Prednisone symptoms and conditions

As a Doctor myself I think drugs are NEVER the answer except in EMERGENT issues in Heroic life saving... YOU however and all individuals are and should be MORE accountable for your own health and STOP DEMANDING the Drugs and look to LIFESTYLE changes in DIET and EXERCISE to achieve the GOALS so necessary for quality and quantity of life.... The tools are at your fingertips ... The almighty internet ... And your OWN imaginative mentation is your TRUE limitation... So TAKE control of yourself and BE accountable .... Sorry so blunt but MORE tough love and Educating people is whats needed.... NOT more drugs....

MDG

September 25,2008 I was told to increase my dosage of Lisinopril from 10 mg to 20 mg and suddenly awoke on October 2, 2008 with a extremely swollen top lip, the degree was enough to get me into the ER room where I was issued Prednisone and Hydroxyzine with Famotidine which I had to take over the course of a few days to a week.

I was prescribed Loestrin FE 1/20 TAB for clotting and having menstruation more often than I should (once every two weeks or so). My first experience resulted in leg pain, after six days. This ended with a Doppler scan to check for blood clots. Well, that was cleared so back on to Loestrin I went. When I picked up my prescription I asked the pharmacist (yes I had already asked my doctor) during consultation about interactions with the other medications I take on a daily basis. Prednisone 10mg tablet and Armour Thyroid 240mg. I was told, not to worry, no issues. Eleven days after starting Loestrin again, I called my doctor because of nausea, vomiting, fatigue, indigestion (like I've never had before) and feeling "foggy." I was told these were "not typical complaints" that they heard. I then checked for interactions on line and found that both the prednisone and Armour Thyroid have interactions. With Prednisone it's side effects can be made more severe than they would be without the Loestrin (never had a side effect in the eight months I was on it, until the Loestrin). I experienced With the Armour Thyroid Loestrin binds to it, preventing the absorption of the thyroid medication. This explains all of the symptoms I was having. Please, beware that you must check on interactions yourself, do not rely on your pharmacist or physician to be aware of these.

I am being treated with Cellcept (1000 mg in the morning and 1000 mg in the evening) for pemphigus vulgaris. Although I am post-menopausal, recently hot flashes have reappeared (yuck), and I am curious if they could be attributed to the Cellcept. I am also on Dapsone, Prednisone, and Valtrex my other main pemphigus medications). I have been taking Cellcept for about 2-1/2 years at this same dose.

I am a loving mother of a 5 1/2 year old boy. He has been on Singulair for over 3 years. In this past 3 years my son has suffered in an unspeakable amount. He came down with Rota Virus and was hospitalized at 2. He then came in contact with Pneumonia in the hospital while he was there. They automatically put him on Singulair, Zyrtec, Prednisone, and antibiotics to treat the pneumonia. Since that day, my son has gone though more tests than I have in my entire life. He has had asthma, sinusitis, leg cramping ( to the point he cannot walk for 2 years), IBS, Acid reflux,(they gave him laxatives for a year that made things worse and addicted to them also), stomach pain, constipation and diarrhea back and forth. He also got Erythema Mulitforme TWICE, while on this drug. All of which the doctors said could NOT be caused by Singulair. He has had several Upper GI's and CT scans. Along with Barium enemas, several hundreds of blood tests, and many many pokes and prodded that were not necessary. All since he has been on Singulair. He now has frequent bathroom trips, depression, confusion, and anger outbursts. He also has to go to the restroom every 5 minutes. He has had genital swelling, and many other aches and pains. None of which his "doctor" ever said could be a result of Singulair. I am 100% sure it was!!!! He currently has anxiety and emotional sporadic issues causing problems in school The teachers and counselors say that it is so strange because there is no TRIGGER and the outbursts are completely inconsistent. His preschool teacher and director are sure he has ADHD. Well, we had him tested and he does not have any part of it. He has no learning disability what-so-ever. So that brought me back to square one. He is in a positive loving enviroment. How could he be depressed and want to hurt everyone around him? He cannot sit still. He cries and says he is 'stupid" and "can't think" like the other boys. He has nightmares and cannot sleep alone. He is scared of everyone and everything. So, as I sit here crying, I realized that this has all been a reaction of his "medicine" Singulair. He never should have gone through all of those painful tests, only to prove they couldn't find anything. So many treatments and sound full advice speeches from his doctors. How could they be so naive and selfish in the life of my son?

