Medicines symptoms and conditions

The CDC/FDA has announced that Tylenol Kills LIVERS ( Acetaminophen is it’s fancy name). Tylenol is one of the safest medicines ever created IF taken as directed on the package for TEMPORARY uses. It’s safer than aspirin. BUT, BUT, BUT, it is used in many medicines. If ANY medicines you are using have the strength written as XX / XXX Example: 50/500 or 25/1000 stop taking them.
Check the Food and drug administration or the Center for Disease Control web sites. Then ask your doctor to change you to a drug that doesn’t have any Tylenol in it. The second number, the one after the slash, is the amount of Tylenol added to each pill.
Many drug manufactures use Tylenol with their medications as a buffer. It is safe to the stomach so combined with their medication it also becomes easier on the stomach.

A very bad scenario.. say you are prescribed 50/1000 of a anti-inflammatory drug, three times a day. Take an adult dose of Nyquil every 12 hours-- that's 2000mg more Tylenol from the Nyquil. Then take a couple extra strength Tylenol for some pain. That could be another 1000Mg up to 4 times a day.
OTHER THINGS with Acetaminophen (Tylenol).Excedrin, Midol, Pamprin, Vicodin, Percocet, and many more.
Also, Liquor and Alcohol hurt your liver.
Don’t kill yourself be careful with this stuff.

J. H.
P.S. Copy and pass this around.

I have been taking Lisinopril for years. Also I've taken numerous tests to find out why I'm so fatigued, sleep all day and more tired afer sleeping even,severe knee pain at night when laying down only... I had also put on a huge amount of weight in a month or two when I started taking it now that I come to think of it. Oh my gosh. As I continued reading everyone's posts I wanted to cry. Has this been my problem after all these years? I sleep my life away for the last few years and I'm only 40. Before I started taking it, I worked out extreme 36 hours a week and worked 50 to 60 hours a week. Now my day is trying to get up to make it to work on time for 8 or 9 hours! I've already sent an email to my endocrinologist to request a different prescription and I am not using Lisinopril anymore!! Are there any class action suits for this? This has really taken a lot from me. I only hope this is my answer, which it sounds like it is! Thank you so much for sharing your stories. I will return after time to reveal my results!

This is not a first-hand experience, yet I would like to share the side-effects occured to my Mom. She was having high blood sugar levels for some time,
The Doc' insisted on Jenuvia though expensive and he said that since it is
produced naturally(from human body itself), there are no known side-effects.
Well I searched for Jenuvia side-effects because my Mom was complaining about increased heart rates, head aches and after going through the experiences on this page, well her joint-pains too can be attributed to Jenuvia.
India is not cautious of the usage of medicines, lack of monitoring authorities,Medics going for quick relief and perks on costly medicines from
Pharma Giants.. and to add a huge diabetic population in need of help..
It could adversely affect lives of millions.

Taking nitrofurantoin Monohydrate/Macro 100 mg for UTI, trying to determine if it is a medicine that can be taken by patients with Type I Reflux, and treated with Zegerid or other similar medicines.

i started using nuvaring about two and a half years ago. i have always had a small problem with eczema (on the inside of my elbows only), though for the past two and a half years, it has consistently been flaring all over my body. it looks awful and has brought me to an emotional low that NOBODY should feel. i have spent thousands of dollars on medical visits (including a patch test - "inconclusive"), medicines (a variety of steriods, protopic, allegra), vitamins/teas/etc, and countless hours reading and online trying to figure out what could be causing this uncontrollable flaring. about two months ago, i decided to stop using the ring and see if it is the problem. so far, things have been clearly up, SLOWLY but there's some hope now. if anyone is experiencing these symptoms, i urge you to try and remove the ring, don't waste as much time as i did and have to recover from two + years worth of damage to your skin.

Im 29 Years of age, male, the doctor gave me AVELOX 400 for chronic sinusitis 2 days of taking it it was ok. the third day is a nightmare. Begin to have bad dreams, confusion, my blood pressure started to rise up and different parts of my skin begin to swell and started to itch. the worse part is my penis started to itch and then afterwards began to swell and lesion on in. so freaking scary. Please don't take this drug. and for those who made this drug. BAYER right? Please recall Avelox. Medicines are supposed to cure people, not worsen the problem. not only BAYER but all other companies who sells drug which have serious side effect to recall your medicines. If i were only a billionaire i will buy all your medicines and burn it all. O well humans sort of Guinea Pigs. Thats the reality.

