Vicodine symptoms and conditions

On for 10 days, off for several and then on for another 20 for sinus infection. Whole body aches and has since second day or so after starting the second course of the drug, however the extreme aches are getting better since final dose. I have also had extreme fatigue to the point that between the aches and the fatigue, I really wondered if my body was shutting down.

Since stopping the drug I have been having insomnia nightly, despite taking Vicodin for the pain at night. Usually, if I need to take Vicodin for orthopedic pain, I will sleep all night without waking.

Joint at second toe on right foot inflamed, whole ball of the foot swollen, but ortho (foot specialist) says he's aware of Achilles Tendon problems but has not heard of Levaquin causing or contributing to inflammation or swelling of this joint, however he said the problem with the toe is progressing "quickly". I did not have a problem that I knew of with this toe and joint until taking this drug.

Face is somewhat puffy, more than usual and fingers are stiff and feel swollen in the morning.

I had the Mirena inserted December 2007 and I thought everything was going great! Then the weight gain started it was like I gained weight in my sleep I went from a size 14 to a 20 and I hate it. My hair stopped growing and started shedding really bad. My face looks blotchy and rough and I've developed a skin rash that itches terribly. I'm irritable as HELL and my sex drive is completely gone. I hadn't had a period since I had the Mirena placed and three weeks ago I started cramping really bad I felt like I was in labor, I couldn't walk or stand up straight. I took some Advil laid down and woke up in a puddle of blood, by the time I could get to the bathroom I had started passing large blood clots. I went to the hospital and they did nothing gave me a prescription for Vicodin and Codeine. As of today I'm still having the same complications with no sign of getting better. Thanks to all the ladies and their post I now know that Mirena is the root of this evil. Thank you to everyone and hope you all find relief because I just called to have this thing removed first thing in the morning!!!!!

six months ago my dentist prescribed 500 mg and 500 mg of penn every eight hours for five days,, along with vicodin for a horribly painful gum infection in my root canal. To this day I wonder if I will fully get rid of all side effects of the Met. After 3 days I was soo dizzy and with extreme blurred vision, the pharmacist and dentist office stated it could not be the ant but the vicodin. I stopped the vicodine and just stayed with Motrin. I had the worst vertigo and blurred vision you can imagine, I felt like an infection was now in my brain, (yet was not) I felt like I had a toxic infection in my body. I would fight to concentrate mentally, I was very fatigued and sick feeling. This went on long after the tooth pain. It took about three months of strining for mental concentration, dizziness, toxic feelong to begin to go away. By the fifth month I could finally feel my personality had returned. Yet my vision has not and has only gotten worse. My dizziness is every so often. During the first months I kept running back and fourth to my doctor with no avail. It was the eye doctor MD that said he was very suspicious that I had an toxic allergic reaction to the Met. Between doctor visits, eye doctor visits, cat scan I have run my medical bills high. I am extremely worried about going blind.
It has now been six months - my health, my vision, my family, my job, my personality have all suffered from this.... Don't take this drug............

I am a mother of a beautiful 11 year old girl, who was a healthy 10 year old little girl until she got her second Gardasil shot! She received her shot on 1-28-08, and started having nausea shortly after (within a few days). She didn't mention it. Within a few months she started having abdominal pain. She was hospitalized on 4-20-08 with pancreatitis. She got out of the hospital four days later. She was on Morphine while in the hospital and went home with Vicodine. She still had residual abdominal pain for the next few weeks, but the doctor said it was normal. She went to school 2 weeks later and started having severe abdominal pain again. We went to the doctor's office where they found out that her enzymes were elevated again. We then were referred to a gastroenterologist. She has had countless blood test..... negative. She has had an endoscopy, a colonoscopy, many CT scans, fecal tests, and now she will be going in for another endoscopy, but this time she has to take the capsule cam. She was so normal before the shots she was boring, but now she has to miss school on a regular basis ( before she was an honor roll student) and has to miss out on some of the most fun school activities. All the doctors act like she is making it up and they think I'm just some crazy mom that wants to drug my kid. They keep wanting to label her with IBS, but she has no signs of IBS other then the abdominal pain. She now has been on several meds. with no help. She now has joint pain headaches, blurred vision, and she says that she feels weird, with no other way to describe it. I feel like everyone wants to turn the other way rather then to accept that this drug is hurting these girls and focus on treating them.