When I called my pediatrician of 5 years, she told me that " parents that have children with behavioral problems will LOOK for something to blame their problems on." She also said "drug companies only put side effects on their labels to PROTECT the drug companies. (as she laughed at me) They are not always valid". Then she said "if you take you child off of Singulair you will be playing Russian Roulette in his life." Then she said that all children around 5 or 6 go though this emotional time in their lives." She told me that if I take my child off of Singulair that she would no longer be a part of his health regimen for his asthma. She told me to see a Pulmonologist for further treatment.
Who is paying who? This is my son's life???????? I decided to go with my mother-gut instinct and get him off of this medicine. No matter what. He has been a different person since. He is currently going though a lot of side effects and withdrawals (leg pain, insomnia, hic-ups, emotional distress) but every day is getting better. How can the drug companies say that this is a "wonder drug?" There are more reported side effected patients then clinical studied patients! How can a "medication" that stimulates the brain not be connected to other problems? This "medication" interferes with the bio synthesis and action of LTs and has been marketed as NOVEL medication against asthma and allergic rhinitis. Who the hell is playing God here??? The pocket books of Merck or our over PAID "doctors?" Who pays the price? Our children? Or us. Thank god I found this before it was too late. I would not be able to withstand the pain of losing my son due to their lack of scientific evidence. They are lucky I am one of the smart ones. I will not settle for less than Justice for the drug companies and their paid "doctors?" You all end up in the same place. HELL

There are 18 million people on this drug. Most of them are children. Please save a life if not your own child's life. Thank You

I have been put through the wringer with Crohn's. 15 surgeries, all of my terminal ileum removed, 1/3 of my large bowel removed, etc., etc,- Those with sever Crohn's know.

I spent years on high doses of Prednisone, Imuran, Sulfasizine and other drugs and nothing worked.

I was even retired from the US Air Force due to its severity.

Remicade has help tremendously. However, some of the side effects listed above, I have also been through. Some of them, have been explained through other factors and those attributed to the Remicade I take other meds to offset them.

For example, Head aches. I figured the head aches were from allergies that I have had for some time. I attributed some of the headaches to the Remicade. The head aches are very sever after my infusions and decrease to a dull roar after that. I take four aspirin and Sudifed PE and this leaves me with a dull roar shortly after the infusions and does away with them till the next infusion - perhaps this will help some of you.

The muscle soreness is horrible and I take aspirin or Tylenol, but that barely takes the edge off.

I started get those little red dots. Then the dots turn to blisters. I get these on my hands, feet and scalp. My GI Doctor said it wasn't the Remicade, but a Dermatologist showed me a recent article that should Remicade could cause Psoriasis. I take Clobetasol Propionate for these and it has cleared them up.

I took the Remicade years ago and then it was stopped - it was the way it was done then - not constant, just three doses spread out over three months.

I got the tingling fingers during those. A neurologist attributed it to the Steroids I had been on. The nerve damage is permanent.

A few years later, they started the infusions again and I experienced no muscle soreness, headaches, etc. and it did not help the Crohn's as it had before. When I talked to my GI doctor he showed me a study that people build anti-bodies to the Remicade over time. They doubled the dose and it started working again. For those who are experiencing the Remicade not working - perhaps this is what has happened to you.

I get the mood swings, but had never considered it might be the Remicade. I will talk to my doctor about this one.

I have the blood pressure decrease during my infusions, but it has not been sever.

More recently, my joints have begun to ache and initially the Remicade had helped to stop the minor joint pains I already had. Come to find out, I have had bone thinning due to the Crohn's.

The one symptom I have started getting this week is random, sever pain in odd locations - not joints.. They have been deep and feel like they are in the bone. One midway up on my shine, one midway down on my foreman and one in my right thumb. Has anyone experienced this. The pain has been horrible and it does scare me.

I also suffer from depression, but have had it for years prior to the Remicade treatments.

Earlier this summer, I developed a case of shingles. It went away, but about a week ago a similar rash broke out. I thought that it was a second bout of shingles, but my doctor assured me that it would be impossible to contract the disease on different parts of my body. Because I am not home with my ordinary doctor, I had to see another doctor, who was unsure of what the rash could be, but nevertheless prescribed with with 50mg of Prednisone daily. I took my first dose today, and am reluctant to continue. I don't want to be a victim of any of the side effects, but am unsure as to whether there is another way to go about getting rid of the rash. Any advice that could be given so as to not have to continue with the Prednisone would be great. I don't want the rapid weight gain, depression, mood swings, etc.