I started taking Avelox 9 days ago. I was prescribed 14 days of Avelox after a round of Ceftin failed to clear up a sinus infection.
I am an avid tennis player, playing 3-5 times a week. My first bad experience happened yesterday when I went out to play and as soon as I walked outside I had a head to toe tingling feeling. This felt like I had chills but no goosebumps were showing. Over an hour or so later, the goosebumps showed up. This was in 90 degree heat!! I first thought it was dehydration, which it may have been, since I didn't seem to be able to get enough water/Gatorade no matter how much I would drink. This is even at night when I am not in the heat!!
I didn't take the medicine today. Played again this morning. I had the same tingling feeling head to toe, but no chills this time. To explain the tingling, I told a friend my skin felt like it was creepy crawly! It was a horrible feeling again in extreme heat!
I, also, have a hamstring that feels a lil tinge to it. I never have these problems and I am guessing this is due to the medicine, too.
If I walk outside, my body temperature feels like it shoots up! Even though I do not have a fever.
I went to my doctor's office and he is out of town! I asked to see another Dr. and he was "too busy to see me" since he was trying to get to the hospital! I was told to call my family Dr.which I did, only to be told he was also booked and I couldn't be seen. So, I gave up! And, not taking the medicine anymore!! Never again. This will be on my list of 'Allergic to.'
I usually have no side effects from medicines.

ive been on prednisone and cortisone..2 doses i woke up and couldn't move my legs at all. the more i walked the more it hurt..the more i sat the worse it was to stand up and walk..idk what to do..i have to take this for the rest of my life..its just terrible to move.and my doctor wont be around for 3 days.

My mother is on levaquin for a urinary tract infection which had gotten worst than we thought . The infection had set up in pockets behind her rectum. She is on levaquin, and other medicines such as; digoxin, metoprolol, lipitor, diltiazem and lasix. I am so afraid she is on medicines that can do more harm than good. She also suffers from congested heart failure. After she returned home from the hospital stay she extremely weak, is this a results of taking the antibiotic ( levaquin or a combination of all of the drugs listed above)?

Until yesterday, I took 14 days of a 4 week prescription of 100 mg twice a day doxycycline for a tick bite rash. I rarely take any medication. The first week I just had mild side affects. Late in the second week I started to notice that I was becoming increasing anxious for no apparent reason. Even after hard exercise the anxiety seemed to be persistent as if an impending panic attack. Yet, I had no external reason to explain the anxiety.

After two additional days the anxiety seemed to keep ramping up and I began to get very dizzy when I moved suddenly or bent down to pick up items from the floor. The pressure behind my eyes also feel like it was increasing. I was afraid my blood pressure was spiking but in actuality it was probably either cranial pressure or simply an fight or flight anxiety response. I also experience some pretty vivid dreams.

I finally searched online and found no official symptom of anxiety for doxycycline but found people complaining about it unofficially. I spoke with my pharmacist who also said she had no listing of anxiety as a known symptom for the drug. She suggested I stop taking it and see if my symptom subside.

It has been 24 hours since my last dose and the anxiety has reduced substantially but not completely. I feel like I have a hang over today but otherwise I do feel an immediate improvement. I am still a little dizzy but not like yesterday.

Like all drugs, you should be very cognizant of how the drug affects your body - even if a physician tells you otherwise because only you can really tell and everyone has different bio-chemistry which reacts in different ways to different drug compounds.

