Insurance companies symptoms and conditions

Straight from Wikipedia:
Metoprolol may worsen the symptoms of heart failure in some patients. Check with your doctor right away if you are having chest pain or discomfort; dilated neck veins; extreme fatigue; irregular breathing; an irregular heartbeat; shortness of breath; swelling of the face, fingers, feet, or lower legs; weight gain; or wheezing.

This medicine may cause changes in your blood sugar levels. Also, this medicine may cover up signs of low blood sugar, such as a rapid pulse rate. Check with your doctor if you have these problems or if you notice a change in the results of your blood or urine sugar tests.

This medicine may cause some people to become less alert than they are normally. If this side effect occurs, do not drive, use machines, or do anything else that could be dangerous if you are not alert while taking metoprolol .

Side effects
Transient effects include dizziness, lightheadedness, drowsiness, tiredness, diarrhea, unusual dreams, ataxia, trouble sleeping, depression, and vision problems. It may also reduce blood flow to the hands and feet, causing them to feel numb and cold; smoking may worsen this effect.

Serious side effects that are not to be tolerated for any length of time include symptoms of a very slow heartbeat (less than 50 bpm) (e.g. persistent dizziness, fainting, unusual fatigue), bluish discoloration of the fingers and toes, numbness/tingling/swelling of the hands or feet, sexual dysfunction, erectile dysfunction (impotence), hair loss, mental/mood changes, trouble breathing, cough, dyslipidemia, and increased thirst. Other highly unlikely symptoms include easy bruising or bleeding, persistent sore throat or fever, yellowing skin or eyes, stomach pain, dark urine, and persistent nausea. Symptoms of an allergic reaction include: rash, itching, swelling, severe dizziness. Taking it with alcohol might cause mild body rashes and therefore is not recommended.

Why on earth do Doctors keep prescribing these medications that are doing more harm than good? They are causing so many other symptoms, no wonder our Health Care in this country is "out of sight". We take drugs that continue to make us sicker , sicker, and sicker, which require more testing, testing and testing....HELLO people...you need to ask yourselves if you "believe" what that Doctors are telling you. I don't, not anymore. They are SOOOO misinformed by the Pharmaceutical Rep pushing drugs that the DRUGS have become the REAL DISEASE! You need to go back to "square one"...and get off of everything.

My girlfriend age 62 was taking 14 different medications that included BP Meds, Cholesterol Meds, and on and on. She's now laying on a Ventilator from all the interactions these drugs have caused her. She cannot even lift her head of the pillow. Her memory is shot! Just another side affect of the drugs. Are there any Doctors out there who can "step out of the box" ? You're killing people with the drugs your prescribing because you don't understand the interactions they have with each other. You just keep on prescribing. You need to study each medication before you keep prescribing them.

My daughter had the Gardasil shots last year. The school nurse talked to these young girls and told them all the dangers of cancer. It is a scare tactic. Doctors tell you to get the shots as well...makes their offices LOTS of money...the insurance companies presently pay for the shots, and the are very expensive. My daughter passed out w/ the first shot. Never has passed out before. (Do not allow your daughter to drive herself to get this shot...for the adult women..have someone drive you if you choose to have this vaccination, although I would strongly recommend NOT.) My daughter, since she was vaccinated with Gardasil, has had multiple ear infections, warts, strep multiple times, flu-like symptoms multiple times...pretty much the immune system took a nose dive. She never missed school before...was exempt from school exams many times because she was never sick. However, after Gardasil, she has missed many days due to all the sicknesses she has experienced. It has been approx. a year and she hasn't been as sick lately. I am hoping the immune system will get back to what it was before the shots but I strongly recommend NOT getting this vaccination. If my daughter gets worse, I am tempted to contact a lawyer. We might should get a count on the women that have been negatively affected by this and go to D.C. This vaccine should have been researched more. Our daughters should NOT be guinea pigs!!

Unfortunately I've had to stop the Lupron injections. I lost my job and with that my health insurance. I am wondering can anyone tell me when I can expect my period to start again?

