Dermatologists symptoms and conditions

at the most minor--occasional nausea and heat flashes for me

reading all these postings scared the hell out of me at first...

As I did, later on, all these people should heed their dermatologists' and doctors' opinion and advice before this website's and others' posts and personal comments (not to defile this respectable website), because they dance around various circumstantialities (percentages and likelyhoods, drug interactions with others, etc, etc). Whether they are of coincidence or not, I believe these people scroll through these posts and feel amazed that they aren't alone in terms of side effects and experiences regarding different drugs that other people have had too...
In conclusion--whether this makes sense or not--these comments and threads gather people together to, analytically speaking of course, scapegoat a placebo for any or all various "common side-effects"

Worst night of my life--woke up feeling filled with anxiety, insomnia, had to get up repeatedly to urinate, felt very agitated, though I felt very peaceful & relaxed at bedtime, feet were swollen so badly I couldn't put on my shoes. I took 10 mg of Benadryl, which did not change how I felt. My internist took me off the Singulair immediately, when I contacted him the next morning.

Despite being on an antidepressant which was recently increased, very recently I felt sad, anxious, and was crying all the time, felt irritable, and was chronically tired. I took 400mg of gabapentin (Neurontin), prescribed for nerve pain, numbness, tingling in both hands & feet at 9 p.m. Just before bedtime at 10:00 I'd take 10 mg Singulair. 1-2 hours later I was wide awake, sometimes not sleeping for hours or at all, even after taking 1-2 Benadryl, without the dyes.

Over the past two years I've had eczema, for which I saw 2 different dermatologists and an infectious disease specialist. Eczema was so bad, I couldn't sleep at night. I consulted with every imaginable doctor, including the allergist who prescribed Singulair & was told it couldn't be the Singulair because Singluair was FOR ALLERGIES. Was diagnosed with fibromyalgia by a neurologist, recently had a repeat of an MRI because I couldn't walk the pain was so bad. My neurologist was unable to find any reason I had pain & difficulty walking, after reviewing the results of the MRI.

I've seen my internist for heart palpitations. When I reported urinary frequency, he had me get a cystocopy (negative) because I had hematuria, blood in my urine, and I had weight loss.

I still have many of the side effects, like the numbness & tingling in my feet and hands, however, I am able to sleep through the night and did so immediately after going off the Singulair. A lot of the fibromyalgia pain I was having has subsided, depression, anxiety has subsided as well.

Have any of you suffered from really bad constipation whilst on Yasmin ???. Im at home now and i look five months pregnant. I keep taking senna tablets but it just isnt working. I eat really healthily drink loads of water. The only thing i can put it down to is Yasmin but im not sure if its just me if noone else has had it on Yasmin. Also have the following:

*melasma on top lip that looks like a moustache.
*cant stop eating constantly.
*really dry mouth, constantly thirsty.
*anxiety.
*feel down on myself

I can only take Dianette as a alternative but put weight on easily on it so im not sure what to do. Did any of you end up putting weight on on Yasmin after the first six months? . I don't know what to do.

Please could you let me know if you had constipation on Yasmin so i now if it is the Yasmin or not. My doctor knows but didn't seem too concerned.

I am writing on behalf of my elderly parent, Carmela, who has been diagnosed with Lupus since 1991. She has been on a small dose of prednisone since her diagnosis in 1991. In the last several months she has developed very many odd hazey type grey spots all over her body. Dermatologists and doctors are not giving her any answers. They took her off predisone because they THINK this may be the cause. She is on an inhaler and does not like it. She wants to go back on the prednisone as she is feeling chest congestion and lethargy. I read an article on the internet that describes prednisone may cause unusual bruising. I'm not sure if this is what her spots are. They are only the color grey and appear to be beneath the skins surface. They are soft or hazy looking. They are small, about the size of a dime. Has anyone heard of this before in Lupus (prednisone) patience. Any info you have is sure appreciated. S. ******

