Propensity symptoms and conditions

I have taken three 500mg doses of Levaquin since Saturday. They were prescribed by my urologist for a "possible" minor prostates that might be affecting my PSA (2.2). The very first night I was unable to sleep, tossing and turning all night. Thought nothing of it, and blamed it on diet or too much sleep the previous day. However, insomnia has continued for three straight nights and last night I woke at 4:30 AM with shortness of breath (had to take long deep breaths to feel like I was getting enough oxygen) that felt like an anxiety attack. Although there was no pain, I felt like my heart was pounding and rapid. Finally got a little more sleep and woke up feeling OK in the morning, but blood pressure was elevated. I continually feel like I'm on a caffeine high. I never associated it, but, I woke up second and third days with a sore throat and have had a few minor muscle twitches in arms, legs and abdomen.

I feel fortunate compared to others on this forum. I have stopped taking the Levaquin and have an appointment with my family doctor tomorrow. As a side note, I had an acute prostates this time last year and took Cipro for over one month with no similar side effects that I can recall. Does anyone know if two drugs from the same group can have such different side effects, or can I expect the same problems if I start taking Cipro again?

I got the Mirena in July because I was bleeding so heavily during my periods and had low Ferritin - not anemia yet, but potentially close to it. SO I chose to have this inserted, and the past few months have just seemed to get achier and achier. I could also have a B12 deficiency which is being looked into, but is this a side effect that has been reported frequently? I've also had more headaches than usual, and numbness of hands/feet, a classic symptom of B12 deficiency. But still - the achiness is freaking me out.

I was on Yasmin from November 2005 to February 2007. I didn't have a period until June 2007, and have only had 4 periods since then (and one was medically induced). I have been to a gynecologist and an endocrinologist. I have had a battery of blood tests done and all have come back normal. I have some more coming up.
Before going on Yasmin, my periods were relatively normal. I didn't have a "set your watch by it" kind of period, but I did have a period every single month (just different times during the month). While on Yasmin, I can't name specific side effects that I noticed. Looking back, breast tenderness increased (and continues), increased propensity to headaches and fatigue, and weight gain were all present. It is going off of it that has really messed up my system. My doctor originally thought I had PCOS, but blood tests have come back normal. I was even convinced, because since going off Yasmin, I have developed some of the classic symptoms. I am at a loss as to why my cycle has not returned to normal.
I am so frustrated, and while it is nice not to have periods, I want to know that I am okay. I am wondering if my being on Yasmin is still haunting me.
Has anyone else had difficulties for such an extended period after coming off of Yasmin?

Hi all,

My first time on this site, it's quite interesting to see how people have very similar side effects. My case is I fought with a Poison Ivy and lost, my left arm shows the battle scars. Before going to the doctor, I tried Calamine, Caladryl, Cort Aide, Ivarest, Aveeno Oat Meal Baths & Tee Tree Oil. All failed to help, so off to my doc I went. After what I told him I tried using, he told me to stop. He noted those things do nothing to help Poison Ivy rashes to go away, he prescribed for me to take 20mg of Prednisone 3x a day for 4 days, then knock it down to 2x for 4 days and then 1x for 4 days. He also prescribed Cortisone Cream and to buy OTC Doneboro to soak my arm, it smells just like vinegar..I wonder! I have been taking Prednisone since Monday, so far the only side effects that have shown up is Insomnia and coughing. I do have A LOT more energy than I used to have, my job is enjoying my spitfire mode. The question is, what will happen once I am off this stuff? I've read and heard a lot of nasty things about this drug and I guess I will find out in another 9 more days, I've never been on Prednisone before, I do watch for changes in my body. Making sure I am not growing a beard or mustache, that my boobs don't expand (even though it would make my husband VERY happy). I am sorry to see many on here are having a bad time with this, maybe some of you should get a second opinion. Some doctors today are babied by pharmaceutical companies to push drugs, with some issues some of you have you may want to research your health problems more. Never take the word of your doctor as concrete, they are human too and make mistakes. I believed one fertility doctor until I researched my condition to find out I would never be able to have children, they milked my health plan until I faced them with my findings of medical research sites and online articles by universities. Never again! Fool me once, shame on you, fool me twice, shame on me. Don't be fooled, research for yourself. I will keep you posted as to my next 9 day countdown.

Alison

I have been SO EXHAUSTED ever since I had my Mirena put in (almost 2 months now). I have a toddler at home and am a single mom, so sure there is already a propensity to be tired, but not like this. I find myself unable to stay awake - I lay down any chance I can, and I sleep in a fog that feels similar to when you're sick and just so "out of it" that you can't imagine being fully awake anytime soon.

Besides that, LOTS of lower back pain, gas pain, abdominal pain. Also, my periods, though much lighter, last FOREVER...10 or more days, and they come whenever they choose, there is no rhyme or reason.

Anyone else feeling extremely tired?? It was so painful to have put in, and I was so looking forward to lighter periods (mine were terribly heavy before) that I'm hesitant to take it out and just keep hoping my side effects go away. Ugh.

I was on Entocort and experienced terrible anxiety, racing of my heart, and would cry at anything. Doctor took me off Entocort cold turkey and put me on anti-anxiety medication which is not really helping. Another reason he took me off Entocort is that i had colonoscopy it showed that I did not have crohn's and colitis like they thought I had. What I was wondering is how long after stopping Entocort will my anxiety and racing heart go away does anybody know. I was on it for 4 weeks.

I was put on Topomax for migraines. I've worked myself up to 125 mg in about a week and a half. (Probably a bit too fast, but the migraines were killing me.)

I went on a trip the same day I started Topomax. I was convinced the entire city made disgusting Diet Coke. Then I got home. Needless to say, it was the Topomax.

Tingling in palms of hands.

Mild, constant nausea. Nausea worse after eating oily food. "Clean" foods such as water, mildly sweet ice pops, blueberries, celery, etc., taste wonderful. I think this propensity for not wanting to eat fatty foods is making my stools just a bit harder than they should be, which causes a bit of tummy pain and gas.

Also, I got my period two weeks early. which is just unheard of for me. That might have been a side effect of going off the beta blockers. (My last preventive migraine treatment.) Just noting it in case someone else has had a similar experience.

As for the migraines, it's a bit early to tell. They were awful when I was on the 25-50 mg dose, but I guess that was to be expected.

Good luck, everyone. Btw, what do you do for the nausea? Phenergan?