Precaution symptoms and conditions

I am 44 years old and have been taking singulair for about 4 years. 3 months ago I started experiencing crushing chest pain, tingling in my lower limbs, and felt very stressed out. I went to the ER last Thursday and was checked out for angina - the ER doctor told me I was suffering from chronic severe anxiety. I took Ativan for 4 days and felt better, but now the drigs are gone and I again having constant chest pain. In doing some research I found that anxiety can be caused by imbalance in adrenaline, and so started looking online to see if any of the allergy/asthma meds I am taking (adviar, singulair, allegra) can affect adrenaline. That';s when I found this website. Although i find the testimony compelling, I wish more folks would have poted about how their symptoms improved (or didn't) AFTER discontinuing singulair. Also I've noticed many of the stories are about children not adults; many people are taking more than one med for asthma, and most people's symptoms seem to come on right away whereas I have been taking sinulair for years and only recently have anxiety. I will stop singulair tonight and see what happens, but am wondering if anyone has come across further research that correlates singiulair with anxiety? My job life is really peaceful, I am otherwise happy, work can get hectic but that's true of any job, and I am out of ideas as to why suddenly at age 44, when I eat right and exercise - why get anxiety? Thanks for the posts, I'll try to remember to follow up after I am off Singulair for a few weeks.

To everyone out there that has issues with doxycycline...
Now i fully understand the old saying that nothing is free in life.

I got it for lyme disease 7 days ago, and it was one of the free prescripts from my grocery store (great i thought). Little did i know how powerful this stuff can be. For the last week i have basically had severe headaches and wanted to give up on life. I didn't want to work out, didn't want to go to work, had chest pains, muscle spasms, and DEEP DEPRESSION....
now i know why this is free, because after it gets you so depressed, they figure your doctor will put you on something to get you out of depression, a money making drug. This is probably the meds talking still (i stopped yesterday after what felt like a complete and utter mental breakdown). Regardless of my silly conspiracy theory, i am glad i stopped taking it, and i hope that i start feeling like myself again.

I've been on Ocella -- a generic form of Yasmin -- since late March/early April. I only started taking it because I was on a different birth control pill in another country (no side effects there) and then moved to the US in December and when the other pill ran out (not available in the US) my doctor in the US prescribed Ocella (Yasmin).

About ten days ago I went to the ER -- I discovered I have Supra Vesicular Tachycardia (SVT) -- apparently a condition a person is born with but doesn't discover until their 20s, 30s, later or never.

Then last night I went to the ER because I was having pressure across my chest. They did EKGs, blood work and then even admitted me to the hospital for the night and did a stress test the next day. Everything came back normal, yet the cardiology nurse prescribed (as a precaution??) an aspirin regimen (this would be to prevent stroke, blood clots I suppose) as well as 0.4 nitroglycerin only in case of chest pains. On the discharge papers it says I should go back to the ER if, after three doses of nitro, the pressure does not subside.

I read the medical insert for Ocella tonight. It mentions "pectoral angina" (chest pain) as well as stroke, blood clots, etc. as possible side effects of Ocella. I'm inclined to stop taking it.

I've also had some bowel issues but I don't know whether those might be caused by the pill as well?

I was given z-pak as a precaution due to repeated exposure to pertussis while working as an ER Tech at a local hospital (2005). I experienced chest pain and rapid heart rate. My blood pressure when I get to the ER was 240/186. I have always been healthy and fit.
All the cardiac tests were performed and were normal except for the chest xray. It showed a 30% pneumothorax. I was so shocked.
Since then I have not been able to keep the BP under control. Even more so I have extreme difficulty urinating. I am not male, but if I had a prostate it would be the answer. I have edema and constant trouble emptying my bladder. No one seems to care. I've been to many Dr.'s and no one will listen. They just put me on more BP meds with little response. 44yr female.

