Liver symptoms and conditions

Ok, caseybo if I were you I would have my bloods checked. It's not a joke since Yasmine may cause a vit B deficiency. Sounds like vit B12 or B6, actually. Get yourself checked up. You can top up your vit b6 easy by introducing some vit. suplements and meaty and eggy diet but b12 as being stored in a liver has to be injected if lacked.I have just come off Yasmine because I had a descreased sex drive up to the point there was no purpose to take a pill.Also bad skin and getting erraticly moody. I have been off for just over a week now after being on for 8 mths. Blime!I soo bloated, have PMS-like symptoms including aching ovaries, back pain, mussle pain, tiredness, overall fatigue and the strangest one: tingling sensation all over my upper body, like something is creeping on me.anybody experienced that?Cannot wait to get back to my old normal. I only hope I won't put any wt on!I do not have an apettite at all as for now.Also want my boobs to get back smaller as DD seems to be to heavy.

2 genetic mutations in the gene that encodes for the transporter protein responsible for moving anti cholesterol statin drugs into the liver to be detoxified. have been identified. This gene is "SLCO1B1" (also referred to in the scientific lit as "OATP1B1"). Drugs must be "detoxified" by organs within the body and then eliminated, otherwise the drug stays in the blood stream, building up to toxic levels. With either of the 2 mutations, statins have been found to be (from various studies) anywhere from 122% to 400% ABOVE NORMAL plasma statin levels. How many people have either of these mutations? (Population genetic studies were done in Finland on Caucasian pop--so all the #'s refer to Caucasian population) 25 % to 38% of ALL Caucasian possess one of these 2 mutations. Thus, for however many yrs someone with one of these mutations has taken a statin, the level of the statin in their blood stream conceiveably could have been 400% ABOVE normal statin levels. ALll those pharmacologic effects of statins--decreased coenzyme q10, depressed manufacture of dolichols, depressed manufacture of selnproteins and thus glutathione, interrupted production of GTPases and glycoprotein function, decreased brain cholesterol levels--neuron synapses and new growth of neurons depend upon brain choelsterol--are intensified unrelentingly for the length of time the drug is taken.

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.

took avelox for 5 days, and developed "drug induced hepatitis", which hospitalized me for several days, and been sick with severe jaundice for 9 weeks, unable to eat, or be around food.
this has been confirmed by many tests, including biopsy's, ultra sounds, and cat scans.
no "liver" side effects noted but they can be severe.........................and should be noted !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

I have a 15-yr old. She's been taking singulair since she was 7. These are a few of the things that I have noticed over the last year but ignored because I too, as many of you have, thought it was because she a teenager.

1. Stomachache .. she complained all the time. Thought it was nerves because it was usually before she went to a training session or game.
2. Restlessness.
3. Headaches.
4. Moodiness.
5. Tired. Fatigue. Weak. Even after she gets hours and hours of sleep. Figured it was because her schedule is whacked. We've had fights over her not going to bed at a certain time.
6. Menstrual cycle changed last fall followed by acne when as before she was perfectly normal with clear skin. Recently put her on BC because of her hormonal change. Blood tests showed she was normal. We tried it anyway to regulate her periods. Took her off of it after she had her period for 3 weeks straight. Probably won't put her back on BC since taking Singulair might be the problem.
7. Tired all the time. Falls asleep in class.
8. Lost interest in her favorite sport which she rocks at. Thought it was because of a 2-month down time due to an injury.
9. Several times, have seen signs of depression but when confronted she says no she's fine. Depression is probably from being unhappy with her appearance. Being on the pill made this worse.
10. Doesn't want to go to school. Whereas before not a big deal. Most kids don't like school, but lately, she talks about how much she hates it. Usually excited to start the new school year, this year not so much, more like dreading it and her attitude hasn't change about it.
11. We argued last week and it was the first time she screamed at me and told me she hated me. She's never done this before. Her thoughts and moods have been horrible but they come in spurts.

After reading everyone's experiences, I am taking her off Singulair. I know it's not an overnight cure and will take some time, but I just want my little girl back. I find it strange that this all occurred within the last year even though she's been taking Singulair since 7. Do you suppose it's in teenagers and puberty?