Hello everyone! I just want to thank each and every one of you for your postings. On more than one occasion I would come to this site because without all of you I probably would have truly lost my mind. I just want to give a brief history of what's been going on with me because if it can help one other person then it's all worth it. In 2005, I go vaccinated for chickenpox, I work in health care, never had them, and wanted to start having children since I'm 36. A month after the vaccine I broke out in a horrific rash ALL OVER and had it until April of 2008. I went to the hospital where I had the vaccine, 5 dermatologists, 3 Infectious Disease, various medical doctors and no one knew what it was. This April, I was admitted to the hospital with Autoimmune Hemolytic Anemia. After 3 hematologists, the last one feels the vaccine threw my immune system into a tizzy. I started with 60mg of Prednisone and eventually got down to 2.5mg. The hemolysis(body produces antibodies that attacks it own body) started again so I went to a new Hematologist and was put back up to 30mg and just got put down to 10mg today. Right now my biggest concern is the hair loss. I use to have such thick hair and now I cry almost daily because I loose so much. I am going to try the Ensure like someone posted just to see if that helps. I drink protein shakes, take Silica, multivitamins (Solgar) that have biotin, and going to try Nioxin shampoo. I have terrible mood swings and now I feel like I am going through withdrawal. It's almost like I want to take more just to feel better. I know that sounds crazy. The big fat moon face, my joints feel like they pop out, confused easily, can't sleep, and just can't really leave my house and live a normal life since April. I HATE IT!!! The only thing that helps me feel better when the daily prednisone "kicks in" is walking and exercising. I feel so bad for everyone this drug is just awful. I get angry because not one person told me what life was going to be like on prednisone. I think that is just mean. That's why these postings are so important. I know this is entirely to long but I feel so much better getting my story out there. Did everyone's hair eventually grow back. I don't know if I will have any left next month. Thank you all so much.
GG

I'm 18 years old and live in Florida, while at the gynecologist for a routine visit my doctor strongly suggested that I start the Gardasil 3 shot cycle. After checking with my mom (who was unfortunately given biased information from my doctor without first doing research on the product) agreed since we both figured that my doctor would be knowledgeable enough on the subject (or you would think since she was the one administering the drug.) The first two shots went fine and I had no reaction at all. After the third shot (in October of 2007) I woke up the next morning with swollen hands and extreme swelling at the injection spot. I immediately returned to my gynecologist where I was told “there is no possible way you can be allergic to this medication” by my doctor, and that those reactions would go away in a few days. A few days following this I developed sores in the back of my throat and under my tongue, however my gynecologist still insisted there was no possible way it was an effect of the Gardasil (EVEN THOUGH IT WAS THE VERY NEXT DAY) & I had no previous illnesses. Within the week following I developed body-wide hives so severe that I cannot sleep and they affect my breathing. I’ve seen several doctors (allergist, dermatologist, primary physicians, and immunologists) none of which can determine why exactly I have these hives, besides that it is a “drug reaction” (it took 11 vials of blood to determine that). However when one of my dermatologists questioned Merck about it they simply said that there is no evidence and I cannot sew!!! That’s all they cared about! A law suit! WHAT EVER YOU DO, DO NOT GET THIS SHOT, TELL EVERYONE YOU KNOW! It has ruined my life. As an 18 year old girl living in Florida I love to go to the beach however because of these hives they get so severe when I’m exposed to sunlight I can no longer go. It’s also extremely embarrassing when people stare at them since they cover most of my body on a daily basis.

Here is our daughter's story, and believe me the tears are pouring down my face as I am writing this.
Our daughter, who had completed her series of 3 vaccinations has been experiencing considerable hair loss. Her first shot was in May 24, 2007, the second on July 26, 2007 and the third and final on November 27, 2007.
Here are the other specifics....our daughter was 13 turning fourteen.
She has had every blood test imaginable to rule out the obvious which may cause hair loss such as thyroid disease, polycystic ovary disease, diabetes, and the list goes on and on. Everything came back negative. We even have a future appointment scheduled with a rheumatologist this coming November 08. We have seen the Endocrinologist and two dermatologists (a scalp biopsy proved negative to any infection, disease, etc. Granted, she had a typical amount of stress during the school year, as any young teen would, but nothing to cause this. Everyday our daughter says to us, "you should see how much hair fell out in the shower today". She's so afraid to brush or comb it because of the extreme shedding. She literally, to date has half the amount of hair she had one year ago. Let me tell you she had beautiful hair. The hair loss is becoming quite visible at the forward part of her scalp. This has been devastating, hair is everything to a teen. (to anyone this is devastating) We must also mention that her periods have been totally out of whack. She went 6 months at one point without one. It finally came back, but it is so sporadic, getting every two weeks, at times extremely heavy, etc...
She also complains of intermitent dizziness. We are reporting this to Merck today (the Co. who makes this horriffic vaccine), along with the FDA. If anyone else is experiencing anything close to what we are, we all need to pull together and make the public aware of what's happening so we can prevent this from happening to our loved ones.
Please share your experiences. Feel free to write me if someone you know is going through this same tragedy.

