Inderal la symptoms and conditions

I am 40 yrs. old and have been on nuvaring for almost 3 years for treatment of PCOS & endrometriosis. Unfortunately, I had to go off the pill after experiencing a number of migraines w/an aura. The first year was great, no pills to remember, but then I started to have discharge and slight yeast infections on occasion. As we were experimenting with replacing the ring 2 months at a time to lessen the migraines, I thought it just may be my hormones adjusting. About 5 months ago, I was placed on Inderal LA to help with the migraines and started to notice hair loss. I instantly thought it was the Inderal and have been off it now for 6 weeks & still have hair falling out - more than before. I'm wondering if perhaps it could be the nuvaring, after reading all these entries. It will be interesting to see if it continues. I don't think that nuvaring has had any worse side effects then any other BC I've been on....it's just what your body can handle.

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?

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 began taking inderal to prevent migraines. I became severely depressed, and would cry about everything. I even cried when my husband made me dinner! I was angry about everything and couldn't control my moods at all. I never associated it with the medicine. I ran out and didn't get to the drug store, and within 3 days of being off the medicine, I was much better! Please

I have very high blood pressure. I was on a beta blocker for years (my heart runs extremely fast) to slow the heart down. Too many side effects - asked the doctor to change. First of all NEVER go off of a beta blocker cold turkey (yuk). Anyway, my heart is really fast (I am on 240 mg). It seems that my heart still is running extremely fast and I have developed the most horrible pain in both of my arms. It is from my elbows down to my fingertips. It feels like someone is squeezing my arm really tight. My fingers are tingly. Is this a possible side effect or has anybody ever experienced this before?????