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Excercise symptoms and conditions

Here are side effects posted by other members, that mention excercise.
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200 Side Effects posted for excercise

September 1th
2009
12:37 PM

I was taking Zyrtec for the past 8 years and I am also on Antidepressants ( Effexor) and on Singulair. I had to stop taking the zyrtec 72 hrs prior to being re-tested for my allergies. I had done this once before and knew that the withdrawals were pretty intense, with itching so bad it made me want to go to the hospital. This time I looked up Zyrtec withdrawals and was shocked at the information I discovered. I stopped cold turkey and I am miserable with the itchiness. I also discovered that I don't get so short of breath( I run ) during my exercise. never going back on that stuff again. I still have allergies and get shots every 3 weeks but haven't had any problems not taking the zyrtec in relation to my allergies.

-- By sabine | Reply | Private Message me

August 27th
2009
10:15 AM

I took this poison 5 years ago and I'm still suffering the effects of it. PLEASE send it MEDWATCH reports so that they can get this off the market.
For all of you just starting your journey into hell, only time will help you. Take hot baths, don't over exercise ( you will tear tendons), change doctors tell everyone you know not to take any FLUOROQUINOLONE (LEVAQUIN, CIPRO, ETC.)

-- By helen950 | Reply | Private Message me

June 23th
2009
1:07 PM

Just like everyone else i had my mirena place at my 6 weeks appt in august 2008. After gaining 30lbs in 8 weeks i had it removed. I am 5'5" and usually weigh around 120lbs. Here i am 8 months later and i have only lost 8 lbs. I diet and exercise and i am depressed over the weight. I still feel exhausted and yet i wake up after 2 hours and lay there all night. i can't wait until my body is back to normal!

-- By mommyof4 | Reply | Private Message me

June 17th
2009
3:46 PM

I'm 15 years old and i've been taking prednisone for a few months, and from what i've read i'm on a really high dose. i was diagnosed with rheumatoid arthritis and another autoimmune disorder concerning my muscles at the same time. my doctor told me prednisone was my only choice; it was either that or i would lose the ability to walk. he told me there'd be side effects, but i had no idea it'd turn out like this or i would have fought harder for another course of action. i started out on 30mg twice a day, and since then was weaned down to 20mg twice a day and now i'm down to 30mg once a day. i've been looking up a bunch of information trying to figure out if there's a way to lessen the side effects or any hope at all that they will get better. apparently there isn't much. after reading a bunch of these stories i gotta say i'm not feeling great about this. i totally understand everything everyone is going through. i'm sure you can imagine what it's like being smack in the middle of high school with a huge puffy face, acne so bad on my face, chest, back, neck, and shoulders that wearing a bra could put me in tears, and mood swings so bad i've lost friends over it. everyone knows how brutal high school can be, where appearance and attitude are everything. and i try to tell my doctor about it and he literally looks at me like i'm a whiny teenager and says "you're just going to have to deal with it." and people like my mom and my closest friends don't get it either. nobody understands how beyond frustrating it is. i'll get into the worst moods and not have a reason for it, but i'll stay angry for hours or burst into tears over someone looking at me the wrong way. it'll get to the point where i have to isolate myself from other people because the abrubt mood changes get so bad. as bad as i hate to admit it, the pain from the arthritis is gone now and supposedly my muscles are doing better too. developing arthritis caused me to have to quit cheerleading, something i've loved doing for 6 years, because the pain got to the point where i couldn't get my arms above my head or bend my knees. however, i'd almost rather deal with the horrible joint pain than deal with the side effects of prednisone. if your doctor gives you and alternative method, take it. i've always been confident in the way i look and really outgoing and happy and now i sometimes catch myself thinking about suicide. that's shocking to me because i've got so much going for me, but this medicine makes me miserable. and when i complain about it, anyone i'm talking to just looks at me like i'm being a cry baby. my mom does too, she'll say things like "you just have to do this. i know it's not what you want but to be honest i'm sick of hearing you bitch about it."
i feel a little better knowing other people feel the same way - like nobody gets whats going on with them. the prednisone does give me days of really great euphoria and days when i feel like i could run a marathon, but waking up in the morning to the acne and huge face puts me to tears every day. i have to pee all the time, usually getting up at 2 or 3 am. i don't sleep well anymore and i do sweat all the time. which also sucks being a teenage girl. i'm always hungry, and when i eat i never feel full so i don't know when to stop. my neck and face have put on so much weight that when people see me in the halls or out and about they ask me what happened. mind you these are people i don't talk to, just ones i know from classes or whatever. and it's pretty bad when teenage boys i've never really talked to ask what happened to your face. kind of a blow to the ego, or whatever is left of it at this point.
i'd like to know if, as my dosage gets lowered, the side effects will diminish and when i'm off the prednisone completely if they will disappear altogether. any help there?
or if there is any way to help the acne or puffy face

