Summer time symptoms and conditions

After reading these posts I am more confused than before, because my experience is so far very different. I was diagnosed with DVT about two weeks ago and now take Coumadin daily; the Lovenox injections have been discontinued. The reason I'm so confused is I now feel the best I have in 5 (five) years.

Before being placed on the anti-coagulants I had memory and concentration issues that were progressively getting worse and greatly affecting my job, and had daily headaches. I had joint pain that made it difficult to get up after sitting for awhile; they felt constantly inflamed. I felt fatigued all the time and my muscles hurt like I had really pushed them; I just didn't have any strength, and had muscle cramps. I was constantly yawning and found my jaws hurt from clinching my teeth, subconsciously trying not to yawn. I was extremely sensitive to physical touch, even hugs hurt. I also felt extremely depressed and cried almost daily. My lips and left cheek tingled, as well as other parts of my body. Plus I would get the feeling of sudden pressure in my head (different from a headache) like it was going to pop off, and I my eyes didn't seem to track what I looking at and had difficulty in remembering or comprehending what I just read.

About 6 (six) days after starting treatment it completely changed and these symptoms are essentially gone. I have talked with my doctor and pharmacist and they are baffled. I am concerned this change, while welcomed, may indicate an underlying condition that is not yet diagnosed. Has anyone ever heard of such an impact from starting Coumadin treatment?

I am a 32 female and on my third day of taking Avelox and its driving me crazy. I haven't slept nearly two days. I am so tired and I haven't been able to eat anything as well because as soon as I put food in my stomach it doesn't want to stay long. I am also so bloated and very jittery and have very bad mood swings and very irritated with things. I haven't been able to do anything I have no energy and as soon as I would stand up I have to sit back down because I get so dizzy and light headed and ready to faint and then vomit. I have been doing that as well. Ive called my doctor and told me to continue to take the med and they are just side effects that will go away in time. Well I can say that these pills made there way into the toilet and are washed away somewhere. And I cant believe that I would spend the amount of money on these pills $120.00 to feel the way that I do. My eyes burn and also cant stand the sunlight. Its summer time and I love being outside and cant. I haven't experienced depression yet and don't plan on it. I guess I will just let this runs its course and eat plenty of chicken noodle soup. I know the next time the doctor wants to prescribe this med for me I am just going to come out and say I AM ALLERGIC to it.. Does it count that since ive been on it that my nose has been itchy and my hair feels like its crawling and I always bite my lip now..I wouldn't advice anyone to take this medicine. Its not worth being more sick then you already are and I am right there with everyone else if there is a lawy suite against this drug I am right there with it

I was prescribed doxycycline hyclate by mt dentist for gum disease. I have been taking it since 3/23/2009. I stopped taking it two days ago. I have found increasing joint pain, especially in the thumbs. It has been getting worse. Also muscle aches from routine yard work, nothing strenuous. Itching all over the hands, arms, legs and back. I had been advised by the pharmacy to watch out for sun while taking it. Since it is summer time, there isn't too much one can do to completely stay out of the sun.

I intend to continue to suspend taking the medication and purge it from my body. This is the second time in the last several years that I was not properly advised of the various side effects.

I was prescribed this medication for dental disease and to take it for a minimum of 90 days. Since 3/23/2009 the gums have stopped bleeding. I just hope my system can purge itself of this RX.

