About Prednisone And Night Sweats
Prednisone And Night Sweats Facts
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Prednisone And Night Sweats Facts in Questions
Has anyone ever had Prednisone Withdrawal? I have asthma, and Friday I had an attack and had to visit my doctor. He gave me a shot of a corticosteriod, to follow up with prednisone tablets. I took 3 x 20mg on Friday. Then Saturday, I only took 2 x 20 mg of prednisone. Today I have taken 1 x 20mg so far with one more to take later on. The problem now is that while my asthma symptoms are alot better. I have very tired and aching arm and leg muscles. I cannot even stand for long without getting exhausted. I can't sleep at night and wake up sweating. My anxiety is also way up. Today is Sunday, my doctor is not in. What should I do?? Please help.....

Monkeymini24 replied: "It is unlikely that off such a small dose in such a short time you are suffering withdrawal symptoms. I also have asthma and have taken prednisolone, or prednisone as you Americans call them, but I had 40mg a day for 7 days then stopped completely. It is possible however that it may be a side effect of the medication (check the leaflet you got with the tablets or if you didn't get one then type prednisone side effects in your search engine). There's always the possibility that it is completely unrelated. Bear in mind that this is not the best place to be asking questions of this nature, it is a public forum and people are not always who they say they are, so if someone says they are a nurse or Dr. please remember my advice. Hope this helps."

stacexx replied: "I would definitely get an appointment with your Doctor for them to check you. Although you seem to be tapering off (which is the correct thing to do with most medications) if you taper off too quickly that could cause withdrawal symptoms. Symptoms include: weakness, lethargy, tiredness, nausea and vomiting, arthralgias, myalias (muscle pains), low blood pressure (hypotension) which may cause light-headedness or even fainting when the affected person stands after sitting or lying down. Here is some more detailed information: What are the possible side effects of prednisone? If you experience any of the following serious side effects, stop taking prednisone and seek emergency medical attention or contact your doctor immediately: an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives) increased blood pressure (severe headache or blurred vision); or sudden weight gain (more than 5 pounds in a day or two). Other, less serious side effects may be more likely to occur. Continue to take prednisone and talk to your doctor if you experience insomnia; nausea, vomiting, or stomach upset; fatigue or dizziness; muscle weakness or joint pain; problems with diabetes control; or increased hunger or thirst. Other side effects that occur only rarely, usually with high doses of prednisone, include acne, increased hair growth, thinning of the skin, cataracts, glaucoma, osteoporosis, roundness of the face, and changes in behavior. Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome. ************************************************************ What other drugs will affect prednisone? Do not take any other over-the-counter or pre ion medications, including herbal products, during treatment with prednisone without first talking to your doctor. Many other medicines can interact with prednisone resulting in side effects or altered effectiveness of the medications. ************************************************************ Good luck and God Bless!"

jomar_who replied: "OH WE ARE FAMILY!! I have asthma too. I USED to take prednisone but after some advancements in medecine, I gave my self a favor and took SERETIDE (fluticasone). this is a very, very good drug against asthma. no side effects like hands shaking. BTW, are your hands shaking??? also, I recommend to you VOLMAX (ventolin). it would do a lot of help to maintain your "short-breath" episodes away. take it from someone who has 20 years of experience about this things. TIP: steroids like prednisone, dexamethasone, betamethasone etc. should only be used for a maximum of two weeks. no extensions. pls. don't rely too much on medecines. try swimming, jogging etc. after you have recovered. it improves our breathing muscles. take care. JOMAR S.T. NDGM '96"

Prednisone reactions? What are some reactions you experienced while taking prednisone? I read the info that came with the drug but I was curious what others have experienced. I'm taking it for a period of 5 days to help me get over my asthmatic bronchitis. I woke up a few times last night SOAKED with sweat. I had to change my blankets in the middle of the night. I did not see this listed as a side affect. Has anyone else experianced this while taking prednisone?

Riley replied: "I know that one of the side effects is excessive weight gain but that won't be a problem because you are taking it for such a short period. I haven't heard of having sweats though. If you have a fever with the bronchitis then that could cause you to be sweating."

