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Would you have Fatigue when you have Chlamydia?

Summary: there is no Fatigue reported by people with Chlamydia yet.

We study people who have Fatigue and Chlamydia from FDA and social media. Find out below who they are, other conditions they have and drugs they take.

You are not alone: join a mobile support group for people who have Chlamydia and Fatigue >>>

 

 

 

 

Chlamydia

Chlamydia (chlamydia is a sexually transmitted disease) can be treated by Azithromycin, Zithromax. (latest reports from 60 Chlamydia patients)

Fatigue

Fatigue (feeling of tiredness) has been reported by people with multiple sclerosis, high blood pressure, depression, rheumatoid arthritis, osteoporosis. (latest reports from 200,694 Fatigue patients)

On Jan, 30, 2015: No report is found.

Do you have Chlamydia and Fatigue?

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- support group for people who have Chlamydia
- support group for people who have Fatigue

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Can you answer these questions (Ask a question):

  • Number of dysponea reports for potassium chloride. jantoven medication
    Having serious bouts of shortness of breath, fatigue, disorientation with minimal exertion---doctor is not convinced symptoms are real.
  • Since starting coumadin i am exhausted all the time and have muscle and joint pain. (2 answers)
    In 2012 I had two PE's and four DVT's; I was diagnosed with a clotting disorder; after several hospitalizations they put an IVC filter in. Within a few months I was diagnosed with RA, Rheumatoid Arthritis. I am chronically exhausted, I have muscle pain - sometimes the pain in my upper legs/thighs is so severe I have lift my leg with my hands to get it into the car. Overtime I lost my livelihood and have become very depressed. Doctors say these symtoms are not related to any of the drugs I am taking.
  • What is the time space for taking l-thyroxine and pantoprazole am dose
    also taking Panioprazole in am forty-five minutes before breakfast,
  • Can nuvigil (vs adderall) be used simultaneously to help wean off 60mg/day of adderall? (1 answer)
    I have been on Adderall 30mg 2x daily for years!! I've had it lowered to 20mg, I've TRIED to go months without it (when not working) however I feel I've built up a tolerance level to the point that it's not as effective as it once was. My personal life has detoured WAY past anything an ADHD medication can possibly help as far as focusing on NEEDED tasks etc. I end up feeling wrapped up in what I'm doing at the moment that my anxiety increases due to all that I haven't been able to accomplish. I take various medications for various reasons, depression, anxiety, bulimia etc., and for the most part the doses have varied based on circumstances and current need at said time of prescription.. MY FAMILY HAS A HISTORY OF HEART DISEASE, And realizing that I'm already on the highest Adderall dosage scares me (and THEN as I think about it, it makes my heart race!). I've also noticed increased muscle spasms as well as extreme and intense pressure on my jaw (TMJ). MY QUESTION IS: does anyone have any experience LOWERING their Adderall dosage AND adding Nuvigil? The research I've done to date gives me impression that it could help balance out the more extreme effects of Adderall (60mg/day) but that the nuvigil would or could potentially help with the EXTREME exhaustion I feel as Adderall wears off. Some days I just crash, some days I sleep fine and others no matter how hard I tryyyy, I just CAN'T fall asleep, therefore making the next day worse! IDEALLY I'D LIKE TO BE MED FREE, right now I need them, but am hoping maybe I can speak with my doctor to lower Adderall and add Nuvigil to help wean me off the amphetamines as well as lower dosage intake. YES, a lot of the anxiety, sleeplessness and depression are related to current circumstances in my life, however, where I am is not where I want to be or where I'm headed.. Life is a journey, and all my meds have become a part of a journey I never thought I'd find myself taking. I don't want life/meds to define me, or create a me I no longer recognize, because scarily enough that seems to be a common pattern. As I overcome each and every daily obstacle, I also don't want to be "hooked" on my meds or needing "more" to wake up/sleep/function.. I'd like to work on finding a solution towards weaning off my meds NOW, and work my way off slowly, primarily the Adderall. I'm hoping by suggesting to my doctor and showing him my research he may agree (IF ITS EVEN A LOGICAL COMBO, CLEARLY IM NOT A DOCTOR) nuvigil could help me. I've already started taking less of my anti depressants, trazadone and xanax without discussing with doc because he is always busy.. My next appt I want to go in fully prepared with a plan and an overall goal to REDUCE my Adderall dose, but overall, I'm clueless!!! I have no idea what other meds other than nuvigil "could" potentially help if at all. I could be entirely wrong, Anyone with any experience using one vs other or both simultaneously, or anyone with constructive input, PLEASE COMMENT/SHARE!!
  • What's the best home remedy for jaundice?
    I started out thinking that I had pancreatitis, had all the symptoms, abdominal pain that went all the way thru to the back & inability to digest food (chronic indigestion). I read about keeping the bodys pH better balanced, bought pH test strips (urine) & found I was very acidic. I began eating more alkaline foods, alkalizing my water, and avoiding really acidic foods. Stopped taking my acid reducers because they actually KEPT me more acidic. I noticed that when my body's pH was up (alkaline) the pain was tolerable but when it began to drop (acid) the pain kicked up again. My doctors say they don't necessarily think it's pancreatitis because the ultrasound doesn't show inflammation & my blood test numbers are only slightly elevated. My liver enzymes are also slightly elevated. The doctors don't Seem very concerned. Today, for the first time in 2 months since this whole thing started I noticed I'm jaundiced. What the heck is this?

