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i have been on prednisone for 5 years off and on and he moon face is there the hair loss the weight i really want to come off it so bad the asthma is a big issue in my life i wish they would come out with a better drug for us asthma patients the withdrawals i have been going through are the hair loss i use to have long thick beautiful hair thin face smaller body i am hoping some day i will get it all back
hopeful

I started SMZ/TMP DS 800-160 tab 2 days ago. I have bad feelings about this drug and today is 4th July and the weekend. I will quit it to get some other drug for my UTI. But it won't be for 3 days because the doctor is out till Monday to get another drug. Someone tell me a drug that does work for UTI. Someone mentioned Amoxicilln? Can that be used? The headaches are awful. I can't seem to empty my bladder at night so I never really sleep since I pee every 20 mins a few drizzles. I also was given that drug that makes the pee orange. It is Phenazopyrid 200mg. It relieves pain, burning or irritation of the lower urinary tract. Someone offer us info on a positive good drug they have used to help UTI. Thanks!

I too had HORRIBLE experiences on Toprol-XL. I was put on it after I walked into a doctor's office and my BP was 235/152. Yep..you read that right! Scary times. I started taking the med, and I too gained 35 pounds with no change in diet. I was tired, weak, groggy - I honestly felt like I was slowly dying. At that point, I decided that high blood pressure was far better than the experience I had on Toprol. It ruined my marriage. Can you say ZERO libido? I decided that I would try a different form of metroprolol - metroprolol tartrate versus succinate. I did this when I went out of town - I honestly thought my heart was going to pound out of my chest - coming off this medication was horrible, and if the other posts are true about this being worse to come off than opiates, I REALLY feel for addicts now. I have been off the Toprol now for about 9 months, and I feel so much better. I've lost what I call the Toprol weight, and I made some life changes. I did the following: (A) I purchased a rebounder (mini-trampoline) and have built up from 5 minutes per day to 15 minutes per day (goal = 40 minutes per day) - there are HUGE health benefits in rebounding and it's really easy on my joints (google the benefits - I promise you won't be disappointed). I turn on the TV or turn on my Ipod and bounce away. (B) I joined Freelife International, and began drinking Go Chi juice (www.pbowen.freelife.com) because it has three scientific studies proving its effectiveness. (C) I stopped drinking caffeinated soda and began drinking a homemade blend of green (matcha) & darjeeling teas (if you want the recipe, e-mail me and I'll send it pamela.bowen@gmail.com), and (D) I bought a device called RESPERATE (www.resperate.com). I HAVE MY LIFE BACK!!! Don't think you have to live the way you are forever!

I had been on Lisinopril for about 5 weeks, first on 40 mg. then I reduced it in half on my own, and have now decided to stop entirely and go back on Avapro. When I started it, I developed flu like symptoms and I thought I was just sick, but my body continued to fill "unwell". I had such terrible vertigo that I fell down 3 times and would get very dizzy when sitting up or bending over. Sometimes, the vertigo comes when I am sitting perfectly still! I became constipated and bloated with bouts of gas, headaches and sore throat in the evenings. My arms and legs were falling asleep during the night, so bad that I had to wake up and massage my hands and move my legs to get them circulating. Also, leg cramps have developed and cramps and shoulder pain that doesn't want to go away.I started to have to urinate all the time, as well! When I went to the doctor's office after being on it for 3 weeks, I complained that I was feeling awful (like I was going to die), depression had set in, I want to sleep all the time and have terrible vertigo, I was told that these were unusual symptoms and to try it for a few more weeks and see if these symptoms subside! Typical!!! It is thru researching blogs like these that I found that my symptoms are not at all unusual, but they are VERY ALARMING! I am a 46 year old woman and am healthy in every way. This medicine makes me feel as if I am being poisoned! I went off of it yesterday and am now doing an herbal cleanse to detox myself. I am also on fish peptides - which lowered my bp substantially in the past, but needed to find a reliable source that keeps it in stock all the time. It is safe and has no side effects.