Exhaustion, joint pain, headache, ankle swelling, shortness of breath, persistent (cold) sores in my nose…

I am 52 years old and have taken Lisinopril for approximately 7-8 months. During the past two weeks, the majority of my joints have suddenly begun to ache. My fingers, especially index fingers, and one wrist are extremely uncomfortable. Other than the side effects listed in the comments on these pages, has anyone lost their eye brows? Sounds crazy doesn’t it but I first thought it was a side effect of hormone replacement therapy. I gradually stopped taking the HRT (ugh!) but continued to lose my eyebrows and now I notice my eyelashes are thinning. After trips to two dermatologists, neither had an explanation and both denied the HRT drug would cause the hair loss. I was and am extremely frustrated. I am not sure what made me research side effects for Lisinopril again but I finally saw something on an internet site saying that ONE percent of people could suffer hair loss. I’m sure my doc will be disappointed that I want off this medication. The only meds I take regularly are Lisinopril and Dyzaide (low dose). I have taken the Dyzaide for several years.

I received my first shot of Gardasil in January 2007. It could have started sooner, but about a month later my hairdresser noticed a bald spot in the back of my head. I rushed back to my ObGyn and asked her if the Gardasil could be the cause as nothing else had recently changed. She said that she had not heard of this, but she referred me to a dermatologist. I asked him if my hair loss had anything to do with the Gardasil. He replied that I had Alopecia areata and one thing had nothing to do with the other. He advised that I continue with the Gardasil and that he would start treating me for the alopecia. I wish that I would not have listened. I don't know what would have happened if I had stopped then, but I didn't I proceeded with the treatment to the end now over half of my head is bald!!!
I don't know what to do. I keep going back to the dermatologist for treatments for the alopecia, but it just keeps getting worse.
If anyone has had a similar experience and would like to share or has found some other treatments that work, please post a reply.

Melissa

I have been using NuvaRing for a little over a year now. I am 38 years old. Over the past few months I have been experiencing incontinence problems...nothing major, I just sometimes felt like I had dribbled on myself. I had to wear pantyliner. I thought I was just getting older and had this to look forward to....I have since realized that the week I take out the ring I don't have this problem. I have also been experiencing major depression and am unable to control my temper...the least little thing sets me off! I want to sleep all the time and have no energy. Three months ago I started having migraines. My husband complains because I have NO sex drive, but when we do have sex I burn so bad afterwards I can't stand it. I have also been to 2 dermatologists for severe acne! I have felt like I am falling apart! After reading everyone's comments, I think that the NuvaRing is to blame.

I am a 30 year old female and have had asthma since I was 3 years old. For years I struggled with it, having to always have an inhaler on hand everywhere I went. About 4 years ago by the prescription of my pulmonary doctor I started taking singulair and advair once a day (before bed) The one thing that I have noticed that concerns me a bit, is that when I miss even one day of the medication (due to my forgetfulness in refilling) my asthma will be worse then before I even started the medication. So it's like I'm dependently addicted to it, which is really scary. Just one day off of it and I have to use my albuterol inhaler at least 5 times a day and I can't even get out of bed sometimes.

The other thing that I noticed was my complexion changed. I have been to several dermatologists who either think I have a mild rosacea, mild acne rosacea or a mild adult acne. I have never had a problem with my skin, it was always clear. However now it is just so tempermental. I recently asked an internal medicine doctor who doesn't seem to feel that there is any link between singulair and skin problems but thought that perhaps it was the advair.

