35 years symptoms and conditions

Took Yaz years ago for some months. Do not remember many side effects. Starting taking it in July 2009 and within 2 weeks was hospitalized with pulmonary embolisms in both lung. Which means blood clots in both lungs. Doctor's could not find any other reason than Yaz. Please DO NOT TAKE THIS DRUG. I was a healthy 37 year old with not history of clotting disorders and now I have to have see a hematologist, pulmonologist and take Coumadin for the next 6-9 months. I never thought that a medicine could destroy me in as little of a time as 2 weeks. I thank God for getting me through it and am writing to warn any future users. Don't take this med.

Hi All, we definitely need a lawsuit. I am finally my old self again after 2 years of hell. My nose shut down after moving into my new house 2 years ago. Went to a local clinic here. My Dr. gave me the Kenalog shot for "inflammation", she did not tell that it was a steroid. I am allergic to steroids. I was suicidal, depressed, had a breakdown, lost 10 lbs. in one week from not eating. Menstrual cycle went from 3 days for 35+# years to every other week for 7 days. OMG, I went thru 2 years of sheer hell. Finally had to have a partial hysterectomy this past May I AM SO ME AGAIN! WE NEED A LAWSUIT against Bristol Meyers. Thank God my husband was beside me, or we would have divorced. Poor Guy.

I am 35 years old and I have high blood pressure. I am taking Inderal and Lisinopril. I have been taking Lisinopril for about a year now. I have had a cough for almost a year now. Have had chest x-rays and ct scans that show nothing is wrong. I was taken off of Lisinopril and put on Diavan but my feet and ankles were swelling so I went back to Lisinopril .
I still have cough, dizziness, light headed, hot flashes, fatigue, weakness and chest pain. I cannot go to the grocery without everyone staring at me coughing and the people at work are getting annoyed with it. I cough to the point where I vomit. My doctor has sent me to a specialist for acid reflux and has even went as far as telling me I have sinus or allergy problems. I will be going back to the doctor next so I will be suggesting being taken off of this drug and put on something else. Thank you to everyone on here. Everyone thinks that I am crazy because I am only 35 and I have all of these symptoms but no one knows what is wrong with me.

My 17 yr old son was prescribed Prednisone along with Accutane for Acne. His two older brothers had undergone accutane treatment when they were each 17 ish, with no major side effects - no mental disorders at all. They did not have Prednisone along with the accutane. I questioned why my youngest son should go on the prednisone but was assured by my trusted dr. of 35 years that his very low dose of 20mg a day would be no problem. We continued the dosage for 3 months and then tapered off for 3 weeks. That's when my son's trouble began. He felt a change immediately - things didn't seem 'real', he has a hard time describing the feelings. At two weeks after discontinuing the prednisone his symptoms really began to be very frightening. He is athletic and was vomiting for extended periods - probably due to the stress of what was going on in his head. We then saw 2 GPs, his Dermatologist and I contacted a Psychiatrist, His father and I didn't want him to progress to antidepressants and he does seem to be improving - nothing like some of the other stories contained here. I just wish we had NEVER gone on this - even at 20mg - for something like acne. NOT life threatening - I should have listened to my gut and just stuck with the Accutane.

Hi Ladies, like all of you I too have my share of Mirena issues. I have had my IUD in since March 2008, so a year & four months now. To start with the positive- I do not get periods. I haven't had a period starting the following month I had it put in. Now for all the Negatives- Bad Acne and usually I have great skin. Not anymore. They are more like red bumps mainly on my forehead, Constant migraines, mood swings, constantly stressed, pain in my lower abdomen, lower back pain (Doctors thought I had a kidney infection- all urine, blood tests, pelvin ultrasound, CAT scan were normal), constant urinating & cannot hold my urine (like a bad UTI), I have noticed when I comb my hair after washing it, I am losing a lot of hair, I get a lot of dizzy spells all the time, painful cramps in my legs, fluttering in my stomach (like a baby moving/kicking- I thought I was pregnant), I have a lot of discharge- I will be walking a big gush just comes out, my sex drive is barely there- I am in my 20's and just about every time I have sex with my husband I will just go dry in the middle of it & just about every position hurts, I have very itchy skin now. I am always scratching especially my legs. I am always applying lotion to help with the itching, I also developed a ganglion cyst in my hand next to my wrist. It was so painful my hands would swell, numbness & tingling in my fingers, pain in my forearm, I just had a needle aspiration done a few days ago. Now that I have confirmed the side effects with this site, as soon as my doctor's office opens I am calling to have this trash removed!!! Thank you Ladies.

