Blood work symptoms and conditions

I know that for every woman, the side effects or various medications and hormones are different. I personally had the Mirena IUD inserted a little over 3 years ago on the recommendation of a friend who, at the time, had nothing but positive things to say about it. I went on that recommendation alone, and now wish that I had done more research into the side effects before having one inserted.

The initial insertion was not horrible, but not great either- a pinch at insertion, severe cramping and pain within a few hours, and a dull aching feeling in my abdomen for about a week. After that, though, I couldn't feel the IUD at all.

It was not long after that when I began to experience side effects. Like many of you, I attributed my symptoms to stress and life changes. I figured that my migraines, back pain, fatigue, dizziness, increasing urinary tract infections, and weight gain were a result of a changing metabolism and high-stress job.

When I went to my family physician to have blood work done (because I was declared anemic when trying to give blood), I was told that I wasn't getting enough iron and I went on iron supplements. (The supplements then made me constipated- sorry if that is TMI, but that was a very unwelcome result!) When I took trip after trip to my ob/gyn for antibiotics to treat UTIs, I was told that the UTIs were unrelated to the IUD. When I saw a urologist to have three separate tests done (one for hormone levels, another for uterine function, and yet another to test kidney function), all tests came back within normal range. Even when I went to the ER one Saturday morning, when my back was spasming so badly that I could barely walk or stand, I was told that my back pain was stress-related.

All the while, my friend (the one who recommended the IUD in the first place) was dealing with similar problems- weekly severe migraines, back pain, etc. She was being told the same things by her ob/gyn- none of her symptoms were related to the IUD. Since she and I trusted our doctors completely, we went on about our lives, upped our workout regimens, tried to de-stress as much as possible, took OTC pain meds when it was all too much to bear- and yet for both of us, our symptoms continued.

Then, in July, my husband and I decided to begin trying for a baby. I made my appointment to have the IUD removed (which was a painless process), and it was only then that I began to research the Mirena IUD online. My former ob/gyn had moved, and my new one seemed ill-informed about what to expect once the IUD was removed. I wanted to know how soon I could conceive, and she knew very little about the process- heck, she didn't even know what the hormone was called that she had given me to jump-start my period (it was progestin, by the way- a very common prescription that my paramedic husband knew quite a bit about, but the ob/gyn didn't even know the name of!).

Once I got online and found this site (among many others), I finally began to put two and two together. I am now firmly convinced that my symptoms were directly related to the Mirena IUD. Again, different women are affected in different ways, but I know that for me- nothing good came of messing with Mother Nature like that.

Now that I've had the IUD out for about four months, I feel like a different human being. I did experience the "Mirena Crash," but once that passed, I almost immediately began losing weight, my abdomen was no longer blown up like a balloon, my energy level and sex drive increased, my back pain is now gone, and I haven't had a migraine or UTI since.

I've since switched ob/gyns, but I now have a healthy distrust of anything medically new and experimental. I will never have the Mirena inserted again, and I will definitely research anything and everything regarding my body. Ladies, listen to your bodies- mine was screaming at me loud and clear for over three years, and even though I knew that something was very wrong, I didn't listen. I'm just happy that I "accidentally" figured it out. (Oh, and my friend will be having her IUD removed later this week. She and I now call ourselves the "sister skeptics!")

I had Mirena since Sept 2008. All I felt was a slight cramp when it was put in and a minor ache for a few hours afterward. I had some spotting for about 4 days after it and then nothing. Periods got lighter each month but the spotting got longer and longer.

I stumbled across this sight a few days ago when I was wondering if the Mirena could cause weight gain. After reading everyone's experience with it, everything started to come together. I got it 3 months after my daughter was born. I had gained 80 pounds while pregnant and lost 40 within 3 months. I then had that damn IUD put in. I gained it all back. I haven't been able to lose anything after gaining it all back. I have trouble just trying to maintain my weight. This is what I've experienced so far: weight gain, facial hair, cramping, sharp abdominal pains, joint pain, constant exhaustion, mood swings, bloating, tingling sensations, headaches/migraines, 15 days of spotting each month, constant hunger, no sex drive... I've had blood work, tests on my stomach and abdomen, iron infusions... All my doctor was telling me to do is change my diet and exercise when I went about the exhaustion. I've done that and gained 3 more pounds!