my doctor just put me on something called methotrexate or something like that to help wean me off the prednisone, and does anyone know what those side effects will do? or if they'll affect the prednisone side effects?
i'm constantly obsessing over gaining weight and what my skin looks like and what i eat and how heavy my face feels and the occasional pressure in my eyes to the point where i just want to be put out of my misery.
and after reading other people's stories i really don't understand why this drug is still given out as freely as it is. but maybe all doctors are like mine, they just don't get it.
best of luck to anyone who's on prednisone, my heart goes out to you; i'm right there with you
sorry this became like a book it wasn't meant to be this long

-- By db1993 | Reply | (12) replies | Private Message me

May 18th
2009
7:35 PM

I have just started my son on Singulair about 1 1/2 weeks . ago. He is also on Allegra plus using the Nasonex. The allergist did warn about all the things that have been reported about this drug. We still decided to try it to see how he responds to it. The number one thing we have noticed is: it has really made a difference in him with his allergies for the good. As in all the things we have heard about behavior issues with others, we have seen an increase in his energy and hyperness but not enough to alarm us yet. We have decided to keep him on it until we see a difference that we feel he is in any kind of danger or anyone else. Hopefully this will not be the case, we all are just getting our exercise which we did prior with him anyways. I hope that a few more positive reports come in, taking any kind of drug you run the risk of side effects. I'm not a fan of taking them but right now they help my son breathe and enjoy being outside where kids should be playing and loving life.

-- By sherry68 | Reply | (2) replies | Private Message me

March 10th
2009
8:42 PM

***Update*** I have posted previously. I am now 6 weeks post removal of the IUD. I have had two normal periods 28 days apart. They were a little heavier than usual but other than that, very normal. All my symptoms are gone. And now that the weather will be getting nice soon, I will start my exercise and diet regime and see if THIS time I actually get results. I just cant wait to lose this weight!
OH, I just got a mammogram and had a normal one last year but this time, apparently something doesn't look right so I have to go back for another mammogram. As swollen and tender as my breasts were all year and as bad as we all got cycts on our ovaries from the Mirena, I wouldn't be surprised if whatever is showing up on the mammogram was caused by the Mirena as well!

Im so glad this thing is out. Hello hair (stopped falling out), hello sex life, hello energy, hello brain, etc.

-- By mrsbarrett | Reply | Private Message me

February 24th
2009
2:33 AM

I had open heart surgery August 23rd 2006 for a conginital heart defeat (Aortic Valve replaced with mechanical St Jude valve). I wanted a bio valve but Drs insisted I should have the mechanical valve because of my age (45 at the time).

Prior to my heart surgery I was a performer, singer/songwriter/actress/comedianne and I loved what I did. It was my life. Now, after 2+ years post-op and on Warfarin (7.5 mg daily for life) I feel like life has ended and I'm just a walking dead person. The effects I feel daily are as follows...