Hi
I am in the UK - where any knowledge of side effects related to Yasmin appear to be non-existent. I was prescribed this to treat my endo after having problems with another pill (constant bleeding and mood swings).
Initially it was like a magic pill - immediately improving the mood swings and stopping the constant bleeding. Then after about 4 days I felt so nauseous I wanted to go home from work - this lasted a few days.
A week and half into my first pack, I suffered continuous asthma attacks - with no obvious cause, this developed in hours to spontaneous vomiting along with a hacking cough.nI was prescribed antibiotics for "infections". The symptoms continued until it was unbearable and I was put on anti-vomiting tablets. and changed onto a different antibiotic.
A week later back at the doctors surgery I had a series of tests - awaiting results as I type, as I have very dark urine, stools that are not "normal" (clay or yellow), pain in my stomach, pins and needles, continue to vomit if don't take the anti vomiting tablets. Have now stopped taking Yasmin and await results...
HOw long does everyone appear to improve after stopping taking Yasmin? Also does this sound like I may have a case of hyperkalemia? (I am awaiting results).
Many thank

I am a few days away from my 19th birthday and i've been taking Yasmin since the age of 11. I was diagnosed with PCOS when i was 11 and Yasmin has been what's keeping my period regular and more or less pain free since then. In May of 2008 i was switched to the generic version of Yasmin called, Ocella and started to notice more and more symptoms and side effects. My stomach pain in the mornings grew greater by the day and when i was on my sugar pill i would gain an unbearable migraine. Thinking it was just part of being a woman i ignored it and went about my life. It wasn't until December of 2008 while out with a group of friends i came into some serious stomach pain. thinking it was just a typical stomach ache that i normally got i ignored it. when i came to be about 4 am and the pain hadn't stopped i started to worry. first thing in the morning i went to the doctor who referred me to get an ultrasound. The ultrasound showed that i had gall stones and that i should have my gall bladder removed before more complications were to occur. Being a college student only a week away from returning to my second semester i opted to wait until spring break to have the surgery. During the 3 month wait i experience extreme diarrhea whenever something was put in my mouth, extreme stomach pain, heartburn, nausea, headaches, sore muscles, the list goes on and on i felt like i had been hit by a truck every day and i still had to go to class. in March of 2009 i had my gall bladder removed thinking that the symptoms would finally stop i returned to school only to find that nothing got better. It's been 7 months since my gall bladder has been removed and i'm still having the same symptoms as before and now i've added depression, stress, lack of energy and interest and many other things to the list. I'm still taking Ocella because i've never been advised otherwise but the symptoms are taking over my life. I am a sophomore majoring in electrical engineering at college and it's just become harder and harder to focus on my work or to enjoy the aspects of college that i should be with the frequent trips to the bathroom or having to opt out of a fun activity because of stomach pain. I was wondering if anyone can help me, maybe point me in a direction where i can get better and get back to enjoying what a 19 should be. Thanks.

Within 5 days after beginning Tri-Clor treatment, I began developing very bad indigestion and panic attacks similar to the feelings I had while recovering from Gall Bladder and liver drain surgery.
The second effect was the sudden arthritic swelling and pain in the fingers of my left hand which is my dominate use hand. I stopped immediately taking the Tri-Clor The indigestion went away in one day. The pain and swelling in the hand mostly the palm and fingers, has persisted for almost a month and does not respond to the usual treatments of Chondroitin and Glucosamine.

There are so many of us with depression/emotional issues from the NuvaRing.

For me, the NuvaRing saved me, only by revealing the MESS it created.

I was diagnosed bipolar in 2000 and spent 5 years on heavy medication in an attempt to manage it. In 2005 I went off the medication and my oral contraceptives in order to become pregnant. Following the birth of my son, I never returned to oral contraceptives AND never followed the typical path of a bipolar mother. There were no PPD issues, and I ended up not returning to the bipolar medication. I was symptom free without an explanation.

In May 2009, after years without anxiety symptoms, I went on the Nuva Ring. Within 12 hours, all of my old symptoms had returned. Within 5 days, I realized there could be a correlation and removed the ring. By the next day, I returned to myself.

With a call to my psychiatrist, who I hadn't seen in over a year, I described what had happened. She explained that the hormones do not process through the liver with the NuvaRing, unlike the oral contraceptives. This direct route into the body made the effects of the LOW dose hormones that more apparent. Thankfully, I learned that my issue all along was the hormonal birth control, and not my mental health.

