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Suppress symptoms and conditions

Here are side effects posted by other members, that mention suppress.
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50 Side Effects posted for suppress

June 13th
2007
5:19 PM

Hi! I am a 36 year old female and have been on this HORRIBLE HORRIBLE drug (prednisone) for 2 1/2 years now..... Hopkins doctors still arent sure exactly what i have. My immune system is attacking my liver so to speak. My body is basically looking at my liver like it doesnt belong and is attacking it with large multiple lesions that is eating it away... the good thing is that it hasnt interupted the functioning of it yet but is leaving horrible scar tissue. I have been in and out of the hospital 13 times, have had just about every test imangable, 12 liver biopsies and they STILL have NO clue! They are leaning towards Church Straus desease and Wegners but the weird thing is i have half symptoms of both. The first year they had me on 80 mgs of prednisone a day which had seemed to put me in remission for about 4 months and then they came back even worse so i was put back on the prednisone, 80 mgs a day AGAIN along with 100 cc's of Methotrexate, another not so nice drug... i had EVERY SINGLE BAD SIDE EFFECT OF BOTH DRUGS!! This second time around was ALOT WORSE for some reason!!! My body DID NOT LIKE IT!! Nausea, hair loss, moon face, gained 40 pounds (and i was in great shape, worked out, i am 5'4 and was 110 pds!), EVERYTHING was swollen, legs, ankles, arms, neck, face, had the camel hump, fingers and especially my belly!!! UGH!!! Have bone, muscle, and SEVERE joint pain! Kaliedescope vision, dry eyes and then had mucus discharge (kindof like pinkeye), headaches, intestinal problems.... VERY CONSTIPATED and then the opposite!!! I literally felt as if i had turned into a man in my behind!!! Sorry to be so gross but thats how bad it was!!! Jaw problems, teeth and gums as well, skin sensitivity and have little bumps all over my skin (kindof like tiny little moles), itchy, broke out with acne and pretty much NEVER had more than 1 pimple a month, had facial hair (VERY DISGUSTING!!!! HAD IT WAXED EVERY WEEK!!!!) and then on top of all of that the swelling of my liver not to mention the PAIN! I was recently in the hospital again with 12 new lesions, pneumonia, and 104 fever. My doctors said the Methotrexate was the cause and i was having a bad reaction to it so they now have me on 100mgs per day of Azathiroprine. I am now finally down to a maintenance dose of 5 mgs of prednisone cause my body was starting to reject that as well. I thank god that i am now down to that dose!!!! It as only been 2 wks and the withdrawl symptoms are horrible worse then they were but i know what is to come =) loosing all this fluid and all of the HORRIBLE side effects i listed above. I will have to be on the maintenance dose of 5mgs the rest of my life and can live with that cause when my body gets back to somewhat normal i wont even notice that im on this CRAP!! I will be on the high dose of Azathiroprine for a few years and then on a maintenance dose of that as well for the rest of my life to keep whatever this is that i have under control.... the scary thing is is that they arent even sure that all of these meds will even work...... im a guinea pig..... The only thing that i am on out of all 25 pills/meds that i take everyday that works is my pain meds. Oh and i also forgot to mention that i had to be put on some "HEAD CASE" medication (thats what i call it =) ) for depression. Its a low dose but it does seem to help... I am terrified of what the future holds but continue to be strong and have an amazing support team... my fiance and family =) I dont even want to think about how i would be without them. I go back on the 25th of this month for my MRI so please who ever reads this keep me in your prayers as for all of you are in mine. I feel for each and everyone of you that has to endure this horrible drug everyday and i hope that everything works out you. =)

Sue =)

-- By sue36 | Reply | (5) replies | Private Message me

April 6th
2007
3:39 PM

All,
I've been taking Advair for 1 year. I'm on the smallest dose version 100/50 which you have to take twice a day. After a month of taking it, I starting to experience loss of voice and a skin fungus (discolorations patches) on my back and chest.

Advair pushes a steroid into your lungs to relax the muscles. After futher research, I discovered that the steriods actually surpress your immune system, leaving you more exposed to ailments that might be applicable to your body type, living environment and family history.

So, I started taking about 3000 mg of Vitamin C everyday. 1000 at breakfast, 1000 at lunch, 1000 before I go to bed.

It has helped with the skin fungus other physical ailments that otherwise, without a strong immune system, I would be suspectible to.

As for the loss of voice, I got off the advair for 1 week. My voice completely came back. Then decided to only take the Advair once a day, and only at night (I know you are not supposed to do that as per the prescription requirements, but I did it anyway). Typically when you get horse naturally, it takes sleeping over night (since your are not talking) to gradually recover your voice. So, I only take the advair a night, so any damage it would cost, my voice could recover too overnight, versus, taking it in the morning, and having to go to work, where I have to talk alot in my job.

I recommend you increase you Vitamin C intake, and do some research on the benefits of Magnesium supplement and it's positive effect in managing Asthma.

As always, remember to consult with your doctor about the supplements you want to take BEFORE you take them.

Good luck to all.

-- By price3322 | Reply | Private Message me


 

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