Medicare symptoms and conditions

I obviously have a COPD situation...last 5 years of shortness of breath etc..there is no question of the relief I got from Adaviar but I have had the constant pain under my rib cage...feels like an elephant is sitting on my chest...but worst of all since I started three months ago I have had 3 teeth break off. I assume there is a bone loss issue involved with the ingredients.
I am on Medicare so I don't have any dental coverage so my dentist is having a great time with my extractions. If there are others with teeth issues please let me know. Adaviar has been around for about ten years but that does not mean a Class Action suit would be out of the question here. I have talked recently with my Primary MD about trying something else but I would not mind so help with my upcoming Dentures.

I have had mine since oct 06, I immediately started to have unusual discharge, so much that I have to wear panty liners or a lite tampon, It's extremely embarrassing to have to go through with it everyday, especially in the summer, when i wanna wear a bathing suit. I also hate to have sex, it hurts so much, I can barely take it. I have been oody and miserable, around the time I do get my period I have very tender breasts. My period is lite and only lasts a few days, so no complaint there. I have enlarged cysts now, and they also contribute to my pain during sex. I have no sex drive whatsoever. Could care less. And I use to have sex on a regular basis.

For the past year I have been struggling with acne, I have never had pimples in my life, so now having the right side of my face full of acne and nothing, nothing will treat it. I didn't have much weight gain at all. Im back to my regular size, but I do workout now, and haven't lost anything either.

I thought for the past 3 years I've been crazy, Im depressed, but nothing to be depressed about, I dont have a stressful job, Im healthy, taken care of. But I can cry over nothing, literally, I cry everyday, and lately its getting worse, I thought I was pregnant, because I felt so emotional, I was feeling flutters in my stomach. Things that I felt the first itme.

I don't have insurance, and make to much to get medicare. I really want to get it taken out. This has affected my life so much, that its ruining my relationship with my boyfriend.

I cant believe how many others are having same symptoms, I should have looked into this a long long time ago. Hopefully I can have planned parenthood take it out.

I was prescribed topiramate (it finally went generic- I've been trying to get this med pre-authorized by Medicare for years) a couple of weeks ago for off-label use related to bulimia, more specifically, for weight loss. I also take lamotrigine, an anti-convulsant, for bipolar disorder.

I began at 50mg/day for 2 weeks then titrated to 100 a few days ago. The side effects I've noticed so far are opposite to most of the ones noted here. I am not lethargic or sleepy at all. It's 3:10AM and I am wide awake, as I was last night. I had an excess of energy today and plenty of words to express my ample thoughts. However, my brain working in a sort of backwards fashion, these are the exact sorts of symptoms that signal mania and are extremely dangerous to somebody who has my condition, so I am on strict notice with the doctors and will most likely be either taken off the topa if this continues for another day or two, or put on an anti-psychotic as a preventative, which of course would be counter-intuitive to the weight loss idea as atypical cause gain. You can see from my writing style of run-on sentences that my thoughts are a bit jumbled.

Also- numbness in the heels, irritability, neck pain, itching.

I shall try to post back if I don't wind up in locked ward :-P

I am in total shock!!! I have been at the hospital with my dad for 9 days now and not one person can figure out whats going on. We came in through the ER with extreme pain redness and joint swelling in shoulders, hands, elbows, ankles. Thought it might be gout so they withdrew fluid from ankle that was milk colored, no gout crystals. He started lisinopril 5 weeks ago at 5 mg per day he was on Inderal LA before with no problems. The pain has moved through out his body and he now has generalized pain weakness. He was taking lipitor but has not taken for the last 8 days so I was thinking if it was the lipitor this would have stopped by now. They ruled out any bacterial infection, labs and blood cultures have all been clear. They started checking for off the wall crap viruses like yellow fever, west nile virus, parvo virus and denguey SP? He has not had a fever what so ever and has not been out of the country for 30 years. I am going to make sure he does NOT take this drug starting in the AM does anyone know how long before the side effects take to go away?

