Steriods symptoms and conditions

I am shocked!! Over the last year I have experienced significant hair loss, mood swings, dizziness, cardiac issues (ended up in an ambulance for a suspected heart attack at age 37) can not go one day without Protonix, if I do I wake up in the middle of the night with horrible reflux and choking sensation. For the last 2 years I have had numerous allergic reactions resulting in shots of steriods and pred-packs..they can not find the cause (mostly when I get hot or flushed and every time I go on vacation). I never thought it could be my BCP. I have taken Yasmin, Yaz and now Ocella for about 2 years. My MD switched me from Yasmin to Yaz....b/c of HA's a year ago, I had a heavy period for 36 days, started back on Yasmin and my MD wanted me to take them continuous to skip my periods b/c of fibroids. My hair started falling out, my skin is dry with dry patches all over my legs and then my hair started falling out..thats when everyone told me I was crazy. I have a cramp in my right side all the time, I suspect from my gallbladder. I am a nurse and really thought of all of the worse things that could cause these symptoms, Thyroid, Cancer, Heart Disease, OCD, Paranoia. I think I will be stopping my Ocella(generic for Yasmin) tonight. I have been on BCP for 13 years straight, I'm scared that my periods will never be normal again? Anyone have any issues once off Yasmin??

I am looking for any information anyone has about the possibility that Singulair causes colitis or that it can lead to inflamed colon and bleeding colon. My daughter is 4 years old and has never been a sick child. In September, she started bleeding from her colon, and a month later, she was finally diagnosed with colitis after having a colonoscopy. The doctor prescribed Prednisone (steriod) and Phlagyll (antibiotic) (spelling?). I decided to stop giving her the Singulair that she had previously been taking because I didn;t want her to have so many drugs in her system as one time. After a few days of the steriods and antibiotics, she was well, with no signs of problems. Everything was going great for a few weeks, but last week I started giving her the Singulair again, and her colits symptoms have come back. Has anyone else experienced this in relation to Singulair?

Male 28. Was diagnosed a couple of months ago with Ulcerative Colitis and was prescribed Prednisone. A large dose to start with then tampered off for 4 weeks. The first week I felt great, better than great, fantastic. The only downside was difficulty sleeping. The following 3 weeks, without any exaggeration have been among the worst I have ever experienced. I think the lack of sleep finally caught up with me, so I was constantly tired and generically felt depressed, also knee ache, eye pain, inability to think clearly (quite a problem when you are an Engineer), lacked energy or strength – and the Acne. Never before have I had Acne like this, and I used to suffer quite bad during my teens. Its just so aggressive, every few hours there seems to be new ones appearing. It seems to occur when ever I step down the dose. I think having this bad skin has really added to my depression over the last few weeks, it has been especially difficult considering I have been in the process of starting a new job. To top all of that my UC seems to be worst than ever! I’m worried that when I go back to see the Doctor next week he is going to put me on some equally-annoying medication or maybe another course of Prednisone if I’m lucky.

Does anyone know of some natural alternatives that are good for UC, very reluctant to put anymore man-made chemicals into my body.

I have had asthma since i was 10. I am 44 years old now. I have never in my life been on prednisone this long (since Feb 2009). It is now July 11,2009. I was admitted to the hospital for IV steriods (prednisone) because for the first time in my life the general 10 course with the pills wasn't working. so there i was on 165mg of pred every 6hrs. After eight days in the hospital i was released and was to take 40mg for five days and decrease by 5mg until done. I didn't do to well and had severe exhaustion where i couldn't even walk 2 steps the next day. so I went to my pulmonary dr. who said he noticed a severe anxiety side affect in me from the drug and said i needed to get off it as soon as possible, he had me drop my dose every day by 5mg. TO FAST! I had breathing problems again, started over going slower, got down to 10mg and had to jump to 40mg again! side effects for me are severe anxiety (which i have to take ativan for) and especially massive painful foot cramps. My hands will cramp to while trying to write, but the foot cramps and the feeling of being wired are the worst. I am still trying to wean off....sometimes i wonder if i will ever finally be off this stuff. I just want to cry sometimes. It feels like being pregnant and going thru post partum at the same time