It's scheduled to come out December 4th. That day can't come fast enough for me!

Lisinopril works! I have been taking 5mg three times a day for years. No side effects. The Dr. told me to take 15mg once a day. Is this a time released tablet? I am 77 years old and a diabetic. I test my blood sugar 6X a day. This way I can control what I eat. Sugar problem was diagnosed 5 years ago with levels running from 40-385. I was depressed & worried about my health. This drug resolved the problem. My best advice is talk to your Dr. and your pharmacist. Friends, family & neighbors mean well. Consider the source!

Panic attacks, ER visit, blood work, shakiness, nervousness, sweating, nausea, agitation. Do not take this drug. I was only on it for about a month. I have heard it has bad side effects. I am hoping to feel better soon since I am off of it. It will drive you crazy.

M.

Panic attacks, er visit, racing heart, blood work, sweating and feeling sick to your stomach, shaking, nervousness. Do not take this drug. I have heard it has bad side effects. Only on it for 1 month and hoping to feel better soon.

By M.

Are there any meds that are safe? I was taking 10mg norvasc. I started taking 20/25 mg lisinopril. I was doing ok on the norvasc but the added lisinopril has almost killed me. They had cut my norvasc down to 5 mg then to 2.5 mg when I started the lisinopril. 4 days ago I stopped the lisinopril and added back 2.5 mg norvasc. Back to 5 mg. The side effects seem to be letting up. Now im wondering is all of my meds are killing me. I can't live without them. My BP sores. Im so scared of what I should do. Im afraid of all my meds.

One of the newest thing my daughter is experiencing is, her joints in her body hurt alot. Mostly in her knees and ankles. Anyone experiencing this?

Please help me I already post my side effects that after taking that med for 7 months I start having a joint pain ,my all body hurts I have no energy left ,I have stopped taking doxy from last one week but I m not recover .does anyone know how I will get normal I m continuously taking Motrin 800 mg for my pain but I'm worried how long I can be on Motrin but if I don't take Motrin I cannot even walk ,does anyone think arthritis but my blood work was negative ...plz help me

I have been taking 20mg Lisinopril for six days for 140/100 BP reduction. Muscle cramps, muscle pain, dizziness, ringing in the ears (which I already had, but this medication has made it MUCH worse),some heart palpitations...generally scary and, on balance, I am going to find some other solution. Frankly, this is like taking a slow acting poison.

I experienced severe chest pains and major mood swings...shortness of breath..12 days i was on it and when i called my obgyn - they said take the ring out and go to the ER. I immediately went to ER...I work at a hospital - so that got me in quicker..the ER doc did a cat scan, ekg, blood work and chest xray - thank god nothing showed up...This birth control was NOT for me and should be taken off the market.

I've been on Yaz for 3 months now and have had lower back pain , and major stomach pains that I'm keeling over in pain I did some research on this pill and see all these comments and lawsuits oh my god .. I went to my doctor and she said that birth control don't cause these kind of side affects and she thinks it could be an ulcer and she put me on meds for an ulcer and I'm waiting for blood work results before I go for a scope I don't know what to believe or if I should stop taking the pill and see if this pain goes away any suggestions out there email me at ******

After you read a representative sampling of this website's testimonials, you certainly ask yourself inter alia: Can this be true? Did thousands of people inject an antibiotic from the fluoroquinolone family, which crippled them for longer or for shorter? Most of us, I suspect, never really get beyond the initial litmus test: Did this medicine poison me or save me? (The answer depends, of course, upon the age, gender, medical condition, and most importantly, the DNA make-up of the individual patient. For hundreds of thousands of patients this antibiotic is a boon. For thousands of other misfortunes this antibiotic is a disaster.) But there is another important question here.

Who gains from self-revelation? To be sure individual sufferers gain certain emotional catharsis from posting their adverse drug reactions (ADRs) to levaquin. E-postings are one-way anonymous tracks that form ruts on a well-traveled trail of tears. Unless these postings are hoaxes written by mischievious gnomes, then they consitute prima facie evidence for a causal link between levaquin injection and sundry crippling ADRs.