Was previously on Micardis HCT; dr. switched to generic Lisinopril HCTZ 12.5 in 11/07 when I went on Medicare & was concerned about cost of Micardis. Since that time I've put on 10 lbs. and had increased pain/muscle fatigue and general lethargy. Unusual, as I've exercised 4-5 days per wk. (incl. aerobics/strength trng/flexibility.) for 20+ yrs. Also, frequently, have problems swallowing pills due to feeling of obstruction in esaphogus tube. In July '08 I awakened to slight numbness/tingling in lips and my lips then proceeded to the swell to the point of pain and my lips (in profile) protruded further than my nose. I received steroid injection and prescription for steroid pack. Diagnosis was possible allergic reaction to new cosmetic product. Today (9/3/08) I woke up with the same symptoms and again had to go to the dr.for a steroid injection & meds. Diagnosis this time (different dr.) was possible side effects of "blood pressure meds." Has anyone else experienced edema of the lips, wt. gain, and problems swallowing?

I was put on Prednisonsone for Uveitis, inflammation of the eye. He started me on 20mg at 9 pills a day, then each week it was lowered to 6 pills then now i'm on 3 pills and then next week it will be 1 1/2 pill and i'll be off. I got the puffy face, my feet swelled, everytime i hate my stomach bloated and hurt, my face and neck turns red, i stayed hungry although i fought the temptation of eating for not wanting to gain a lot of weight, which I don't think I've gained any. But now I wake up in the middle of the night and severe knee pain, it feels like my knees they are in some kind of device that is crushing my bones they hurt so bad. i caught a bad cough and it's been around now for about 2 weeks and won't go away, i told the nurse about it and she says, i probably just got what everyone else has gotten, just a bad cough, well what's if it's some kind of infection? I look like a chipmunk, my face is so puffy. When i get off these prednisone in another week I WON'T BE going back on them, no matter what the case. I'm in more pain being on them and have more side effects while on them than the problem i was having with uveitis. I think some co workers thank I'm over reacting, but they're not here they don't see all the pain and frustration i'm going through while on this drug. The leg pain just started this weekend and i Know i can't deal with waking up everynight like this in severe pain. Everyone just makes me feel like i'm over reactin and it's nice to know that somebody out there is going through the same thing. Any comments will be great.

Have taken Zocor for 7 or 8 years.. with no muscle soreness... suddenly.. in Jan 2008 leg muscles got sore.. sitting for a half hour and getting u, first few steps were wobbly.. can't blame Zocor unless there's a delayed side effect with it occurring after years of use... am going to stop taking it tonight and give it a 30 day rest and see what happens... could be something else... after all, I'm in my 83rd year.. anything could be happening.. I'll hold off seeing my doc.. she'll probably tell me to do just what I plan to do.... and.. Medicare won't pay for a primary physician visit....

after using Lipitor for 5 years,after my doctor ignoring my muscle pain complaints for over a year one night my neck muscles started to convulse
like a dog coming out of a lake
this immediately led to a severe bout of vertigo,could not move my head with out fainting for 3 to five hours
doctor diagnosed it as rheumatoid arthritis what a joke
the next day i could not get out of bed, my leg and arm muscles failed me
after about a week in bed i was able to get around on crutches and after 10 days could get around but in pain
doctors treated me like a leper of old,HIGH BLOOD TURBIDITY LEVELS
no one would commit to a diagnosis publically EVEN AFTER MEDICARE INQUIRED
they spent 50 k trying to prove it was not lipitor,THEY FAILED
after 3 months of memory loss,hallucinations weakness in all muscles
there was small improvement,NOT SO MUCH DEPRESSION,NOT DEAD TIRED ALL THE TIME,STILL NEEDED EXCESSIVE SLEEP TIME
thank god that some doctors i know came down with it so i was able to find out what it was LIPITOR
NOW A YEAR AND A HALF LATER I AM RECOVERING
MAY PHIZER ROT IN HELL, ONLY CURE IS TO GET OFF THE POISON
AND HOLD OFF ON EXERCISE UNTIL YOUR BODY DEMANDS IT