They think that I have either crohns or ulcerative colitis. I have tried antibiotics, lialda, mesalamine enemas, with no improvement. After another colonoscopy they put me on prednisone at 40mgs, 30, 20, 10, then 5 decreasing weekly. Well the first week was okay. I had some of the side affects, insomnia, extreme hunger, and crazy. I could deal with that. But then when I decreased down to 30mg, my body flipped. I awoke from the middle of the night with burning pain in the knees. So bad I took 4 ibuprofen and threw myself in the tub with epsom salt. I thought okay that was weird because I have never had a joint pain in my life. I saw the gastroenterologist that day bc I was still having abdominal pain. He totally blew off the knee pain and said he had no idea what that was. I thought okay maybe it will go away. A few days went by and nothing. 3 days later and I awoke one morning crying in pain because of my legs. I called the on call doctor who also said he had no idea and go to the er. So I went crying hysterically for 4 hours. Even after 3 rounds of dilaudid I was still in pain. They suggested a Rheumatologist. So I went to one a week later who said I was going through steroid withdrawals. And there is nothing we can do but treat the symptoms of pain. I am now down to 10mgs have been out of work for 2 weeks and am absolutely miserable with severe leg pain, muscle weakness and fatigue. He also adjusted the drop down increments to 5 instead of 10. Anyway I will never take this drug again and I think they rushed to this one. Just wanted to share. I am glad I found this website because I went from a fully functioning physically fit 28 year old to a crippled crying crazy person. I think I was scaring my husband, honestly, until we both read some of your postings which were similar.

I have a history of sinus infections. After two rounds of Augmentin did not clear up my latest one, my doctor finally gave me the steroid pack and Avelox. He had tried to avoid the steroids. I have had them so many times. I finished my steroids 5 days ago and my Avelox yesterday. I read the side effects and did as it suggested. Since it mentions low potassium would not be good I ate a banana every day and had some orange juice to keep my potassium levels up. The drug warms against taking any pain killers such as Aleve, Advil, etc. One earlier reviewer admitted taking Aleve and had a bad reaction... well.... bad move.... I have had no real side effects that I can say for sure are Avelox related. I did feel a little less focused at times, but was not obviously groggy or woosey. I did have a little abdominal discomfort that I usually do not have with drugs, but it was short-lived and only occurred 3 of the 10 days. Many people have bad effects because they do not follow the warnings against anti-acids, pain killers, low potassium, etc. Some people are more likely to react to any medicine, while others like me rarely have a side effect. My tendons did not hurt... nothing.... People who are out of shape, have a poor physical life style, etc. sometimes help contribute to the drugs reactions by being in basically poor physical health to begin with. America is one of the fattest, out of shape nations out there due to our abundance of everything. The majority of persons can take Avelox with no real issues. I will take it again. I truly feel concern for those who had problems, but sometimes we are partly guilty by how we don't take care of ourselves when we are well...... As with any drug, some persons will react no matter what... It's often just a matter of inherited genetics...... Be safe everyone, and take time to evaluate how you take care of your body and really decide to do better. For the record I am almost 58, 5-9 158 pounds and work out semi-regularly.... Take care of that temple God gave you. Its the only one we get on this Earth,,,,,,

Im so glad I found this site. I thought I'm going crazy. I have been using Advair for 2 years now, and started taking it 2 times a day 3 months ago. I experienced severe depression, frequent dental visits due to loss of bone (im 39, thats far too early and I never had problems like that before).

Back in October last year i was having really bad pain behind my eyes - they hurt on movement. I went to my doctors 8 times within two weeks - he kept giving me pain killers saying it was a tension headache. The last appointment i had with him id lost the vision in my right eye - they eventually referred me to the hospital. After loads of tests and questions they finally put me on Steroids and strong antibiotics via drip and i had MRI scans but by then i had lost my sight completed and was told i would never regain my sight as my nerves were severely damage. After a week or so on Prednisone my sight was getting slightly better in the left eye which was great i could think about seeing my son again. I have been taking Prednisone along with loads of other tables one for my bones and nerves and folic acid and very strong painkillers etc for months. I tried to reduce my dose as directed and my condition got worse the pain behind my eyes came back and they they said i had C.R.I.O.N so now im back on a high dose and im also taking azathioprine. I have experienced all the side affects of this drug - Round Face (moon face) server muscle cramp - i was unable to walk for 8 hours a few weeks ago i was in so much pain. Terrible bad back - shoulder blades hurts. Terrible spots. Really bad heaches. Eye pain. Water retention. Sleeping problems. Mood swings. Theres to many to list. This drug helped me regain my sight but i cant wait for the azathioprine to get into my system so i can start to reduce the steroid and start loosing some weight and get rid of all the other side affects.