My 12 year old son has been on 60 mg of Prednisone for two weeks now. His side effects have not been bad at all up to this point. He's gained about 6 pounds. His brain is unusually active right after taking the drug, and this effects lasts a few hours. He's always been a wildly creative kid but prednisone seems to intensify is creativity and the productivity of his brain. He has Tourette Syndrome and his tics waned overnight after beginning the meds so that is a big bonus if prednisone is responsible for that. He has always been an insomniac since he was a baby but prednisone makes him sleepy, so sleepy he takes naps during the day and goes to bed early, sleeping soundly all night, so soundly he had an accident and wet his bed last night. His head sweats when he sleeps. He has infrequent periods of mild irritability. His appetite has increased but not unnaturally so. Seems like he finally has a sustained healthy appetite. He goes to 45 mg for two weeks tomorrow so I'm interested to see what new side effects this brings on. No stomach problems despite taking this along with very high doses of antibiotic. Maybe the prevacid he takes with Lactobacillus is helping with that and the fact that he takes his meds with small meals or lots of fluid.

what did anyone use as an alternative???....my daughter is currently having a severe wasp reaction, has been told to take prednisone, and I don't want to give it to her.

I have Crohns and had a flare up so I'm back on 40mg of Prednisone. I've been on 40mg now for 3 weeks and I start to tapper off in another 3 weeks. Well every time I start the prednisone again I get new side effects. This time, my gum are bleeding all the time and the pain in my knees are horrible! I still get the regular side effects, ie: Mood swings, joint pain, sleeplessness, sweating, swelling of my legs and hands, wanting to eat everything under the sun, moon face and my hair falls out! I wish the drug manufactures could develop a drug that would not be so hard on our bodies. I have to struggle with the pros and cons with every flare up. Do I want the weight gain, mood swings and hair loss or do I want to look good and be very sick! I'm 37 and was 16 when I found out I had Crohns.

While I am sure that Singulair has adverse effects for some children/teenagers/adults, I took Singulair for 2-3 years (until my asthma symptoms improved to the point where I didn't need to take it) while I was a kid and had no adverse side effects. Started back on Singulair in April after having severe reactions to my new puppy (I am now 21). Since then, I really haven't had any side effects at all. I agree that they should black box Singulair and possibly not prescribe it to some children/teens, but for some people (like myself), it works, and shouldn't be taken off the market completely.

I'm a 35 year old stay at home mom and graduate student. Since taking a 10 day course of Avelox for a nasal cavity infection I have had severe hives for the last three weeks. The hives started about a week after finishing the Avelox course. The doctor that prescribed me the Alevox told me that it is what is causing my skin irritations. I have good days and bad. Sometimes I wake up with swollen eyes and puffy lips. The hives are extremely irritating and look like a chemical burn. They cover about 75 percent of my body. The worst irritation seems to be on my feet, legs, arms, face and hands. The only thing that takes away the discomfort are oatmeal baths; however the hives are quick to return. I don't know how long I will suffer with this skin condition. I am on my second course of prednisone and I take antihistamines around the clock, but still no relief.

I am a 60 yr. old woman and was on simvastatin for several years before I realized that all of my aches, pains, and muscle weakness could be because of it. I stopped taking it in March, and had very little improvement until June when I started taking 100 mg CoQ10 twice a day. I am now pretty much pain free but the muscles in my thighs are still very weak, and I am still very fatigued. Anybody have any suggestions?

I just finished a 10 day (4xday) prescription of Flagyl (250 mg) prescribed by my Gastro doctor for treatment of (SIBO) Severe Intestinal Bacterial Overgrowth. Two days after finishing Flagyl I broke out in hives all over my body and my upper eyelids were very swollen. Now my dermatologist has me on Zyrtec and Prednisone. Has anyone broken out with hives and had swollen eyes from taking Flagyl?

I took prednisone for 6 days ( the pack). Six the first day and five the next till day six I had one pill left. I have never experienced hair loss like this. I have a patch of hair that fell out in a circle the size of a 50 cent piece. I didn't notice it really falling out but noticed a bald spot and I freak out. I came on line to get info about this medication. This drug was ordered for me because I have severe pain in my back due to osteoarthritis, sciatica and back surgery. I was told taking this would help with the inflammation and might relieve some of the pain symptoms. Well, I think the pain would be better then the side effects that I suffer. I had loss of appetite and acne on my face. I feel dizzy and bloated. I pee all the time and seems like i visit the bathroom much more often for other reasons too. I have felt like a crazy lady and have less patience than normal. I hope that this does not last for ever. This is a small amount of the medication. I am sorry for those of you that have experienced a long period of time on this medication. I pray for you that they will find another alternative with less effects to your bodys.