November 6, 2008 was my last injection and it was a 3 month dose. It is May 2009, I am 39 years old and I have not yet had a period. My fibroids ae back to their large abdomen filling size so I am very worried.

Not having insurance or adequate funds has reduced me to the internet for research first before venturing out to a doctor as a "self-pay" patient.

They had me on a 600mg dose to begin with, which I cut way down to 200mg daily.I have high blood pressure and tachycardia and it does lower all that quite well. However, I am scared to go to bed at night, because I wake up shaking like I'm having seizures, I feel like my whole body is twitchy. Leg cramps, ringing in my ears, vomiting, nausea, dizziness, hot sweats, cold sweats, dark spots on the wall, (my blood pressure was normal), thirst, panic and anxiety, not caring about life or the house or bills, and horrible dreams, no appetite, then increased appetite, insomnia,and this all started about 3 days into the meds. Let your body adjust to it, yeah, it's getting worse so we'll see.

I am 22 years old have been taking birth control for five years now and have used three different brands. The first one that I was on was too low of a dose and after six months my body became used to it and my periods became irregular. After that, I took Yaz for a while and loved it but once I switched insurance companies, it was $60 a pack. I then went on to Loestrin 24. I have been taking it for a little over a year now. I have not noticed weight gain or an increased appetite but have had many other problems with it. There have been months where I miss my period entirely and then have a very heavy period or two separate periods in the next month. As well, I think it has made my skin worse and my PMS a great deal more noticeable.
I often have unbearable cramping for two days prior to and on the first day of my period. Sometimes I have a "period" that lasts about 6 hours and is not more than just brown spotting on the Saturday before I am to start a new pack.
Currently, I have missed my period the last two months and have had to continuously purchase and take pregnancy tests to be sure that I am not pregnant. My breasts/nipples are swollen and extremely sensitive and painful. I will be purchasing a pregnancy test today because I am unsure of what is going on.
Suggestions for women looking to go on birth control: try other brands of the pill prior to Loestrin 24. Yes, it does give "shorter and lighter" periods...but often causes missed periods. I know that we all hate those days during the month where we feel like absolute crap and do not want to leave the house because of our periods...but (at least for me, a 22 year old student) I would much rather have that monthly reminder than to spend more money on pregnancy tests each month than I do on my birth control.

Currently on month three of side effects. LIghtheadedness, head pressure and tingling, feeling like I am going to pass out, awful Castro pain, gas, belching, chest pain. Tendinitis in both knees and left wrist with swelling. Weak, tired, sick 80% of the time. I have been scoped, had mid section ultrasound, heart stress test, numerous EKGs, blood workups, all within range except for low potassium. This is poison and it just goes on and on. Most Doctors are skeptical although I have found two that believe this is a result of Levaquin, after seeing a half dozen including my internist, Gastro Doctor, urgent care Doctor, ER Doctors, cardiologist, etc. I would think the insurance companies would want this off the market. My medical bills are out of sight and my deductible which is rather large was met two months ago.

Only on it for 1 month so far and already having issues. I apparently have the worst case of endometriosis all my doctors have seen, including a cancer specialist that had to do all my surgeries because of the severity. Granted, I am only 31 years old and have had a full hysterectomy. So, after 3 surgeries I am still having severe abdominal pain and bleeding (don't know where that is coming from since I don't have a uterus anymore) so they said try Lupron and I finally gave in. Now I started getting such severe pain in my lower back that I can't stand for longer than 15 minutes and terrible side aches. I started getting headaches (which I already take pills for for years now),and have gotten the hot flashes as well. What are we to do ladies? I am so sick of complaining to the doctors about pain. You feel as if you are a big cry baby. What are my options here and does this ever stop?

Hi, I am a 36yr old mother of 2 boys aged 14 & 12yrs. I had the mirena fitted in 1 1/2 years ago.. had all the bleeding at the beginning, but unfortunately it carried on for months. had very heavy bleeding in months 7 & 8, so heavy it left me feeling nauseous and faint. then it went back to 3 weeks of bleeding out of 4. and thats now how long i bleed for all the time. have heaps of discharge (eww), zits, feeling constantly like crying over nothing. Had hard cyst, which went on its own. got referred to a gyno (cause of heavy bleeding) which i saw 3 weeks ago. he has no idea why i had the heavy bleeding, has no idea why i am bleeding 3 weeks out of four (not heavy) but he is now booking me in for a vaginal hysterectomy.!! I still have the mirena in, only because i am told that if they take it out, my periods will be a lot worse than before i had the mirena inserted!! argghhhh. anyone else being put forward for a hysterectomy??