I've been on lipitor and other generic forms of it for the last 8 years since the age of 26. I started on 10mg then 20mg and later 40mg. About 4 years ago I started with severe stomach cramps. The pain is so bad that I have to go home in the middle of the day, I can't walk or sit straight the pain is that bad and NOTHING helps. On a scale of 1 to 10 I would probably put this at a 7 or 8. I would also be nauseous and be really tired. I have had countless opinions and tests done and doctors keep telling me it is an "enigma" and there's nothing wrong with me. We've treated it through coeliac diet, exercise, lots of water, but it never helped. About a week ago I stopped drinking my meds by pure chance. I have not had one incidence of stomach ache. My doctor tells me that it's not possible for the lipitor to be the cause. I am sure he's wrong. Has anyone had a similar experience?

I have been on prednisone since I was two years old (I am now sixteen) because I have Autoimmune Hepatitis IIa. I would like to point out that there is still a life worth living being on prednisone, maybe I say this because I do not know life without it, but at least we're alive! Last year I had a flare up of the AIH and had to 6x my dose of prednisone. It sent me into a spiraling depression of constant sleep, crying, hopelessness etc....but I made it through. Just PLEASE keep hope that things would get better, because I know what it's like being on the dreaded drug better than most.

I was started on Advair HFA about 35 days ago. A little background about me is that I'm 35 years old, in good physical shape. I'm a competitive cyclists doing road races anywhere from 45-100 miles, I work out 2-4 hours everyday. I've had lifelong chronic asthma, but have fought the disease with my healthy lifestyle. I also play the saxophone.

Since I've been on Advair I've developed a constant sore throat. Been coughing up stuff constantly when I'm out training on my bike. Can't seem to sleep for more than a few hours at a time. The worst side affect has been the leg cramps which are killing my training for up coming races. I have constant leg cramps that force me to get out of bed over and over to work them out. My energy levels have dropped to the point that I can't do even half a workout without being totally wiped out. This is coming from a guy that averages 60miles a day on the bike, the other day I couldn't even do 15 miles and had to stop from the constant cramps and tiredness. This stuff is a nightmare. I've gone back to using nothing but my albuterol inhaler. I'll continue to do lung exercises 4 times a day and completely clean up my diet and basically get this stuff out of my system. Let this be a warning that you can't get something positive without something negative as well.

My husband, a 55 year old diabetic who is currently on dialysis was initially prescribed 20 mg Lipitor about 5 years ago. He began experiencing leg pains, but continued to take the drug. In May 2007 in suffered a minor stroke (clot). Upon release from the hospital, the neurologist prescribed an 80 mg dose claiming studies showed those who have had a stroke benefit from the higher dosage. He recovered from the stroke and was able to return to work in August 2007. On December 31, 2007 he suffered another stroke, however this time it was a full blown cerebral hemorrhage. After he suffered this stroke, I searched Lipitor on the web and to my surprise found an article that stated the higher dosage of Lipitor could cause brain bleeds in people who have suffered a prior stroke. I truly believe this high dosage of Lipitor was the cause, however the neurologist and his regular doctor say no. Of course they would say that, since they are the ones who put him on it in the first place. They blame it on the fact that he has other health issues, however he has been on dialysis since the beginning of 2004 and was able to work and function normally. Needless to say, when he was released from the hospital, Lipitor was no longer one of his prescribed medications. They wanted to prescribe a low dose statin of a different brand, but his cholesterol levels have been excellent without them and I won't let him take another statin. The damage is done, he has difficulty walking, has lost his balance and was forced to go on permanent disbility. He was an active volunteer fire fighter for 35+ years and the fact that he can no longer do all the things he use to do depresses him.