Scared, Help Do I have Lymphoma or cancer? Help, back in the beginning of February I began to feel bad. Not wanting to eat, abdominal discomfort,indigestion. Thought was my Crohns disease and began taking prednisone. I went to ER three times. Have had 3 abdominal/pelvic ct scans in feb, 2 chest xrays in feb, a small bowel follow through in march and upper and lower gi series in march. I was up to 80 mg pred and have now tapered off completely to zero for last 4 weeks, during the last two months i have developed a rapid heart beat, sweats and off and on fever. I have kept insisting to doc that i do not feel myself, he insists that its in my head or the crohns. He says all my scans and blood work come back ok. In last 4 days my fever has been getting more pronounced and having night sweats. Went to doc yesterday and he gave me antibiotics, told him i was worried about lymphoma and he look at my neck glands and said everything look ok, have all the signs of lymphoma scared could the prednisone have hid the lymphoma from the scans? Thanks for your answers I did have my thyroid checked and that was fine..He said the antibiotics were in case i had an infection.

cam replied: "It could be a hormone issue, an infection, thyroid problem and so on. You have the right to go to a different doctor. If you are not comfortable with what you are being told I would recommend switching doctors or getting another opinion."

barthebear replied: "Well wouldn't you have a palpable node perhaps in groin area or underarm? The prednisone could affect your blood counts but now that you have tapered off it you would have regular blood work. Did the Dr say why he was giving you antibiotics? Did he do a blood culture if he thought it was systemic infection? Hmm. Well dont try to diagnose and please dont panic; but you may want to get 2nd opinion if you arent feeling right about this."

bitchsdontknowaboutmydiabetes replied: "haha your gonna die"

quijibored replied: "I am guessing that you are having prednisone withdrawals from tapering off too quickly. Resume prednisone at 2 1/2 mg daily and then taper off very slowly at 1/2 mg per week. I bet within 12 hours of you taking the prednisone you will feel just fine. Ask your Dr for approval before you try what I suggested. "

Char replied: "If the antibiotics have no effect, you may have a problem. [that was the clue for me] Stay in close touch with your doctor until you get the answers you need. Here's the best site for info: Best wishes"

How soon should I get relief from Prednisone & Ventolin? I started coughing on Sunday night (6/7/09) and I went to the doctor on Wed (6/10) feeling like my breathing was compromised and I had semi-productive sharp painful coughs and he said he thought I had bronchitis - he gave what was supposed to be really strong cough syrup (Rx w/ hydrocodone) and a "Z-pack" for the antibiotic. I felt like I had a little more energy for a day or two, but the syrup didn't relieve the cough and I was having trouble sleeping because of that (syrup made me a little fuzzy, but didn't help me sleep). Now it's 6/19 and I went to the doctor again yesterday because now in total I've missed 5 days of work since last Monday (my cough was no longer productive) he did the lung function test and my capacity/power was about a third of what it should be. He prescribed Prednisone twice a day for 5 days and Ventolin every four hours. I started both at 6pm last night now today my cough is worse than ever, i feel more fatigued, same breath capacity, constant wheezing, have little bladder control (assuming from coughing for two weeks straight), have had a headache for almost a week straight, constantly sweating and uncomfortable (the AC is set at 70). Is it going to take a couple of days on these meds to feel any relief or increase in lung function? I just want to feel a little better!!!! Thanks, everyone! So if the Ventolin is supposed to work immediately and it's not relieving my wheezing or coughing, should I keep using it?

Matt A replied: "Ventilon should give you some relief right away. Prednisone will take longer, from several hours to several days."

William replied: "Lets start off with the Prednisone. That is a steriod that is used to decrease the inflammation in your lungs. It may be what is causing your fatigue but also you may be getting less oxygen into your body. The vetolin should give some relief almost right away. You may want to talk to your doctor about using a nebulizer. This is a small air compresser like machine that blows air into a small cup with liquid ventolin. This will get the medicine into your lungs better than the puffer. Talk to your doctor about using Advair. This is a 2 medicine combo that helped me ( severe asthma). Good luck and I hope you feel better."

