Short term disability symptoms and conditions

IN DEC 2008 I CAME DOWN WITH CHRONIC BRONCHITIS, MY DR. PRESCRIBE 750MG OF LEVAQUIN ONLY 5 TABLETS FOR FIVE DAYS. AFTER ABOUT THE SECOND DAY I STARTED HAVING SEVERE PAIN IN MY SHOULDER, FOREARMS ,HANDS, BACK ,HIPS AND KNEES. I MADE A APPOINTMENT TO SEE MY DR. AGAIN . COULD HARDLY GET IN OR OUT OF THE CAR THE PAIN WAS SO BAD. WHEN I WAS TOLD TO GET UP ON THE TABLE THE PAIN WAS SO BAD I WAS ACTUALLY SCREAMING. SHE KNEW RIGHT AWAY THAT IT WAS THE LEVAQUIN AND KEEP SAYING I AM SO SORRY, IN AWAY I WAS RELIEVE TO KNOW WHAT WAS CAUSING THE PROBLEM THINKING I WOULD BE GIVEN SOMETHING TO MAKE IT GO AWAY . I WAS AT THE DR. ABOUT EVERY OTHER DAY THEN XRAYS MRI AND FINALY AFTER THREE DIFFERENT DR. I HAD TO SEE A ORTHOPEDIC WHICH STARTED A SERIOUS OF SHOTS , NINE SHOTS GIVEN SEVEN DAYS APART AT A COST OF OVER A THOUSAND DOLLARS. I WAS OFF WORK FOR FIVE MONTHS . STILL MY KNEE GIVES ME PROBLEMS BUT EVEN BEING ON SHORT TERM DISABILITY I WAS LOSING MONET AS I HAD TO PAY 500.00 ON MY MRI , 25.00 FOR EACH OFFICE VISIT WHICH WERE MANY PLUS 10.00 EVERY VISIT FOR THEN TO FILE PAPERS FOR MY SHORT TERM DISABILITY AND IF THEY WERE NOT SATISFIED WITH HOW THE FILE , THEY WOULD NOTIFY ME AND I WOULD NEED TO PAY ANOTHER $10.00 FOR THEN TO REFILED.I WAS ONLY GETTING 60%OF MY PAID MINUS MY SHARE OF THE INSURANCE . I STILL DON'T HAVE ALL OF MY ENERGY BACK BUT TO KEEP MY JOB I HAD TO RETURN TO WORK ONLY PART TIME FOR THE FIRST COUPLE OF WEEKS ,AND NOW THEY HAVE ME BACK ON FULL TIME AND IT IS VERY HARD THERE ARE TIMES WHEN I DRIVE HOME AND GO TO GET OUT OF THE CAR I CAN HARDLY WALK. IT HAS BEEN A NIGHTMARE, I HOPE THAT THEY TAKE IT OFF OF THE MARKET.