Dizziness
Severe Headaches
Blurred vision
Memory Loss
Fatigue
Weight Gain
Trouble concentating
Fluttering effect in my head/ears- Hard to explain
Hair loss
Unexplained pains in chest & left side of my body
Unable to sleep well
Tiredness- even when I've done nothing to be tired for
Nausea
Gas & Diarrhea off and on
teeth pain- Like I've drank something very cold
feeling in my head similar to a brain freeze- like you ate ice cream too fast
Night bleeds in my month- wake up with a mouth full of blood daily
What do think, is that enough??

I'm going in tomorrow for a cat scan because the headaches have been so bad they feel I need to be checked for brain tumor and/or internal bleeding. When I tell the Drs I think this is due to Wafarin they pratically laugh in my face as if to say, "Silly silly woman, don't be foolish! We know whats best for you. Remember, we saved your life!" Really? Did you?!

I want nothing more than to get off this rat poison and regain my life, but to do so could mean a stroke or heart attack. I would go under the knife again to have the mechanical valve removed and replaced with a biological valve, but do you think my insurance company (Kieser) would pay for a "silly" thing like that? Right!

Welcome to the greatest country in the world!

I'm going to start a website to help people like us. I want your stories, please send me your info, together we might make a change, what can it hurt to try? Email me ******

B.

-- By beverly4help | Reply | (8) replies | Private Message me

November 10th
2008
11:47 PM

I am a 65 year old female taking 20mlg of lipitor for almost 10 years. All of a sudden I started having severe pain, shaking and weakness in the calf muscle. The pain is unbearable. Doctors after doctors including a cardiologist, rhoumatologist and internist don't know the reason. I have stopped lipitor for 3 days. I cry and pray to god to help me everyday. I cannot exercise which is my passion for many years. I am hoping the lipitor is the reason and not something else. I have to wait and see. But I suspect it is.
SR
I do have nausea, depression and low back pain and arthritis and frequent headaches.

-- By achoo44 | Reply | (5) replies | Private Message me

October 14th
2008
12:04 PM

I have been feeling most of these symptoms for a while but thought it was just in my head or that I was going through early menopause but I am only 38.
Immediately I gained weight in my stomach area which made me mad but I dealt with it. I have have really long periods where I used to have a 3 day period. Now I have anxiety and mood swings where I just feel like being mean. I hate how I am to my husband, mom and kids. I feel like I can't concentrate and I can't remember a conversation that I had 2 days ago. I really feel like I was deceived of all these bad side effects. I just called to have this bitch removed and the nurse said she has never heard of any bad side effects. I guess I am one of the unlucky ones. I also exercise and diet constantly and can't seem to lose the extra weight I put on. It's so frustrating when I try so hard.Now I am a little nervous about getting it taken out. I plan on taking a xanex b.c it hurt so bad when I had it put in! I also am a little nervous about what birth control to use next. I don't want to deal with hormones again. It's not worth it. Also the sex drive is very low for me. I really wish I would have seen this blog ahead of time. I would NEVER of had the mirena inserted and I wouldn't have wasted a year and a half of my life on being miserable!! I'm getting this removed 9am on Friday!!

-- By reallymad1 | Reply | (5) replies | Private Message me

September 20th
2008
1:58 AM

I was on Luvox since it became available in the United States;Over 12 years. I was prescribed Luvox mainly for my OCD and as the years passed, I noticed obvious emotional blunting, lethargy;Mind was in a fog, retarded ejaculation, the works.

Have slowly reduced dosage from 300 Mg/Dy to 100 Mg/Dy with INCREDIBLE RESULTS such as greater energy, weight loss, feeling less "detached" and "cold," SOME anger (harmless & intermittent), lucid thinking-NO change in OCD symptoms whatsoever. Less impotence-All positives.

Will soon begin taking Choline and other B-Vitamin supplements to ease the final stages of withdrawal from this highly addictive drug that thankfully has the shortest half life of the SSRIs.