Eczema extemely itchy at night...can't sleep? I've had eczema since I was a baby, and have been on various medications, usually topical. Right now I use steroidal creams which have ceased working and only make my skin thinner in areas, so it just comes right off, causing more pain than necessary. The past few months though I've had extreme eczema flare-ups, and so I took prednisone I was prescribed, which usually dampens the eczema enough that I can get it under control. Unfortunately, even while I was taking it, I was miserable with eczema symptoms. I wouldn't mind the itching so much, except that I wake up and realized I've clawed myself have to death during my sleep and am then in extreme pain, and can't go to sleep. Even when the pain is there, I can't stop scratching. Or rather, I can't stop itching. I do take hydroxyz for itchiness and it doesn't help at all. I've taken benadryl, and other antihistamines. The worst part is at night when I go to sleep, my neck becomes extremely hot and itchy. It does not resemble the eczema on the rest of my body, which confuses me. I've tried sleeping with my hair up to keep it from causing my neck to sweat, tried sleeping on my stomach so that it doesn't rub my pillows, bought new hypoallergenic pillows and pillowcases, and still, it just itches and bleeds and hurts so much. I have done everything it seems....from trying various cleansing teas to everything doctor recommended. I'm particular to avoid allergens, and I use hypoallergenic soaps and detergents, as well as tar shampoo. When I use oatmeal baths, it only makes me itch more. I've tried vaseline, and taking lukewarm showers. I can't shower everyday or it dries out my skin entirely. During the day it is not as bad, but I do know that any kind of sweating or humidity automatically worsens it. Is there anything strange out there that I haven't tried? I need something to help this go away... Edit: I've even had sleeping medications prescribed to me, which only make me drowsy but do not cause me to sleep through the pain. I also keep my nails very short, but that, once again, does not seem to hinder my night-scratching.

Tayyyy. replied: "I had eczema too. But I usually only get it in the winter, because in the summer when I am in the sun the sun seems to help it a lot."

Wally G replied: "The main cause of eczema is overreaction of the immune system. Identifying certain foods, chemicals, etc can be very helpful in battling this disease. I try to avoid soy and milk products which trigger my flare-ups. After using number of pre ion drugs I've turned to the natural treatments. Now I use herbal remedies from serenaskin.com, which aim at the root of the disease - the immune system, and are steroid-free. After about 2 weeks of using ointment and spray my skin has been cleared up and now I just continue with anti-eczema extract, which controls the immune system. My skin has been clear for months now. It is the only treatment I have found that provides me complete relief when I use it as directed."

The One And Onli replied: "hy urm...iv also got eczema. iv had it ever since i was 3 months old. now im 14. When i was around 5-8 years old, my eczema got worse...it was just like yours...actually, i think that it was MUCH worse than yours. i looked like a zombie!...all my skin was all red and i was itching all over. i even had eczema on my face. it was more worse on my face, than it was on my body. I couldn't even talk coz i had broken skin near my lips..it hurt soo badly...just like YOU, i couldn't even sleep at night...i kept itching and scratching...my attendance in skwl got worse by the minute. When i was around 10-12 years old..my skin improved sOO MUCH..it got better...it got better because i was given a cream ( cream name = elocon) by my doctor. he told me to use elocon over and over again. my skin got much better, once i started using the ointment. i was soo glad!. my eczema seemed as if it VANISHED!. even tho i did use the cream...i still had a few eczema marks left. those also kind of faded away coz i started using coco butter. when i was about 13...i stopped using the cream coz i thought it was alll gone. but unfortunatly it came back.. so then i started using the cream AGAIN..then, my eczema lukily wiped out again :)..i was soo happyy :D Now...i would definatly reccomend u to use elocon and butter cream to get rid of that horrable eczema. once youv started using it, dont stop....carry on using it and ul be fine :D....i hope i helped you out... REMEMBER, USE ELOCON OINTMENT/ CREAM AND BUTTER CREAM!!!! :D"

Ulcerative Colitis..? For the past three nights I havent been able to sleep very well at all. That's pretty unusual for me. Im getting concerned because for the past two nights ive been waking up drenched in sweat. Ive never had night sweats before and am wondering if anyone has ever experienced this with taking Prednisone or Remicade for Chrons or Ulcerative Colitis. Ive been on Pred. for about a week now and I had my second infusion of Remicade about a week and a half ago. Has anyone experienced night sweats? Ive also woken up this morning to a runny nose, an itchy throat, and the back of my throat burns when i breathe in.

superstarr replied: "Sounds like you might have an allergy to one of your medications. I'd ask you doctor about this, just call. Or even call ask a nurse- if you don't want to go in."