I am just in shock. I have been on Avelox for 7 days now, and I can tell you that the side effects are not worth it. I still feel sick and have the bad cough. Now, I also have Thrush. But the weirdest and most upsetting part of this was that I didn't notice any of the other symptoms. So I went all week, talking a mile a minute, sweating, dry mouth, hallucinations, etc. Then on Saturday, a few of my friends staged an intervention. They actually believed that I was taking Crystal Meth - ICE. I was heartbroken, confused, and mad. I knew I had not done any illegal drugs, but several of my friends were convinced.

I went to the doctor today and found out that it was the Avelox. However, I had already taken today's dose. I even told the doctor about the situation with my friends and asked if this drug could be related. He said no, it must be the steroids and sent me on my way. As luck would have it, the pharmacist saw me in the store and approached. I asked him if Avelox could make me feel the way I was feeling. He told me that I should have never been prescribed Avelox and Effexor as they had drug interaction issues. He also told me that my symptoms were disclosed on the pamplet. The problem was that I got the Avelox as samples after the Augmenton didn't work.

So, I came home took the meds for the Thrush and watched tv. I haven't slept since Thursday, nor have I eaten since Saturday. I am hearing and seeing things. Now I am scared to go to sleep because I may not wake up. My heart is beating fast, I can't stop talking, dizzy, blurred vision, disoriented but extremely happy given the circumstances, paranoid, jittery, extremely thirsty even though unable to pee.

This is just horrible. I am not a drug adict and do not do Meth/Ice or any drug like that, but now my best friends are doubting me. They don't understand or believe that an antibiotic could do this and how am I supposed to prove it to them? It looks like, just because I got sick, I may lose some of my closest friends... Remember, most drug adicts and alcoholics DENY it first. Great, huh. Now everyone is going to be watching me to see if I am on drugs. I feel violated because evidently I got all high on this antibiotic, didn't enjoy it, and now am suffering the consequences.

What makes it worse is that people I love now don't trust me, and I didn't even know what was going on

I was diagnosed with Ulcerative Colitis in Aug of 2005 and in remission for 9 months. I came out of remission in May of 2006 and have been on prednisone since then until right now. I would go on high dose of steriods, try a new medication, and try to ween off and get sick right as I went off the steriods, so I'd have to do this rollercoaster all over again. For a year now, I have been on steady, high doses between 60-100mg daily with no break. I tried to go below 20 and got really sick again and have run out of medication to try, so I had my colon removed. Right now, we are trying to ween me off the prednisone (since i dont need it for my disease anymore) but have to go over 3-4 months and very slowly since I've been on it so long to prevent the body from doing all the fun things it does when you stop prednisone cold turkey, like a coma and stuff. I'm SICK of the side effects this drug has had on me! I have had countless sleepless nights, heartburn, night sweats, weight gain (i went from 140 lbs to 215 lbs right now), the moon face to where i can't even recognize myself, red face, weird skin, sensitive teeth, thinning hair, hungry ALL the time, stretch marks, all the weight is in my stomach, the buffalo hump, high blood pressure and high eye pressures etc. These are all the side-effects that have been horrible on this miserable drug. I'm sure there are a lot more I am forgetting, but these are the ones that come to mind. Hopefully they will go away once I am able to finally get off this drug!

took the drug for only 4 days and ended up with MAJOR hives. My doc said he's never seen this side effect before and even took pictures to share with his collegues. It did get rid of my sinus infection, but what a price to pay. I took prednisone to get rid of the hives and that did work, but I still have faint scars where the hives were bad. This was back in May of 08.

