Liver problem symptoms and conditions

October I received my mirena in 2006, if I had known then what I know
1st now I would never have gotten it. My husband and I share 3
2008 beautiful children, 2 being twins, since the risk of having another
8.30am set of twins was high, and his refusal of a vasectomy, my
doctor assured me this was the best thing for me. During the
2 years that my mirena was in I gained 20 kilos and continued
to gain blowing me up to 130 kilos. I have always been chubby
but no efforts to lose weight would work. I suffered depression
and the same doctor started me on medication for that,
still saying nothing about my mirena as the possible cause for
my problems. I was suffering excessive sweating, and not the
nice smelling kind, terrible tiredness and fatigue, aches and
pains, pelvic pain and complete loss of periods. It was only
when I went to my doctor a few months ago and demanded
that the mirena be removed, that I have started to improve. No
more sweats, I am still on my depression medication and am in
the process of weening off it. I have started to lose some weight
but unfortunately have now been blessed with liver disease. If
it's not one thing it's another. I have been researching to see if
mirena has contributed to my liver problem as I did not have it
before the mirena was inserted ????????? My experience has
not been a happy one, but losing trust in who I thought was a
good doctor really sucks. Don't take what they say as truth!!!!
Now I have to convince my husband to have a vasectomy and
so far he is proving quite difficult!!!!!

How interesting to find this site! I, too, was diagnosed with temporal arteritis on February 29 (no more leap years for me!). Because I was already blind in one eye (had no idea) and losing sight in the other eye, I was put on 100 mg daily of prednisone. I had no idea of what I was in for. Since that time I have been able to taper down to 42.5 mg daily, but I don't think I've missed a single side effect. Horrific headaches. A 25-pound weight gain so rapidly it was unbelievable, moon face like I've never seen, was thrown into diabetes right away. My blood pressure went haywire, my cholesterol went haywire (had never had problems with either of them). I think I agree that the most debilitating has been the muscle weakness and leg cramps. I have no balance, have had 3 serious falls. The latest is my skin is breaking down and I'm losing my hair. What hair I have is like somebody held a match to it and frizzed it. I'm short of breath, keep trying to exercise and it's like climbing a high-altitude mountain. Swelling of my feet to where I can wear NO shoes except for Crocs in about three sizes bigger than I ever wore in my life. Now I have a liver problem, am being sent to an "ultra-specialist" for this. The good news is that my remaining eyesight has been stable, and I am very thankful for that. I have been assured by multiple specialists that I would have been blind by now if not for the prednisone. Although it is very difficult for me to read by the time night arrives, and that was my chief "hobby." The other part of this whole sad saga (ha) is how much money my husband and I have been out this year -- unbelievable. Lab tests or doctors every single week and sometimes every single day. I am now under the care of 5 different specialists (ophthalmology, rheumatology, cardiology, hepatology and internal medicine), and it has been so incredibly expensive. This is even with fairly decent insurance. I have been told that I have at least six more months to go on this treatment, and then possibly another year on methotrexate. Thank God I have NOT experienced the depression that seems to be a common thread here. I am trusting in Him to get me through this itme and to come out on the other side completely cured. But it does get difficult in the meantime.

If you have any other course of treatment, take it. It has been 6 years since my last injection of Lupron. Between the ages of 26-36 I was given a total of 18 injections( 3- 6months treatments), to try and treat my endometriosis, It did not work, I ended up having my ovaries removed. I was not aware or told of the effects from the Lupron I would have(* except for TEMPORARY hot flashes and no period) to tolerste over the years. My short term memory is gone almost, I feel like an idiot most of the time. I can remember what bathing suit I had when I was five, but I can't remember a what subject I am talking about when I am on the phone or talking to a person for example. I am 43. Because of all the Lupron I was given, I had to start getting a yearly mammogram when I was 30 because of the hormones, so I get an added bonus of a 10 year head start on radiation form the x-ray machines. Besides the memory loss, I have insomnia, hot flashes, vision problems, fatigue, and LIVER problems ( I am not a drinker or a drug user). I know people would think this is a normal part of menopause, however, I have been having all of these symptoms, even with my ovaries and never had any of these symptoms until my 3rd injection of Lupron. I refuse to go on PREMARIN, (why would I want another hormone, and one made from pregnant horse urine!) If Lupron works for you, wonderful, but my doctor, said the symptoms would be gone within 4 months after my last shot. HE WAS WRONG. Good Luck