Turns out that Luvox leaves the brain BEFORE it leaves some of the internal organs it "lingers" in before total clearance from the body.

Plan to deal with my OCD and severe depression with a combination of therapy;A serious attitude change, nutrition, SENSIBLE supplementation and exercise.

Will STAY on my Klonopin (2 1/2 Mg/Dy) because I have a phobic mindset RE: My panic attacks which the Klonopin has kept at bay for the most part.

ALL psychotropics, neuroleptics and other "mind candy" is toxic and usually only MASKS the symptoms, giving the illusion of "treating the symptoms" of a particular disorder (set of).

And for what its worth, I USED to be super-pro medication. Just too many bad side-effects from various medications, including Luvox over most of my life.

Plan on going off of the last 100 Mg of Luvox VERY, VERY SLOWLY;Don't need any "Seretonin rebound syndrome."

-- By dumbfounded | Reply | Private Message me

September 19th
2008
1:49 PM

This is unbelievable... i thought everything that's been wrong with me, has been in 'my head', sex drive, weight gain, fuzzy vision, mood swings...

I honestly think this should be taken off the market. I cannot believe everyone's comments about this contraception. I have taken the pill over the years, depo provera, and thought my mood swings were bad then, but what really is the kicker, is the sex drive, hot flashes and weight gain/bloating.

At 29 years old, i have never felt the way i've felt on this, i've been trying to explain to my boyfriend 'it's just me' !, now i realize why.
as for the weight gain, i have always been conscious of my diet and exercise. for the past two weeks i have especially been trying to lose weight, but to no avail. hot flashes, it's insane. Please after reading this, look for another form of birth control. This should never have been approved. I took it out immediately after reading other's comments.

-- By clee8 | Reply | (1) replies | Private Message me

September 13th
2008
12:30 PM

Prior to getting the Mirena IUD i was at a healthy weight for 40 with two kids. I followed a daily exercise routine and ate properly. I had the IUD placed and almost immediately started to gain weight. I have put on a very frustrating 35 lbs in the last year and a half. My exercise and eating have NOT changed. My mood has!!!! For the worse. I can not wait to get this horrible thing out of me.

-- By jojocoolmom | Reply | Private Message me

August 18th
2008
2:42 PM

What a Godsend this website is. I am a 48 year old female, and I have been taking Advair (the lowest dose) for about 2 months now, with steadily worstening side effects. Although I have to admit, my first dose of Advair was like a much need "breath of fresh air", the side effects are not worth it. In fact, I just got off the phone with my doctor, telling her I will no longer be taking the Advair. These were the side effects I have experienced: rapid heartbeat, rib pain, joint pain in my legs and fingers, loose bowels, and a noticeable change in weight / body shape. I have always been complimented on my tiny waist and flat stomach, but as of late I have noticed my waist size increasing, despite my usual exercise. In addition, the most serious and most disturbing side effects are insomnia and the onset of severe depression / anxiety / paranoia. I had issues with depression as a young woman in my 20's with anorexia, with no relapse until I began this medication. Yesterday, I had to pull over to a store parking lot to cry for no reason! If it were not for this website, I would have blamed myself for some sort of mental weakness or unhealthy thinking. Also, I have never experienced anxiety in my life, and while on this medication I have had several episodes of intense panic, where I was convinced I should immediately draft a last will and testament. My vision has been blurring in and out considerably, my voice sounds as if I have larynxitis daily, and I have also experienced profoundly increased thirst and urination. I have not had my blood pressure checked, but I feel like what must be an increase in this, as well. Lastly, the past few days I have noticed severe hair loss, which, until I read this website, I attributed to my recent dieting. (I have been desperately dieting and increasing exercise to try to regain my figure that this medication is apparently ruining. Until this time, I have weighed the same and had the same or stronger body than high school school (5'4'', 115 - 120 lbs.) God bless everyone who has contributed to this website to educate others about the horrors of this medication. My doctor wants to see me to "give me something else", but I am going look into alternative therapies (yoga, breathing exercises, teas, etc.) The comment that made the most sense on this website was the person who wrote "break up with your asthma...begin by taking a deep breath and telling yourself you no longer have asthma." Also, I have seen that God / Jesus can heal anything, so I am going to turn to Him in prayer instead of the doctors. After all, Who created our bodies to begin with? I will add you all to my prayers, and that God will help us all heal from this... both the asthma and the suffering created by Advair.