I was on Lisiniprol for 91 days as an ACE inhibitor for diabetes and kidney protection. All was find except for a constant feeling of burning blood all the time. It was tolerable though.

But on day 91 I developed hives. 14 days after that I was broken out from scalp to sole of my feet -- feeling miserable and no relief in site.

Dr. told me that I was allergic to something and to take benadryl. 3 doctors later I was told that I had hives and had to learn to live with it. He increased my benadryl.

I took myself off all my meds except insulin -- not knowing what was going on. I researched and discovered the this drug should NOT have been given to me because I also have SJOGRENS (an autoimmune disease akin to Lupus).

The hives got worse, my benadryl was increased by the drs. Finally I passed out due to benadryl toxicisity (overdosed) and they put me on prednisone.

To this day -- 6 months later -- I still have hive outbreaks that are miserable. I have missed a day from work every 7-10 days. The prednisone helps, but as a diabetic it sends y blood sugars through the roof. My rheumo has put me on doxepin (an antidepressant) because it has an antihystamine property that seems to be helping.

It is also useful for the rheumotoid arthritis that comes from Sjogrens and such. I am sleepy a lot -- but that could be from the doxepin.

I will never take Lisiniprol or any other ACE inhibitor. I am suffering and the worse part of it: the doctors and medical profession don't care and simply tell me to learn to live with it.

I was given Biaxin for a sinus infection that never cleared up. So the doctor gave me Bactrim. I took one before I went to bed. I woke up all jittery and full of anxiety. Sometimes this happens, because I do have agoraphobia with panic disorder. I took my second dose with breakfast. About 3 hours later my gums started to burn; like I ate too much salt. It was irritating, but did not realize it was from the antibiotic. Then my teeth started to hurt really bad everywhere, and it felt like electrical shocks going down my body. My skin turned all colors of blotchy purple and yellow. I started to shake so bad that it hurt. My Dad rushed me to the emergency room. I was given epi, steroids, and an anti-inflammatory. Then monitored for 2 hours. Which was hell, because I have agoraphobia.

I was sent home with prednisone and benadryl. It has been six days since this has happened, and I still have the chills. I feel like I have the flu. My teeth still hurt, and advil won't even help it. I have a constant headache. This medication should be banned. I only took 2 doses and became so ill. When do the side effects finally stop?

I have been io Lisinopril for several months, and the only side effect I can say is a VERY ANNOYING rash on the inside of my upper thighs. It comes and goes and gets worse with warmth, like a heat rash. I also have now developed a rash on my butt that is looks to me like shingles. Very itchy, to the point of bleeding from scratching. I treated with diaper rash ointment and triple antibiotic ointment to not much improvement. Reently tried a jock itch ointment which seems to be working. Also took myself off Lisinopril 2 days ago, and things are getting better, but very slowly........

MY FATHER WAS DIAGNOSED WITH TEMPORAL ARTHRITIS. HE HAS BEEN ON PREDNISONE FOR ABOUT 5 MONTHS NOW, STARTING FROM 80MG/DAY. HE HAS TAPERED DOWN TO 40 MG/DAY,,BUT TH SIDE EFFECTS ARE STARTING TO BECOME UNBEARABLE.
WATER RETENTION,,SWELLING, MUSCLE PAIN,,WEAKNESS.
HE IS 80 YEARS OLD,,AND IT IS REALLY TAKING A TOLL ON HIM. IF ANYONE CAN GIVE ME ANY HELP OR INFO TO COUNTER SOME OF THE SIDE EFFECTS(MUSCLE PAIN AND WEAKNESS MOST IMPORTANT) IT WOULD BE GREATLY APPRECIATED.
THANK YOU.