I am a 44 yr old female. I have been on Zocor for 2 yrs. I have never had high cholesterol. I have a family history of heart disease and after my 44 yr old brother had a heart attack and the transplant, my doctor put me on Zocor as a precaution. I have had problems over the 2 yrs and have been to the doctor many times only to be dismissed as Oh, I need to lose weight, I need to get out of the house more, I need to exercise, It must be my depression....and on and on. I have never had a kidney or liver test in 2 years. I never knew I needed on and my doctor never tested me. I have over 30 symptoms/side effects of Zocor. I only looked into the side effects after my mother-in-law had muscle break down, an intestinal blockage and a ruptured bowel and almost died a few weeks ago. I couldn't believe what I found on this site. I immediately stopped the Zocor. I started to feel better right away but it was short lived. i felt great for 1 week and then it all crept back in on me for a week and then this last week I am back in bed with dibilitating fatigue and muscle weakness. I will now list my symptoms/side effects.
Shortness of breath; heart palpitations; droopy eye lid (left eye); eye lid twitch (right eye); optical migraines; numbness & tingling of my arms (from the elbows down) and my hands; My hands "fall asleep"; Itching all over; severe muscle weakness ( I have dropped things); muscle pain; joint pain (even the little ones in my toes); leg cramps; critically anemic (on 3 iron pills per day); ruptured ankle tendon (left ankle, currently being treated with a brace trying to avoid surgery); hot flashes/flushing; cold hands and feet; dizziness;, loss of balance; headaches; blurred vision; mental fog; confusion; loss of memory; loss of concentration; extreme and debilitating fatigue; insomnia; trouble staying asleep (wake every hour); huge weight gain; swelling of calves, ankles and feet; dark colored urine; gas; upset stomach; diarrhea; stomach pain; depression; anxiety; hair loss; bruises; mouth ulcers; back pain; tingling on top of head; heaviness in my thighs; EXHAUSTION! I feel like I am 100 yrs old. I have had nights that I thought I was dying and had panic attacks that I would not survive the night. I have 3 young children to take care of. I can not even put conditioner on my hair or shave my legs in the shower because I have to get out so quickly due to exhaustion. I have to lean on one elbow at the sink to brush my teeth. When I get out of the shower I can barely breath, I am wheezing, my heart is pounding and I feel like I will collapse so I have to get out and rush to my bed. I home school my 3 children and most days we do school in my bed. Everything is an effort. I can never plan anything because most days I am incapacitated. I may have a good day and can actually go out to dinner or Walmart once or twice a month and then I can't wait to get back home and get in bed because I am so worn out. I don't see how this drug can actually remain on the market. I am so angry and upset that my doctor never told me this could happen. When I asked about side effects I was told "oh no there aren't any really". My doctor never ran tests on me. I just can't believe this. I go tomorrow for blood work and I go to the doctor on Mon to discuss the results and all of my problems. I am so afraid that I have permanent damage to my muscles and possibly my heart. I went tot he doc months ago with shortness of breath and swelling and she did an EKG and said my heart was fine and I was not having congestive heart failure. I fear I was and still am! It is not normal to be out of breath just brushing your teeth and combing your hair. I hope we all get the answers we are looking for and that we all recover from this horrible drug. God bless you all!

My son (14 years old) was given levaquin for a sinus and ear infection
2 weeks ago. Around the same time he began practices for his high school baseball team. He complained about his legs being stiff and aching. We assumed it was the intense practices causing his muscles to ache. After a week on the drug, he could barely walk and his knees were swollen. We were very concerned and looked up the side effects of levaquin on the internet. We were shocked and angry when we found out that levaquin should not be given to children under the age of 18 because on the possibility of joint and tendon problems. Today we went to the orthopedist and he drained a lot of fluid off of both knees (it looked like about a 1/2 cup from each).The doctor thinks it has to be a side effect of the drug, because the symptoms began at the same time. He doesn't
think after examining the knee and having him perform certain tasks that he has damaged any tendons. He has all the symptoms of rheumatiod arthritis. He is very athletic and plays competitive sports and we are praying that his knees are not permanently damaged by this drug. Parents please research all drugs and there side effects before giving them to your children! Doctor's DO make mistakes!! The pharmacist failed us too.