My option is now a non-hormonal IUD, which has it's own messy issues, but I embrace fully in exchange for the emotional instability.

I feel that I have one of those stories that women need to hear. I do believe we are not realizing the full effects of these hormones. I took it as far as one can take it, with a full diagnosis and years of medication. I have to wonder how many women are experiencing milder effects and just don't realize that it could be the hormones.

I have been on Nuvaring for 2 months now and after the first month I went back to the doctor and she said that the side effects were normal and would go away after a few months. I don't think I believe that, cause I just feel so bad. I use to never fight with my boyfriend and now it is an every day occurrence. I get headaches all the time now it seems almost everyday. I feel so depressed and before I got on it I was happy go lucky and the peaceful one and now I am just on edge all the time and I hate it. I get nausea and for a moment i was thinking maybe I am pregnant but I am not and it is just frustrating and irritating. The best things about the ring is I don't really get cramps and no period pimples and no weight gain and no pill everyday. I never had there problems on the pill lo overall or on the patch. I must say though that it feels great to know I am not alone cause I was beginning to think it was just me and also i don't know if anyone has this but does your chest or heart feel tight at time like a palpitation? I am 24 and I never had this until now and I am so tired that all I want to do is sleep and I feel faint from time to time. I feel like i have all the bad symptoms except a few and no yeast. I honestly think this is my last month on this and thank you all so much it is such a relief to know I am not alone. Oh and I do get hot too and everything.

I'm 23 and just started Loestrin 24. I noticed the negative side effects immediately- nausea, cramping, constant headache, breakthrough bleeding, and severe depression. In general, I feel sick and unwell; ironically, I feel like I'm in the first trimester of a pregnancy. My doctor told me it may take a few cycles for me to adjust to this pill but I don't think I want to commit to a pill that causes this many adverse health problems. I think a baby would be less hassle!

Treated for a staph infection, I was 12 days into my 14 of 2X 500mg/day on Bactrim and Cephalexin when I started having chills, nausea, migraine-level headaches, fever, swollen lymph nodes and disorientation. I went to the doctor on the 12th day expecting that I had the flu (Swine/A and influenza B are here)...both were negative. My doctor prescribed Tamiflu (thankfully I chose not to take it) hoping this would ease the flu symptoms. Three days later I'm still battling these symptoms and frankly concerned about damage to my liver, kidneys, etc. as a result of the Bactrim. The doctor said that I likely am having a reaction to the Bactrim - thanks for telling me two days after the fact.

I run a small business and missed 4 days of work as a result. I'm hopeful that two more days off of Bactrim will get my body back to normal but I feel like I was poisoned by this drug that shouldn't be on the market.

Wow, I decided to google nuvaring and leg cramps. I haven't had a charlie horse in 11 years, but I had one two weeks ago and I have noticed my legs are always achey. I have rheumatoid arthritis and my other joints don't even hurt this bad. After reading this I took it out. I rather have long periods than leg cramps. Guess I will call the doctor on Monday and let her know. I can't take oral pills because it goes through the liver. This sucks. I just wasted 35.00 after getting the mail order people to drop the one prescription from 67.00 to 35.00. I am anxious to see if my leg cramps go away. :-)

I have been taking Levaquin for four days now and am suffering from serious lower leg pain, weakness in my right hand, nausea, my skin feels so hot all the time and not able to sleep. I am sure the Levaquin is causing this as this all started right after taking the first pill. I did not get an information sheet from the pharmacy that there were serious side effects to this drug. I was prescribed Levaquin for a sinus / ear infection because I am allergic to Zithromax (my liver reacts negatively with this antibiotic). I will not be continuing the course of antibiotic and hope the pain stops.