Does anyone here ever had any tingling issues? I had total thyroidectomy in Feb. 2009. Felt good the first month or two and have gone down from there! Some days are good, some are bad. Never know from day to day how Im going to feel! I started out for about a month and a 1/2 on 125 levothyroxin.....then my doc lowered it to 100.......as of July 14th, Im now taking .88. The tingling Im getting is all over my body, different places, here and there. Ive had some heart rate issues for a couple of months now too and finally had my regular doc send to me see a heart doctor.
Thought maybe the tingling could be from low calcium.....it was normal, CBC was normal, ECHO was normal.....waiting on the holter test results right now. The heart doc gave me a prescription for Toprol. I told him I wasn't going to take it cuz sometimes my heart feels like its barely beating and Im afraid it will make it worse. Im glad I didn't get it! Ive read of too many side effects.
Palpitations, kinda fast heart beat with pounding.....sometimes it feels likes its barely beating! Most of this occurs when first laying down......every now and then while sitting, etc. I do not exercise.....and should but just don't find the time. I switched jobs around the time I found out I had several nodes on each side of my thyroid. I was getting tired a lot and just thought i worked too much. I went from a physical job to a sit down, 12 hour, graveyard shift. Since the surgery, Ive felt it more. Im tired of feeling like crap all the time......I was already going thru some perimenopause stuff before all of this! Before I ever found out about my thyroid, I did have real light pounding of heart when laying down and tingling every blue moon, but very mild as well.
Now with no thyroid.......and medicines with all the side effects......IM GOING NUTS!!! Right now the moodiness and tingling are whats bothering me the most. Some days Im really tired, others Im ok. My body gets hot off and on, no fever. The past 3 days my calves, feet, and ankles have started to swell........never before! Plus I get some throbs and pains in my legs and arms and under my arms here and there. I probably need a new doc and I change of medicine......but Im afraid.
For one, Ive decided to go back to a physical job........and hopefully it wont screw with my heart rate even more. Ive read up on tingling........Im guessing maybe its from all the damn stress since my calcium was normal. Does anyone here have any suggestions?????

About 4 months ago I took 7 days worth of Levaquin after my sinus surgery. It was a preventative measure, I never had an infection. A few days into the prescription I started having tendon pain in my knees & ankles. I couldn't sleep, I was having nightmares, I was emotional, anxious and drained. My doctor told me to stop taking the Levaquin immediately. 4 months later and I am still suffering from entire body tendonapathy, neuropathic pain, joint pain, skin sensitivity, severe migraines, temperature sensitivity, twitching (muscles convulsing), basically my entire body hurts. Some days are a little better than others but not by much.

I have been to rhuemetologists, neurologists, pm & r doctors, physical therapists, acupunture, orthopedic surgeons, & allergists (in Chico Ca, & @ UC Davis in Sacramento Ca). NONE OF THE DOCTORS KNEW WHAT TO DO. My general physician actually told me to "go home and wait it out" because there was "no hope of finding help" (I'm not kidding). I've had tons of blood tests with fairly normal results. Thankfully I have a wonderful neurologist who has taken some interest in my situation. All of the other doctors told me that my case was very rare & that they had heard of such side effects but had never seen any patients with them! After some research on the internet I seriously doubt that my condition is as "rare" as they claim.

I am only 28 years old, I can't walk, I can't work, and my life has been turned upside down. I was very healthy before, I don't have a family history of health problems, nothing like that...it was the Levaquin.

Here is what I am currently taking: Lyrica for neuropathic pain, twitching, not being able to sleep etc., and oral morphine for the severe pain, Milk Thistle to promote glutathione (important because it helps your liver detox), Magnesium Malate (also helps detox), a multivitamin, vitamin c, and fish oil pills. I also attend acupuncture 2x per week (honestly feel some relief from it). Also, I heard that glutathione infusions are helpful but I haven't tried them yet. At this point I will try anything.

IF YOU HAVE HEARD OF ANYTHING OR ANYONE WHO CAN HELP WITH THESE DEVASTATING SIDE EFFECTS PLEASE LET ME KNOW.

~J.

I have used Nasonex for about two years. Last spring, I developed vision problems which I didn't attribute to the Nasonex. In the fall, I was diagnosed with a cataract and glaucoma in my left eye.
I did not have any known risk factors and take very few medicines, so I believe the Nasonex caused the cataract and glaucoma. The first eye doctor never mentioned that the Nasonex could be causing my eye problems so I continued to take it until recently when I discovered it was probably to blame. I am now facing cataract surgery and the new eye doctor I went to told me I have the eye of someone 20 years older.