Wow! Let me tell you my story: I was first diagnosed with HBP (170/140) during a high school sports physical in the beginning of 8th grade (I was about 14 years old). I was in top shape and a very healthy eater. I had probably (from what I remember) every test done to see what was the cause of this hypertension - and the only thing found was that my kidney's produce too much rennin (the hormone that increases BP). I was then put on Lisinopril 10mg. Everything continued well for about 6 years - I also stayed in shape and ate healthy. However, throughout those 6 years, I did notice my curly hair turning straight and my incredibly (can't do nothing with) thick hair started to thin and become style able. Now...I do know this is my fault, but in the past 2 years my healthy eating habits have slipped, I've gained weight and started smoking - plus have a sit down, don't move kind of job. However, about 1 year ago, I had a slight spike in my pressure and my doctor added a diuretic (HCTZ 12.5mg) to my lisinopril. Ok, that brought the pressure down and all seemed well. Then..... In December 2008, not long ago, I started not feeling well. Thinking I was sick, I went to the doctor's to find my blood pressure to be 190/140. Immediately, my does was increased to 30-12.5mg. That brought a quick drop in my BP down to 110/66 - I was so darn dizzy I could barely function. I was also but on short-term disability because all this caused me to be off work for so long. Unfortunately, when my dose was adjusted to 20-12.5mg and the dizziness stopped I went back to work. Now, I can't go back on S.T.D. for many, many weeks. And....... The past month has been complete HELL!! My hands (mainly fingers) and toes are almost always cold, I've been dieting for over a month and am struggling to lose weight, my hands and feet go numb more often than usual - I never used to find myself waking up in the middle of the night because of pins/needles feeling, my hair is thinner than ever and stick straight - I'm afraid I'm not going to have any left, I have UNBEARABLE headaches (sometimes all I want to do is sleep and sometimes, like tonight -it's 4:12am- I can't sleep), I have acne like a teenager - mind you, I never had more than 1 to 2 pimples at a time growing up, and that was rare (I was lucky)... Thank god for FMLA or I would have lost my job since I've spent so much time home since I thought all was good and went back to work. Only wish I could make a dollar again. Now to top it off...I was referred to a nephrologist (kidney specialist) who after seeing me only once for about 30min and reviewing blood work from the end of January (I had a high calcium level as well as some others that deal with the kidneys) wants to take away the diuretic (HCTZ) part of my medication (hopefully to reduce the calcium level) BUT DOUBLE MY MG OF LISINOPRIL. HE WANTS ME TO TAKE 20MG TWO TIMES A DAY. I was starting to think all these new symptoms that came on so quick were a result from the increase of lisinopril - now I think I'm sure. I'm not changing my medications until I can talk this over with my PCP - I'm going to ask we try a medication change. Does anyone have any suggestions? Or any suggestions why a 20-year-old has blood pressure as high as 190/140 with no family history of HBP or really any health problems? Any suggestions why the kidneys are producing too much rennin? Any meds that drop the pressure and we don't get headaches - I can live with cold limbs and numbness - it's the headaches that are rendering this 24-year-old helpless :(

Wow! Let me tell you my story: I was first diagnosed with HBP (170/140) during a high school sports physical in the beginning of 8th grade (I was about 14 years old). I was in top shape and a very healthy eater. I had probably (from what I remember) every test done to see what was the cause of this hypertension - and the only thing found was that my kidney's produce too much renin (the hormone that increases BP). I was then put on Lisinopril 10mg. Everything continued good for about 6 years - I also stayed in shape and ate healthy. However, throughout those 6 years, I did notice my curly hair turing straight and my incredibly (can't do nothing with) thick hair started to thin and become stylable. Now...I do know this is my fault, but in the past 2 years my healthy eating habits have slipped, I've gained weight and started smoking - plus have a sit down, don't move kinda job. However, about 1 year ago, I had a slight spike in my pressure and my doctor added a diuretic (HCTZ 12.5mg) to my lisinopril. Ok, that brought the pressure down and all seemed well. Then..... in December 2008, not long ago, I started not feeling well. Thinking I was sick, I went to the doctor's to find my blood pressure to be 190/140. Immediately, my does was increased to 30-12.5mg. That brought a quick drop in my BP down to 110/66 - I was so darn dizzy I could barely function. I was also but on short-term disability because all this caused me to be off work for so long. Unfortunately, when my dose was adjusted to 20-12.5mg and the dizziness stopped I went back to work. Now, I can't go back on S.T.D. for many, many weeks. And....... The past month has been complete HELL!! My hands (mainly fingers) and toes are almost always cold, I've been dieting for over a month and am struggling to lose weight, my hands and feet go numb more often than usual - I never used to find myself waking up in the middle of the night because of pins/needles feeling, my hair is thinner than ever and stick straight - I'm afraid I'm not gonna have any left, I have UNBEARABLE headaches (sometimes all I want to do is sleep and sometimes, like tonight -it's 4:12am- I can't sleep), I have acne like a teenager - mind you, I never had more than 1 to 2 pimples at a time growing up, and that was rare (I was lucky)... Thank god for FMLA, or I would of lost my job since I've spent so much time home since I thought all was good and went back to work. Only wish I could make a dollar again. Now to top it off...I was referred to a nephrologist (kidney specialist) who after seeing me only once for about 30min and reviewing bloodwork from the end of January (I had a high calcium level as well as some others that deal with the kidneys) wants to take away the diuretic (HCTZ) part of my medication (hopefully to reduce the calcium level) BUT DOUBLE MY MG OF LISINOPRIL. HE WANTS ME TO TAKE 20MG TWO TIMES A DAY. I was starting to think all these new symptoms that came on so quick were a result from the increase of lisinopril - now I think I'm sure. I'm not changing my medications until I can talk this over with my PCP - I'm going to ask we try a medication change. Does anyone have any suggestions? Or any suggestions why a 20-year-old has blood pressure as high as 190/140 with no family history of HBP or really any health problems? Any suggestions why the kidneys are producing too much renin? Any meds that drop the pressure and we don't get headaches - I can live with cold limbs and numbness - it's the headaches that are rendering this 24-year-old helpless :(

