At week 5, I was put on the new drug Victrelis (Boceprevir) and within 3 weeks my body rejected the drug. I could not think, I could not walk/sit/stand without pain, I thought my head would explode, my eyes were on fire, and then I had a series of 3-4 brain seizures. I was released from the hospital 2 days later, and then within 7 hours had a final seizure and was rushed back to ER. Is there anyone else out there who has experienced this? I feel so alone, and the hospital diagnosis was a sore neck! I'm so furious that 1-no one did a CT scan while I laying flopping about on the gurney, and 2-now I have to prove I had seizures by getting an MRI and EEG for disability. My husband and I are dumb-founded. I have been taken off this drug, and continue with the Pegasys/Ribavirin combo for a full 48 weeks. I was undetected at week 4! Please tell me I'm not alone! Anyone???
Wow this is really wild! This is the first time I am hearing of this particular side effect. On a more positive note I saw on another thread you were UND at week 4 which is really great news. I hope you remain so for the duration of you treatment on dual therapy. :)
Thanks for your comment. I just found out my girlfriend got rid of her Hep C naturally by drinking liquid milk thistle for a year. If this treatment fails, I will not repeat it but will try what she took. I hate these side effects.
Milk thistle does not cure Hepatitis C. Hopefully, you will attain SVR (cure) with this treatment, but if you do not, then there will be new treatments in a few years which you can try. However, milk thistle is not one of the cures. Do not be fooled. Only the approved treatments for Hep C will cure Hep C.
I thought it was too good to be true. I am UNDETECTED at 4 weeks! I was on triple treatment with Victrelis but my body rejected the new drug. Now I'm back on Peg/Ribavirin for the full 48 weeks. Only 36 weeks left. I hate the side effects, but I take it day by day.
Now they are saying it was "muscle spasms", and to have a brain seizure you need to be unconscious. I asked for an MRI, but they won't send me. I am 100% it was the Vic, as those particular side effects disappeared within 24 hours of stopping. I can walk, ride my bike, and think again (no more brain fog), my hair is not falling out, the pressure in my head is gone, and the white puss is gone from my eyes. My body totally rejected Vic. I don't mean to scare anyone with the word seizures, but that's what it felt like. I thought I was going to have a stroke on the left side.
Are you seeing a Hepatologist? If not i would switch to one. If you are you might want to consider another one. There is a huge difference between " muscle spasms" and "seizures". If you were at the ER and they thought you had a seizure the would have immediately taken you to CT/MRI for confirmation. Doesnt make sense
As others have said, I am really sorry for what you went through. Diana has a good idea, you can call the help line, speak to a nurse.
I have read that others have had lowered threshold for seizures though they had had seizures before tx.
The inf can do a lot of crazy things, I don't know much about Victrellis
I hope you continue with the UND all the way to SVR
I did contact Victrelis. The nice lady asked me questions, then told me the side effects were not related to the drug I was taking! She said they will report it to Health Canada,and I told her that I am also reporting the adverse side effects to Health Canada. Victrelis will not admit to anything.
I am seeing an epidemiologist who put me on this treatment. Last week, I asked to be referred to a neurologist so I can get an MRI and EEG. I have nerve damage now and my hands tremble. I have not heard of a Hepatologist, and I believe I'm in good hands but if they don't give me what I want, I will definitely seek help elsewhere. Thank for all your input.
I am now convinced months later that the side effects of Victrelis gave me Cerbral Edema.
The doctors said I had an anxiety attack and the final diagnosis was muscle spasms! I was so angry back then. Why did I not get a CT or MRI? I asked to see a neurologist and was denied. Most of these symptoms went away after I stopped Victrelis but my head hurt to touch it and fell soft and squishy from March to the end of the year.
Taken from webmd's website:
What Are the Symptoms of Brain Swelling?
Symptoms of brain swelling vary, depending on the severity and the cause. Usually they begin suddenly. You may notice any of these symptoms:
Neck pain or stiffness
Vision loss or changes
Inability to walk
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