Shortly after beginning Yaz, I began getting dizzy at random, messy vision, fainting spells and an arrhythmia. I spent 2 days in the hospital and none fo the doctors attributed any of the side effects to Yaz, but that was the only new thing in my lifestyle. I also had been having incredible abdominal pain in the upper right area where my liver is. I have always been incredibly healthy and I started taking this to help the PMDD. Instead I am afraid that I have a frigging pending stroke coming my way or blood clot hiding in my brain making me pass out. Im scared and incredibly angry that all I did was try to get some help and instead had my life and my family's well being threatened. I am fighting to get an MRI on my head just to be sure nothings in there. I know I sound paranoid but suddenly getting an arrhythmia and passing out at random is scary. I am afraid to hold my daughter because If I faint, she'd get hurt. Another thing is at the beginning, I would dry heave a lot, but my doctor kept telling me to stick with it. She is STILL telling me this. Im stopping it tonight and joining a class action suit.

lower back pain, hair loss,joint pain, complicated migraines, vertigo, palpitation, hormonal imbalances (lowered DHEA, increased aldosterone-it affected my adrenal glands and kidneys), epigastric pain, bleeding, extreme fatigue, anxiety,pulmonary failure etc. I had to go through ER, 2 CT scans ( abdominal and brain), 2 MRIs, neurologist, endocrinologist, GI, gyno etc. I threw my Yaz pills in the trash after the first CT scan that revealed multiple tumors in my liver and left adrenal gland ( i took the pills for about 3 and 1/2 years)... the past 6 months have been a hell, but there are no more migraines, anxiety or other neurological symptoms at this point. By the way, one of my best friends who just started on Yaz recently ended up in the ER last week with a blood cloth in her left lung. Please stay away from that drug!

Dear Medications.com:
I cannot thank you enough for this site. Just yesterday I was prescribed Cipro for a nagging UTI which seemed to only partially get better with Doxycycline HYC. After only 3 Cipro pills I am stopping!! And will never take Cipro again. I take responsibility for rushing back to my doctor at the emergency care clinic and asking 'now what' after the Doxycycline was finished--we Americans are so quick to want the next candy pill with more strength! So even though my initial urinalysis showed no dangerous / STD bacteria present, because I was still urinating too frequently my doc suggested Cipro. I trusted him and took the first pill last night--I got a terrible headache, woke up promptly at 3:30 AM and had trouble returning to sleep. Got up this morning, took the 2nd pill and by early afternoon, was so tired and aching I had to lay down for 1.5 hrs..I felt miserable. Then this afternoon, after taking my 3rd pill, that's when I began to feel occasional tingling in my joints, hot pain in my knee capsules, continuing low-grade ache to my head, the feeling that my esophagus was shrinking, etc..... EVERYTHING you guys all have reported.

I got on the internet and thank God I found your site. After 2 hrs of my own research and the testimony of so many people, including tons of once-healthy, athletic persons whose lives have been destroyed irreparably by Cipro, I took my healthcare into my own hands, called my pharmacist and said 'I'm finished touching Cipro...never again will I take it.'.

This drug is more toxic than anything I've ever taken, and the way my body has begun to react in only 24 hrs, it is obvious that the drug co's are playing with fire on this compound. We as people must stand up and take action, and educate our doctors. I am taking some info. into him tomorrow, telling him i will be on a strict cranberry juice and kidney/liver tea detox program for the next few weeks to see if these 'natural' methods might help me rid my system of the bacteria.

In any case, I refuse to use Cipro ever again and hope that many more people will read these pages before ingesting any or too much of this dangerous drug.

d. r.
48-yr old sporty, and very healthy guy who wants to stay that way!

THis website has been a tremendous help for me. Two days after I was prescribed 500 mgs of Bactrim twice daily, I started feeling really odd. First the achiness, then my left leg began to swell. I am not taking the meds anymore, but am now so fatigued, and sore, I feel as though I have had the flu for a week. I honestly do believe that it also has a negative effect on the liver. Just from the almost constant ache , I have on my right side. I just want to sleep all the time. I have not taken the meds for two days, and yet, the effects remain. Beware of this nasty medication. I don't know why the FDA allows its distribution!!

I started taking this garbage in May of 2009. I would go to the Dr and my BP would be 180/110. Let me say im still on Lisinopril BUT stopping tomorrow. Let me tell you my story.

35 year old male, diabetic and HBP. After years of not taking care of my self i went to the doc, i started taking Lisinopril. With in weeks i got a hacking cough and my BP was still crazy high. They up'ed my dose to 20MG and then hell started.

