Iv therapy symptoms and conditions

I've been on Advair for 12 years.I'm 27 years old and fed up with all this medications that doctors prescribe.We are so brainwashed into thinking that we misbehave if we don't see a doctor.Let me tell you what: The majority of the doctors, only know to prescribe medication.They get bonuses from the pharma industries every time they prescribe their "new discovered"medicine.
Advair is supposed to be preventive, what you don't know it's for how long.Exactly!!!.....'cause it's not meant to cure Asthma, it's meant to keep you hooked for the rest of your life.
My worse symptom is a very fast heart beating.I'm a martial artist and every time i exert a fast burst of energy(while i'm sparring for example), my heart goes into pumped up mode.It beats very, very fast and i have to stop because it hurts.Sometimes i keep going no matter what and feel like i'm exercising for two people.When i stop, i breath very deeply for 5 minutes and all of a sudden it stops and beats regularly.
It's not fun, and one more thing: I'm from Argentina and my mom sends me the medicine from there cause it's way cheaper, sometimes i run out(i procrastinate sometimes), i'm left off with no medicine for a few days and boy.....I'm a wreck.The time you stop you go right back to where you started.I've been researching about an alternative to this "S***".I'm afraid 'cause i don't want to feel discomfort with my lungs anymore, but i strongly believe that there should be a natural alternative to all this laboratory drugs and i'm on a mission to find it.

Has anyone had the experience of previously taking Levaquin without side effects, then when taking it again, developed severe headaches, joint aches, muscle pain and weakness, etc? I am currently going through this. I've taken Levaquin before probably 2 or 3 times due to upper respiratory problems and not noticed any side effect but this time, I've taken 5 days worth, 3 in hospital 2 as outpatient dose and can hardly move. I had the same experience in 2004 with zithromax. Had taken it without side effects, then suddenly when taking it again developed such bad chest pain, I thought as did my doctor, that I was having heart attack and spent a week in hospital before figuring that one out.

My story about the Mirena started from 2002. I had my seconnd Mirena placed 2 years ago. Having them put in and taken out are extremely painful you need way more then advil I had to take painkillers given to me by my doctor. I never knew about all the side effects I was never told and now know that everything that has happened to me is because of the mirena thanks to your blogs and my doctor. The first problem was serious stomach issues so bad that they had to remove my galbladder. Well that didn't work so I have had 2 upper g-i's and 5 colonoscopies the last one they found colitis which they could not explain why I had it. I still have stomach issues so bad that I run to the bathroom after eating. With all that being said you think I would lose weight well no I have gained 15 pounds since the last one was placed. My heart I have had an extremely fast heart beat since having the mirena so fast that I have passed out numerous times; the cardiologist said its definitely hormonal but would never tell it was from the mirena. I went through 22 different tests for my heart, evern wore a monitor for an entire month. Sex drive is not there, I never am in the mood. Exhausted I am constantly tired I have to fight laying in bed, but at night I can not fall asleep even on prescribed pills only get about 4 hours of sleep; before the mirena I could sleep 10 hours with no problem. Last but not least is the headaches and neck pain they have been so bad I have had 5 nerve blocks since having the mirena. I have gone into the hospital 3 times since 2002 for severe headaches which they have run every test known to man on me and can not tell me what I have. I have had to recieve iv therapy for the migraines that you can only receive in the hospital with a nurse watching you for 48 hours since you have to receive 3 doses of it. I could not walk, talk, or even look at light. My stays at the hospital have ranged from 3 to 7 days. I have gone to specialist after specialist and no one would tell me the truth or knew what to tell me. Finally 3 weeks ago I went to the neurologist and he told me straight out after looking over my medical history and speaking with me that without a doubt it was from the Mirena. After 7 years,11 specialists, my galbladder being removed, numerous hospital visits, and endless procedures I finally know the truth. I hope people read my story and think twice about using mirena; you could end up like me. I am only 28 years old, married with twin daughters. I have had to live like this for 7 years; I will never get that time back but once I have this removed I know I will have my life back.

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?

I've been taking doxycycline (100mg, twice a day) after a meal for Lyme for about two weeks now. So far my stomach has been pretty good, got a little nauseaous a few times but not too bad.
The main problem I've been having is a tingling feeling in my hands, arms, feet, legs and sometimes my lips (almost like I had novacaine six hours ago). It feels like the blood circulation is poor, if I get up and move around the tingling goes away. At night I've been having trouble getting comfortable due to this, feels like my arms are falling asleep.
Can anyone tell me how long this will last after I finish the doxy? I have about two weeks left. Thanks!

I took Levaquin from May 1, 02 until July 19,02 for an infected hip prothesis. I developed severe pain in my fingers, knuckles, hands, shoulders and TMJ joints. The Dr. said it would go away. As of May 9, 03 I still have the problem and am seeing a rheumatologist. He, through blood test said I have ANCA Positive vasculitis which is caused from taking Levaquin. The course of treatment is steroids. I took steroids and the raised havoic with me, and only made matters worse. His next course of action is massive doses of steroids. IV therapy for three days followed by 100, yes 100 days of taking 15 mg prednisone daily. He treated his only other patient with ANCA Positive and it did not work.
I'm currently waiting to get in to Mayo Clinic, Cleveland Clinic or University of Michigan Medical Center.
My question to anyone out here is if there is a class action law suit going against the manufacturer of Levaquin.
jcoleman@shianet.org