Knowledge is power symptoms and conditions

The best drug out there !! No I am not ignorant enough to make these cart blanche statements like some of these posts---Millions of people have used this drug successfully like I have. Just because it works for one individual they should not recommend it to the world nor if it causes you personally some harm YOU SHOULD NOT POST A STATEMENT THAT INFERS IT WILL HARM EVERYONE--IN-OTHER-WORDS GET A LIFE!

Significant hair loss has caused thinning around my face & entire hair line. Within weeks of taking Ambien CR... Woke up daily with headaches, mood changes, depression.....

I am a licensed NYS Cosmetologist. I know what is normal hair loss & what is not. It started with itching on my whole scalp, there was a lot of white greasy almost dandruff substance on my scalp. It didn't flake off like normal dandruff though. Then I noticed my hairline was not what it would normally be. Each time I brushed my hair the brush was filled with more hair daily... I stopped taking the Ambien CR, the itch went away almost immediately & so did the hair loss. I thought I'd give it one more try & took 1 pill one night. The next day the itch came back, so did the white greasy substance on my scalp & my hair started to fall out again.......... Went to my Dr told her what was going on & she didn't even blink, just asked if I wanted something else for sleep. I said no thank you not after this experience. Went back on Advil PM, not sleeping as well as I was, but at least my hair isn't falling out any more. Just keep hoping it will grow back in, has anyone had their hair grow back???

Hi Ladies- I promised I would post to let you know how I am doing WITHOUT Aviene. I posted the Sept. 10 comment entitled Thanks ladies because I felt your posts have helped me.

I stopped taking the Aviene on a Thursday and all side effects stopped and no new ones occurred. All is well, I enjoy life without being a freak show.

In a DAY AND A HALF WITHOUT AVIANE MY HEALTH RESTORED.

I mentioned the 20 pound weight gain within a few weeks, by the following Tuesday I lost 9 pounds and today is the 26th and I lost 15 pounds. No anxiety, no irritation, no face issues (in a week it cleared up), no mood or energy issues, no excessive thirst, burning of eyes, chills, fever, rashes, itchy -nothing. I was allergic to it and my body wasn't breaking down the coloring agents etc whatever the hell is in there b/c it's not like you get a box or product descriptions. This isn't personal comments, I spoke with pharmacists, doctors, doctor friends, nurses etc. I work at a hospital I have great resources to share with you.

Whatever your side effects are, let's do this. Let's listen to our bodies, listen to experiences and draw your own conclusions.

I know my body, I know myself, and I know my life changes, mood changes, physical changes were due to this pill.

Please consider when being worried about what will happen if you quickly go off it that the consequences of staying on it are more severe. For me, and for many of us, the side effects didn't stop but kept adding and if you are reading this and are just curious or feel something is off with you do not take it any further. I am sharing that I am not a sensitive person and do not experience side effects... and I completely broke down physically and mentally from the amount of side effects and had to self defend.

Many of your comments helped and let's face it if you read that some ladies lost their hair... come on... obviously something is wrong with this pill.

Take care ladies, my sincere hope is that my post will help you, as you have helped me.

So you know, I went back on Alesse and all is well. My drug company didn't cover Alesse but ALESSE HAS A PATIENT CARD FOR THOSE WHO DO NOT HAVE INSURANCE AND FOR THOSE WHO DO BUT THE COMPANY DOESN'T COVER ALESSE RATHER THE GENERIC AVIANE. Your patient Alesse card you get will cover the difference that your insurance company may not. I paid $ 2.89 for my monthly prescription which is less than if the insurance company covered it. Check with your pharmacy location site if they participate in the program and it is not hard to find one that does.

You may not like Alesse, I can only share my experience with Aviane that did make my life a living hell. Happy to be OFF it!

Please take care and self defend your situation and reach out to those around you.

Hi everyone,

i need to tell you about what just happened to me, because it seems most people are definitely not informed of all the possible side effects of prednisone - not only just relating to the dose of prednisone you take but also for how long.

I have been using prednisone for almost 14 years now, the doctors all tell me i'm unlikely to ever get off prednisone now because i've been on it too long. I know all about it's usual side effects (water retention, mood swings, thinning of all tissues including blood, acne, anemia, etc etc).

One side effect i was not advised of, not even in any educational material about prednisone either, was that long-term dependence can lead to Acute Adrenal Crisis. Which is deadly if not diagnosed and treated promptly. Thus i nearly died two weeks ago. I became rapidly ill with vague symptoms that i now know are symptoms of acute adrenal crisis. *THE ONLY REASON THE ACUTE ADRENAL CRISIS OCCURRED WAS BECAUSE OF LONG-TERM USE OF PREDNISONE*. Not many doctors will warn patients in advance of this. It is however, very very important that people are aware that long-term use of prednisone needs to be very carefully weighed with the benefits of using prednisone (i was started on prednisone in 1995 to treat severe Crohn's Disease).