I had Mirena inserted in 2007 due to a lack of tolerance to birth control pills. The experience was very painful for me. However, the doctor explained that the initial insertion process is different for every woman as we are not all designed the same. My cervix/uterus is oddly positioned. According to the doctor they are "crooked". As a result, the doctor had a difficult time properly inserting the mirena, which in turn resulted in major pain! But, this was just my personal experience. Not every woman will encounter this difficulty. However, I would recommend taking at least 2 ibuprofen before the procedure. Throughout the past 2 years, I have experienced a range of symptoms. Major depression, severe mood swings, acne, lack of energy, excruciating lower back pain which mocked mild labor pains, and the overall inability to function normally. I begged the Doctor to remove the Mirena 6 months ago, but she convinced me otherwise considering I cannot tolerate birth control pills either. Nevertheless, I am 35 years old, have one child already, and do not plan on having more. Well, last week, I was basically confined to my bed due to excruciating lower back pain, and severe bleeding. I called the Doctor, and they finally saw me today. I insisted on having the Mirena removed once and for all, and already feel 100% better just 12 hours later! The purpose of my message is not to discourage anyone, as we all have different levels of tolerance when it comes to pain, medications, etc.....Yet, I felt compelled to share my personal experience as it was not a positive one for me! The only "positive" symptom I obtained from the Mirena was a lack of periods. Unfortunately, there was a downfall to that as well. Due to a lack of a regular menstrual cycle, I felt extremely bloated, and had difficulty losing weight despite working out 5 days a week, and eating a proper diet. I sympathize with each and every one of you, and appreciate your efforts in sharing your experiences. Upon stumbling upon this website a few days ago, I finally found the courage to have this thing removed so I can once again "feel normal!" Good luck to all of you!

I have been on Toprol-XL (BRAND) for 3 months. I took the generic for 2 months with no change in BP so I requested the brand name. I found your website by surfing the web looking for answers to my complaints. I have weight gain, vivid violent dreams, extreme fatigue, my breathing is slow and I am just dragging around in a fog. I felt better when my BP was high and I didn't take all this medication. Currently, I am taking first, Lisinopril, then added Toprol XL AND then added Clonidine. My BP is still not properly controlled. I am going to the doctor today to have my medication changed. Thank you for sharing your comments.

This post is directed to anyone who has contacted me regarding a possible class action lawsuit, which I was trying to initiate, as stated in my Oct 17th, 2008 post.
After contacting as many as 10 law firms, from NY to San Francisco, I have virtually "thrown in the towel". In essence, what they are saying is, this will be too expensive to litigate. The pharmaceutical companies have "teams" of lawyers, and I believe they are reluctant to go up against them.
I find it diabolical that this drug Kenalog is causing so much suffering, some emotional, some esthetic and some, like myself, sheer physical pain...but nothing can be done about it.
For all of you who have emailed me and I was unable to return your ems, I apologize....but I have been waiting to hear something positive feedback to relay. Unfortunately, that was not the case. If anything does develop I have stored your information and will get back to you. I would hope you would do the same.

On October 18, 2007 I started taking Symbicort. It worked GREAT!! As far as breathing better. About a week later I noticed upper back pain, dizziness, and nausea. I continued to take this inhaler. Then on November 5, 2007 I was rushed to the emergency room with a collapsed lung. (Spontaneous Pneumothorax) Still even after surgery I continued to use this inhaler until June 2008. When I finally thought may be it was this inhaler. I don't know to this day. I still feel strange from time to time. At the time of surgery I was only 35 years old.