Hi my history started from last couple months when I realize my bp went up very high(160/100) so I started metoprolol succinate 25mg,for couple days i felt fine and my bp went down but I noticed some pain in my right side so i thought maybe is the liver problem and i started to get off.After a week i was suffered from withdrawal(first week i decreased dose to 12,5mg)then my bp was very high so i called doctor and he prescribed metoprolol 100 mg and lisinopril 25(i never used this one)and hydloxiazyde 12,5 and i felt better for couple weeks then I started to get heart palpitation and very low bp so I quit hydroxiazyde and now I'm on toprol xl (oryginal brand) and still have chest tightness (i switch metoprolol to toprol one day ago)and how you guys divide the tablets to get exact amount its hard

Was put on citalopram for depression as have liver problem. My face started to bloat

I'm posting my comment here on the Levaquin site because I too was poisened by this drug one year ago. I experienced horrible joint and tendon pain and even a year later I am still experiencing problems with both Achilles tendons. What I wanted to talk about today is Levaquin's horrible sibling Cipro. Here it is...the honest facts...In late Dec 2006 my dad was diagnosed with chirrosis of the liver. On Jan 8, 2007 he was admitted into the hospital to have fluid drained from his abdomen as a result of his liver not functioning well. My dad was given 400 mg of Cipro through an IV over the course of one hour. I wasn't there with him at the time because I would have never allowed the doctor/nurse/whomever to administer that to him. He was released from the hospital two days later and was ok by all accounts. On Jan 18, 2007 my dad was rushed to the hospital ER where we were told he was in complete kidney failure (renal failure). His liver was also failing. My 70 year old dad died on Feb 13, 2007 from complete kidney and liver failure. At one point over the weeks he was slowly dying I looked up Cipro on the internet and was horrified to read that Cipro is notorious for causing acute renal and liver failure. Another Flouroquinolone, Tequin, was taken off the market last year for causing the same thing. My dad had a "sick" liver to begin with and I cannot comprehend whay a doctor would prescribe a drug to him that is known to cause liver failure. Yes my dad had a liver problem, but besides that he was in excellent health. I do believe that one day my dad would have died as a result of having liver disease, but I truly believe that the Cipro he was given caused his kidney and liver to fail so soon and so rapidly. Beware my friends....beware. May God bless us all who have been affected in one way or another from this crap that is STILL on the market.

ive been taking 1cc of 50mg winstrol every other day, but after the frist bottle, ive been having back problems( i think its my liver), i was wondering if its liver problem, and i had a couple of drinks recently as well.

Started on Lipitor 10 mg 6/16/03 Thought only side effect to watch for was liver problem. Noticed muscle pain (and I mean SEVERE muscle pain--could not sleep because of it and literally crying every day. I blamed it on the fact that I'd gone off hormone replacement therapy.) in late August/early Sept, but didn't associate it with Lipitor until a friend mentioned he'd had problems. I stopped taking it right away and saw my doctor. She tested me for rheumatoid arthritis (came back negative). I've been off it for little over a month. Some days I think I'm getting better and other days aren't so good. The big question I have is: How long before I will be "normal" again?

I have been taking 3500mg of Neurontin for 3.5 years to reduce sever pain caused by cirvical disc degeneration (injury caused in severe car accident) Neurontin reduced the amount of pain and seems to reduce painful outburtsts of unvolentary movements & phantom numbness and pain. I am able to reduce the amount of daily pain-killers that I need to get through the day. I am currently questioning the relation with Neurontin and a liver problem recently discovered. Of course, blood tests indicate cholesterol, and blood sugar problems. Is there any documented relationship with the long term use of Neurontin and liver and/or kidney disorders?
Thanks