I am absolutely amazed at all the side effects that may be a result of Lipitor.I have been on Lipitor for approx.4 weeks. Accdg to my blood work, my cholesterol was extremely high...possible genetic factor.(father had hight cholesterol).My diet is fairly low in fat, exercised regularly, etc. I have had muscle, joint, breast, and all over body pain, nausea, headaches,decreased energy. I actually think I am having heart attack or stroke pain....I have become very anxious due to these symptoms. Having lipid profile done tomorrow, see the doctor next week. I am going to go off the Lipitor and see about an alternative from a health food store.(I am also a registered nurse)

Hi everyone, I am a 36 year old with severe endometriosis. I was diagnosed at 17 and was offered a hysterectomy at that time, since I would never have children (So they said, 5 miscarriages but 2 babies, later, I had them all fooled). I have had 6 surgeries throughout the years for severe pain and endo growth. Finally, I asked for a hysterectomy to avoid all of these problems. My Dr. asked me to try Lupron first for relief. I have to say, I am so glad I did!!! I have felt better on the Lupron than I have in years. In addition to this, I have been taking 5mg Aygestin as back therapy (Norethindrone) and I take Calcium replacement daily. It has been wonderful. I have felt good, LOST weight, but do have annoying hot flashes the first week after the shot, but they go away. Additionally, I have had fibromyalgia for the last five years, and my pain symptoms have gone away with the Lupron +add back therapy. I think the 5mg of Norethindrone is the key to preventing the terrible side effects that Lupron is noted to have. I would recommend the shot, only with the additional Progestin- along with a multivitamin with calcium. I am GLAD I did! A hysterectomy may still be in my future, but for now, I have options.

I have been on Synthroid for about a year. I had high blood pressure and the doctor did a number of tests and found a thyroid deficiency. I started with 75 mcg and was moved up to 100 mcg.

I have gained weight in the last year - at least 15-20 lbs. It is all in the stomach. I look like I'm pregnant. It is very hard to get rid of! I am exercising my tail off, and giving up snacks, sweets, etc, and it's not going away.

I also never had problems sleeping but I do now. I'm glad I found this discussion group, because I see many others have had weight gain problems.

In June I found out I had actue renal failure. One of the many medications I was given was prednisone. After a few weeks I grew so weak, tired and in a lot of pain. I even had to take a medical leave from work(4 months).
I was told to expect the moon face, hunchback, the acne..However, my sypmptoms worsened to point I didn't want to eat(lost 30 lbs) could hardly move and had to be hospitalized(almost went on dialysis). They flushed me out for a week at the hospital and avoided dialysis.
Once out of the hospital I proceeded to keep the weight off, but the side effects just mounted. I had thrush in the mouth(the worst feeling), sleeplessness, I had every side effect listed and I mean all with the exception of hallucinations and depression. The miracle was that what I was expecting weight gain, moon face did not happen.
Around September my doctor started weaning me off prednisone b/c I told him I cant take it anymore. Wouldn't you know it the minute I started getting weaned off the medication I got the moon face and acne. I cant beleive how much acne I have and the moon face and extra chin that came along with it are not cute. In 3 days I gained 10lbs and feel like I'm gainiing everyday. This might bring on the depression that has yet to occur. Why is this happening now that I'm being weaned. I started at 80mg a day and now I'm down to 30mg and next week down to 20mg.
I know this drug did its job and I pray that I dont have to be on it at all once the weaning process is over, but this is hell. I really feel doctors should tell you everything that you can expect. I didnt know enough about this drug(I know there is the internet I should have used it) and had I known then what I know now I seriously might have asked for some alternatives. This drug may be a miracle in the medical community, but for those of us who have to take it, its hell. Does anyone know how long it will take for the moon face, acne, and weight gain to go away?