I also have experienced strange mood shifts that sort of go back to the time I started the medication. I fight a lot more with my husband and just feel very anxious, fearfull, reclusive, depressed. I feel like another poster, that everything is going to go wrong, or is always wrong. I'll have extreme anxiety about small everyday things. I am an actress living in LA. I have a commercial agent and was quite active in auditioning but this has dwindled as the years have passed.
Is all this due to the medication? I cannot say obviously, and like another poster said, you can't attribute side effects that some people have had to all the millions of people that must take this medication.And, it is true that during studies conducted of medications anything that someone experiences has to be listed as a side effect. I was taking a medication for my possible ADD symptoms, concerta, and one of the side effects is "Accidental Injury" what does that even mean! I asked my doctor about it and he told me, that if someone so much as accidentally bumped into a table or tripped during the study it would have to be listed as possibly being associated with the medication.It's a legal thing I'm sure.

But in any event who's to say that it isn't causing these symptoms. I certainly hope that it doesn't. I can only vouch for my physical symptoms for sure. I know whether or not I can breath or not and that it's due to not taking the medication since being on it is like I don't even have asthma. But as for the emotional stuff, they are just that emotional and there are many other things in peoples lives that could be contributing factors. The greatest test would be to stop taking the medication to see if the emotional symptoms improve.

So I started taking YASMIN in December 07. I switched to YAZ in January 08 and just quit a week ago. So about 4 months of bc. A week ago, I broke out in hives and rashes. I would itch one spot and then others would form. The areas get hot and the welts raise up my skin. It started when I was out in the sun but it couldn't have been sun poisoning because I never got burnt. I am diagnosing myself rather than a doctor because they do NOT know everything. After reading into the YAZ and YASMIN side effects, I am not risking anymore problems. Oh and I got an upper respitory infection along with the rash. This lingering cough has a weaze and phligmy sound. My friends are concerned with it too. I have never been the type of person to suffer from any major sickness or skin problem. I am tough skinned and have never gotten any kind of food allergy. I am 24, 5'6'' and in semi-athletic shape. I am an actor and model and I cannot afford to get rashes and a bad horsey cough! YAZ was great for 2 months and now bam! Downfall happening. Temporary relief-cortozone cream and antihistamines like benadryl.
YAZ benefit-clear skin, no PMS
YAZ side effect-rash, no sex drive/libido loss, difficult/no orgasm, appetite like a hog! Food #1 thought. Packed on pounds quick.
YASMIN benefit-clear skin, lost weight quick
YASMIN side effect- a little loopy, speech impediment, no sex drive/libido loss, no orgasm, couldn't even fake an orgasm!

I am going to be 42 in April. I had the Mirena inserted in 2005. Initially I was aware of the side effects. I did not linked all of the side effects together until coming to this site and searching for reasons for having extensive hair loss. I have experienced the back pain, the skin itching, horrible acne that looked like mountains forming on my face, night sweats, headaches, depression and nausea. I used pain medicine like crazy......Out of all of these the hair loss drove my search for answers. I made an appointment to see a dermatologists who proceeded to shoot my head with approximately 30 cortisone shots and subsequently provide me with cortisone cream to trigger hair growth. I could pull on my hair and end up with a hand full of strands. It was unreal! It has been two weeks since I have had the Mirena removed. It was not painful at all and I had very little bleeding. Just spotting. My body is now suffering from Hormone Naive. My stomach is bloated and I am craving food. I feel like I am pregnant. The good is: I am no longer suffering from the headaches, back pain, the acne is gone, hair breakage has slowed down a great deal, and my mind is clear. I can put words together that make sense. I recommend to all women to have the Mirena removed and want to thank you all for this site. I would have never put all the pieces together. It is not worth the damage to our bodies. Because of my age, being divorces and not wanting more children (I have two) I will be getting my tubes tied in the near future.

I to have a huge dent in my right butt cheek. I would be interested in a class action suit. This is ridiculous! It has been about three months since I received the shot. Has anyone noticed their dents getting better with time?

Did anybody suffer from a skin rash post labor??? This is my second labor, and after both labors were induced 2-4 months after the labor I found myself with an unexplained skin reaction which resembles Herpes Zoster and the urticaria. Dermatologists could not find the cause and I am currently on Prednisone to control symptoms. The only link could be the drugs given in hospital.