bt replied: "steroids knocks your immune system, making you more susceptible to colds, so that's probably what that is. common side effects of remicade do include fever, chills, muscle pains... so it's probably that. it'd be a good idea to call your doc and check because you want to make sure it's not anything else. you have to be careful because you don't want to get really sick while your immune system is knocked out by the steroids."

carl b replied: "The drenching sweats are from the Prednison. They will happen (mostly at night) until your off the Prednison a couple of days. I have used both Remicade and Prednison. The sweats only happen with the Prednison, but the Remicade doesn't seem to work so well without the Prednison. The throat stuff sounds like something else. Hope you feel well soon."

sethwoods101988 replied: "hmm. see a doctor"

jo jo replied: "i had these the night sweats its the steriods wants you are of they will stop the steriods attack your imune systoms so lots of colds is the norm if you are on steriods you must not go near anyone with chicken pox i also got chrons its a horrid illness put it will get better when on steriods"

could hiv show up in the saliva before blood?could hep c cause a false positive result for a antibody hiv test? ok i went to a free clinic to get a rapid hiv saliva test done and it came back non reactive.a month later i went again with my partner just so we could both get tested together and know each others results.his saliva test came back non reactive and mine came back reactive.we walked all the way there in the heat and im pretty outta shape so im not sure if that could of threw off the test.the lady who did the test said the line was very faint and showed up towards the end of the test.they took my blood and sent it to the lab to confirm my results.my blood test came back negative.i was with my partner and only him for six months when i got a reactive result but a neg blood test.i haven't had any symptoms of hep c but am worried.is it possible that it could of been a bad test and my health is fine?ive never used drugs or been with anyone who does.im now with a new guy that ive been with for about 3 months.i know he's clean but 2 weeks ago he broke out in really bad hives and went to the er.they gave him prednisone 10mg and he started taking them.about 2 days into taking them he started having high fevers that were only at night.the er told him to stop taking the meds so he stopped.that day he got into a car accident and had a neck and back injury and put him on anti inflammatory,pain,and muscle relaxer meds.but he was still running a fever only at night along with back pain and some mild shortness of breath.also he started running a low body temp(96.7) and sweating only during the day.he started to look pale and a little yellowish(to me) but he is puerto rican but the whites in his eyes were fine.he went back to the er and his white blood cell count was normal but his heart and liver enzymes were slightly elevated so they kept him over night to evaluate him which went back to normal.they couldnt figure out why this happened or whats causing it along with running fevers only at night but no night sweats.the dr did ask him if he wanted a hiv and hep c test done which he agree to.we have to wait 5 days for the results and im so scared he has hiv or hep c!!!and i might have it even tho i have no symptoms.any thoughts or answers would really help.please im just so scared and worried!!!!thanks for your time.

Pearberr replied: "No and No. HIV can't be detected in Saliva, ever, unless you mix saliva with the actual virus. You produce a completely different anti-body in response to Hep than you do to HIV, so no."

Chronic cough and excessive mucous? I've had Asthma since I was 10 months old. In November, I was diagnosed with Bronchitis and Asthma Attack, due to chronic cough and excessive mucous. I was given the basic antibiotic and prednisone treatment and within 1 week I was feeling better. Well, in 1 months the chronic cough and excessive mucous came back. I was rediagnosed with bronchitis and asthma attack and give another antibiotic and another dose of prednisone. Well, since November this has been happening every month. Chronic cough and excessive mucous (which makes me feel like I'm closing up and difficulty breathing, the only way to clear it is to clear my throat and cough), always comes back and I'm alway rediagnosed with bronchitis and Asthma attack, and I'm always put back on antibiotic and another dose of prednisone. I always feel better within a week, but then it always comes back within a month. I do not believe this is reaccuring bronchitis and asthma attacks, I'm beginning to get scared. I am a 23 year old female with a history of Asthma, Myotonic Dystrophy Type 2, Sinusitis, Allergies, and a positive TB test. After the TB test turn positive, I had a chest x-ray done, which showed that I wasn't contagious. I have no symptoms such as fever, chills, or night sweats. The only thing I'm experiencing is chronic cought and excessive mucous which makes me feel like I'm closing up since November. There is a family history of Sarcoidosis. As for those of you who say go to the doctor, my husband and I are both without work and have no insurance. I am going to try and go to the doc, if I get to bad, this week; I'll just have to pay payments. We have no free health clinic in Greencastle Pa, so that's not an option either. I just want to know what some of you think this could possibly be. Thanks.