-- By vke | Reply | (1) replies | Private Message me

July 14th
2008
7:19 PM

IN RESPONSE TO THE PREVIOUS POST:

STAND UP FOR FELLOW WOMEN

Because this is exactly the type of thing M.D.s will feed you as they're pushing pills. "I used it myself, it worked great for me... it must be something with your lifestyle change... it can't possibly be the hormones!"

Isn't it lovely, how even female doctors can so inadvertently seek to compartmentalize what should be a free-thinking, myriad of personalities and body types?

Here is my reply:

"you: "...I have not gained any weight...of course I diet & exercise about 5 days a week....do those of you who have experienced weight gain exercise regularly?..."

The NuvaRing does not cause weight gain. That's absurd. There's only one way to gain weight (as your self proclaimed fit self must agree) and that is to take in more calories than you burn.

But, the hormones in the NuvaRing, however, DO cause appetite change, and DO cause dizziness associated with these changes if the "food" (for lack of a better word) the hormones causes one to "crave" is not consumed. As you can imagine, this messes with a work out routine.

Which leads me to this, SWEETHEART... I DO exercise regularly. I'm a healthy size 6, 140 lbs, 5' 8" I am 21 years old and graduating from the University of Pittsburgh. I have helped my friends and family with diet and exercise plans since I made the goal to become fit (I was not a healthy weight in high school). I run a mile every week, and work out at the gym every other day with a trainer.

First of all, why are you even on the "side effects" page if you're so happy with the product? There are ongoing investigations as we speak concerning NuvaRing related stroke and death, and incident reports are on the rise. I have always been a stickler for healthy sex lives, hormonal birth control that works in conjunction with a woman's body, and safe sex practices. Let me just give you my two cents: I assure you, I am as in touch with my body as I am in touch with my inner self. And I will not hesitate to let you know... that I KNOW when something's off. NuvaRing was great for me for a while (we're talking a good 8 months... how long have you had yours?)... but then it took over my life. I am not young and naive, I am not unfit or unhealthy, I don't smoke or mess with drugs and rarely drink, I am a not mentally unstable, nor do I have any unmentioned medical conditions. I'm glad that the NuvaRing works for you, but to begin a post so cheeky as to assume that those of us who have posted here are unnecessarily blaming hormones for our own unhealthy lifestyles is infuriating. You think everyone here hasn't considered that it may be "something else"? Something eating at us?

you: "ALL birth control effects everyone differently. I'm not saying this for everyone, but sometimes a lot of people like to blame certain actions & physical changes on something & maybe this is the case...for some people. I've been on the pill before & I always got off it b/c of weight gain....well, it was b/c I wasn't eating properly or exercising. I liked to blame my mood swings on the pill as well, but once I thought about it, I still had those before & after taking the pill."

The above paragraph you have written may have redeemed the post, were it not for your still underhanded tone in relation to the "healthy lifestyle" aspect or - as it seems - "theme" of your post. And, yes, I too know and understand depression and anxiety as it has personally affected me through its looming presence in and around immediate family members. Hormones can affect seratonin reuptake and such and do very much affect the mood in many instances.

So, if you are so certain that "some" of the women here blame their sorry unexercised asses on hormones, I will return the favor and say that perhaps it may be a good idea for YOU to look into cases of depression and anxiety as you are so SURE that the nervous system of your brain has not in any way been affected by hormones.

Thank you for placing the women here in such a pigeon hole! This is so easily a perfect example of something I'd hoped our society would work on... All of us are built differently, of different ages and gene pools... how can one expect a mass-produced commercial drug to work "as directed" to a world of unknowns?