I was prescribed CIPROFLAXACIN 500 mg 28 tablets twice a day. I developed Achilles tendon on my right leg
while playing volleyball. I am using crutches and off from work with short term disability. This drug did not cure my existing problem
but created new problem. Even when such side effects were known to the Physicians and Pharmacists I was not made aware of this. As a United States of American citizen I am requesting FDA to please ban such drugs
that cause such side effects.

I received a Kenalog injection on my face on September 19, 2006. Since then my life has become a living hell. Tbis was to relieve the inflammation from a cyst. Hah!! I have severe redness and burning on my face and it hurts to this day. Every cream and even prednisone failed to take this away. I saw a plastic surgeon yesterday, who said the effects may be permanent. This includes changes in pigmentation (which I've noticed), slow healing, etc. I suffered a severe depression and had to go on short term disability from work. The surgeion has recommened IPL as a way to treat the redness. I'm going to try to get a lawyer. This injection was given by an incompetent PA who never warned me of any of the side effects. Does anyone know of ANYTHING that can reduce the redness and burning? I'm desperate.

Huh, you guys should be happy you don't have a crazy doctor like mine. I'm 5'7" and 160lbs and my doctor wants me to take 20mg basically cause he thinks I talk too much. Not only that, but he wants me to take it indefinetly. My mother had originally wanted me to see a doctor and take some kind of medication because I was having somewhat of a nervous breakdown about a year ago when I lost my job. Now she's just wanting me to get off the medication completely and I can't agree more. Yes, my body has gotten used to the 5-10mg that I take (what did you think I was really going to take 20mg? I'd never get out of bed) and I feel ok taking it but do need lots of coffee in the morning to get my brain working. But I feel that this drug may permanently alter my brain chemistry if used for a prolonged period of time and I'm just going to have to get off of it. I've been weening myself off it for a couple months now. After about three days of not taking the drug it get's really tough. My sensesk, especially my hearing get hyper sensative and always hearing high pitched shrilly noises in just about everything. This in itself gives me a paranoid like feeling. Hot flashes all the time, no eating, hard to sleep. I can't understand why my doctor is so crazy about taking so much of this stuff. Not once has he even mentioned that this drug is for short term use. I'm going stop taking it now and not see him anymore. Hell, he put me on short term disability a year ago cause he said I was in no state to have a job. I wonder if he failed to realize this was because he was giving me 20mg!!! Where did this guy learn medicine? Well, the disability insurance has ended because they state that "the information in my file indicates I have recovered," and I'm going to get my life back to the way it was before and without any medications. Especially cause without medical insurance I'm looking at a $450-$600 a month medication cost. No thanks. Oh and as far as the smoking question. Nicotine and smoking cigarettes is ok and actually increases the metabolism of the olanzapine significantly. So your probably just getting a reaction to intial increased metabolism of the drug. My biggest complaint about the side effects of this drug is the blurred vision, constant sleepyness and just not being able to think clearly.