Constant blinding chest pain, strange electrical shocks in my back and head, went to ER and was admitted, they said i may have had a PAST hart attack Weeks of in and out of the hospital a 3 day stay in the cardiac ICU! Then i had a CT angiogram with dye and that reviled MY HART WAS FINE. I still had this horrible pain in the chest and legs and hands and my gut, electrical shocks and night mares and freak out for no reason at all. Problems with erections and slow hart beat. Unreal panic attack that i think i was about to die or GO insane. The past few days i have had intense pains in my upped back and gut. I went to have some blood work done to see how my new diet is doing. All the numbers were amazing, BUT my LIVER IS HURTING! Now i do not see a doctor for 5 day to review it all BUT i know this pill has mad my life hell for the past 2 months. MY LIVER WAS FINE BEFORE i took this pill.

I was able to make my diabetes VANISH with diet, i must try that with HBP. STAY AWAY FROM THIS PILL.

I had the Mirena put in almost a year ago now .. At the time my doctor whom I trust very much .. and myself felt it was the best thing for me at the time because I was having on and off times of very heavy bleeding that wouldn't want to stop .. so to try and reverse that we went with trying putting this in .. It was a little difficult getting it put in ..but nothing all that bad .. as Im reading this site .. I have called my doctor and asked for her to call me ... Because .. I have recently had blood work done .. I have lupus so its taken often anyway in June my liver readings where high in the 70's so we waited one month and had them rechecked .. I was just told on fri I need to have a ultra sound done on my liver because in one month them readings went from the 70's to now being 125/135 and no one seems to know whats causing it .. soo i am grasping and looking into anything I can think that could cause it .. now im wondering if I didn't go from one problem right into another by getting this .. I hope im wrong and I hope for all of you having problems you feel better and get on the right track soon ..
God Bless .. V.

I had the Mirena put in July 3rd 08 at my 6 week check up after I had my second child. I did not have much pain during insertion. However now (about a year later) is a different story. I am glad that I found this page, and I am not alone. I have the common side effects that others list on here like weight gain, mood swings, irregular periods that are different consistency (clots, stringing, heavy flow, light flow), extreme fatigue but unable to sleep, lack of interest in normal activities, and breast tenderness. I know I expected the mood swings, weight gain (but did not think it would be the 18lbs i gained while i was eating healthy and working out) and cramping for a few months after insertion. However the past 2 months I have had a lot of pain in my pelvis. Cramping is not the right word for it, it feels like pressure on my pelvis. Like someone is standing on what feels like my ovary. This is also with the occasional flutter in my stomach that feels like a baby kicking. I have gotten what I believe is my period and took a pregnancy test that was negative. The pain is mainly on the right side which goes around to my hip and sometimes up to my shoulder. It has now turned into a stabbing pain in my lower middle abdomen (this is all with no other bleeding other than my 3 day period). I am calling to doctor tomorrow to get myself checked out. I feel the strings in the same place I always have but the pain is something I can no longer take. I am not sure that this is worth it anymore, I think its time to talk to the husband about a vasectomy!

My daughter has this vaccine and was severely ill. Migraines, hair falling out, pneumonia, dehydration, you name it ... She was super healthy before this vaccine. You need to detox to feel better. Western medicine cannot help much - unless they understand the eastern side of medicine as well - trust me - I'm in a yahoo group Lets Talk About Gardasil.

You need to go gluten-free/sugar-free/casein(dairy)-free, drink bottled or distilled water and introduce extra vitamins. (B12, D3, magnesium, folic acid, and a liver boost, which you can find at a vitamin shop). There is lots of information at the yahoo group - so please join so you can get healthy. Gardasil is a GMO (genetically made) which has problems all its own - but you need to get the metals out of your body which are in this vaccine and in many foods you eat - start reading labels! No high fructose corn syrup and lots of rest. Please check out the chat group - and please file a VAERS report - that is URGENTLY needed to get this vaccine off the market.

