In July I was given Levaquin 750 mg, the following day I was in so much pain. I have HVC and MS. I also had my neighbor look at my blood work done prior to this "follow up" visit this doc. If he had read the test he would have known there was no respiratory trouble.
First it appeared that this drug hit my throat, sore lymph nodes, my legs were so weak, and then a very sharp pain hit my right side under the breast plate.
I had my gallbladder removed, but this nasty drug had attacked my liver too.
I am looking for someone who can give me heads up on this biopsy report. I am trying to get into the San Antonio Texas medical group for liver transplants and problems. I would like to have some knowledge or at least an idea before i go.
"The liver shows approximately 4 portal tracts present to evaluate, The portal interface hepatitis is moderate and continous around most of the portal tracts (3/4). The confluent necrosis is focal in some areas, (highlited on the reticulin stain) (2/6). The focal lytic necrosis/apoptosis and inflammation is one focus or lesss per 10x objectives (1x4)
Portal inflammation is moderate around most of the portal areas (2/4). No distinct lymphoid follicllies are identified
There is focal bile duct inflammation The PAS stain highlights the glycogen content and dgree of steatosis which is variable ranging from 5% to approx. 20%. No abdormal inclusions are seen on the PAS-D stain. The trichrome stain highlights the portalal- to portal and portal to central fibrosis. However, the entire tissue represents subcapsular tissue which can over estimate the degree of fibrosis. The iron stain is folcal and minimal in a few kupffer cells and hepatocytes.
1. Liver wedge biopsy
Chronic hepatitis with fibrosis consistent with Hep C
Modified Ishak HAI grade; 3, 2, 1, 2, =8/18 and stage 4/6.
Mild steatosis (5 to 20%)
Iron stain is 0-1 +/4
I also have MS and am constantly juggling what disease to treat first. I have survived Hep C for 20 years, When I found out I had this I stopped all activities, drinking. I have taken 2 treatments, the first interferon helped both the MS and the HEP C, but the Ribfiravin, and PEG, did not respond and I was very sick on these drugs. The doc I was seeing at the time said that if I was not responding to the drugs that his choice was not to treat.
Prior to all of this I was improving with my MS and I felt my enzymes were under control, they were never over 100. I appreciate anyone's response to this, I am alone and I am lost.