I am 19 years old and I recently was taken off of it 2 years ago when I switched doctors. Prior to the switch I had been on it for 16 years. I prob have some of the worse side effects. Because it causes an increase in appetite I ate but I didn't eat all the time, and I ended up gaining over 100lbs. I have a black-brown ring around my neck and for the longest time I thought it was dirt that wouldn't come off so sometimes I scrubed my neck sometimes to the point that it was raw.I have bad acne on my back and its just horrible.I cry every single night because of the side effects.I just want to know if anyone on here can help me.

I'm a 37 year old female and have severe asthma and allergies and have used pregnisone on and off for 30 years. I believe I am the poster child for the long term side effects. My immune system is shot to the point that my normal medicines for asthma (ventolin, advair) and allergies (tylenol sinus, claritan, visine A) and ezcema (elidel, hydrocortisone, etc. - - NOTHING works!

In the past 6 months, I have developed various infections that the doctors have not been able to identify. My eyes are swollen and red with large amount of white/yellow secretions. Vaginal secretions. Face swollen. Skilled covered in a rash with ezcema out of control. Sharp pains in my back and stomach. Constant asthma. Abnormal hair growth. It is to the point that it is impossible to function and each doctor just wants to prescribe more pregnisone. I feel as if my body is a walking time bomb and it is so full of all the cortisone from over the years and has just decided no more.

I admit that I too readily believed in the doctors when they would rapidly prescribe the pregnisone. Only now am I paying attention to the long term side effects.

Has anyone had tests done to test their immune system and other organs for damage? Thanks and best to our pregnisone club.

I am 21 years old and was recently diagnosed with rheumatoid arthritis in my hands, fingers, and wrists. My doctor put my on 60 mg of prednisone at first and then had me slowly go down to 20 mg a day. I have since been trying to go off of it myself. I can't stand the side effects any longer. I have this constant charlie horse pain in my hips and legs, i am so hot and constantly flushed, i feel so depressed ( i am normally a happy all smiles kind of person ) i have done nothing but cry everyday for the past week because I just feel like so many people don't understand or believe anything I am saying. I thought maybe some of this was all in my head until I found this site. Is there any other medications out there that don't have all these terrible side effects? I feel as though the pain from the arthritis is far less worse than this.

I was on prednisone for 6 days 60mg the first day and then 40mg for the remainder and beginning the day after the last dosage for the following 3 days my body would crash. I would go through these severe mood swings I would be fine one and then about 1/2 an hour later feel very depressed for a while. I also felt swollen and heavy. I knew it must have been the prednisone because I have no other reason to be depressed and then somone else I knew had similar emotional side effects

I've took a very high dosage of prednisone for 6 years, from the age of ten years old. 17 years later, i still have an extreme moon face. The only thing that has ever helped me was a facial exerciser (a microcurrent devise), but those results can be hard an expensive to maintain. As anyone else ever had a moon face that wouldnt go away even after stopping their prednisone usage after a long period of time? Does anyone have any advice for me, on how i can finally get rid of this horrible extreme moonface? my face and all my facial features are swollen, including my eyelids, this has been goin on for years. I also have suffered for years from severe chronic diarrhea from an illeostomy reversal. Please help me.

My Mother was diagnosed with Rheumatoid arthritis 30 years ago. She has been on prednisone at low doses since then. About 3 years ago she started imagining things, and hallusinations. About 2 years ago her prednisone dose went up to 60mg a day due to a stroke of the optic eye nerve. She has since been tapering down, now at 15mg a day. But tapering down makes her arthritis more painful. She has developed diabetes, loss of sleep, loss of apetite, loss of muscle tone. When she gets bumped, it's a big opened gash, rather than just a bruise. With the higher dose she was more moody & would get angry easier. The hallucinations & paranoia continue & are making me more & more concerned. I haven't read about this in any of the stories. Has anyone else experienced this side effect? I spoke with her Rheumatologist who suggest a psychiatrist to prescribe anti-psychotic drugs. She's already on 11 pills a day, does she need another?
Please let me know if anyone has experienced this as well.
Thank you.