More questions for: Chlamydia, Fatigue

You may be interested at these reviews (Write a review):

  • Prostatitis and prostate cancer acceleration due to anaesthetics
    Caught Chlamydia in 1978. Interestingly, the partnered girl's sister worked in an aviary; and I found out later that Chlamydia originates from handling birdshit and birds are the carriers. Chlamydia was undiagnosed at the time, so it was listed under 'Non-specific urethritis'. Chlamydia wasn't named until about 8 years later. I was given tetracycline and told to stay off alcohol and sex. Yeah, really?

    I was 24; highly sexed, and in night clubs and pubs most nights. I laid off the alcohol and after two weeks, I was good. The laying off sex, I understood, because of contamination of others (condoms were little used in 1978 in the singles arena); so I masturbated one night... and that caused me immense in my prostate, and pain and suffering for the rest of my life.

    The ejaculation was extremely painful, and chronic prostatitis started. I was on and off medication for two years. I got light-sensitivity, which means in sunlight, I came out in burning rashes. I became allergic to tetracycline.

    The message? Consultants are generally poor at communicating what not to do, and why not. Lay off sex he said. All he had to say was no sex, no masturbation; or you may suffer for the rest of your life. That would have done it.

    No-one has been able to help me with this chronic prostatitis. In the early years it would come and go, but as the years have gone on, it has become more frequent, and now it is constant.

    Four years ago I went in for major foot surgery, and flat-lined. I was in intensive care for 2 days, on a morphine drip for the pain.
    When I awoke, I knew immediately I was suffering with my prostate. It was aching badly and I was urinating frequently. The nurses were amazed with how many 'bottles' I filled in such a short time.
    For the next few months, I was in agony. I have tried every possible drug going, as well as prostate massage and the indignancy of a urethragram whilst female students were watching.

    In November 2011 I went to see another consultant, who suggested a biopsy. I was diagnosed with prostate cancer. After much research, I now know that my diet and lifestyle, coupled with inflammation of the prostate with prostatitis, has caused prostate cancer. Yes, there is a direct relationship between prostatitis and prostate cancer.

    I am now beating it, without drugs and without surgery. I have changed my diet to a vegan diet, no sugar, very little alcohol, and a lot of supplementation.

