other than asthma. Why did they do that after hearing about the Lipitor? Do they know something? Are there doctors who believe that statins are killing and seriously injuring people? I'm so angry. Even as I sit here typing I know when I stand up I will have massive amounts of pain that I will have to "walk off". My quadriceps have not recovered, and remain ridiculously weak.
If I can stop one other person from going through this I will be happy. Thanks everyone for taking the time to list your symptoms. It makes me feel better to know that someone believes me, and knows what I am going through.

I started nuvaring after being on the pill for 6yrs and trying ortho evra for a week and ending up in the hospital for nausea. After about a few weeks on the ring I was feeling exhausted all the time, even after 12-14 hrs of sleep. I was moody, in a super depressed mood, and I had no sex drive. I was driving my boyfriend crazy because I was like a different person, and I was miserable. I talked to my doctor about switching again, but she suggested that before I switch I try taking a multivitamin with B complexes and iron because birth control can cause vitamin deficiencies that manifest as all of these awful symptoms. I took her advice AND IT WORKED!!!! Since taking the multivitamin daily, I have had no side effects with the Nuvaring for 4 months, and I feel better than I have in a long time. So before you run to switch to something else TAKE A MULTIVITAMIN! It might save you a whole lot of time, money, and trouble.

I love the vitamin...23 y/o not trying for pregnancy but was looking for a multivitamin, Prenate Elite was recommended by my doc. I've been using for about 6-7 months and I've seen extra growth in my hair and nails. The pill goes down easy and doesn't have a bad taste either. Is not too hard on stomach and has also relieved my occasional constipation.

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

My daughter has been on Yasmin for a year and a half - it was prescribed for irregular periods and spotty skin. She is 15 and has had a year of nausea, leg cramps, hair loss, headaches, elevated heart rate,fatigue , irritation,angry outbursts ,dehydration severe moodiness and depression and lately- uncontrolled crying for no reason. She also sees black dots after exercising. She has gone from a happy girl who loved exercise to a grumpy couch potato! The doctor diagnosed it as a viral infection and suspected glandular fever - she missed a lot of school!
Today she had a day from hell - fought with a teacher and cried for hours. She also takes Ritalin as she is ADD- so I thought it was that - I decided to look up Yasmin and am so glad I did! What a great website! She has just taken a multivitamin and mag.phos - NO MORE YASMIN!!! Any advice on what she can use for her skin? and irregular periods?
A million thanks
Caron

I am 32 years old, and still have acne. I have been taking it for almost 14 years now. I know that Lamictal causes skin rashes. I asked my neurologist if Lamictal causes acne. He said no. I will never be able to get rid of acne, as long as I keep taking it. I have been seizure-free for over 2.5 years now. Dad won't let me get off of it, and be on primidone only. It's more important to keep driving seizure-free, than to have clear skin.

HI guys I was given pred at 60mg then over the next several weeks I tapered off. it is now about 3/4weeks since I took the last tablet. Whilst i was on them I developed quite bad hand tremors/shakes and since taper off to a low dose I have started with muscle twitches all over. Has anyone had experiences like these? And how long did they last?

I was prescribed prednisone for cronic sinus infections along with antibiotic for 30 days. I was not weaned off just stopped completely after 30 days. It has now been three weeks and I am suffering from swelling in feet, lower legs and hands. Any suggestions on what I can do to reduce the swelling and how long this may continue? I