Was previously on Micardis HCT; dr. switched to generic Lisinopril HCTZ 12.5 in 11/07 when I went on Medicare & was concerned about cost of Micardis. Since that time I've put on 10 lbs. and had increased pain/muscle fatigue and general lethargy. Unusual, as I've exercised 4-5 days per wk. (incl. aerobics/strength trng/flexibility.) for 20+ yrs. Also, frequently, have problems swallowing pills due to feeling of obstruction in esaphogus tube. In July '08 I awakened to slight numbness/tingling in lips and my lips then proceeded to the swell to the point of pain and my lips (in profile) protruded further than my nose. I received steroid injection and prescription for steroid pack. Diagnosis was possible allergic reaction to new cosmetic product. Today (9/3/08) I woke up with the same symptoms and again had to go to the dr.for a steroid injection & meds. Diagnosis this time (different dr.) was possible side effects of "blood pressure meds." Has anyone else experienced edema of the lips, wt. gain, and problems swallowing?

I started taking Levaquin on Aug 8th for bronchitis 6 days after taking medication I was awoken about 2am with severe shoulder pains in both shoulders I went to the ER to find out why I told them that I was taken Levaquin they took an X-ray of my shoulders and said they were fine prescribed percocet for pain. Pain got worse went back to ER was given a shot for pain and was told to get an appointment with bone and joint Dr. On the day of appointment my right forearm, wrist and hand swelled up. I told my Bone and Joint Dr.that I was taken Levaquin I told him that I stopped it immediately after reading side effects He prescribed an anti-imflammitory Pain got more severe went back to ER was given EKG and took blood and urine test all test came back fine. Went to another doctor he then checked me for Lyme disease. which came back neg. I then went back to first doctor that prescribed the Levaquin. she thought that I had arthritis. 8 different blood test were given all came back fine. Ended back in ER because by the end of day I could not walk, had high fever, sore throat, severe head ache, and was sick to stomach. Several more blood test were done. all came back fine. ER doctor prescribed prednisone which seem to help some. I went and seen another Dr. Still no one knows what is really wrong. I believe it is the LEVAQUIN it has messed me up bad.

I'm a physician. Usually Kenalog injections can be avoided and oral steroids used like prednisone. The local dimpling effect may occur if the injection is too shallow, actually there is a temporary "disolving" of the subcutaneous tissue, the muscle and joints are not damaged. It is usually viewed as a "cosmetic" adverse effect. The Kenalog injections was primarily designed for joint injection and the kenalog or similar depo form stays active in the joint for a few weeks. All steroid medications can cause irritability and this is usually temporary for a few days. Steroids can cause muscle weakness- this is usually associated with high doses for prolonged use like being on prednisone for 3 or 4 months. Steroids can have an adverse effect on menstruation, but this is usually associated with chronic use. The most serious problems with the steroids result in bone weakness(osteoporosis) and serious damage to joints like the back and hip. Steroids can also result in weight gain, diabetes, high blood pressure and cataract formation. I don't think Kenalog is any different than other steroids such as Medrol or Prednisone in terms of the side effect profile. These are dangerous medications that can also be very helpful in saving lives and diminishing pain.

I was prescribed Prednisone along with an H2 Blocker and an Antihistamine for a severe chemical reaction to using old lotion in a tanning bed. I only laid 2x, but I am severely paying for it now. I was only prescribed Prednisone for a 9 day treatment. By the 3rd day I had the acne. I suffered with Acne all of my life until I was 18 (I am 27 now) ... and haven't looked back at that terrible part of my life since... well, now I am faced to stare right back at it. Literally. I have only been off of the prednisone for 2 days, but I can not WAIT to get my life back. If I could take back the last 2 weeks over something so stupid and cosmetic as tanning, I certainly would. I have never had any previous problems with any of this, and this is the first time I have really had an allergic reaction to anything.... typically, Benadryl would have cured me. Although this time incurable with Benadryl and Cortisone, I regret the Prednisone. Severely. I hope this goes away within at least three weeks.. as my husband is coming home from Iraq and that is not the welcome home I want him to have (even if he is much less superficial about it then I am). Sigh.

I got an infection on my leg from an bite and went to the er to get it checked out and they opened my abscess and prescribed me Bactrim. I made sure i was talking it to get rid of the infection and didn't want to go through that pain again. Then 4 days later I started running a high fever and nothing I did could get it to stop. It would go away for an hour or so then come back. I assumed I was getting the flu cause I had a fever, bad body aches, and I had nausea and stomach ache. But I could not figure our why I had chest and back pain. Well then the next morning I woke up with a major rash all over my body. From my head to my toes, I went straight to the emergency room and they told me to stop taking the bactrim and gave me Prednisone and Benadryl. This has been the worst experience of my life. I don't think they should use this drug at all. It has the corst side effects and they take a long time to recover from.