I am 65, suufering from ulcerate colitis. Imuran kills my lever, I had to take a strong dose of prednisone.up to 60 mg. now after ten days I am on 30 mg.
it helps for colitis but I am not sleeping. I took sleeping pills, I can sleep about 2-3 hours in 24h.
Who could help me to be able to sleep again ? What kaind of sleeping pills or tranquilisers are recommended ?
Thank for answering also directly to my Email ******

Thank you.

Hi, I was on Prednisone for a little over a month for Crohn's disease. I had minor side effects while taking it: couldn't sleep, no patience, dehydrated, dry eyes. It is the side effects from AFTER stopping prednisone that concern me. I''ve been off Prednisone for 3 weeks and I think I am losing my hair and getting acne-that I didn't have before or during taking Prednisone. Anyone experience side effects that started after stopping the med?

Can someone email me and tell me if this pill really makes you gain weight because honestly thatz what i want..

I am really hoping someone can help me with the side effect issues I am having after taking Prednisone to cure a tumor on my larynx.. I was on the drug for six months.. taking 60 mg a day. It saved my life and at the same time it was just about to kill me, I am not kidding. The horrible effects it had on my body was really worse than the tumor that was taking my life. It would have almost been easy to die.
But today I'm very grateful for the miracle it did on my throat. I did not have a voice for many years.. today I can sing and that makes it's a great gift.
I was wondering, after being on it for so long and coming off nice and slowly, should my joints be in this much pain? My body aches are horrible.. all the muscles hurt and that never seems to go aways. Is this normal?

im not a member of this website but here's my story. I am 23, healthy, and in good shape. Never really had anything serious. I came down with a sinus infection almost 2 weeks ago and was prescribed amoxicillin, which i immediately had a reaction to. broke out in a rash.. I was then prescribed Zithromax and Prednisone. I was taking prednisone and felt weird then looked up the side effects and decided not to take it. After my Z-max, I was not feeling any better and returned to the doctor yesterday. He prescribed Levaquin and Duramax. I decided to check the side effects BEFORE beginning taking the medicine. I went to medicinenet.com, and no serious side effects were listed. I took the levaquin on an empty stomach, and about an hour later, my mood shifted from Happy/Playful to Zombie-like and confused. I wanted to cry but I wasn't sad about anything. I couldn't sleep that night, and woke up after having a nightmare. I came to work today and researched it and found multiple websites of people complaining about this medicine! What is going on!?

major itching, welts, and rash. I have been taking wellbutrin for three weeks and I am not taking it anymore! Class-action is in my future! and to the guy who said "you just need a drink" - your implication that everyone is just nuts (as the drug inherently suggests) was really off the mark. You must be an investor in the companies who develope these meds!

I have had constant problems with my throat/tracheal area ever since using Advair over 9 months ago.

Symptoms began the first week of using Advair: Symptoms included loss of voice, thick phlegm, loss of gag reflex and itching/pulling at the back of the throat.

(AdVair usage was for 2 months only while it felt like all it did was collapse my lungs and make me unable to breathe more and more)

Symptoms for 2 months later included: Thick yellow/green or red/brown phlegm, constant rippig feeling at the back of my throat, supposed Sinusitis/Post-Nasal Drip, dryness of the mouth and constant loss of gag reflex (while pushing the back of my throat would help relieve the aching and pain)

Symptoms from months 3-9/Present: Pulling, pushing sensation at the back of the throat, terrible acidic taste in the morning as well as the taste of food during the day, constant popping & gurgling of the esophagus, uncontrollable burping, pain on the sides as well as the tops of the areas near my lungs, constant trouble breathing, dryness of the throat (warm water feels good for this-cold water only makes it worse), constant scratching/painful feeling on the back of the throat, a barbed wire feeling at the back of my mouth and Severe trouble sleeping.