Acute adrenal crisis can happen over weeks, months or years - in other words, it can come on so slowly that by the time you know there's something wrong you're already very very ill and in great danger.

I am very glad to have found this website and i hope you will all refer anyone who has any experience with prednisone to this site - education and knowledge is power - the power to stay alive.

(by the way, the treatment for acute adrenal crisis is to load up on prednisone - seems i'll probably never be free of this drug unless i can get my adrenal glands to begin working again (as prednisone "takes over" for the adrenal glands and they effectively go to sleep, and this is especially true for long-term use)).

My sympathies to everyone who has to go through the many nasty experiences with prednisone, especially the young children (I had to start it when i was 16). It really does mess with your body and mind, and in my case, became lethal.

Please pass on all your information relating to use of prednisone to everyone you can - it really is that important and seems to be the only way to avoid most of the disasters related to prednisone use.

take care everyone,
Linda
(Australia)

I have been taking Lamictal since October of 2007. I experienced some of the symptoms (muscle pain in the head and neck) before I started the medication. I have experienced panic attacks since July of 2005. I have had mild heart palpations since I was in my mid 20's (I'm 36 now). I have had what I would consider a below normal energy level since my mid 20's also. Ok so like everyone else I am thinking I'm a hypochondriac! However, I was diagnosed August 28th 2007 with having Lyme’s Disease and also Hyper-Thyroid (same time, same lab-work). Two weeks later I was diagnosed with Bi-Polar Disorder (this is one thing I knew I was battling but didn't know how to handle it). My physiatrist started me on Lamictal and I did the standard ramp up to 200mg. I also was started on a 90 day treatment of Dyoxicycline for the Lyme’s and Methimazole for the Hyper-Thyroid. I was very very weak and was only able to stay awake for short periods of time (4 to 5 hours max). Just an fyi, I am not overweight, lazy or unmotivated. I have the physical appearance of perfect health. This, I think works against me as the Dr's seem to think I'm just whining. Mater of fact; my Primary Care Physician never tested me for Lyme’s. I went to an Urgent Care Center which tested me for Lyme’s disease and I came back positive (they also tested my Thyroid levels and found the problem with my THS levels) I told my Dr the results and he insisted I have same test done again. Guess what, new tests, same results.
My symptoms today are very similar to what I have seen posted many times. Muscle pain (entire body, some areas worse than others), heart arrhythmia, racing heartbeat, intense palpitations, nausea, foggy “un-plugged” mind, fatigue, weak muscles, muscle cramping (especially after repetitive motion, such as strumming a guitar), panic attacks (much more severe) and the latest addition to the group, Insomnia. Muscles pain in my head, fore-head, jaw, temple, neck (front and back), shoulders, is terrible to say the least. The pressure in my fore-head (right under my brow) makes me feel like I need to close my eyes or rest (resting does not relieve anything). The front of my neck is so tight at times it feels like my jaw is being pried down. I could go on and on.
On my quest to find out what else is going on with my body I have had 2 Echocardiogram’s on my heart and abdomen, 2Nuclear Stress Tests, blood work out the wa-zoo, MRI of my brain, 2 CT’s of my Head and Neck, Chest X-rays, Endoscopy, Colonoscopy, and all revealing nothing.
Most doctor’s I have encountered seem to want to treat the symptoms, not the problem/disease. I believe I know why; we (the ones who are there for solutions) tell them what the symptoms are (how we feel). We of course are thinking “this will help with a diagnosis of the problem/disease”, when in fact (I feel); the doctor’s thought process stops there. They don't know what’s wrong with you but they do know what your symptoms are so....bingo, let's treat the symptoms. Don’t misunderstand what I am saying. I’m not saying, “Most doctor’s don’t know what they are doing” or “don’t take your meds”. I am saying you and I are one of the 20 to 30 patients most doctor’s see daily (100+ weekly). They may be caring and good people but they are just as human and fallible as you and I. My advice is this; (and I am taking my own advice) don’t always “pop” into your body what the doctor suggests/prescribes, without doing your own research. Heck most of us won’t buy a car or more importantly, send our kids off to a college with out doing your own research (we just don’t trust those shinny brochures). Your body and your health are worth you doing your own research. Just keep in mind, Pharmaceutical Reps are always at your Dr.’s office (sit in the waiting room for 10 minutes and I’m sure you will see one). Reps are paid to do one thing; encourage (push) the Dr.’s to promote use of the Pharmaceutical Companies drugs.
My wife and I have been doing our own research on Lamictal (after a year of taking this stuff) and the side effects associated with this drug. We have searched through many (many,many) web sites for information and we have talked with pharmacists and Dr’s for opinions. Although I’m am not thoroughly convinced that Lamictal is the cause of all of my symptoms, my wife and I have decided to lower my Lamictal slowly from 200mg to 100mg. I am now taking 150mg daily (three days now) and plan on staying at this level for a total of two weeks before lowering to 100mg. I do fear dropping the dosage to quickly (potential side effects) or lapsing into a mania. To help avoid a manic episode my wife and my immediate family are all “up-to-date” with my course of action. They are on “Red Alert” and have promised to keep a close eye on my behavior patterns and moods. (I don't want to put them through another hyper-mania episode, its much too devastating). I do want so badly to feel healthy and alive again and at this point I am rather frustrated with the Dr.'s ability to help me achieve this goal. Remember it is called “Practicing” Medicine. So now I’m going to practice a little, very carefully and cautiously.
As a foot note; I have recently (past two weeks) been re-tested for Lyme's with a negative response. I am keeping in mind Lyme's test are very inaccurate (still hoping this one is accurate). My thyroid is under control and normal, so.... let's see if dropping below 150mg of Lamictal will eliminate some of these other symptoms. I will keep you posted.
Erik