I am scared to death after reading what everyone is going through. I was put on Levaquin for 10 days and got to day 9. My joints ached so bad I thought I had arthritis, and even had my Dr. do blood tests for it (I had no idea it was the Levaquin). I am only 35 years old and never worried about arthritis before this. Also, within 5 days I started developing hives all over. Again, I was stupid and didn't realize until day 9 that the hives were because of this med. I told my Dr. and he told me to stop taking it which of course I did. I assumed the hives would go away after the med was out of my system. But a week later the hives were unbearable. I was put on prednisone (another issue altogether) and that helped the itching, but now every time I try to go off or back off the prednisone the hives come back- and they are terrible! Now my Dr. thinks the hives were from something else because there is no way that the Levaquin is still in my body. But after reading what other people are going through on this med, I am convinced this stuff is as everyone says- POISON!! I am so worried about the joint and hip pain that was so bad I couldn't stand for long without excruciating pain in my right hip. It felt like I had a one hundred pound weight just sitting on it. And my hands were the worst. I have a newborn and could barely pick him up without worry that I'd drop him. I don't know what to do.. Is there anything to do?? I'm still on the prednisone, and have been for a month. I need to get off of it but every time I do I itch so bad with the hives that I cannot function. Also because of the prednisone I noticed last night that I am getting "moon face" my face is swelling up and there are a million side effects from that drug too. How long does this last? Has anyone else fought the hives that come with this? Please help me, I am so scared!

I had my thyroid removed because of cancer. I was 18 years old. At that time, I was put on Armour thyroid because that was the only thing available. I am now 56. Somewhere along the line they figured out how to make chemical thyroid and of course I was put on it - for the next 35 years. Blood checked so many times I can't remember, dosages changed. Always a runny nose, hot and cold always a problem. I drink something hot and I start sweating, I drink something with ice and I get the chills. Back on Armour now - not the absolute best - but certainly much better than synthroid! Still what do you do when you have no thyroid? Also to let you all know, after the thyroid was removed I was treated with Radioactive Iodine, and told that I probably could not have children. Well, I am stubborn - I have three boys - had them at ages 23, 25 and 37! Many, many problems through the years ( oh yeah, the radiation treatment that I had at 1 month old fried my thymus as well as starting the cancer - it took 17 years for the cancer to develop. It was only after all this that they began to find out the you really did need a thymus too. Oh well, I could go on and on. So find me a solution to my thyroid that is gone. Can we regrow it like they are regrowing ears, fingers, etc?? Something to look into for the medical profession...

I am 35 years old and recently have had a string of ovarian cysts, which did not disappear at the end of my regular menstrual cycle. After three menstrual cycles and continued cysts, my gynecologist recommended I go on birth control to rid myself of the cysts. As I had tried Loestrin in the past and disliked it, she thought I might appreciate a low estrogen solution and not a pill. She recommended the NuvaRing.

I started taking it 7 days ago. By the 4th day, I felt I had a yeast infection. By the 5th day, I was in such pain I could no longer walk. I felt itching inside and out, as well as incredible burning. My vagina is so swollen, I cannot wipe myself with toilet paper or dry myself with a towel after showering. I took it out on the 7th day and almost within 2 hours I felt the burning stop. The following day the swelling started to lessen. I can walk now, but the itching and inflammation may take some more time to go away. It is clear with my sudden improvement that the NuvaRing was the culprit.

If you experience burning, itching and swollen privates- STOP taking it!

on aug. 11, 2007 i quit smoking after 35 years. i had a massive heart attack. was on patch in hospital. dr. put me on chantix on aug. 14. for some reason i needed only half a dose. at 3 weeks i asked cardiologist if i could stop taking since i felt i didn't need it. said no 2 more weeks cause he was concerned about the stress on my heart. so i stopped using 2 weeks later which made me on the drug 5 weeks. was great! the strangest thing i got from it is ever since taking it, smoke smells horrible. i mean worse than anything i have ever smelled! it continues to this day. great side effect! no way i would start smoking again. i can't stand being around anyone that has been smoking. lost some friends over it. drug was great for me. only problem-- i have very good insurance and chantix for 1 month was $100. a little pricey but worth it. others have told me if you stay on it 2 months full dosage is when you develop dreams and etc.

i'm 35 years old and started taking yaz one month ago. i have felt as if i have had PMS for one month straight! i have spotted or bled the entire month, have been extremely moody with my husband and children, my breasts have grown by a full cup size (and no, i'm not happy with this development), i've gained about 5 pounds (all i want to eat is Christmas cookies all the time!), and headaches. i have never been on the pill before and thought i might try yaz for pms and acne. my skin does look better, but it's not worth my sanity!