Tests have included: Barium swallow, upper esophageal testing, the regular scope, the looking at my vocal cords and beginning of trachea through my nose, Bravo pH Test, CAT scan, 2 X-Rays, Prilosec, Zegerid, Levaquin, Mucinex, Moxomicillan, muscle relaxant and finally Reglan.

Ruled out diseases include: GERD, Post-Nasal Drip, Sinusitis and basically all other diseases of the esophagus.

Current diagnosis from around 7 different doctors: Unknown, try to take the Reglan and wash the back of your throat with Listerine.

What should I do? It's been 9-10 months now and no doctor knows what this is -- I will be posting this on any Advair side effects as well as Trachea/Esophageal site -- email is MistaLM@gmail.com, if anyone else has had the same side effects or for lawyer inquiries.

I have had constant problems with my throat/tracheal area ever since using Advair over 9 months ago.

Symptoms began the first week of using Advair: Symptoms included loss of voice, thick phlegm, loss of gag reflex and itching/pulling at the back of the throat.

(AdVair usage was for 2 months only while it felt like all it did was collapse my lungs and make me unable to breathe more and more)

Symptoms for 2 months later included: Thick yellow/green or red/brown phlegm, constant rippig feeling at the back of my throat, supposed Sinusitis/Post-Nasal Drip, dryness of the mouth and constant loss of gag reflex (while pushing the back of my throat would help relieve the aching and pain)

Symptoms from months 3-9/Present: Pulling, pushing sensation at the back of the throat, terrible acidic taste in the morning as well as the taste of food during the day, constant popping & gurgling of the esophagus, uncontrollable burping, pain on the sides as well as the tops of the areas near my lungs, constant trouble breathing, dryness of the throat (warm water feels good for this-cold water only makes it worse), constant scratching/painful feeling on the back of the throat, a barbed wire feeling at the back of my mouth and Severe trouble sleeping.

Tests have included: Barium swallow, upper esophageal testing, the regular scope, the looking at my vocal cords and beginning of trachea through my nose, Bravo pH Test, CAT scan, 2 X-Rays, Prilosec, Zegerid, Levaquin, Mucinex, Moxomicillan, muscle relaxant and finally Reglan.

Ruled out diseases include: GERD, Post-Nasal Drip, Sinusitis and basically all other diseases of the esophagus.

Current diagnosis from around 7 different doctors: Unknown, try to take the Reglan and wash the back of your throat with Listerine.

What should I do? It's been 9-10 months now and no doctor knows what this is -- I will be posting this on any Advair side effects as well as Trachea/Esophageal site -- email me at MistaLM@gmail.com (I know I'll receive spam, but if there are lawyers as well or anyone of interest concerning AdVair -- feel free to contact me)

It doesn't work, nothing has helped for my allergies, including this shot... is there anything stonger that any of you know of? Please email me devannielsen@gmail.com

when on vacation last november, i started having palpitations, where my heart literally paused/ skipped a beat. i went to the er and they did a bunch of tests and i now have a med bill of 10K+ for one day in hospital!

no blood clot (air travel and oc's within the previous year made them suspicious), but they found a very small asd/ pfo (heart).

my thyroid hormones were totally whacked, a blood clotting enzyme was elevated and my oxygen level upon exertion was low (dyspnea). i'm tired of seeing docs so i try to destress and exercise more.

the only thing i was on at the time was the flonase...i had been on it for more than 2 weeks and for the 2nd or 3rd time this year...my ent told me it was okay. yasmin is also a suspect in my drama, but that posting is on the yasmin side effects page.

write to me at ******, if you have had similar symptoms or have questions.

My 4 year old experienced night terrors and extreme night sweats from amoxicillian. She also got rather drowsy. My son broke out in hives the very first time he had it, which is extremely rare and means he's severely allergic to it.

Seeing as both me and my husband are allergic to it as well, we'll keep our whole family away from it.