The first time I heard the word prednisone was late Dec 07 when I was hospitalized for severe pneumonia. I started off with a bad sinus infection that quickly advanced into pneumonia in a matter of a couple weeks. I tried 3 courses of antibiotics but I continued to get worse and got to the point where I was unable to breath on my own. Within a day of being at the hospital I felt like I was living in a dream world and from there I continued to get more stoned by the minute. I had no idea I was being pumped full of prednisone intravenously, along with my antibiotics. I was given a dose of 250 mgs daily, and obviously it was way too much for me. As I progressed into my dream world, I had a couple of “episodes” where I acted completely out of character, and got really paranoid and highly emotional. I pulled my IV out of my arm the one night and sat and watched the blood dripping from my hand, not really understanding where I was or what was going on. Later on I got really paranoid that the nursing staff was conspiring against me and talking about me behind my back (lol) , which I normally would not care about, but for some reason it made me really upset and I sobbed uncontrollably at times. I also tried to leave my room in intensive care a few times, as I was convinced that I was not supposed to be there and wanted to go home. My doctors were really freaked out so they gradually lowed my dose over the last few days I was in the hospital, even sent me for a CT scan of my brain in case I was going crazy. Prednisone is an extremely strong and evil drug – that is why I had the adverse reaction!! Not because I’m crazy! And one should never be given a drug like prednisone without their knowledge!! A few weeks after leaving the hospital I started going down hill again and the doctors realized that what I had was an immune disorder and not just pneumonia per se. After a few months of on again off again prednisone (never longer than a week at a time), I was put on a daily regiment (50 mgs) of it starting in May. Since then I have experienced all of the same side effects noted by everyone on here, weight gain, sleeplessness, anxiety, hair growth (the worst is on my face and fingers!!) dizziness, confusion, trembling hands, tooth aches, and the worst of all , big time MOON FACE! I feel like a complete freak most days. I am now tapering and am down to 10 mgs. So far I have seen no improvement in the side effects, accept now I have withdrawal side effects on top of everything - nausea, headaches, flu like symptoms and trouble breathing. I HATE this drug, even though I know it ultimately saved my life in the hospital and my kidneys – as I had complications caused by the autoimmune disorder. I see my doctor next week and I want off this drug completely. I am not sure the benefits out weigh the side effects to be honest. I want to feel normal again and be able to recognize my own face in the mirror  People should use extreme caution when using this drug and it should only be used to save people’s lives, not used for minor things like poison ivy. That is unconscionable!!!! Good luck to all who are on this drug.

My 8-year-old son started on Singulair 6 weeks ago. Soon afterwards he had severe problems falling asleep--often up until 4 or 5 am before drifting off, but I didn't make the connection. (Thank goodness it's summer time and no school!)

About 2 weeks ago, my doctor recommended Singulair for me, too. The first day I was unbelievably sleepy, but after that I, too, have had severe problems with insomnia. I have also noticed involuntary muscle twitching, restless leg syndrome, and my mind feels like it's turning to mush. I used to tutor statistics; now I can't even do basic multiplication! Scary!

I have just thrown out both my son's and my bottle of Singulair. I hope stopping it will reverse this crap.

Has anyone had the Mirena taken out and immediately replaced with the copper IUD? I'm having this procedure done on May 20, 2008 and I'm really scared that doing this will further hinder my weight loss effort. I've had the MIrena for a little over 2 years, and like many many women I only have very recently started to connect Mirena with side effects I never imagined. It was inserted Feb. 2006, and immediately I turned into a horrible, moody, extremely emotional basketcase. I never even thought twice about the Mirena being responsible. My husband and I thought I was postpartum depressed. I lost everything, meaning my husband, my home, my life, and my mind within 3 months of insertion. I had already had one child, and after she was born I had PPD, but not to the extent of attempting to kill my husband and turning his mother in to Social Security. This was a horrible time in my life and I wish I had known that it wasn't just postpartum behavior. Recently I've noticed the increase in my weight....a problem I never had before and I don't like it. My skin is a big oily blemish nightmare, also a problem I never had before. I'm always nauseated, I am depressed still and now summer time has become dreaded because I can't stand to look at myself and it's too hot to cover all the way up. I'm terrified of removal because I have read many stories saying that you go through a worse emotional roller coaster to get the hormones out of your body, but I suppose I've done it once, I can do it again. If anyone has had the Mirena removed and replaced with the copper one, can you please tell me what to expect??

HI,
I stopped Lisinopril since "August 1st. It took until last week for the heart palpatations to go away. For the last week I finally can sleep a full night again without waking up with a racing heart beat. I feel so much better, it is unbelievable. The hair loss people mention, which I also experienced, is caused by the rise of lithium levels, which in turn messes with your thyroid function, this causing dry skin, flaking scalp and hair loss! I just knew that I never had dandruff in the summer time, but never connected this with the hair loss and of course lisinopril.
Good luck to all of you!

hmmm , i really like the ring, i'm at the end of my 3rd month and i've actually lost weight (but i think that may be because its summer time and i've been eating a little less), and my boobs arent sore at all, none of the usual BC pill side effects. the only thing i can say is that i get dizzy sometimes when i get up too fast, and i've been wondering lately if i am depressed. i've also been wondering if its even working because i seem to be getting my normal PMS (crying, and food cravings) toward the 3rd week. i'm gonna wait a couple more months i think, because this is the best thing i've tried yet. :[