Insomnia effect of Prednisolone

I have had a severe inflammation on my eye for a few weeks now. After drops, ointments and cortisone-containing eye drops did not help, I got the tablets prescribed. 60 mg a day. I do not feel hungry. I’m pretty relaxed I do not care. I’m not tired, I have sleep problems. Diarrhea started on the 4th day. So far, the inflammation has not improved.

Fatigue, insomnia, depression,

Earache, fatigue, loss of appetite, slackness, impulsiveness, insomnia, concentration disorder

Tachycardia, complete insomnia, anxiety, nightmares, panic states, sweating, thoughts of suicide, depressive mood, stomach ache, back pain, pimples, itching. After 2 weeks I slowly skipped the 7 week therapy because the side effects were so extreme. Never again would I take this medicine !!! I still have stomach problems 3 weeks after the last tablet!

Tinnitus is still there, and high blood pressure, back pain, tremors, insomnia, as well as calf pain!

After getting 3 cortisone infusions first, I was given pills. Scheme: 5/4/3/2/2/1 / 0.5. Already after the second infusion, the urinary urgency increased. After the first tablet intake, it became more and more and on the 3rd day of tablet intake I could hardly get enough fast to the toilet. In addition there were strong mood swings with sudden outbursts, heavy sweating, insomnia (extremely during the 3-day infusion, then slightly improved), unexplained nervousness and of course the familiar bright red face associated with heat sensation (as in a very strong sunburn). Helped the drug, but the side effects were extreme. At the next acute hearing loss, I will probably wait a few days, if the symptoms disappear as well. Because the side effects have burdened me a lot and limited, especially the constant Urn urgency and partially uncontrolled urine output.

In case of sudden tinnitus without physical cause. Taken 10 days, starting at 30mg. The stuff changed my psyche so much that I barely recognized myself. Hopeless, timid, dejected, close to the water. Restlessness up to panic attacks, palpitations, insomnia (also due to tinnitus), frequent flushing, depression. Sorry, it has nothing: /

After a weeks-long torture of the diagnosis. I got the diagnosis Autoimunne hepatitis. At the beginning I got 75mg prednisolone to get my liver values back down. Which unfortunately did not work out as hoped. Already after the second revenue I got violent stomach cramps. Since the 5 day I have violent heartburn, nausea feeling. Pressure in the chest and abdomen. Ever since the 7th day, I have been feeling worse and worse and have almost no feeling of thirst. Since the second week I am extremely sensitive to headaches and insomnia. First I could not sleep through then it was only 3 hours of sleep per night with many interruptions and meanwhile sheep I partly not at all or only in the minutes area if it will be 30 min in one night I am meanwhile already happy. In addition, I am the corresponding permanently powerless but have an extreme urge to move and can not resist accompanied by hunger pangs and corresponding weight gain on average 3 kg per week. Now I take it for 5 weeks and have for 2 days an unpleasant feeling of heat of the facial skin and since 4 days, the skin in the genital area dried out and brittle which, for example, when washing is very painful because the foreskin gets each time entry. The worst thing for me is that my friends and family are suffering because I am constantly irritated and accordingly fast as the HB male go to the ceiling. Now I am in the process of sneaking out the prednisolone. From 75mg down to 50mg and continue in 10mg steps and then replace it with another drug.

Fressatakken, no satiety, weight fluctuations, starvation, hair loss, full moon face, acne, water retention, insomnia, aggression, body aches, sweating, increased hair growth, cycle disorders, depression, nausea and acidity of the stomach, dry mucous membranes, maritime disorders,

prednisolone acis was prescribed for my crohn’s disease. It is one of those medications that you know have tremendous side effects, but you have to take them because you can not help it. When my crohn started three years ago, I had to take the drug for almost a year, up to the highest dose of 100 mg per day. overweight, full moon face, bulls neck, sweat attacks, hyperactivity, insomnia – all this has happened to me. after that it was slowly faded out. Now I take it back since yesterday days, because my chron has deteriorated rapidly and I can not stand it from pain. And lo and behold, an hour after taking the miracle happened, the intestinal rebellion came to a standstill, I cried with happiness, because this pain that drove me mad, subsided. I start to become human again. That’s why I accept all that there are side effects. until just a better, lasting solution for my illness is found and the pain of the drug humira, which has cost me almost three years of life quality because useless in my case, is over. Cortisone, like many other medicines that are just awesome, is important and good. the goal and purpose is that you can live reasonably well again, however. I am grateful that there is such a thing.