dee replied: "well from my understanding of things you may have an allergy to dairy its quite common in undiagnosed or treament resistant or recurrant coughs and upper respitary infections. due to the fact that u had a positive tb test a broad spectrum antibiotic may be needed but as for wat u can do u should look at ur diet and eliminate dairy or dairy products and see if that helps ofcourse along with watever ur doctor or healthcare provider prescribes. it may not necessarily be dairy but anything that you may or may not be allergic 2 that could be contributing to this"

Are these symptoms Wegener's? In November of 2002, my husband was selected to be deployed to the Gulf when it was discovered that someone with his expertise was needed. Due to the last minute nature of his selection, several inoculations were administered together in the fall of 2002. He immediately became very ill, and fluid was found to be in his lungs. Antibiotics were required due to bacterial infection. He was not deployed at that time due to the illness. A few weeks later, on February of 2003, he had been sick for three days and saw a physician. At that time, symptoms included headache, nasal drainage, cough, weakness/achy, nasal congestion and wheezing. He was again diagnosed with pneumonia. A few months later in December of 2003, he was again seen by his physician after being sick for four days. He had blood in his sputum due to oral lesions, nasal drainage, and chest symptoms and was diagnosed again with pneumonia. (Diagnosed with pneumonia 3 times in about a year). In September 2004, he was seen by his physician with symptoms involving lesions (spots) on both ankles. The lesions were misdiagnosed as spider bites and he was treated with prednisone and colchicine. He saw his physician on March 13, 2005 after being ill for six days. Symptoms included: cough, fever, nasal drainage, and chest symptoms. He was diagnosed with acute bronchitis. In 2005, we relocated. He saw a physician in November of 2005. Symptoms included: painful lesions that had developed on his legs, severe pain in joints in legs up to hips, swelling in left ankle, nausea, severe stomach cramps and flu-like symptoms (body aches, headaches and feverish sensations). All of this was preceded by bronchitis three weeks prior. Around the time the upper respiratory symptoms resolved, severe stomach cramps started and he believed he lost about twenty pounds in this time frame. Additional symptoms at that time included: significant decrease in energy, some intermittent dizziness during flu-like bouts, diminished urine output, course sounding breath, nosebleeds and discomfort in hands and shoulders. After seeing a rheumatologist, it was determined that he had purpura and intermittent abdominal pain consistent with an autoimmune (vasculitic) syndrome. He was prescribed prednisone which was very helpful at that time. On December 22, 2005, he was seen by a physician and had the following symptoms: chest filled with fluid, lots of clear phlegm, left foot felt asleep, right foot felt tingly. Most recently, in February of 2008, he experienced the onset of right extremity purpura again. Symptoms since February 2008 have included severe joint pain, recurrence of lesions, vision problems (blurred vision, burning, itching, painful eyes), bulging, painful and itching and very enlarged veins in hands and feet, hot flashes/night sweats, severe fatigue, nausea, numbness/tingling in extremities, numbness in upper spine and anterior scalp, muscle weakness (particularly the legs necessitating use of a stick to aid in walking and cant walk very far), mood and anxiety symptoms (depressed mood, hopelessness, suicidal ideation, loss of interest in activities, difficulty concentrating, short term memory loss, loss of appetite, weight loss and fatigue: for which he was prescribed an antidepressant), urinary problems (painful and difficult urination followed by milky discharge, severe pain in right testicle/groin area), migratory pain, insomnia, muscle twitches, new smaller red spots on legs and painful nasal lesions. During the last few months, he has had to take stronger and higher doses of pain medication to manage his pain. In August of 2008, his symptoms have significantly worsened, the prednisone has not been as helpful (currently 60 mg.), and he appears to meet criteria for the diagnosis of Wegeners granulomatosis, fatigue and neuropathy. (Differential: midline granuloma; upper airway malignancy; relapsing polychondritis; goodpastures; polyarteriis nodosa and other vasculitis). ANCA tests and kidney biopsy have not shown what they need for diagnosis to be definitive. They've tried tapering him off Pred. at least twice, but have to increase it again due to symptoms becoming much more severe. He wants to try Methotrexate or Cytotoxin, doctors want to taper him AGAIN. Unable to work at this point. Still trying to get a diagnosis and treatment. Some sinus issues on MRI.