Curiously, this e-forum cannot be used as a tool for organizing thousands of potential litigants who might coalesce under a class action lawsuit. Yes, we can analyze each other's anonymous revelations to see if they muster our respective sense of the "ring-of-truth" re: levaquin toxicity, and we may contact each other one-on-one, but no-one can harness this intoxicating communication's technology to reach simultaneously all respondents en masse as a bloc.

So, who wins? The emotionally unburdened e-poster who learns belatedly that s/he is not alone and that prescription medicine likely caused more pain than the underlying malady for which s/he is being treated? Or big pharma that continues to manufacture and market a medication that poses downside risk to many consumers who unwittingly incur more damage than therapeutic value?

Indeed, who wins in a forum where consumers anonymously reveal their symptoms and unconfirmed suspicions? The answer is big pharma wins. Pharmaceutical companies data-mine our postings to estimate the frequency and bredth of ADRs about which consumers complain. House statisticians estimate the ratio of active complainants : silent complainants, i.e., the ratio of complaints who show up on this website to the far heftier percentage of complainants who never post on this website because either they are technology-challenged or they are incurious. House actuarians proceed to estimate how much operating profits their employers must set aside to cover losses in out-of-court settlements or in awards made to plaintiffs in class action lawsuits.

I think this is how the game is played in a behavioral sink where billions are made in a deregulated marketplace that allows predators and prey to interact anonymously. Sorry to be such a downer, but I fathom only the desperate plight of tens of thousands of levaquin consumers for whom no monetary award ever will compensate them adequately for their suffering, and the hundreds of millions of dollars at stake in court awards if consumers ever brought to bear their aggregate numbers and draw a bead on their big pharma tormenters.

I think it a true horror and shame that pharmaceutical companies have not devised a test which determines in advance which patient safely may consume levaquin and which patient's DNA places him or her at risk. I suspect the genome technology is available, but would dig too deeply into big pharm's bottom line. The economics of "parachutes-for-everyone" is infeasible. We are all guinea pigs in a B-grade movie featuring Russian roulette, billion-dollar pay-offs, and an FDA that pretends not to know.

I just turned 21 this month and went to the gyno for the first time just before my birthday. she gave me a trial pack (one month) of loestrin. a few of my friends are on yaz and told me about the horrible side effects, so i figured this one would be better since it's the lowest hormone dose and my body is super sensitive. i started them last week and since then i've been even more moody than usual, go into these random bouts of hysterical crying for no reason, and the worst part is that two days ago my "breakthrough" bleeding started- only it's not just spotting, it's basically like a full-blown period. i got blood work done (almost a month ago) at the gyno's, and i called last night because i hadn't gotten a call since. waiting to hear back this morning because there was a slight abnormality with the pap smear.. needless to say i'm pretty pissed with this doctor for not following up, and for leaving me in anxious suspense about what's wrong with me. is this normal to bleed like this? i went on birth control to regulate my severe, debilitating periods, and now i feel sick and have been bleeding for the past two days pretty heavily. :( really disappointed & upset.

Just had to comment on these side effects I'm reading about Lipitor and other Statin drugs. I don't take anything and I never will after finding this site. Guess what, I have had high cholesterol since I was in my early 20's. When I say high... it ranged from 240 - 260...remember when 250 was OK? Well folks, it's 30 years later, my cholesterol is just about the same range, and Oh My GOD...I'm still here without any drugs.!!! They lowered the range so they could pass out the pills!!! Greed, greed, greed. Do you wonder why our Healthcare system is out of control? Well, when you keep feeding people medications that are presenting the side effects they do, making them sicker, they just keep testing and testing and testing for other things. Let's do blood work, MRI's, CAT Scans, Spect Scans, Pet Scans...Scan away...and guess what...all comes back OK...hmmmm why not look at the drugs you're prescribing. We need to see "all the side effects" listed. Not just some. They're misdiagnosing, Alzheimers, Fibromyalgia, MS, Lupus, Dementia, Arthritis, and on and on when it's been the drugs causing the diseases!
Ween off everything and anything you can...take your chances...when God wants you, he's going to come and get you no matter what you're doing...right or wrong!