I have been on prednisone continuously now for 15 years. I was put on it in March of 1995 for a lung condition called chronic eosinophilic pneumonia. I was 122 pounds when I first started prednisone. Now 15 years later I am 197 pounds. I am 35 years old with osteoporosis. I have dealt with depression, terrible headaches, stomach ulcers, hormonal imbalance, hair loss, swollen feet and ankles, I now wear glasses when I didn't before, I have thin skin now that looks older than my 35 years, I deal with night sweats, and in the summer out in the heat my very round moon face turns red as a beet. But, no one can get me off the prednisone. I have seen many specialists, and within 1-2 days of starting to wean past 10mg I get so sick I have to be hospitalized, I literally can't breathe or live without it. I hate this stuff and what its done to me, but I have no choice but to take it or I will die. Doctors have tried alternate medications, nothing but prednisone works. If there is ANYONE who has had to be on it as long as I have or have had success in getting off it after being on it for so long, I would love to hear from you.

I am 21 years old. I have been taking Yasmin for 3 years with no problems. For the last two months I have used the generic brand of Yasmin. My breast size has increased, I feel bloated and have put on weight. Nothing else has changed. I exercise 6 days a week and eat the same. I have stopped taking Yasmin. Has anyone stopped taking it and lost the weight and if yes how long did it take?

I am 35 years old and I was put on Methylpred 4 mg for an allergic reaction to Sulfamethoxazole (septra). I broke out in bad red spots from head to toe. My doctor prescribed this medication for the reaction. I took the last of my 2nd day pills. Two hours later I woke from bed with a painful burn in the bottom of my feet and palms of my hands. It then went to my legs which I took a luke warm shower to see if that would help. I then continued to ad aveeno cream an didn't work, it then started to go through my body in 10-15 minute intervals in different parts of my body. Now when I itch it feels like I'm burning. I can't eat anything cause I have the taste of this pill in my system. This is the only side effect that I have been having with this medication. I noticed today the 3rd day of my pills that the red spots are starting to get lighter. I will never take this pill ever again.

I am 35 years old and I live in Jacksonville, NC. Five days ago I was prescribed Levaquin for a serious sinus infection. After taking the first pill, I kept telling my husband I felt weird. Like I was numb. This was Saturday. By Monday I had no feeling in my face, no sense of smell or taste. It was horrible. By Monday eve my heart was pounding. I felt like it was coming out of my chest. I was so dizzy and I found it hard to concentrate. I woke up Wed. morning telling my husband I felt weird. I felt like I couldn't move my eyes and I couldn't feel the left side of my body. My lip on the upper right was swollen with blisters. Not to mention they were so dry because it seemed like no matter how much I was drinking I could never stay hydrated. By lunchtime Wed my left side of my body became very hot to where I was actually sweating under my armpit on the left side and my right side was cold. My heart began to race very badly, I became very dizzy, I felt like I couldn't breathe, my throat felt like it was swelling up and I couldn't swallow, then I started to shake uncontrollably, my body broke out in the horrible hives/rash. My blood pressure soared to 198/109 my pulse was 148. Then everything went black and I lost conscious. When I woke I was told I was unconscious for nearly three hours and that they injected me straight in the neck with epinephrine and injected me in my arm with 50 cc of Benadryl. They told me that they believe I suffered a serious reaction from Levaquin. It is the day after, cant even go to work, so weak and have the worst case of diarrhea you could possibly imagine. I was not even aware that the FDA put a black box warning on this drug. Meaning it is the worst warning you can have without removing it off the market. What the hell is wrong with these doctors? Why the hell would you keep giving that poison to us if you know it has such severe reactions. I am a mother of five and yesterday I thought my kids were going to be without a mother, that is how bad it was. I still have the bouts of paranoia and swear I am seeing things. My mind is a blur to most of yesterday. I still have no feeling on the left side of my body, or my face. I still cant taste or smell anything either. I am having bouts of dizziness and anxiety. I only consumed four of the 750 mg tablets, they gave me seven. They have prescribed me a different antibiotic, however because of yesterday, I am petrified of taking any medications, even Tylenol.