I have had my mirena for 3 years now and for the most part enjoy it. The only side effect i have had is i get bacterial vaginosis (BV) quite often. I never had BV in my life until i had the mirena for about 1 1/2 years. i do like the fact that i don't have to worry about taking a birth control pill daily or worry about getting pregnant. It definitely is affective considering my partner and i never use precaution when having intercourse. i guess i would prefer dealing with BV for a week then another child for a lifetime!

I have to say that I have had the total opposite experience with Mirena. After several weeks of research and careful deliberation, I chose to have it inserted. The live journal website "iud divas" provided so much information, and mainly showed me that all women have different experiences. Sure the insertion was painful, but it was also brief. I took the rest of the day off work as a precaution. I was a little nauseous for a while and had some cramping and spotting. It has been over 3 weeks since my insertion, and I have nothing but positive things to say about Mirena. I feel great and it's wonderful not having to take a pill every day. Instead of cautioning about the dire consequences of using Mirena, I would advise women to bear in mind that every woman's body is different. I would also advise looking at the iud divas live journal so you can see that there are many many women who have had positive experiences with both Mirena and Paraguard.

I just quit YAZ. I too thought it was great at first. Raved about it. Not sure if it was working or if just the promise of the potential benefits that made me think that. I have a history of Lupus symptoms that I am only now tying together. I was feeling SO BAD that I started researching lupus and found that it can exasperate the symptoms. i was having heart palpitations lasting for nearly 20 minutes, shortness of breath doing small tasks, inability to take a deep breath, NON EXISTENT sex drive, SEVERE depression, and the last straw was the constipation/diarrhea cycle. i too had slurred, stuttered speach...but did not correlate the two until reading comments. my motor skills seemed to be effected. doing what i absolutely needed to do in a day was all i could manage. this may be a combination of factors coming into play, but there IS NO DOUBT that the timing of me starting this pill corresponded with the exasperation of these symptoms. i quit less than a month ago. hopefully things will improve. doctors need to take more precaution in perscribing this. my doctor was new to me and was quick to perscribe, no hesitation. i encourage you to insist on lots of tests before trying this. check your liver, kidney, potassium...be sure, then try at your own risk.

I want to post this because this site has given me good perspective on this Rx and side effects experienced by others; its good to know I am not alone. As far as an agenda, I have none, in fact I was all for the Singulair initially, because it seemed to be a good alternative to inhaled steriods which I had read could interfere with normal growth. My son, 4 yrs. old, with a diagnosis of Asthma, started Singulair about 2 weeks ago. Asthma seems to have been improved by Singulair. Within a couple days of starting it, though, he reported vivid (but not nightmare-ish) dreams, a week later he dropped his afternoon nap, which we were expecting to happen eventually, so didn't think much of it. He is a wild child generally, but we also noticed an uptick in bad and aggressive behavior within a day or two of starting the Singulair; we really clamped down on him though, so that effect has been somewhat muted. He has always occasionally complained of indigestion stomach aches, but these complaints have increased to several times a day in the last week, also complain of lower abdominal pain which he says is "different" than his earlier indigestion stomach aches. Last week or so he's been up late at night, had trouble going to sleep, looks a little pale with dark circles under his eyes ("he's becoming a Goth" I joked with my wife). Last night he got out of bed late, appeared disoriented and seemed to be half awake, half asleep. He was talking, but not making sense and seemed to be upset and/or confused, but when pressed he assurred me nothing was wrong and nothing hurt--put him back to bed and this morning he remembers getting up, but also keeps telling me he had a "weird" (not scarry) dream and that he keeps seeing it while he's awake. Luckily this weird dream was not scarry for him, but he was clearly a little freaked out by seeing it again this morning. He seemed o.k. heading off to preschool, but we are taking him off the Singulair as a precaution. My advice to anyone else out there seeing similar symptoms in their kids is to go with your gut -- I always tell people that a Doctor's job is to tell you the odds, like only 1 in 500 or 1 in 1000 kids will have a certain reaction, or condition, or illness, it is the parents' job to be sure that their kid is not that 1. So I'm taking my kid off the Singulair because I think he may be that 1 kid who experiences these unusual side-effects. How wide spread they are, I have no idea. I will get on my soapbox and say I think it's time for the FDA to require drug companies to conduct long and short term clinical studies on kids for any drug that will be prescribed to kids--entrusting our childrens' health and well being to a drug company's own short term study conducted on fully developed adults is foolish and insane.