Alex V replied: "That was very long. If you're in doubt, you can get a second opinion from another doctor. Diagnosis over the net isn't a good idea."

I am a 32 year old, up until recently, generally healthy female. Took a trip in Feb. to AZ and came back with? a cough.Then had some teeth pulled. They put me on amoxicilian,a steroid and pain killers. Then everything started falling a part. By day 3 on the meds I began to have swelling in my whole body. Day 4, I was like a round ball.Gained almost 20 pounds in water weight.So swollen the skin under my feet were cracking and bleeding.I began having extreme pain in the right side of my jaw.Went to the E.R,after calling the dentist he said I might be having an allergic reaction to meds. Never had a problem with penicillin before. The hospital kept me for 3 days. I.V. antibiotics and steroids.Tested my blood for everything from Lyme disease to Lupus to rheumatoid arthritis. They said I was now allergic to penicilan.All blood work came back normal. Extremely high white count though. Said I had some sort of infection.They sent me home with a months worth of Doxycyline and more pain meds. Went to reg. doc. they did more blood work came up empty,except for slight anemia,always had that though. Then I began with a weeks worth of prednisone,still on the Doxycyline, pain meds and sleeping pills. Still hadn't slept through the night for about two weeks. Now begining to get extreme fatigue,then developed night sweats and chills and more swelling and alot of pain. Went back to the doc for more blood work,still all normal. Then developed a painful red bumpy rash ONLY on chest and started coughing up blood.Not alot just dime sized every couple of days. Then getting dizzy and seeing white blurry spots sometimes. They sent me to the specilist,he came up with Valley Fever. Went for that blood work and cultures and also diabetic blood work. Now 2 weeks later the cultures haven't grown anything, all the blood work has come back normal and have had 2 more trips to the E.R, with all those symptoms and having chest pains,numbness and tingles in my left side of body only. Also having moments of forgetfullness. Everytime I have been to the E.R they did chest x-rays and blood work all kept telling me it was normal. Now on my last visit to the E.R they said I have pnuemonia.Last two chest x-rays were three days part. The first one they said was clear. They are sending me to a Pullminary doctor. Except for having mono in high school and a severe case of pnuemonia 2 years ago(hospitilized for a week) I have never been sick.I have not had fevers or weight loss. Though my appetite has decreased I am still gaining weight. I am only 5'2" and almost pushing 190 pounds. NOT normal for me. I am not pregnant,had four children then had my tubes tied. I do smoke but am trying to quit. Down to less a pack a day. Can anyone PLEASE PLEASE give me some ides. The doctors have told me they don't know what is wrong and only treating the symptoms and not the PROBLEM. I have a family history of Lupus,diabetes,heart disease. It all runs rampant through both my parents sides,,them included. Let me clear up any confusion. The first specialist I saw stopped all the steroids. As of right now I am taking only Naproxen for the joint swelling and pain killers. He is the one that thought I had this Valley Fever. But the cultures have come negative. They keep dumping me from Doc. to Doc. because of all my tests comming back negative. No one seems to know what is wrong. They are trying to handle only the sypmtoms and not the underlying problem. One says now I have pneumonia. I am not sure about that though. I had it two years ago and it isn't anything like that.

galadriel19823 replied: "could be a allergic reaction to steiroids,they shouldnt have put you on that. I know someone who had this same problem. I would stop the steiroids completely"

Jenn replied: "Could any of the medication throw off your test results for lupus? I think maybe some of you symptoms are a result of the lack of sleep or allergic reaction to the medications. Which is also throwing the doctors off. Can you think of anything you might have done/eaten that would have put you at risk of getting something while out there. What symptoms do you still have since you've been back, why did you have your teeth pulled. I would seek a second opinion, or fourth. I wouldn't stop any medication unless your doctor tells you otherwise."

George replied: "The last time I was on Amoxycillin it played havoc with my immune system. I was ill for weeks and weeks, and I felt awful. I couldn't sleep. It's quite a strong drug and I think the body becomes reliant on it, causing you to become ill when you stop taking it."

Best replied: "My doctor recommended me to use and it is showing me noticiable results."

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