It might be a good idea to examine your female conscience. But, I suppose that might be hard to do from the point of view of the interior of your ass."

-- By mtv6357 | Reply | Private Message me

July 14th
2008
11:04 AM

I cannot disagree with these negative postings more. I absolutely love the nuvaring. I have not gained any weight...of course I diet & exercise about 5 days a week....do those of you who have experienced weight gain exercise regularly? I have also had an INCREASE in my sex drive...I have been with my fiance for 5 years, and for the past 3 of those, I have had no sex drive whatsoever. I got on the ring & bam, it's there with a vengence...the only problem with that is that we're getting married in 2 weeks & I wanted to make it special & stop having sex a couple of months before the wedding...but I just can't get enough of it. I have dealt with depression & anxiety my entire 27 years of life, so if the nuvaring is causing that...it's not any worse than normal. The only side effects I've had is the discharge, (which yes, is very annoying) and tender breasts...but I can deal with that. Although I have noticed that I cry a bit easier...but I was always a crier as well. I cry when I'm mad, sad, happy...always have, so nope...guess that's not from the ring either. ALL birth control effects everyone differently. I'm not saying this for everyone, but sometimes a lot of people like to blame certain actions & physical changes on something & maybe this is the case...for some people. I've been on the pill before & I always got off it b/c of weight gain....well, it was b/c I wasn't eating properly or exercising. I liked to blame my mood swings on the pill as well, but once I thought about it, I still had those before & after taking the pill. The only reason I quit the pill was b/c it did give me acne. Anyway, just my thoughts....& I wanted to post something positive for the ring.

-- By lilyjaymes | Reply | (4) replies | Private Message me

May 27th
2008
5:24 AM

After reading this site I'm so ridiculously upset with my allergist. I was specifically told that the 100/50 dose of advair had such a small amount of steroid that it shouldn't have any adverse effects.
In the 5 months I've been taking advair I've gained 20 pounds, and I've been unable to lose even an ounce of it despite diet and exercise. After reading this page I decided to cut down to one dose a day, and magically I dropped 3 pounds. I'm going to my doctor tomorrow and just let him try to tell me that advair doesn't cause weight gain.
Oh also, I'd been feeling very down and depressed lately, and I'd even considered going to a psychologist. I just attributed my feelings to issues in my personal and work life. Well, as soon as a I cut down on the advair I went back to feeling like myself again. I hadn't even noticed how much I had changed until I suddenly felt a million times less irritable and able to smile and really laugh again.
I'm worried about just quitting the advair (I'm paranoid about side effects) but I feel so much better without it that I don't know if I can bring myself to take my next dose.
What a choice - breathe perfectly and be miserable or constantly suffer with asthma and not even be yourself.

-- By starshine3500 | Reply | Private Message me

May 17th
2008
2:07 AM

After having been floxed back in December, I am finally able to say I'm symptom free. The only permanent damage I have is a floater in my right eye. I'm grateful that I have it because it occurred on the third day of 750 mg levaquin and because of it I stopped immediately. I also had tinnitus, ruptured tendons in my ankle a torn rotator cuff. I had pain in my rib cage that felt like someone punched me in the lungs. I had an eczema like rash on my elbow, neck and back but that went away in a matter of days. I had a low grade fever and night sweats. I noticed real improvement at the four month mark (things were the worst at the 2 month mark) and now at nearly 6 months, I can say I've completely recovered. Make sure to eat organic meats, dairy, eggs and produce because they put fluouroquinolones in non-organic animals and once you've been floxed it only takes a small amount to cause a reaction. I also take supplements--a good multivitmin, extra C, Acai juice, glucosamine and chondroitin with ASU (to stave off the inevitable cartilage erosion) SAM-e and MSM. I'm able to do vigorous exercise with no ill effects and I'm sleeping well. I will not take any prescriptions nor will I trust any doctor unless it's a matter of life or death. As long as we continue to have a "for profit" health care system, our well being will be secondary to the obscene wealth gained by pharmaceutical companies and the entire health care industry. It truly is caveat emptor as long as we live in a country where corporate profits trump the public good.