I'm 15 years old and i've been taking prednisone for a few months, and from what i've read i'm on a really high dose. i was diagnosed with rheumatoid arthritis and another autoimmune disorder concerning my muscles at the same time. my doctor told me prednisone was my only choice; it was either that or i would lose the ability to walk. he told me there'd be side effects, but i had no idea it'd turn out like this or i would have fought harder for another course of action. i started out on 30mg twice a day, and since then was weaned down to 20mg twice a day and now i'm down to 30mg once a day. i've been looking up a bunch of information trying to figure out if there's a way to lessen the side effects or any hope at all that they will get better. apparently there isn't much. after reading a bunch of these stories i gotta say i'm not feeling great about this. i totally understand everything everyone is going through. i'm sure you can imagine what it's like being smack in the middle of high school with a huge puffy face, acne so bad on my face, chest, back, neck, and shoulders that wearing a bra could put me in tears, and mood swings so bad i've lost friends over it. everyone knows how brutal high school can be, where appearance and attitude are everything. and i try to tell my doctor about it and he literally looks at me like i'm a whiny teenager and says "you're just going to have to deal with it." and people like my mom and my closest friends don't get it either. nobody understands how beyond frustrating it is. i'll get into the worst moods and not have a reason for it, but i'll stay angry for hours or burst into tears over someone looking at me the wrong way. it'll get to the point where i have to isolate myself from other people because the abrubt mood changes get so bad. as bad as i hate to admit it, the pain from the arthritis is gone now and supposedly my muscles are doing better too. developing arthritis caused me to have to quit cheerleading, something i've loved doing for 6 years, because the pain got to the point where i couldn't get my arms above my head or bend my knees. however, i'd almost rather deal with the horrible joint pain than deal with the side effects of prednisone. if your doctor gives you and alternative method, take it. i've always been confident in the way i look and really outgoing and happy and now i sometimes catch myself thinking about suicide. that's shocking to me because i've got so much going for me, but this medicine makes me miserable. and when i complain about it, anyone i'm talking to just looks at me like i'm being a cry baby. my mom does too, she'll say things like "you just have to do this. i know it's not what you want but to be honest i'm sick of hearing you bitch about it."
i feel a little better knowing other people feel the same way - like nobody gets whats going on with them. the prednisone does give me days of really great euphoria and days when i feel like i could run a marathon, but waking up in the morning to the acne and huge face puts me to tears every day. i have to pee all the time, usually getting up at 2 or 3 am. i don't sleep well anymore and i do sweat all the time. which also sucks being a teenage girl. i'm always hungry, and when i eat i never feel full so i don't know when to stop. my neck and face have put on so much weight that when people see me in the halls or out and about they ask me what happened. mind you these are people i don't talk to, just ones i know from classes or whatever. and it's pretty bad when teenage boys i've never really talked to ask what happened to your face. kind of a blow to the ego, or whatever is left of it at this point.
i'd like to know if, as my dosage gets lowered, the side effects will diminish and when i'm off the prednisone completely if they will disappear altogether. any help there?
or if there is any way to help the acne or puffy face

my doctor just put me on something called methotrexate or something like that to help wean me off the prednisone, and does anyone know what those side effects will do? or if they'll affect the prednisone side effects?
i'm constantly obsessing over gaining weight and what my skin looks like and what i eat and how heavy my face feels and the occasional pressure in my eyes to the point where i just want to be put out of my misery.
and after reading other people's stories i really don't understand why this drug is still given out as freely as it is. but maybe all doctors are like mine, they just don't get it.
best of luck to anyone who's on prednisone, my heart goes out to you; i'm right there with you
sorry this became like a book it wasn't meant to be this long

Sever Urticaria on the 10th day of a 15 day course of Nitrofurantoin for chronic UTI. The urticaria has already lasted 2 weeks and has not subsided yet. Taking Antihistamines. This is the third such instance of urticaria after taking Nitrofurantoin in the last 7 years. In the previous 2 instances urticaria started weeks after finishing the antibiotics course hence could not associate it the drug. Doc feels it could be drug induced liver cholesterol which is causing the itching. I am a 34 yr old female

I think I'm going to die... I took pill #6 (100mg) which translates to 3 days and I think I'm going to die... I just got back from ER with liver/stomach pains... even though I repeatedly let the nurses know I was taking Macrobid and Xatral, the doctors never EVER got wind of it and treated me as if I had an indigestion. After taking my 6th pill, my throat is swelling up like mad, I have funny heart beats, strong stomach pain, funny tingling pulses in the fingers, and I feel like I'm going to pass out, I'm out of breath, and I feel so dizzy and lightheaded and I'm afraid of passing out for fear I will stop breathing when I do...