    In December 2013, I went in for more foot surgery. I was unaware about the morphine at this time, so didn't consider it being a problem. I talk to the anaesthetist, who wanted me to have an epidural (injection in the spine to numb my lower body). At no point did he talk to me about my prostate history.
    In recovery, I sensed a problem as soon as the anaesthetic began to wear off. It was like my prostate and testicles wanted to explode. I knew I was going to have problems. My intuition reminded me of three years ago with the morphine, so I asked the surgeon if he knew of these complications with morphine, but he didn't.

    I spoke to the head of the post-operative ward and asked her if she had any experience of post-operative patients who suffered with prostatitis after surgery, and she confirmed she had. So here was a nurse who knew of the problems, but the surgeon and anaesthetist didn't. This is typical in the health service... the lack of sharing.

    Not only did I suffer with the chronic prostatitis (and still am 11 month later) I was incontinent. It took 6 months of 4-times daily legal exercises to get back control of my bladder.
    For me, morphine has a dire effect on my prostate.

    Bear in mind that your prostate is designed to eliminate toxins, so it is flooded with morphine. I will do my best to ensure I check for morphine in any drugs or anaesthetics in future.

    My first PSA level was 18, 3 ears ago. I brought it down to 13.5, then 10.4, 10.3, 10.9, 11.3, 14.3 and after the last surgery it spiked at 17.5. As a result, I have gone back to a stricter, greener raw diet to bring it down again.

    Oh, and anther tip; you need to get your vitamin D3 blood count above 200n/mols (UK measure) to have any chance of not getting prostate cancer. Mine was 32 when I was diagnosed. Today it is over 200, from supplementation of 10000 ius a day. Minimum in the UK, recommended by scientists, is 75n/mols, and it's too low. OK if you have a great immune system, but not if you want to fight prostate cancer and prostatitis.

    Black African males in the Northern US states and in Europe have twice as much risk, due to lack of sunlight. Sunlight on skin promotes vitamin D3, which is essential for the immune system and production of calcium.

    Black African males need more sunlight to produce the same amount of vitamin D3 as a caucasian male. Also, any male who is bald and fat has a higher risk, so a Black African, obese bald male, has an extremely high risk of prostate cancer, unless they get their immune system in order.

    The main way to fight all this, is on a clean, raw vegetable diet, pure water, no alcohol, sugar, processed or refined food, no meat, no dairy, no vegetable oil, no exceptions, and some breath-taking regular exercise. Just like we did 100 years ago. Go figure! Look at chronic disease studies of 100 years ago. 85% of all disease was from infection. Today 85% is from chronic disease.

    Your prostate eliminates toxins, and today, we are overloading it. Remove the toxins (and the stress and anxiety) and things will improve. It's a hard road; but with it is you want to be healthier and live longer.

    Good luck.
    Glenn.
  • Diagnosed with postural orthostatic tachycardia syndrome after mirena
    After getting the Mirena put in, I got really sick. I went home and got super dizzy, nauseous, and tired. I felt so sick and could barely function. I called the doctors office and they said it couldn't be from the Mirena. She said that I must have the flu. Well, I kept it in for a little while longer. I then started losing my hair. I went back into my doctors office because they thought I was experiencing the symptoms for the Mirena going through my uterine wall. The ultra sound was fine. She reassured me that the Mirena could not be the cause of my complications. So, a week a later I went to another doctor to have the Mirena taken out.
    Never quite felt like myself and a year later I got diagnosedI with Postural Orthostatic Tachycardia Syndrome, after a tilt table test was performed. It's weird to me that my symptoms started almost immediately after the Mirena was put in.
  • Mucinex dm and advil congetstion
    I noticed another female with simlar age and side effects; and a third female who in addition was under active thyroid. I have taken both drugs independently and had no problem with them. I am prone to low blood pressure & dizziness due to the thyroid problem
  • How an integrative wellness approach cured me of insomnia, ibs, and more (1 response)
    For 10+ years, I suffered with insomnia and a host of other problems including intestinal distress, headaches, psoriasis, anxiety, cognitive issues, hypothyroid, chronic itching, restless leg, etc. Traditional medicine, aka taking drugs, was not working to heal me. Since childhood, I’ve had IBS, headaches, and upper respiratory problems. Then, in my early twenties, after childbirth, I begin to suffer with panic attacks. I managed to get the panic attacks under control, but the insomnia never went away. I took both Ambien and Clonazepam at different times in my life. When I expressed my concern over taking these meds, my doctor reassured me and told me that some people just have to take sleeping meds for their entire life. I read literature on insomnia and tried most everything – no late night eating, no TV or electronics before bed, sleep in a cool room with complete darkness, meditate, sleep labs, etc. etc. etc. Even with the sleeping meds, I never got restful sleep. Most days, I felt like it was all I could do just to get by. For at least the first half of each day, I felt that I was in dazed stupor until the meds in me would start to wear off. I was first on Clonazepam and then switched to Ambien. When I made the switch, I suffered through withdrawal for about a week. It was horrible -- no sleep, hallucinations, etc. For years, I had silently suffered – my family, friends, and colleagues having no idea to what extent. I felt that mentally, cognitively, and physically I was slowly slipping away. My love for my child and my desire to nurture and provide for him is what kept me going. Without this purpose in my life, I fear that I might have given up somewhere along the way.