I have been reading a book on anxiety and phobias,it says that the Gene # 23 is shorter for people pre dispositioned for anxiety,If this is the case it makes sense as this drug works genetically,,so i wonder the % of short 23 to long 23, and that would give Merck its % of adverse side effects...betting its more than they are saying.As far as the doctors still saying this is a small %,they are just not asking the right questions,The insurance companies should have a record on clients that filled prescriptions for singulair and anti depressants and adhd drugs.If we all cn figure it out in a week ,Well what does that say

After having the third shot I noticed my hair began falling out (July 2007). It is now over a year later and after having numerous blood tests, visiting a dermatologist and doing tons of research, I have concluded that gardasil must be causing this. My hair continues to fall out, I have bald areas around the crown of my head and my mood is very depressed by this. I also experienced soreness in my legs and joints but these are not constant. My periods also are out of whack. They can be between 28-50 days apart. I would not recommend anyone getting this vaccine. I wish my OBGYN had not sold me on it. I was 31 when I got it but she said age didn't matter, she said one day insurance companies would cover this vaccine for all women no matter what age they are. I paid $190.00 a shot and now I have a thin head of hair that may one day soon be bald if it doesn’t stop falling out. I think they should take this vaccine off the market. If anyone else has had severe hair loss, has it stopped falling out after a certain point?

I had the Mirena inserted a little over a year ago. Over the last year, I've grown increasingly not myself...wanted to crawl into bed and do nothing. My relationships with everyone changed-husband, parents, children, neighbors, work. I became a hermit. My skin looked unhealthy, it actually hurt to the touch, my body ached like an 80 year old woman. I felt hot all the time. I felt 4 months pregnant. Could hardly climb the stairs often. I weigh currently 155 and am 5'6". At my 6 week checkup postpartum, I had lost all but 8 lbs of baby weight. Couple of months later, had mirena inserted, and voila gained 15 lbs over the next couple of months. It was a cumulative effect...over the next several months, my face was swollen, my hair, skin, chest was extremely gross oily. I couldn't think straight, my and get through the day. I couldn't remember simple things. What got me out of bed was knowing that my children had gone outside and I didn't want them to run into the street. I knew something wasn't right, but it didn't occur to me that it would be the mirena. I went to my general doctor complaining of EXTREME fatigue. I thought maybe it was my thyroid. The doctor ran 3 blood tests...TSH, mono, blood count. All came back normal. Doctor wanted to put me on anti-depressants and recommended therapy. Not that I'm opposed to the recommendation, but it just didn't sound like the solution. I went to another doctor for a second opinion. Also wanted to put me on antidepressants. I didn't want to mask whatever was going on. I wanted to get to the bottom of this. There was a reason for my feeling this way. I just was not myself but truly didn't think antidepressants were the answer. Meanwhile, I scheduled my annual gyn appointment. The IUD hurt at times, I was constantly aware of it anyhow with sharp jabbing pains, and my husband could feel it during intercourse. So I went in thinking I was pretty sure I'd ask for it to be removed. Still not attributing all these dramatic changes to the mirena. When I saw the dramatic weight gain after the IUD insertion, it sealed the deal in my mind. I wanted it out right then and there. Much to my surprise, joy and relief, I instantly felt better in my abdomen. That night, I put my jeans on and they were actually looser. My body was in constant swelling/PMS mode - due to the artificial progesterone. Within a couple of days I had lost 5 lbs and my jeans continued to get looser. It's been only 6 days now, but each day I feel more and more like myself. My weight is dropping, I have more energy. I want to garden again, a hobby I no longer enjoyed whilst having the IUD, I want to take walks again and exercise, which I had no energy to actually do. It feels better to "be in my skin" - weird to say, I know. Before the IUD was removed, my skin felt uncomfortable. My neighbors noticed the weight loss and the already noticeable change in my complexion. I'm able to engage with my children and meet their needs, whereas before I was barely getting by. It's going to take more time I know, to get rid of this awful acne, remaining weight, greasy skin, etc. but I am 100% certain all these changes to my body and mood were because of Mirena. Today, I have a headache settling in. I think it's because my body has been artificial progesterone heavy, suppressing the estrogen, natural balance. It's got to learn to kick in with my own normal hormone function. I'm expecting some ups and downs, but am thrilled that it's out and I'm on the road to recovery. One thing I question is why doctors so highly recommend the Mirena? I asked for the copper IUD and they steered my toward the Mirena, even when I was nursing. Why don't doctors warn patients of the likelihood of depression and the whole host of other problems that I had and so many other women report? I'm very glad I didn't start taking antidepressants because they come with their own side effects, and I would have had a harder time getting to the root of the problem. Only when I had the IUD removed did I google mirena side effects and realize that thousands upon thousands of women have been through the same thing.