Ive only been on Advair for almost a month. I couldn't believe how quickly my asthma disappeared. I was using my inhaler daily and tried other things but nothing helped. I went to a pulmonary specialist and prescribed Advair for a month. I'm so glad i have to go back and see him this Saturday b/c I want to tell him I will no longer take this. I'm 26 years old and had developed asthma when I was 7 years old. It went away when I was 14 and just came back full force 3 years ago. I would have tried anything to be able to breathe normally again.
I've had the hoarseness in my voice and a bad cough where I'm spitting up mucus everyday since I've been on Advair. I figured if this was what I had to live with to have the chance to live a normal life asthma free that id take it, it wasn't so bad. But this past week I've had blinding headaches non-stop. Ive been nauseous, sweating, coughing, I've been sore like I just finished a long workout, chest pains, tightness in my chest and my legs have felt so weak. This morning I woke up with the worst cold too; which I know Advair weakens your immune system but this is crazy. I stopped taking Advair this morning & I'm going to tell my doctor I need to try something else.

Hi, I've just had my Mirena taken out ( thank Heavens) and can now get my life back. The only good thing was no periods for five years. The hormones gradually ran through my system and all the side effects crept up on me.
My allergies got MUCH worse.
My skin thinned.
I felt three thousand years old , ALL the time.
It stripped a goodly amount of calcium from my body, my teeth started crumbling.
( after two months post removal, my bone and teeth density has improved out the site! WITHOUT supplements My dentist and doctor are now a lot happier)
I had NO sex drive at all.
My weight crept up with NO lifestyle change, 30 kilos! - I have lost on average half a kilo a week since removal. NO diet change, NO activity change.
I've always had slight hormonal acne on my face and nowhere else... with Mirena I had it all up my formerly crystal clear back and diarriere, bust and even scalp.
Lots of other minor crap.
Please, if you have sensitivities to the pill and other hormone treatments, DO NOT go here. I thought I was just aging rapidly- bull dust! I'm just glad that my husband gave me all the support I needed to bring this tragedy to my doctor and Gynie's attention. For so, long I thought it was just me.
Now I'm having my tubes clipped. Hormonal interference just doesn't work for me

Question...I have had migraines for most of my life, the first one I remember was when I was 7. I cannot stomach narcotic pain relievers and was thrilled when Imitrex came out. I took it for years. The only side effects I had were a warm rush, like an alcohol buzz, and sleepiness. Then, 5 years ago I was diagnosed with severe mitral regurgitation. My doctor took me off Imitrex right away and switched me to Maxalt, which I also love. It works great. I had open heart in 2001 to fix the mitral valve, then early in 2005 discovered I have tricuspid regurgitation. No surgery as of yet, thank God. I am on disability for the first heart problem and medicare and medical assistance will no longer cover the Maxalt, only the Imitrex. I took one the other day and almost had to go to the ER. I could barely move, breathe, or speak. Thankfully, after an hour or so, the symptoms subsided. But it really scared me. Now my doctor is giving me all the samples he can of Maxalt that they get in the office.
I am wondering if there is a connection between vavular disease and Imitrex? Has anyone had any of these problems?

My mother took her first dose of Fosamax last Thursday, Friday her legs had swollen up, her right more so than the left. The doctor advised us to go to the ER to make sure it wasn't a blood clot. All her blood tests were fine, checked for heart failure, it was fine, ct scan of her chest, all fine, next day we got an ultrasound on her legs, that was fine too. It's been a week later and they are still swollen, she has NEVER had this problem in her whole life and usually avoids doctors but she pulled a muscle in her back and finally broke down and went to a doctor. Since she is 70 he immediately wanted her to take Fosamax. She will not take it anymore and he is at a complete loss as to why she swelled up, but I know the Fosamax caused it. But I'd like to know who is going to pay her medical bills from all of the testing she had done...Merck? She's on a fixed income and Medicare doesn't cover everything. Perhaps Merck rushed and manipulated research on this medicine to get FDA approval?