This is an evil drug, far more dangerous than most illegal drugs. It ruined my life. I wish I had never been put on it. It was the first drug I, a teenager, was put on, having just been diagnosed with my disease.

I hadn't tried other drugs or other treatments; medical guidelines, I know now, say not to use this drug unless the disease is both severe and other treatments have failed. Well, I hadn't tried other treatments yet, so I shouldn't have been put on this drug. And yet the doctor I was assigned, Dr. Anne Sullivan at the University of Iowa's hospital, thought I needed to be on it, told me it was safe, that it didn't have any side effects, and that I would be completely healthy again in a few weeks.

If I had been told about the side effects, as doctors are supposed to do, according to both legal and medical standards, if my doctor had honestly answered my questions about side effects, I never would've taken it. And I'd advise others to never take this terrible drug. I would rather die than take this drug again.

It did nothing for my disease, but it did give me quite a few side effects, some which, according to the doctors I've subsequently went to, are permanent and long-lasting and there's nothing you can do about them; they're just permanent.

People don't talk about the psychological effects of steroids, but they should; they're serious. And, no, they don't just go away when you stop taking the drug. If the drug makes you bipolar, you're not just going to just go back to being you're regular self. Bipolar disorder, depression, anxiety, these things don't just go away on their own.

I had no problem with mental illness before taking this drug, and yet I'm still severely depressed to this day, part of that, perhaps, is from what the drug did to me, that is, the physical side effects, but part of, I suspect, is just that it changed my personality, like it changed my brain chemistry.

Go here-******to learn about the psychiatric effects of prednisone.

Excerpts:

"Although a powerful therapeutic option, corticosteroids are associated with serious adverse effects, both physiologic and psychiatric. While the somatic adverse effects of corticosteroid therapy (Table 1) have been extensively researched and widely described, the neuropsychiatric adverse effects have received less attention."

"In our literature review, we found that the potential psychiatric adverse effects of corticosteroids span a symptom spectrum from subtle mood changes to full-blown affective syndromes and frank psychosis."

"The most commonly reported corticosteroid-induced psychiatric disturbances are affective, including mania, depression, or mixed states."

"Cognitive deficits, particularly declarative or verbal memory deficits, have been well documented during both long- and short-term corticosteroid therapy."

"More severe cognitive impairment consistent with delirium or dementia has also been described."

"In a case-control study of 20 patients receiving long-term low-dose corticosteroid therapy (prednisone, 7.5 mg/d for >6 months) and 14 volunteers with similar illnesses who were not receiving corticosteroid therapy, Bolanos et al9 found a 60% lifetime risk of corticosteroid-induced mood or anxiety disorder."

"The corticosteroid dosage is the most important risk factor for the development of psychiatric symptoms."

"Psychiatric disturbances can occur at any point during corticosteroid treatment, including almost immediately after initiation and even after cessation of treatment."

"Corticosteroid-induced psychiatric disturbances are common and include mania, depression, psychotic or mixed affective states, cognitive deficits, and minor psychiatric disturbances (irritability, insomnia, anxiety, labile mood)."

"It is important that clinicians in all specialties become aware of the potential psychiatric adverse effects associated with corticosteroids and explain these effects to their patients."

"Which patients will experience corticosteroid-induced psychiatric disturbances cannot be predicted. Dosage is the most important risk factor for the development of adverse effects, with patients receiving less than 40 mg/d at minimal risk, those taking 40 to 80 mg/d at moderate risk, and patients receiving more than 80 mg/d at high risk. Most patients will develop symptoms during the first week of treatment, and more than 90% will develop symptoms by 6 weeks."

Side effects: mixed bipolar disorder/manic-depression, suicidal ideation, cystic acne, scars on my face, panic attacks, severe anxiety, rage, euphoria, sadness, impulsiveness, confusion, memory loss, hard to concentrate and remember, thin skin, delayed healing ability, bruises, premature aging, rapid heart beat, heart palpitations, high blood pressure, higher cholesterol, thyroid disease, sweating all over, itching all over, joint pain, increased appetite, massive weight gain, stretch marks, hormones out of balance now, dry eyes, so dry my eyelids stick to my eyes, so dry I can't wear contacts any more, permanent red eyes, blurry vision, vision worsened, eye pain, eyes sensitive to light, migraines, and yellow skin.