I was on toprol-xl for almost 8 years without many problems. i also take isosorbide mononitrate.A few months back I was switched to the generic version (metoprolol succinate er by sandoz) now i have many problems.First I have to say I am disabled with severe COPD. Although I do not feel depressed I have a lot of symptoms of depression. Remember I had no symptoms what so ever until switched by Walgreen's or HMO or Doctor to the generic version. Not sure what to do I have a doctor that does not truly listen,plus he did not want me on toprol xl to begin with. Even though it was good for me. Good luck people!

Been taking Topamax 300 mg a day for the past 4 year. I also take 450 mg of Wellbutrin. This is to help with migraine. Although my total count of Zomig pills I took last year was 120 pills and some of those I broke in half so I wouldn't have to use a whole pill for a migraine. So that mean, with the Topamax and Wellbutrin combined, I still had at least 123 migraine this past year. Three months of migraines. That's insane. I can't stop the "Dopamax" because my doctor says it would be really bad with it. I have terrible memory loss, forgetfulness, and loss of words that is embarrassing. The nurses did not inform me of the side effects when I first started taking it and I thought I was going crazy. I started looking up ADHD on the computer thinking I had developed it as an adult. I was made at the nurse when she asked me how I was doing remembering things and and if I was stumbling for word......I wanted to slap her off her stool.........at that point it was NOT funny.

What a wonderful site.. thanks for all of you and your stories. I too was a Lipitor user ... 20mgs/day for at least 6 years. I didn't notice any problems until last summer. I couldn't grip a golf club so I didn't play all summer. My doc told me it was arthritis. Strange, no history and never had any problems til then. As the months went on, things got worse. Burning in my upper left arm muscle, so intense it would cause me to have to sit down. Heart racing, pain in back, shoulder and jaw, I thought I was having a heart attack. Started reading about Lipitor and told doctor I wanted off. Of course he said no way and he did an MRI thinking it was skeletal. He sent me to a neurologist, who immediately told me I have statin myopathy. Cause...Lipitor!!! Amazing he admits this, also told me his own doc prescribed it for him and he will not take it because he sees too many patients with these side effects. I am liking him and his honesty. I have been off Lipitor for 2 weeks now. Hands are much better but muscle weakness and burning and sometimes tremors persist but I am optimistic that this may take time but I will recover.

I had my Mirena inserted after a misscarriage in December it was inserted Dec 31/07 anyway since then it has been non stop bleeding heavy with clots, I have headaches and dizzy. The doctor says oh this is normal...whatever. They prescribed me some estrogen pills to stop the bleeding and of course its still on heavy course.

Anyway going to see the GP today asking to get it out, I only had the thing put in because my husband who doesn't want any kids with me because of what his ex did to him wanted it. He will not get a vasectomy and due to malignant hypothermia tubal for me is not a first option.

I had a question though when the Mirena comes out how long do you bleed for I am soo tired of this bleeding, and yeah the lack of sex as my sex drive is quite high and we are both getting frustrated by this bleeding mess.