I am 20 and have been on Yasmin a year and a half now and to be honest I am still not 100% completely convinced that Yasmin is the root of all my evils. To all of you who are having horrible side effects after a few days, give it time. Your body is trying to adjust to all the hormones you are putting into it and it’s doing its best to get back to normal. My first month was semi-bad, some nausea here and there and a little tenderness, but not enough to stop my life over. My doctor recommended taking the pill right before I went to bed so I could hopefully sleep though the nausea, which I usually did. After the first month I was perfectly fine and back to my normal life. I then switched to taking my pill in the morning so it was easier for me to remember. After reading countless “horror stories” on this website even I started saying, “oh my gosh, I have that….i have that too….and that!...its all because of that horrible Yasmin!” But then I had to take a step back and realize Yasmin is not to blame. Sure, I have panic attacks sometimes, but I have had those way before I started taking birth control and sure I get depressed sometimes, but what woman hasn’t at least once in their life? I didn’t lose or gain weight, my acne perhaps got a little better, and my breasts didn’t change an inch. My only questioning factor is that I don’t really have that big of a sex drive, but then I realized I never have. Now, before you all start yelling at me, I am not calling you liars in the least, I believe you and I feel sorry for all of you who have experienced bad things because of this or other birth control pills. For those of you who are thinking of taking Yasmin and are scared after reading all of these articles, remember, every body reacts to pills and medication differently. Thousands of people die every year from taking Tylenol and aspirin, but does that mean we should take these medicines completely off the shelves? Of course not. All I am saying is for every one Yasmin horror story there are thousands of very satisfied customers. Give it a try, you only have three months of your life to lose and so much to gain.

Dear Howard, just like to let you know that you may be in the 10% category who suffer from the adverse side effects of Singulair, but such is the ignorance of educated men like yourself who take what is given by a physician and swallow it down with a smile, I'm sure you would be very familiar with the saying knowledge is power, so empower yourself and read up on the side effects of any other drug that you may be taking. Further more I would suggest to you to ask your doctor about Symbicort, its only one inhalation twice a day(an oral steroid) very potent and powerful with an excellent safety profile, you normally taper that drug down to one dose a day or when you need it. Next time Sir College Educated Professional, report the event to the drug and safety of the company or the FDA.

I am a 35 year old male, college educated, professional. I started on the Singulair for Asthma three months ago. At first I thought this was a miracle drug, making my Asthma almost disappear. After 3 weeks I noticed a sense of paranoia, always wondering if persons were speaking about me, how my co workers perceived me, worried about my wifes perception of me, my bosses opinion of me, almost totally unbearable. This carried on until I read this sight.

I have been off the drug for almost two weeks, I am beginning to feel better now. Thank you all for the information. To any parent that has a child on this drug: take them of it! As an adult I was going crazy, can't imagine how a child would be.

My 9 year old daughter has been on sigulair since she was 5. She just recently started having trouble with concentration and behavior. She is always sad and cries alot .She is an honor/gt student but just recently has been having trouble with her school work.She has also begun to hurt her brother and talks about how she wishes she was dead.We are really concerned and she began counseling. Her nuerologists says it could be depression but im thinking i should take her off singulair.She has had headaches,stomach pain,depression ,mood swings and weight gain.

I have pain in my left hip flexor when taking Lipitor. I was on 40mg/day and went on a daily walk with my wife after her back surgery. My left hip flexor would cramp. Sometimes it would cramp so bad, I had to quit walking and catch a ride home.

I had a month holiday off of Lipitor and could run after a week with no pain.

I started back on 10mg/day and the pain has returned, but not as bad.

I did an experiment- Laying flat on my back, I could lift my left leg one foot off of the floor. I stopped the Lipitor for seven days and could lift my left leg two feet off of the floor.
Can anyone help me?