I am a 44 year old female with diabetes. I have high blood pressure and as a precaution was prescribed simvastian(zocor). I have only been on it for about 3 weeks...I have been feeling tired and very moody lately...but yesterday I woke up with my right leg swollen from the calf down my foot with severe burning pain and numbness. Now I have experienced Neuropathy in my left foot for years and somehow thought maybe this pain and numbness and swelling had to do with that...until this morning when I woke up to a severe pain in my right calf ( I immediately thought blood clot).. well I have a doctor's appt tomorrow to see what this is....right now Im sitting at work in so much pain and discomfort I want to cry...my feet are burning, my right leg and right shoulder are in burning pain...and my hands are numb and burning and in pain. I have to sit for hours at a time and cant just take a break when I need too...Ive only been taking this medication for 3 weeks and can not believe that all this pain and burning is from one little pill. Has anyone else had severe swelling from this medicine. Any other diabetics taking this medicine and having the same side effects? Im certain they are going to want me to stay on this medication and at this point after reading all these wonderful post, Im going to stop...Im even having difficulty in typing this post my hands hurt so bad. Im so angry that when I asked my Doctor about side effects he never mentioned these. he told me about being nauseated, constipated and so one...Ohh and I have also gained about 10 pounds in 3 weeks without changing my eating habits...anyone else have that? Thank you for letting me vent here. I was scared to death until I found this site. I was seriously considering leaving work and going to the ER room...Now Im just going to stop taking it and waiting this out till tomorrow....

I am not currently using nuvaring anymore because of a side effect I haven't really found anyone else experiencing. I would like to share my story and if anyone has had the same or similar symptoms please let me know because I am totally bewildered about it. I started using nuvaring after the birth of my daughter in December. I was on the ring for about one to two weeks. At first everything was fine but I started to experience very unique chest pains. The best way I can describe them is they felt like they were in the tissue and flesh in between my skin and my rib cage, and it felt like the area was being squished in a vice, and then my back would start to hurt alot. They first started about once every other day, but then got more frequent to the point when I stopped they were constant. I could not sleep because the only comfortable position was to sit down hunched over with a pillow on my stomach, with my back up against my headboard. My husband brought up the point that it could be the ring, and at that point I was willing to consider anything. I quit using the ring, and the pain stopped, for a little while. But it is still ongoing to this day. Although it only happens about once or twice a month, the pain is no less severe. I am sure it was the nuvaring or the ingredients in it that has triggered this because I have never had this problem before using it. Please if anyone has any advice or ideas, your help would be very much appreciated.

knees have swollen pockets and are excruciating as are ankles. Upper arm spasms do not alow me to push pull or raise my arms at all. Hands feel like there are spained and certsin fingers swell. Dr dismisses lovastatin as the cause and increased the dosage, increasing the problems. Sortness of breath and tight chest and jaw have now been added to my misery. Any one else experiencing thhis let me know. I have stopped taking Lovastatin for 2 weeks but symptoms dont seem to be lessing yet