I am scared to death after reading what everyone is going through. I was put on Levaquin for 10 days and got to day 9. My joints ached so bad I thought I had arthritis, and even had my Dr. do blood tests for it (I had no idea it was the Levaquin). I am only 35 years old and never worried about arthritis before this. Also, within 5 days I started developing hives all over. Again, I was stupid and didn't realize until day 9 that the hives were because of this med. I told my Dr. and he told me to stop taking it which of course I did. I assumed the hives would go away after the med was out of my system. But a week later the hives were unbearable. I was put on prednisone (another issue altogether) and that helped the itching, but now every time I try to go off or back off the prednisone the hives come back- and they are terrible! Now my Dr. thinks the hives were from something else because there is no way that the Levaquin is still in my body. But after reading what other people are going through on this med, I am convinced this stuff is as everyone says- POISON!! I am so worried about the joint and hip pain that was so bad I couldn't stand for long without excruciating pain in my right hip. It felt like I had a one hundred pound weight just sitting on it. And my hands were the worst. I have a newborn and could barely pick him up without worry that I'd drop him. I don't know what to do.. Is there anything to do?? I'm still on the prednisone, and have been for a month. I need to get off of it but every time I do I itch so bad with the hives that I cannot function. Also because of the prednisone I noticed last night that I am getting "moon face" my face is swelling up and there are a million side effects from that drug too. How long does this last? Has anyone else fought the hives that come with this? Please help me, I am so scared!

I am 34 years old. I am a pharmacy tech. I have asthma and allergies. I have taken singulair pretty much every day since it came out on the market. I've had asthma since i was about 10 years old. I took theophylline as a kid. Steriods on and off especially during times when my allergies are bad. I still use Advair during the fall and spring. Every drug has a side effect. However breathing is pretty good damn thing. Do I have days when I feel low? Yeah. Do I sometimes have nightmares? Yup. Are "natural" products the answer. Not always. The fish oil that some of the posters are touting can also cause GI problems. Some of the natural products contain herbs and other plant derivatives that can be harmful for a child that suffers from allergies. Not proactively treating asthma can be deadly. Some of the parents are suggesting steriods as the answer - those can cause weight gain, growth suppression and can lead to a worsening of asthma.

Singulair has never made me feel like I've wanted to kill myself. I was more depressed and angry as kid when my asthma did not allow me to partipate in normal childhood things. I was sad and hated life when I couldn't keep up with friends at recces because I was having trouble breathing. You have to outweigh the costs with the benefits. I am more irritable when I have asthma flareup then I am on a normal day. For me, I choose to breathe. And singulair has been helping me for almost a decade.

I'm not saying the medication isn't causing these symptoms but maybe there is an underlying cause to your child's depression.

Any drug has a side effect. But without medical research and the medications that come with them - people would still be dying of simple diseases and we wouldn't have vaccinations. As a society, as a whole, we are a culture that looks to someone else to fix things and then blames the people who try to fix it. We need to stop being the "hot McDonald's coffee'" society.

I want to post this because this site has given me good perspective on this Rx and side effects experienced by others; its good to know I am not alone. As far as an agenda, I have none, in fact I was all for the Singulair initially, because it seemed to be a good alternative to inhaled steriods which I had read could interfere with normal growth. My son, 4 yrs. old, with a diagnosis of Asthma, started Singulair about 2 weeks ago. Asthma seems to have been improved by Singulair. Within a couple days of starting it, though, he reported vivid (but not nightmare-ish) dreams, a week later he dropped his afternoon nap, which we were expecting to happen eventually, so didn't think much of it. He is a wild child generally, but we also noticed an uptick in bad and aggressive behavior within a day or two of starting the Singulair; we really clamped down on him though, so that effect has been somewhat muted. He has always occasionally complained of indigestion stomach aches, but these complaints have increased to several times a day in the last week, also complain of lower abdominal pain which he says is "different" than his earlier indigestion stomach aches. Last week or so he's been up late at night, had trouble going to sleep, looks a little pale with dark circles under his eyes ("he's becoming a Goth" I joked with my wife). Last night he got out of bed late, appeared disoriented and seemed to be half awake, half asleep. He was talking, but not making sense and seemed to be upset and/or confused, but when pressed he assurred me nothing was wrong and nothing hurt--put him back to bed and this morning he remembers getting up, but also keeps telling me he had a "weird" (not scarry) dream and that he keeps seeing it while he's awake. Luckily this weird dream was not scarry for him, but he was clearly a little freaked out by seeing it again this morning. He seemed o.k. heading off to preschool, but we are taking him off the Singulair as a precaution. My advice to anyone else out there seeing similar symptoms in their kids is to go with your gut -- I always tell people that a Doctor's job is to tell you the odds, like only 1 in 500 or 1 in 1000 kids will have a certain reaction, or condition, or illness, it is the parents' job to be sure that their kid is not that 1. So I'm taking my kid off the Singulair because I think he may be that 1 kid who experiences these unusual side-effects. How wide spread they are, I have no idea. I will get on my soapbox and say I think it's time for the FDA to require drug companies to conduct long and short term clinical studies on kids for any drug that will be prescribed to kids--entrusting our childrens' health and well being to a drug company's own short term study conducted on fully developed adults is foolish and insane.