I find it extremely annoying and offensive that people have the nerve to comment things like: You are all complaining or whining, read the side affects before you use it. why do any of you think that you are more educated or better than any of us? of course we all knew the side affects but people react to medicines (etc) differently. i find it very hard to believe that all of these symptoms are coincidence. 99% of us have given birth and raised children which is the hardest, most challenging, emotional roller coaster and im sure we are all able to deal with a headache now and then and mild cramps but that is not the case with us. its a problem when you wake up every morning with migraines and back pains. it is also a problem when women are so depressed and tired that they aren't able to take care of their children and husband. we all have one thing in common. We are suffering from these side affects. I appreciate everyone who has opened up and told their experience and i will not let someone comment about any of us and tell us we are making this up in our heads or that we are whining. if you feel any of those no one is making you read these stories.. so GET LOST!!!
for those of you that have had a great experience with Mirena why are you even on this site?? you are no help to those who actually need help and those that are suffering.
bottom line is no one is right or wrong but this forum is made for those who want help not someone adding their input to make us feel even worse.

I was prescribed Simva 30mg to replace Lipex which is no longer government funded 6 weeks ago. Since taking this medication I am waking up with tingling in my elbows and fingers blurry eyesight and what really worries me and no one seems to have mentioned is low body temp 34.2 and then a reading of 34.8 now averaging around 35.2

Please is anyone out there suffering from low body temp

My main side effect was because they had me on too high of a dose at first: I had severe abdominal cramping to the point of needing to go to the ER and needing a muscle relaxant (bellatal - sp?). My endocrinologist said that was not possible, but the second he put me on the right dose, it went away. Many people have idiosyncratic (personal to them and abnormal) reactions to medicines.

All I can say is that some experts believe that the synthetic hormones can give false results on the blood tests, making everything look fine, so I have opted for real thyroid hormone and take Armour Thyroid. My thyroid problem symptoms all completely went away within 6 months (many by 2 months) after starting the Armour Thyroid. I spoke with at least a hundred women online before switching who all had the same experience: doing much better on Armour Thyroid. Some doctors are hesitant to prescribe it because there is some bad press in the AMA that some doctor's buy into about it, but it's all misrepresented and untrue.

i have had my mirena for about 1 1/2 months now, and so far i love it, i have had the spotting for the first month which doesn't bother me and now my period is on and i do have very bad diarrhea which im sure is associated with the period more than the mirena itself. haven't had any lack of sex drive in fact i 've wanted to have more sex, and i haven't' been irritable or anything else, so some of the side effects i believe everyone is having may be made up, think about it if you read over and over and over again how bad the mirena is your going to begin to feel that way i know if i tell myself that my arm hurts all day long then eventually it feels like it hurts..neways all im saying is relax stop reading these scary ass posts and do something to take your mind off of it, i know 3 other people who have the mirena that live down the road from me and NONE of them have had any of these problems...ladies i think you are just trying to find something to blame it on...

I am on two 500 mg doses of cephalexin daily to help heal a bug bite..Still waiting for the biopsy to come back. Doctor suggested could be a brown spider bite. Definitely want to stop the skin deterioration and get the wound from where the bite was removed healed but the itching started on day 3 on my stomach and has now spread to entire torso, back, insides of arms and legs. I have tried aveeno baths, benadryl (knocks me out) and eucerin itch-relief. Today I coated my entire body with 1% hydrocortisone with little relief. HELP - I am scratching to the point of bleeding and now that I have read these other comments will NOT take another one of these pills. Any other OTC relief anyone has found?

Last December I was also prescribed Doxycycline Hyclate 100mg for mild acne. I am 17. After a few weeks of taking it my acne appeared to have been getting better and I felt quite relieved. However, after about a month and a half of taking it, I woke up one morning with what felt like extreme heartburn. My stomach felt like there was a lump in it and in the middle of my chest where the esophagus and stomach connected, there was extreme pain whenever I swallowed anything. At first I thought this was just due to excessive acid in my stomach, but as it turned out it was the medicines reaction to a virus/cold I was getting -- the symptoms were nearly like an ulcer (which is what we initially thought). After stopping the medicine for about a month, I was fine and I started taking it again. Now it's been about the same duration of me taking it, and once again I feel as though I'm developing another case of what feels like extreme heartburn/an ulcer. Has anyone else had this problem?

I have a central disc bulge in lowest back I have tried many many types of medicines Tramadol worked and at first I felt a pinched feeling in the center of my skull I told my doctor and we gave time to adjust to medicine. Shortly after I started sweating heavily and I used it still as I was able to sit and stand and had greater mobility. I then started to get shaky alot and confused finally my groin started hurting and about a week later went numb my doctor then put me back on hydrocodone . Eat before use to avoid heavy nausea.