-- By patty8865 | Reply | (1) replies | Private Message me

April 10th
2008
8:17 PM

UPDATE: Our nightmare with SINGULAIR has not ended! After reading "conerned citizens" report discussing the possiblility of Singulair causing asthma blew me away. My son was put on this drug for food allergies not asthma b/c they thought of his two anaphylaxsis episodes in 5 days. 1 food related the other unknown (maybe outdoor mold?) He had no prior issues with breathing.

He has been off of it for almost 2 weeks however over the last week he has slowly developed some breathing issues. After getting off of it, he still has his ear infection from the second day of being on it and last Friday after playing some basketball began to seem like he was winded so I brought him in. He was having trouble breathing. I called the Dr. and he said it could be excercised induced asthma. He is a very active boy who runs non stop and has NEVER had breathing issues before Singulair! It seemed to pass after a few hours. The next fews days he coughed a few times when playing and I thought what the heck is happening to him. Monday at school they didn't go outside so he was fine b/c he didn't run around. Tuesday, they came to get me b/c he was having trouble breathing and one of his teachers whose son has asthma said I think you better give him an inhaler. I called the Dr. ASAP and he approved us to borrow another child's. He freaked out and wouldn't let us give it to him. After 2 epi-shots in the previous weeks, he wanted nothing to do with that. At school the next day, we made him take the inhaler if he wanted to go out to playso he did. He didn't cough but a few times. No excercise at all. Then last night, he got really bad. He started to cough and couldn't stop to the point of gaging and it seemed as though he had developed a ton of phlem and kept trying to swallow. We ended up in the ER where we were told that he has asthma! I am so furious! I don't get this at all! If this report is accurate and my son got asthma by going on it - this will be devastating. We kept him home today from school and took him into the Dr. b/c he continued to cough all night. He is now on Flovent, Albuterol and has an enebulizer. I'm probably the only one of all of us who child did not have asthma to begin with.

Has anyone who did not have asthma before singulair now have any issues? Please let me know!

-- By njcukett | Reply | (7) replies | Private Message me

January 3th
2008
2:44 AM

Shortness of breath after mild exercise

-- By ericc | Reply | Private Message me

December 11th
2007
1:16 PM

I read up on Lupron and was very hesitant in taking the shot, However, my doctor convinced me that it would be helpful with my Endo which is a stage 4. My doctor said well any medicine is like a restaurant if the side effects are bad then everyone knows just like if you get bad service.
Well I got my first shot about a month ago and I think I should have listened to myself, I traded one pain for a ton of others.
I have severe depression at times and the bone pain is almost more than I can bare. I live on Advil to keep the pain under control. I can barely get out of bed in the morning b/c I hurt so bad and I can barely walk. I am losing hair and it is thinning out horribly. I too have put on weight with regular exercise and watching my diet.
I get heart palpitations to where my heart feels like it is going to jump out of my chest and this is the first month. I am afraid of what the next month will bring. I am only 35 and didn't want to get a hysterectomy.