I have severe allergies and cronic sinusitis... like a lot of people on here I have taken all the allergy drugs they make for the past 9 years... Ive had tons of procedures done and sinus surgery last Feb '08. Nothing helps. Ive taken oral steriods many times but recently my new ENT decided to give me a Kenalog shot in Sept. Nothing was explained to me other than it was a steroid. The nurse put it in my left shoulder. I have had all the symptoms people are describing on here except the indent. I have been progressively getting sicker and feeling worse and worse over the past few months. I feel like I could go to bed and just stay there. Now this past Monday he gave me another Kenalog shot in my left shoulder. I heard something on a tv show that it causes depression so I jumped on this site and feel sick about all the messages I have read about people's terrible side effects. I feel like my doctor who I trusted let me down. I am so worried that my shoulder is going to have a big grey dent like everyone is describing on here. I am just so tired of being ill.

I was given a shot in I think January of 2008, not knowing exactly what it was, because I had a fever and the doctor said it would jump start my recovery. At first there seemed to be no problem with the injection site and I felt great just days after.

A couple of months later, when I was working out and losing weight and keeping a very close eye on my body because of it. Suddenly, I noticed that I had a deep indentation and discoloration on the left side of my lower back - right where they gave me the shot. It seemed like it appeared over night. It got deeper, and darker as time passed.. I was scared to press my finger in it because when I did, it just kept going in..as if there was no fat OR muscle in that spot.. I was FREAKED out. I'm a model so this fact that there was a bottomless whole in my lower back was devastating. I also feared that there may be something life threatening going on. I mean, a chunk of you just doesn't disappear overnight..Unless someone stole your kidney, but, I didn't wake up in a bath tub full of ice.

I typed in "Injection that causes Indentation in the lower back" and I found this board. Everyone here suffered the same exact symptoms from this shot and worse. I was certain that it had to be Kenalog. It seemed to cause death of all tissue at the injection site, depression, lethargy, moodiness, insomnia, pain and all sorts of other symptoms after this shot. I started to suffer from all of them soon after the shot and I didn't really know why or where it came from. I was in so much pain and was so tired.. I stopped doing everything I loved and I could barely sleep because of the pain.

I don't know what to do about this. I'm extremely broke and I don't have health insurance(and they wouldn't fix anything considered to them as "cosmetic" anyways).. My parents are in no position to help me anymore and I could never afford an attorney to try to claim against this.

How can I go about fixing this with no money? Is there any way to fix this to begin with?

Any advice, insight or experiences would be GREATLY appreciated!