Re my post #14305 on Nov. 15, 2005: SAW MY PSYCHIATRIST RIGHT AWAY ABOUT ALL MY SIDE EFFECTS. SHE CHANGED MY LAMICTAL DOSAGE TIMES TO 100 MG IN THE PM AND 100 MG IN THE PM, NOT ALL AT ONCE, AND TOLD ME TO TAKE CLONAZEPAM .5 MG THREE TIMES A DAY TO CALM ME DOWN. THIS WORKED! ALMOST ALL SIDE EFFECTS ARE GONE! EXCEPT THAT I STILL WAKE MYSELF BY YELLING. SHE THINKS I AM HAVING VIVID DREAMS I DON'T REMEMBER AND THAT THIS IS CAUSING THE YELLING WHILE I'M ASLEEP. I AM HOPING IT WILL SUBSIDE. OTHERWISE, I FEEL ABSOLUTELY WONDERFUL!!!!

FOR GOD'S SAKE, READ THE LITERATURE THAT COMES WITH LAMICTAL OR GET SOME LITERATURE FROM YOUR PHARMACIST IF YOU DON'T HAVE IT. THE RASHES SOME PEOPLE GET ARE REALLY TERRIBLY DANGEROUS AND SHOULD BE REPORTED TO THE DOCTOR IMMEDIATELY! THEY CAN BE FATAL! IF YOUR DOCTOR DISMISSES IT, FIND ANOTHER DOCTOR WHO KNOWS WHAT THEY ARE DOING AND GO IMMEDIATELY TO THE E.R. OR AN URGENT CARE CLINIC, AND MAKE SURE THE DR. YOU SEE KNOWS ABOUT LAMICTAL AND THE SIDE EFFECTS! THE MEDS SHOULD BE STOPPED IF YOU GET A RASH. NOT ACNE, BUT AN ACTUAL RASH, LIKE HIVES OR ANYTHING THAT APPEARS TO BE A RASH! BE SURE YOU SEE A DR. WHO KNOWS ALL ABOUT LAMICTAL OR WILL AT LEAST READ UP ON IT. I HAD ONE TRIP TO THE E.R. (BECAUSE MY DR. WAS NOT AVAILABLE AND HAD NO BACKUP) ABOUT TERRIBLE SEVERE SIDE EFFECTS OF LITHIUM I WAS ON AT THE TIME AND HE DIDN'T KNOW S--T ABOUT LITHIUM, I WAS TREATED TERRIBLE BY THE NURSES AND I JUST GOT UP AND WALKED OUT. THEY BILLED MEDICARE $958 FOR MY 2 MINUTES WITH THE DOCTOR. I FILED A COMPLAINT WITH THE HOSPITAL AND GOT NO RESPONSE WHATSOEVER. IF THIS EVER HAPPENS AGAIN, I WILL NOT GO TO THE E.R., BUT TO AN URGENT CARE CLINIC. EDUCATE YOURSELF! DON'T JUST HANG OUT THERE IN THE WIND, WONDERING....

I have cusining's disease. I was on Kenalog for arthritis in nec and shoulders for almost two years. The doctor stopped the shots abruptly and put me on VIIOX till it was taken foo the market. I have been on predisone for a year now and continue to decrease my dose. I have every symptom of Cushing's from Moon face, buffalo back and neck. And weak muscles, joints and so much pain. My wuestion is my teeth. I have lost 3 molars and have 4 more indanger. Can you give me some documented information on steroids and my teeth after prolong use. I need my dentist to receive this info so the insurance company will help with the expense. Any web sites, written documents would be appreciated

Regards,
P.J.