-- By hineyone | Reply | (2) replies | Private Message me

November 30th
2007
6:08 PM

I have been on Lupron Depot for a year and a half, and it has been terrible. I am a stage 3 endometriosis patient; I was diagnosed last year on my first day of school. They did a laparoscopy, D&C, and cystoscopy. I have experienced nausea, weight gain, mood swings, paranoia, night sweats, hot flashes, dizziness and have had to be hauled out of school in a wheelchair on many occasions. This is all while on Lupron Depot. It has barely taken my pain away, but I will say that at first it worked amazingly. I don't know if my system is just immune to it now, or what. I had to leave school today because of chest pain and my pulse was 111 bpm. Before I started Lupron, I was told that I "may experience some mild hot flashes at first, if anything." The hot flashes are absolutely brutal. I went from being a straight A student to barely scraping by, trying to get weeks of makeup work done. I have always been a sane, calm person, but when i went on Lupron, after about a month also had to go on Prozac because I was so incredibly paranoid and mood-swingy. I also went from a size 2 to a size 7 in about 2 months! I exercise regularly, I ride my horse everyday, and I eat right. I've always been in shape, but Lupron made me gain so much weight!!! I wouldn't recommend Lupron, but I don't really see what other choice there is, since they have already tried the pill and that stopped working after about a month. I'm so frustrated, and I can't take it anymore! Menopause and pain from endo are making me miss my life. I can never go out, I always have to call in to work, and I haven't been in school consistently for about a month.

To anyone considering going on Lupron Depot, I would think long and hard about whether you are ready to deal with the side effects of Lupron.

-- By joiedevie128 | Reply | Private Message me

October 30th
2007
12:23 PM

I have been on Lamictal for almost a year now and everything seemed to go okay until almost three weeks ago when I had to increase my dosage from 100 to 150mg and my Lexapro to 15mg. In the last couple of weeks, I have gained 7 pounds and I am really depressed. I have an eating disorder (bulimia) and because of this, I profusely purge my food in fear of gaining a dramatic amount of weight again. I am going to see my psychiatrist next week because all of this is going to cause me to crash.

-- By leaforever32 | Reply | (4) replies | Private Message me

October 24th
2007
7:06 PM

I have been on the pill for about 2 and half weeks, before I was on Ortho Tri Cyclyn. I swiched bc on the other pill i started to develope craps again. I have recently notice that my fingers have been swelling up, and my stomach looks like I just ate a thanksgiving dinner..i started to research the pill and now i am freakng out bc i think it might be bc of the pill. I have just started to excercise more bc of my feeling of being bloated. Now after reading all of your coments i am freaking out even more bc i am a college cheerleader and i connot have a 5 or 10 pound weight gain! WHAT SHOULD I DO?

-- By haleyb1 | Reply | Private Message me

October 17th
2007
9:28 AM

I was on Paxil for about a year and have stopped taking Paxil about 5 months ago. I had to stop taking it because I do not have health coverage BUT my main reason is because i've been depressed and have fought anxiety my entire life and I do not want to be medicated my entire life. I did it for one year, it worked somewhat but coming off of was hell, but I feel that I want to fight my anxiety and depression with God and myself, not any drug, I excercise more now and EVERYDAYYYY! is a struggle! I feel droopy still from the after effects of paxil, im not doing well in college because I have a hard time concentrating, my eyes are always glossy, im nervous in large crowds (going to the groceery store is HUGE for me) and I feel like Ive done something to deserve this. But I know it is a battle that I need to overcome without a drug, I understand some people need to take it, but as for me, I may be struggling in school or feel tired all the time but if I have to struggle and fight through, I want to do it!

Another thing, I soemtimes feel alone when it comes to talking about anxiety and depression and being medicated on Paxil. It is sooooo NICE to write to other people and hear there stories. It makes me feel sooooo much better. THANK-YOU! God Bless!

-- By kristenhop | Reply | (1) replies | Private Message me

October 8th
2007
12:18 PM

I am a 45 year old and in August of 2007 I was given this medication as to
an alternative of the expensive blood pressure medications I was taking at
first. However, after a week on this medicine I began to notice some changes
in my sleep, and I had gotten a dry cough (which I still have) and when I would try and excercise and walk, I became real short of breath and very
weak after each incident. I had another episode on Saturday, October 6 and this one was worse to the point that I just could not catch my breath right away and now I have read these experiences from other people who are on
the same medication as I am and it very scary to know that something that is
suppose to help you is really causing your problems. How is it that?

-- By elleanor1 | Reply | Private Message me


 

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