So basically this is my story.. I am 19 and have had severe asthma every\ since I can remember. I took prednisone up until I was 14, and from what I can remember I just stopped taking it around then. Then when I was about 18 I started up again because my asthma got worse. Between the time period of 14-18 I still had asthma, but started working out and became very active and healthy.I lost alot of weight had VERY THICK long hair. Then at 18 I got very sick and my doctor put me on prednisone knowing my asthma history. After being on it for a month my hair has become thin, I have gained weight, my face has rounded, my skin used to get tan very easily but now just flushes. I have headaches all the time, can't sleep at all during the night, then crash during the day. I am constantly depressed. I always have to pee. I can't be at the gym for more than 30 mins and then I just die im so tired. I can go on and on. I have tried so many time to get off but like I have read from the above comments,I become very sick and lazy I literally can't move. But what I need answers for, and what I was wondering, has anyone started to get hives/rash after coming off or being on prednisone. Every time I try to wean off of it I get them all over my legs!! NOTHING and I mean NOTHING makes them go away except when I start up prednisone again. My doctor thinks its okay and no other doctor can figure out why im getting these hives but its so obvious its from that because when I go back on it goes away. This is not a good medication to be on. I haven't seen hair loss as one of the major side effects but has that happened to anyone else. im praying to god i can wean of this drug if anyone knows anything pleaaaase let me knowwwwwww

I URGE YOU TO PLEASE SUBMIT ANY ADVERSE EVENTS OF THIS TERRIBLE KENALOG DRUG TO THE FDA--JUST CLICK THIS LINK AND COMPLETE THE FORM: http://www.fda.gov/medwatch/. The FDA is responsible for assuring safety of medications. Therefore, it is imperative that the FDA recognize the adverse effects to provide any credibility to a class action suit. Please consider forwarding your case to the FDA to force them into action and begin addressing these atrocities.

Here's my case: I am also a victim of having the Kenalog injection administered over a year ago to alleviate poison ivy itching symptoms. Prior to having the injection, I was not informed of any side effects. Not only did the injection not alleviate the symptoms, but has resulted in a discolored and uncomfortable indentation in my left buttock area and psychological anguish because of disfigurement of my body. It is over a year later and the indent remains and continues to cause discomfort. The dermatologist who administered the injection stated that there was nothing I could do to reverse such effects. I reported my case to the FDA (Food and Drug Administration) Med Watch and strongly urge others to report their adverse event to the FDA (see link above).

I made an appt. with my gyno. about six weeks ago because my period was going on for two weeks at a time. Around that time my husband noticed a dent in my butt cheek, and since then it has gotten worse. I was looking up indentation on the butt and came across this information. I JUST called my Dr. and asked them when I was in there for poison ivy what they gave me for a shot, you guessed it KENALOG 80MG. This was five months ago. The indentation is getting worse. Will it ever stop, and what kind of Dr. do I go see about this? Will my periods ever regulate?

POLL: If you or your child have been adversely affected by Singulair could you please reply to this and let me know what ethnicity you are and skin tone. (fair, med., dark, etc.) I'm interested in the demographics of this drugs effects.
Thank you!

I had one injection of Kenalog to treat anal itching. Doctor did not know how to treat it and used Kenalog as her last resort. It did not make any difference. Eventually another doctor diagnosed me with Herpes Cold Sore and treated me with Valtrex.
However, Kenalog messed up my menstrual cycle so badly and I haven't had ovulation for the last three months. What's upsetting is that my doctor knew that I was trying to get pregnant and did not inform me of such side effects. When I called the doctor later and told her what happened, she sounded very surprised and said that she had never heard of such a thing.
Doctors need to be better informed about side effects before recommending any medicine to their patients. And the lesson learned for me is to not trust doctors any more, always do research beforehand. Oh well, hopefully the ovulation will come back soon, it has been way too hard emotionally to deal with the overall situation.
Hope it's helpful.

I don't know if it was the two kenalog injections but I began to menstruate-three years post-menopause. I immediately was seen by my endocrinologist, trans-vaginal sonogram and endometrial biopsy done. i just received a call tonight informing me that a polyp was found and I will need to have a D & C. It sounds like endometrial hyperplasia and this is a very sudden onset - I had the same sonogram in February and all was fine.
I have now found out that steroids can "wreak havoc" with our hormones. I was schedule to have epidural injections of steroids for back and neck injuries. I will not have them now or ever- they are not as benign and helpful as many doctors would have you believe.

I have a 3 year old that was taking Singulair until today after I read the horrible side effects that I was seeing in my child. He is also taking Flonase, one squirt in each notstril every morning. Are there any concerns I need to know? Is this truly safe for a 3 year old?

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.