I posted a question to anyone who used Tri-Sprintec before, but now it's been several months & I'd like to let everyone else know how it's worked for me! Tri-Sprintec has been the best birth control I've ever taken. I have been on other birth controls over the years, and up to this point Yasmin was good but I still had some side effects. I've just started my fourth month on Tri-Sprintec, and I feel more like myself again. I don't have any crazy mood swings, my skin has cleared up, my periods are regular again & my appetite has gone back to normal. I recommend Tri-Sprintec to anyone who is looking for an affordable & reliable birth control (it's offered at the Wal-Mart pharmacy for $9 a month if you don't have insurance.)

I was diagnosed with asthma after 34 years of a very athletic life. My dr. prescribed me predisone, proventil, singular and ADVAIR!! Although the predisone was for a 7 day period, the other three meds. I was to take indefinetly. For someone who has never been on any medication, this was a very hard adjustment!! I took all meds. for about 6 wks. but my gut feeling was just telling me to stop, so after blurriness of vision, weight gain, shakiness, loss of sleep,mood swings,loss of concentration, severe heart burn(especially at night), breast tenderness, back pain and the need to clear my throat all the time I took it upon myself to get off the drugs!! I stopped about a week ago and am feeling a slight shortness of breath but I'm going to stay on top of it and work out on building up my lungs and flushing all these medications out of my system. Sometimes doctors are to quick to diagnose a person and put them on unnecessary medications. I believe on our bodies having the capability of healing themselves with natural elements. I'm on my way to a natural product store to find a healthier way to heal my body. Thank you all for the comments!! I'm relieved to know that I made the right choice on stopping ADVAIR!!!!

PLEASE READ MY STORY!!!....Part 2. My Nephroligist put me on an ARB-Angiostein II Receptor Blocker-Cozaar@50mg.

He said in his opinion, " the medications on the market in both classes of ACE Inhibitors & Angiostein II Receptor Blockers (ARB's) are similar in regulating high blood pressure and helping the kidneys to function better." He went on to explain that "ARB's have less side effects, are a much better quality, and more expensive." "The insurance companies don't want to pay the higher price." "Cozaar is one of the best." I told him that's what I wanted, "The Best." I had a good feeling about this Doc. He knew what he was talking about and recommended what he felt was best for me given the problems I had with Lisinopril HCTZ. He's monitoring me closely and I'm to call him ASAP with any weird or unusual side effects.

I did more research on the ARB's and have personally concluded for the time being, that the ARB's make more sense to me in "how" the medications regulate high blood pressure. Of course there's different types of variables one must always consider before starting these medications or any other medications for that matter. Everybody's medical condition isn't the same and the medications are NOT a "one size fits all" and shouldn't be addressed as such.

I've been on the Cozaar for 3 days and so far I feel great! I'll keep you updated for any side effects. Anyone out there try any of the ARB's? If you're currently taking or have taken, I would certainly appeciate if you would please email me and let me know what your experience was like in regulating your blood pressure and/or any side effects you had.

I had been on Ortho Tri-Cyclen for 6.5 years and NEVER eperienced any problems. I got on Femcon because I was moving to a new state and inbetween insurance companies. My doc gave me a 6month supply before I left so that I could still be on the pill. I'm on the first two weeks, and like everyone else I have experienced break through bleeding. I haven't gotten headaches or mood swings. But as a teacher and a coach, I can't afford to have any of these problems. I'll stick it out for a little bit longer until my new insurance kicks in, but then I think I'm switching back. Anyone know how long this bleeding will last??? did anyone stay on it long enough to see if things setteled down afterwards?

My husband took lisinopril for only two days and had to stop. His side effect symptons included headache, muscle and joint aches, fatique, insomnia, fever and chills, loss of appetite, and THE cough. All of these symptons were severe! It has been two days since he stopped taking lisinopril and he is still flat on his back. I am really amazed that this med ever passed FDA approval, and why any doctor would even prescribe it. I wonder if the docs prescribe it because you can get it at Wal-Mart and a local grocery store pharmacy for only $4.00 per month. Makes me think that the manufacture is trying to push this drug inspite of the horrible side effects by dropping the price, which the insurance companies really love.