After bith my childrens births I have experienced a enigmatic skin disease / disorder which has been unclassified by dermatologists and specialists. First I experienced blisters on my torso, which crusted over and followed with severe urticaria-like wheels all over my body. Doctors placed me on Prednisone 5mg tablets ( 40mg daily) for 4 months, in which time the symptoms subsided , but the side -effects for this Mother was terrible!!! I experienced a 12kg weight-gain, uncontrollable appetite, excessive sweating, dizziness , shortness of breath and extreme hairloss. My skin thinned and OI bruised very quickly. No diagnosis could be made. After the induced -birth of my second child now, I have the same episode and had been placed on Prednisone for the second time just to cope with the swelling.

I am currently in my 7th week of using 10mg - 15mg daily with an anti-histamine. I hate the re-occuring side-effects and am very scared of all the long-term damage. Does anyone have any idea how to boost your own natural immune-defence system while being bombarded witha immuno-suppressant like Prednisone??!!!!

I believe that your own body ws made to heal itself or be healed by natural means... but how and what?? I am desperate, and have been following a anti-candida like diet ( no yeast + sugars + preserved foods) Thus far I have not been able to kick the symptoms. Any help out there would be much appreciated. Have someone experienced the same sort of symptoms???

i received a kenalog shot about 5 months ago on just one single pimple on my left cheek. about 3 or 4 weeks after the shot i got this huge indentation and discoloration. mind you the rest of my skin is completely clear with no acne nor scars nothing so this indentation stands out even more. the discoloration went away completely and the indentation filled some but not all the way. i went to 5 different dermatologists and all say the same thing that it will eventually fill in on its own as the skin regenerates itself in close to 2 years. the dr who gave me the shot gave me no warnings and now im stuck with this unsightly dent in the middle of my face which apparently will correct itself. i have gotten all the fillers like restalyne and collagen but it doesnt work all it does is push the dent to the surface of the skin and its obsorbed in about 2-3 months anyway. if any one has had this experience before particularly on the face please tell me there is hope that my skin will go back to the way it was before or if you kno of any sort of treatment please let me know.

I got my IUD placed in about april of 07 i have seen than experience crazy skin problems such as ance i've never had a problem with ance and i'm 25 i have very bad mood changes that are unexplainable now that i have reread the side effects of Mirena i now know why all the side effects began around the same time and now i'm figuring out why! I will be getting it removed. Has anyone else experience really bad mood swings i was so ready to get on depression medications now i'm going to get it removed and will take it from there!!! Please let me know if i'm not the only one

I too experienced an indentation from a kenalog shot. My experience is a little different though, because I received the shots on my face for acne. I received four shots and two out of the four depressed / indented. I was EXTREMELY depressed and felt hopeless after reading it would take 6 months to a year (or more) to have my skin gash-free. I stayed up for two days straight searching for some sort of help on the internet and found a medical article about something called saline infiltration. It is a relatively new procedure and was created by "one of the best dermatologists in the country". I was so desperate, that the next morning I drove to see him in La Jolla, Ca (I live in LA). I received shots in the problem areas. It is now two days later and my indents are about 80% better!! He told me to give it another couple of days to see complete restoration, and if not, said that one more treatment should make everything 100% normal again. Needless to say, I am thrilled!! I do not know if this will work for any of your situations (being that the dr. is a dermatologist and the shot was initially given for acne), but I thought I would share my great news and hopefully help at least one person out there dealing with this mess.

I too experienced an indentation from a kenalog shot. My experience is a little different though, because I received the shots on my face for acne. I received four shots and two out of the four depressed / indented. I was EXTREMELY depressed and felt hopeless after reading it would take 6 months to a year (or more) to have my skin gash-free. I stayed up for two days straight searching for some sort of help on the internet and found a medical article about something called saline infiltration. It is a relatively new procedure and was created by "one of the best dermatologists in the country". I was so desperate, that the next morning I drove to see him in La Jolla, Ca (I live in LA). I received shots in the problem areas. It is now two days later and my indents are about 80% better!! He told me to give it another couple of days to see complete restoration, and if not, said that one more treatment should make everything 100% normal again. Needless to say, I am thrilled!! I do not know if this will work for any of your situations (being that the dr. is a dermatologist and the shot was initially given for acne), but I thought I would share my great news and hopefully help at least one person out there dealing with this mess. Good luck to you all - I feel for your situations.