I AM PREDIABETIC...TYPE 2 - FASTING GLUCOSE OF 112-120 OVER THE LAST 10 YEARS. I HAVE WORKED NIGHTS FOR THE LAST 35 YEARS SO MY EATING HABITS ARE OUT OF WACK. MY HEALTH CARE PROVIDED PUT ME ON METFORMIN 850 MG 2X DAILY AS A PRECAUTION TO KEEP MY GLUCOSE LEVELS THE SAME OR LOWER. I DO NOT HAVE ANY SIDE EFFECTS PER SAY, BUT IS THIS MED SAFE FOR ME??? HAVE NOT FELT ANY SIDE EFFECTS BUT WOULD LIKE TO KNOW, ARE THEIR ALTERNATIVES FOR ME??
THANKS

I just realized I am not alone.... what a trip! Birth control. I think I have tried a lot of things in the market, pill, injections, IUD, NUVARING; I am 35 years old and I am exhausted of this never ending pregnancy avoidance. But it is inevitable. I want to live my life the way it is.
I have used Nuvaring for over a year now, and it has successfully helped me avoid pregnancy, however, in the last couple of months I have had an increase in the frequency of the migraines accompanied by weakness, shakiness and deep emotional struggles. I get super irritable, or super sad; which is not very normal for me, I am somewhat balanced, I have noticed this marked mood swings around the times of my migraines. I am just exhausted, because I am intolerant to higher levels of hormones and also intolerant to latex. My boyfriend said we should just be "natural", but I think that would just make me more scared than anything else.
Another side effect is that sex is somewhat painful sometimes, I enjoy sex more on my week off the ring, it might be psychological, but I think it is also physiological.
Oh, well, I am glad I am not alone, I am going to talk to my doctor about it. I just want to be at peace with this.

I just started Toprol XL on Friday (four full days ago). I was put on it to decrease heart rate and palps, I have Inappropriate Sinus Tachycardia. I am 35 years old. I was prescribed to take 50mg twice a day, and I am on the generic. Almost immediately, stomach upset started with diarrhea. I still had some palps at 25 mg. twice a day, which the MD told me to start with for about two days. So, after doing the 25mg for two days twice daily, I went on to the 50mg twice daily. Last night I slept for twelve hours straight, and then felt like I had a sedative after I got up. After taking my next 50mg dose this morning, I got so sleepy again, and felt like sleeping and was in a fog after the twelve hours of sleep last night! I can't imagine mixing anything else with it that causes drowsiness, you would pass out. I feel like I can't think clearly,and feel more crabby and irritable. I called the MD this am. and was told to go back to 25mg twice a day, and that side effects would lessen over time. I have had this sinus tachycardia problem for years, and got diagnosed with it officially in 04. It is very annoying, with shortness of breath, pounding heart,and feeling like you are running a race which sitting still. I have also had an increase in feeling like it skips a beat. All this prompted the Toprol usage. It does help the heart rate and palps, but now I feel so tired I can hardly put one foot in front of the other. I try to walk for thirty min. at least five days a week, and today it was all I could do to make it. I have to watch my twenty month old daily, and I can't keep up with his energy now for sure. I plant to go back to the 25mg twice a day starting tomorrow, and maybe eventually get to the 25mg once daily. I never would recommend anyone stopped something like this cold turkey, you could find yourself in the ER, never play with any heart meds!! I pray that a slow decrease will be the answer to finding some symptom relief of my condition, yet still being able to function daily. Thank God also I am a stay at home mom for now, starting this and trying to work, I would be sleeping on the job!