My 4 year old daughter was taking Singulair before bedtime (for asthma) and developed vicious bad dreams. I took her off the Singulair and the bad dreams disappeared. Through web forums I learned that this side effect has occurred in many children. For the past 2 months her asthma has been completely controlled through the use of a nebulizer and inhaler. I found out the Pediatricians and Nurses and our care facility were not even aware of this side effect. Why is such a mind-altering drug being prescribed to children? And why does a medicine that produces bad dreams require it to be taken before bedtime? She was also taking Zyrtec to control allergies. Her doctor mentioned that it could be taken any time of day, so we gave her the Zyrtec in the am and the Singulair in the pm. One morning during allergy season we forgot to give her the Zyrtec in the morning, so we gave it to her at night. Five hours later she was crying hysterically! It took hours to get her to calm down, and this girl is a very happy, social, well-behaved and well-adjusted child. I stopped both medicines the next day and within one week the bad dreams disappeared. So I would also cautious parents about Zyrtec as well.

About a month ago I was given Levaquin, for Pneumonia. After about 5 days my face and neck swelled up, Then came the Prednisone at the hospital. I have never in my 38 years not been able to control my own body. I do take Zoloft,and Xanax for anxiety. No one said I would have a problem walking (legs are not working properly) eating,sleeping, Buzzing in my head. Unable to lift my 3 year old let alone care for her, I get extremely fatigued easily. My Husband has missed a week of work, and if your like us....NOT GOOD. Even trying to type is hard I must look at every letter, It's like I REALLY have to think to make my body move.My kidneys feel like balloons in my back when I lay down,Uncontrollable crying. I can't believe this has happened. We have been going through this the whole month of May.Is anyone able to control the shakes? Even my head is shaking??? I suppose if I had tried hard drugs ever, this might be what it's like. I Pray someone can help me. I am so afraid of what is happening to my body. By the way, when they put me on the Prednisone they did not give me a taper... Had to see another Doctor for that. So as I sit here today, hands shaking, head shaking, knees feeling to loose to walk on them, Hard to breathe, or even to think the way I could a month ago. SOMEONE PLEASE HELP ME...

I am a male, 61. and have a history of switching around cholesterol meds, most recently because of cost due to my high number of medical conditions and large number of medications for, but not limited to: CAD. CHF, diabetes, hypertension, renal impairment, and herniated disks. I have barely been on zocor a month and have experienced extreme weakness, pain in neck, shoulder, hands, legs & feet. Because I have both cervical & lumbar herniations, I was somewhat uncertain until I began reading these posts. I took myself off zocor yesterday and emailed my doctor's nurse. It also occurred to me that after any length of sitting, my legs hurt upon standing while i was on Lipitor, but don't really recall other symptoms. Sometimes, when you have a number of health issues, you come to believe this is "as good as it gets," but now I believe differently, otherwise why bother with the meds at all.

I thought my fatigue and mild depression symptoms were something separate but after reading these posts, it sounds like they could be linked to taking Synthroid? I've been on it for 2 years now. At first, I felt great. I started feeling tired again & my dr. upped the dosage. I just saw him today & complained of feeling tired, depressed, and getting light-headed and off balance at times. He wrote me a Rx for anti-depressants and changed my blood pressure Rx. I'm thinking about trying a Naturopathic Dr. to see if I can get the results I need without all the side affects. It couldn't hurt to get another opinion.

I was diagnosed with Rheumatoid arthritis at the end of 2007 and have been on prednisone since then. I started on about 105mg a week and am currently trying to reduce it but it is really hard as the moment the dosage goes down I lose all mobility and cannot even get out of bed. I am only 23 years old and really feeling the disease to the extent that I cannot even cope with my life. The prednisone has really taken its toll on me and the side effects are crazy! I just want to go back to my old self as I am finding it sooo hard to get through a single day. My side effects include:

Insomnia, tooth sensitivity, depression, anxiety, mood swings, moon face (my face is so swollen that I cant stand looking in the mirror anymore, dizziness, temper, feelings of uselessness, nightmares, night sweats, water retention, and to top it all off the arthritis is getting worse and I am in constant pain. Is there anything anyone can suggest then please help me!