I am a few days away from my 19th birthday and i've been taking Yasmin since the age of 11. I was diagnosed with PCOS when i was 11 and Yasmin has been what's keeping my period regular and more or less pain free since then. In May of 2008 i was switched to the generic version of Yasmin called, Ocella and started to notice more and more symptoms and side effects. My stomach pain in the mornings grew greater by the day and when i was on my sugar pill i would gain an unbearable migraine. Thinking it was just part of being a woman i ignored it and went about my life. It wasn't until December of 2008 while out with a group of friends i came into some serious stomach pain. thinking it was just a typical stomach ache that i normally got i ignored it. when i came to be about 4 am and the pain hadn't stopped i started to worry. first thing in the morning i went to the doctor who referred me to get an ultrasound. The ultrasound showed that i had gall stones and that i should have my gall bladder removed before more complications were to occur. Being a college student only a week away from returning to my second semester i opted to wait until spring break to have the surgery. During the 3 month wait i experience extreme diarrhea whenever something was put in my mouth, extreme stomach pain, heartburn, nausea, headaches, sore muscles, the list goes on and on i felt like i had been hit by a truck every day and i still had to go to class. in March of 2009 i had my gall bladder removed thinking that the symptoms would finally stop i returned to school only to find that nothing got better. It's been 7 months since my gall bladder has been removed and i'm still having the same symptoms as before and now i've added depression, stress, lack of energy and interest and many other things to the list. I'm still taking Ocella because i've never been advised otherwise but the symptoms are taking over my life. I am a sophomore majoring in electrical engineering at college and it's just become harder and harder to focus on my work or to enjoy the aspects of college that i should be with the frequent trips to the bathroom or having to opt out of a fun activity because of stomach pain. I was wondering if anyone can help me, maybe point me in a direction where i can get better and get back to enjoying what a 19 should be. Thanks.

My experience with Mirena has been great! I previously had extremely heavy periods (we're talking soaking an overnight pad in an hour) and Mirena solved that problem--I have almost no period at all anymore. My five years just came up, and I had it replaced. Any "side effects" I've experienced I have attributed to perimenopause. I'm 42 years old, and early menopause runs in my family, so any minor weight gain around the middle, low libido, headaches, I attribute to that, since my doctor's office has confirmed low estrogen through blood work. I love Mirena and plan on continuing with it!

Started taking Lisinopril approx. 6 years. ago. Shortly afterwards I started a spiral downwards for no apparent reason. Did not connect this med. Shortly after starting it I was put on Synthroid for low thyroid. Started having loss of balance, dizziness, vision problems, muscle and nerve pain. B/P went up instead of going down. Have been to every type of Dr. (Neurologist, Dermatologist, Endocrinologist, Internist) and every nerve & muscle test and blood work came back negative. I have extreme cold in my hands and feet, increased back pain. headaches. This past week I have broken out in a rash on my torso and down both legs. The doctors answers are that I'm suffering from depression. The irony is that when the symptoms first started I questioned if I could be having a reaction to the medication and they flat out said no. After reading some of the comments as of today I am discontinuing the Lisinopril and will searce for something natural. I'm fed up with doctors and really short on cash from all the money spent trying to find an answer.

WOW! My Mom is 65 and having a lot of these same issues, rash, swelling of the hands and feet, itching, tired ALL the time, depression and she is really "foggy". Her feet are so swollen she cant walk! Her Dr acts like she is just seeking attention and just orders more blood work! After reading all of your comments I am sure its the Lisinopril! Her doctor told her she should NOT stop taking the meds because she could have a stroke! I am angry he is using this scare tactic. I live 2000 miles away but I ready to make a road trip to get this madness to end! She really needs to find a new Dr and stop using this dangerous drug!
Thank you all for posting these issues!