Hi there... I have just found this site and I'm very grateful to everyone who has taken the time to sit down and tell us their story mine is very similar. BELIEAVE me I feel like I am pushing my family away and I'm losing my relationship with the one person who used to make me feel like I was the most beautiful woman in the world.
I'm a 40 yr female have or maybe had a great job that I loved... On April 12 I noticed a small red rash on my lower right leg no big deal went to the Dr. gave me some cream and sent me home well I went to work and by the afternoon things just seem to get bad my legs began to swell and little blisters started to pop up so I went to the E.R. they had no Idea what was wrong with me got me an appointment to see a skin DR. so I went home but the pain from the swelling was so bad I could not walk any longer went back to the E.R. they gave me some pain meds and called in some other DR. things had gone from bad to worse my feet had gotten to big I could not put on shoes and I had bruised completely across the bottoms of my feet they put me on 30mg of PRED. and it seem to be under control sent me home after 3 day in the hospital things were good for about a day or so I thought I would go back to work well that was not a very good idea.... My sister had to come and take me back to the ER where they did 2 biopsies and still have no idea what is wrong with me. so now they put me on 60mg of PRED the rash has gone, lots of scaring on my feet because of the blisters once they broke and dried out but I can live with that....
It's the side effects that they don’t tell you about,
MOON FACE I can't look at myself cause really that’s not me anymore,
WEIGHT GAIN I have always been thick but I can't handle the extra 30lbs I've gained,
MOOD SWINGS are unbearable,
PAINFUL JOINTS, CAMEL HUMP, BLOODY NOSE, BRUSING, SORE TEETH/GUMS, DRY EYES, FAITIGE, and worsted of all
I don’t have a support systems in my life so I'm fighting this by myself everyday, I have 3 kids that I have tried to explain all this to but they don't get it and well my boyfriend he tells me he understands that its the meds pushing him away but if I can't figure away to control this I will lose every thing including my job. I cant even get the energy together half the time to make it up and down the stairs which also comes with the pain of just trying to lift each leg up to climb the stairs, I also have the camel hump which I find very painful, The acne and the hair growth that I have to get wax off once a month cause I feel like a man I feel like a loser and as of the last couple of days I just want to give up I am now down to 20mg per day but I find that I am feeling so sick I cant think straight I hope and pray for each and every person out there that has to take this MED that you get better and I do hope that my symptoms wont come back. Thanks for being here and I’m glad I found this site. I know now that I’m not losing my mind completely. Elizabeth.

SINCE ON THE MEDICATION ALTACE & MAXIDE DERMATOLOGISTS TESTED FOR ECZEMA. LARGE PATCHY SKIN RASH ALONGSIDE OF MY FACE AND MOUTH. I HAVE NEVER HAD SUCH A BAD EXPERIENCE. I HAVE ONLY BEEN OFF FOR TWO DAY, WE SHALL SEE. ALTHOUGH MAXKDE HELPED WITH FLUID, AFTER READING THE ARTICLES, I AM SKEPTICAL ABOUT WANTING TO BE PUT BACK ON MAXIDE.
I AM ALSO A RUNNER AND I CAN FEEL MY BODY SWELLING ALREADY.

I'm so happy I stumbled upon this website! I was prescribed Linsinopril in 2004 and within a few months began to feel lousy. The drug never seemed to lower my blood pressure to "acceptable" levels and I developed a rash, which sent me to three dermatologists in six months until I finally decided to go to an accupuncturist. The accupuncture treatments seemed to work at first, but the rash returned. Then my leg started giving me problems. In fact, my hip/leg hurt so badly I was considering hip replacement! It felt like my leg was going to fall off. Rising from sitting positions made me feel like a cripple and the pain was excruciating! Xrays and ultrasounds showed nothing. I finally begin going to a chiropractor but I'm not getting better -- I'm just managing the pain a little differently. All along I kept thinking it must be something I'm ingesting that's giving me these problems. I have suffered the same symptoms as many of you, though the coughs weren't nearly as bad. Last year a new doctor (I "fired" the other one because her bedside manner sucked and I wasn't getting any better no matter how I tried) took me off Lisinopril and prescribed Enalapril maleate and even though the rash has gone away (somewhat) the pain in my hip and leg is still awful, and that hacking cough is still there -- in addition to the fatigue, dizziness and swelling. I think this medication isn't much better than the Lisinopril. Since I'm also taking furosemide, I'll stick with that until my next appointment and see whether I can feel like my old self again.