    Finally, a few years ago, I went to see an integrative medicine doctor. After years of being in the darkness, I am finally living again. My IM doctor put me on natural supplements, a natural thyroid replacement, and, most importantly, tested me for food allergies/sensitivities. My test results yielded that I could not tolerate wheat, gluten, yeast, and dairy. I took these results seriously and I completely eliminated these things from my diet. After two weeks of adhering to my new diet, I already felt better. In fact, I felt so much better, that, one evening, I decided not to take my Ambien. I have not taken it or any sleep or anxiety medicine since. My doctor was as surprised as I was and did not really anticipate that the diet alone would cure my insomnia. In fact, he had told me that, since I had been taking sleeping meds for so long, eliminating them completely would be a long process that we would have to work through together. Nearly all of the symptoms I listed have disappeared. I continue to take my natural thyroid replacement and the supplements my doctor suggested. I have the occasional migraine and a few patches of psoriasis -- but nothing like the severity I had before. I am 47 now and I am on a journey of healthy transformation. I eat healthy foods, exercise regularly, and truly feel healthy, younger, and physically stronger than I have in 15 and maybe 20 years. Jokingly, my husband used to refer to me as "fragile." Well, not anymore. In fact, he has told me that my body seems like a completely different one. He has had a front-row seat to my transformation and he is as much "in awe" of the changes in me as I am in myself.

    Ten years ago, I was not optimist about my future. Today, I am full of hope, wonder, energy, and excitement. I believe we have the ability to heal ourselves, but we must be diligent in our pursuit of knowledge, persistent and strong in our will to make lifestyle changes, and patient that results will come as long as we are doing all the right things. By the way, giving up foods I had eaten my entire life was not difficult at all once I did it long enough to realize the tremendous benefits of not eating them.
  • Depo provera overdose
    Dr acidentially gave me something like 9 times the normal dose of depo provera. My life has been miserable! I have fought excessive weight gain, infertility, severe cellulite, and acne for 20 years.

More reviews for: Chlamydia, Fatigue

Comments from related studies:

  • From this study (2 days ago):

  • The symptoms aren't necessarily a result of the listed medications

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  • From this study (2 days ago):

  • I have a history of pituitary brain tumors (one as an infant, surgically removed and treated with chemo, and one at the age of 7 treated through radiation). I had another brain tumor (miningeoma behind the eye nerves) that has led to these latest bouts of headaches and my rethinking of my health. I have always struggled with weight and am on every hormone replacement due to the effect on my pituitary. I am currently on a mostly vegan diet, which I have generally enjoyed but am starting to reevaluate.

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  • From this study (3 days ago):

  • Vegan diet
    Hormone replacement therapy through drugs for almost entire life, since first brain tumor in 1992

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