I had the Mirena placed in 2004 after the birth of my second child. I had weight gain, mood swings, hungry all the time (i would sleep eat), depressed, joint pain and was tired all the time. I eventually got it removed 3 years later and my symptoms got even worse. I was severely depressed, my sleep pattern was abnormal, my mind was fuzzy, couldn't concentrate, joint pain worsened and had absolutely no energy. I started itching and having tingling sensations and "bug biting" pain/sensation especially in my extrementies. It was weird. It stimulated a hormonal response that affected my central nervous system. I know it did. I will never be convinced otherwise. It was a shock to my system. There needs to be studies done in this. I finally drug myself to the my general practitioner 3 months later and I thought that I would get admitted in a psych ward. I was hardly functioning. No kidding. I had no reason to be depressed. My life was better than ever. I was not admitted, but I was put through the ringer for tests and my healthcare bills became outrageous. I had tons of blood work, sleep studies, saw a neurologist, had a myelogram, mri, and put on several medications which added to the weight gain. It has been almost 2 years now and I am just now starting to feel like myself. All of the tests were inconclusive. The neurologist dx was something neuromuscular. I am not on any medication now, but am not 100%. But I know that damage was done and I am older. So I'm afraid that I will never feel great again. I wish I had never had the Mirena. Never. I know I miscarried once and suspect that it happened twice. I didn't have a period for those 3 years but it was not worth it. This product should be recalled.

i went to the doctor for blood work because i was tired all the time, no energy, cold even when it was 80 degrees, and i had breathing problems, so i thought i was anemic. the doc wanted me to have an xray and i got diagnosed with pneumonia. i didn't even know i was sick! so i got prescribed avelox for 10 days 400mg, i feel worse now then what i did before. im extremely tired, i sleep all day, i feel like a stoner, i get dizzy at times and confused. i cant seem to go to bed and iv have dream after dream i even had one about a potato.last night i just started crying about nothing and could not stop then when it was over i just stared off and it was like i was a crazy person. im on the 8th day and im going back to the doctor. oh and im only 18 and i read tests haven't even been done on this drug for 18 - ppl.

I am 24yrs old i've had my mirena for 3 1/2 years and for the past year i have had severe acne,weight gain, mood swings, depression and fluttering feeling. recently ive been nauseated and really tired. When the acne started i went to my obgyn and she put me on tetracycline, when i reported the weight gain she sent me for blood work and a thyroid scan. when i said i think its the birth control she said noooooooooooooooooo there is no weight gain with the mirena and said i should try a diet. Mood swings she suggested i was under stress and may be i should make an appointment to talk to someone. After reading all the blogs and post this thing has to come out NOW !!!

I had the mirena put in at my postnatal visit in may 2009. I bled for a month then things were good. Did notice the "fogginess" Its been 4 months now and so far my marriage is heading south, I'm yelling more, getting dizziness, nausea/vomiting, and I've had my first ever migraine and don't forget the hot flashes about 4 - 5 times a day. I had blood work done today no thanks to my ob/gyn. She can't see me or give me orders for blood work for 2 1/2 weeks. I should find out my lab results soon but suspect it will all be normal. Reading these posts makes me realize I'm not crazy and it is comforting others feel the same. I think after reading everything here I'm gonna have it taken out so I can get back to my normal self and enjoy my family!

Wow, amazing that I am not the only one with Lisinopril side effects that are life affecting! First off, I am 26 years old, overweight but never had HBP until my son was born 4 months ago and now it won't go down. I average in the 130's/80's. I have only been on Lisinopril for 9 days and I have been having extreme weakness in my limbs, horrific anxiety, and my chest feels like I am about to have a heart attack. Had an echocardiogram 2 months ago and all was normal except trace tricuspid insufficiency, which the cardiologist said was nothing to worry about. I ended up in the ER yesterday thinking I was having a heart attack because I almost passed out and was so weak in my arms and legs. Blood work was all normal and I had two EKG's, which were normal despite a slightly elevated heart rate, because I was freaked out. I decided I am going to stop taking the Lisinopril and see how I do. I will control my own HBP with exercise and weight loss.

I have been on Diovan 80 mg for 3 years and have experience a lot of symptoms listed above. 8 weeks ago I got very sick and had constant diarrhea (my stool looked like it had oil floating on the water) and lost 40 lbs. After numerous blood work, ultra sounds, ct scans, colonoscopy and many stool samples I found out thay my pancrease was not working properly. The doctor told me that diovan had caused the problem with my pancrease. I now have to take a medication not to help me digest food and they have changed my bp pills. I am hoping this will work because I have missed a lot of work in the last 8 weeks and they tell me where I got so weak it will take me months to recover from this. Anyone having stomach problems please consult your doctor to see if you are having troubles with your pancrease.

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!