I started taking Mobic 7.5 mg about a year ago like everyone else I'm having some of the same side effects. Skin rash on arms, knee pain that wasn't there, tired and groggy, insomia, and forgetful at times. I have had severe back pain for over two years. Diagnosis, osteoarthritis, osteporosis, degenrative disk disease. They can't even tell me for sure what is causing my pain. Insurance companies like to keep us sick and in pain. Want to do water exercises but there are not many facilities out there.

When I piked up my latest wellbutrin prescription I was surprised that I was given the generic subsititute, budeprion. 3 weeks later I was having symptoms of depression. I didn't associate the symptoms with the medication since I was told that the generic is the same medicine. When I called my dr. the first thing he asked was if I was given the generic. He said the generic is chemically different than the brand name wellbutrin--that's why the name budeprion is different from bupropion (Wellbutrin). It IS NOT the same. He gave me samples of Wellbutrin and after a few days I was back to normal. Now I guess I'm going to have to fight my insurance co. to get the Wellbutrin.

My husband was given a sample of this for a month-long bout of bronchitis and we are now thinking it has done permanent damage to his vocal chords. He only used it 5 times, got thrush (yeast infection) in his throat and is still hoarse after a week of being off of it. Does anyone know the history of this drug and has the word "class action lawsuit" crossed anyone's mind besides mine? I am amazed at the way pharmaceutical companies run the healthcare business in this country!

I don't want to go off on a rant here, but are people aware that a large portion of the FDA's operating budget is provided by pharmaceutical manufacturers? This isn't our first experience with this type of thing and I'm about to launch a grassroots campaign to educate the public. Maybe they'll stop believing all the marketing hype.

I'm thinking that the pharmaceutical companies ought to heed the Hippocratic oath - FIRST, DO NO HARM. Wouldn't it be a remarkably different world if they would take all the money they're spending on marketing and use it to lower the price of orphan and AIDS drugs? They keep saying that research is expensive - and advertising on every possible television show, radio and magazines is cheap? Hello? Are we going to be sheep or are we going to be citizens and hold these companies responsible for what they're doing. Thanks for letting me vent. Please contact me if you want to do something about this. And no, I'm not an attorney, but I'm a writer and I think I just found out what my first book is going to be about...

DO NOT TAKE THIS MEDICINE IF YOU DONT HAVE TO. I too have experinenced all the negative side effects of lupron. Ladies!! We must stick together. If you have Endo, join a local support group. There are some in almost every town. Search the internet. You will find them. I just want to bring up alternative options that have helped me. Maybe they can help you too. Dont want to sound too new age but yoga has really helped my back pain. Also looking into Acupunture which has helped me before but unfortunitly is not covered by my insurance. (Even though its proven to help). My chiropracter is covered so she is trying to incorporate acupuncture and massage therapy. Evening primrose oil can help. For severe pain, I take Naproxin which helps me much more than than Ibuprofen. There is a convention every year on Endo, Im going to try to go. We must communicate and be vocal to our insurance companies and to the public. There is just not enough press about this female disease. I also found out that I have Hypothyroid, dont know if its
all related. Its all hormonal and would not suprise me.

On 200mg twice a day morning and evening about a year now for neuropothy(sorry about spelling). Hands and feet. Used neurontin for about 8 years and put on weight. topomax initially took off about 30 lbs. I weight 300 male. Anything carbonated tastes bad, beer soda etc. I prefer water, lemonade, tea, coffee. Now neurontin's patent is about to run out and the makers have come up withtheir subsitute which is Lyrica. Your dr will be suggesting you try this one. It works basically the same as neurontin, maybe just more potent so you take less and they have a new patent. Probably add the lbs too. It affects my sex life in that cannot seem toget to an orgasam as easily so I avoid it. Many drugs for my condition have this affect since they affect seratonin in the brain and thus have a bad affect on sex life of men who still want to be sexually active. Sorry to be so frank. Actually, the topomax does not help all that much with the pain I experience but I do not want to be too quick to switch drugs. Lyrica is still not available through insurance companies in this country although I here they are working on it.