I know this is tough, tough on the girls and young women that are effected, tough on the parents, and tough on everyone who loves them. Please, just remember that you are not alone! I will fight till I die to try and find out what is wrong with these girls. Just remember that you have options, if you do not want to get your child vaccinated, you can visit ****** and there you can find out what legal rights you have to not vaccinate your children if you don't want to. They have the forms that you need and you can download them there.

I am so sorry for all of you that have been effected by this drug! You will all be in my thoughts and prayers, as always. Just please, spread the word, the more we talk, the more that don't have to be hurt like this. Thank you all so much for sharing your stories! They help more then you know!!!!!!

I have asthmatic bronchitis. In June 2006 I came down with an infection in my lungs, which also set off my asthma. Between the two I was hospitalized and put on 240 mg of intravenous Prednisone and the antibiotic Levaquin. I was cured of the infection and was able breathe normally again but it took a great toll on my body It took me 3 months to taper off of the Prednisone and almost a whole year to feel myself. I was a strong, physically active person before this happened to me and I have not gotten my energy level and endurance back to what I was before I was sick. When I was released from the hospital I went from 160 mg of intravenous Prednisone to 80 mg of pill Prednisone. That step down was too severe and I went through intense joint and muscle pain in my body that it woke me from a sound sleep in the middle of the night. I luckily had an old Vicodin that I took which only made the pain bearable. I should have upped the Prednisone to make it go away but I wanted off. This pain lasted one week with each day getting less. The side effects I experienced from then on were so plentiful that I almost can't remember them all. The physical problems were, thin skin that bruised or ripped and bled profusely with the slightest bump, blurred vision, sensitivity to light, muscle cramps in my legs and hands, sleeplessness, dry mouth and frequent urination. My stomach bloated and got stretch marks. I didn't have any before that. The muscles in my thighs and upper arms atrophied so bad that I could not walk up stairs w/o using my arms to help. My arms were also very weak and I got hemorrhoids; another muscle that was affected. I had a bad case of the drops. I couldn't hold on to anything and broke many glasses. I got moon face that took a couple of weeks to go away after I was off the Prednisone. Because I was on such high doses, my hair died and stopped growing. About 40% of it fell out in one month. It took 6 months to grow back and it all grew back curly. On January 30, 2008 my bronchial tubes closed again due to a sinus infection. Again I was hospitalized with 240 mg of intravenous Prednisone and Levaquin. This time I responded much better, because I jumped on the infection/asthma instead of waiting. I stepped down from 240 to 180 to 90 to 60 and decrease 5 mg a day until I was off. This time I did no lose my hair land did not get hemorrhoids. The other physical effects were pretty much the same but much less severe. However, this time the emotional effects of Prednisone were much worse than last time. I was not a nice person. I was short tempered and argumentative and even had to stop myself from resorting to violence a couple of times. That is definitely not who I am. Prednisone stops your adrenal glands from working and adrenaline is you chemical way of coping with stress. I have been off of the Prednisone for one week and still find it hard to cope with the slightest controversy. My brain is still in a fog and I get confused easily. I cannot handle too many questions at once and forget things. My face is still round. Both times, I have found it the hardest dealing with the Prednisone at the very end and even after I finished taking it. I think it builds up and even though the chemical is suppose to be out of your body in 24 hours, it's effects stay a lot longer. I thought I knew what to expect but the second time was different again. It is a horrible drug but my trade off was breathing. Sometimes I think, that if I have to go through this a few more times, the side effects will kill me before the asthma. I wish all you Prednisone users loads of luck and stay positive.

I have active Rheumatoid Arthritis and am currently on Methotrexate, Celebrex and Vicodin to alleviate the symptoms. My rheumatologist at the beginning of December gave me a flu shot due to low immune side effect of Methotrexate and also gave me an injection of Kenalog (80 i think) for the pain. She told me it was a cousin to the cortisone shots I had in the past but that it was much more effective and with a lot less side effects. I did feel better after a few days. But now 2 months later a large apx 3" long by 1 1/2 inches wide jagged edged discoloration has appeared the entire area is indented almost to the bone apx 1/2 inch deep in the center. This occurred during one week time. last week was not there, this week it is. Very worried looks just like some of the melanoma pictures on the internet. Glad to have found this site. I am seeing a doctor tomorrow morning will update this site once it is diagnosed, hopefully it is from the Kenalog shot - it is in the same area, left arm starting just below the ball and joint of the shoulder.