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SVR, Decrease Meds and Retinopathy Questions
Female, mid 50's, RN, Geno 1a, started with 15 million load, mod liver damage, inflamation & fibrosis. I am on week 6 of triple therapy: Miricle drug Incivik, Pegasys, Ribavirin.
I had Ribavarin decreased to 600mg/day after three days of tx. due to elbows swelling & becoming red & hot , one large hive on my arm and blotchy red rash on torso & limbs.
Thank GOD I still obtained "undectable" status at 4 weeks of Treatment!
I have experienced weakness, nausea, severe headaches, fatigue, rash, flat affect, no energy, decreased cell counts, high blood pressure, increased pulse and higher body temp side effects. All of which I knew could happen and am willing to deal with it. I am scheduled to see an oncologist for the low hgb/anemia.
Also I recieved an opthamologist referral because I am experiencing blurry vision in one eye. The doctor fears retinopathy. He has decreased my pegysys now from 180mcg sub q to 135mcg weekly.
Has anyone experienced a decrease in pegasys on tiple therapy and maintained/achieved SRV?
Has anyone had retinopathy during therapy? How was this treated? Did you have to stop treatment? This was an option suggested by my doctor. I do not want to turn back now. Any insight to share?
Thank you!
I had Ribavarin decreased to 600mg/day after three days of tx. due to elbows swelling & becoming red & hot , one large hive on my arm and blotchy red rash on torso & limbs.
Thank GOD I still obtained "undectable" status at 4 weeks of Treatment!
I have experienced weakness, nausea, severe headaches, fatigue, rash, flat affect, no energy, decreased cell counts, high blood pressure, increased pulse and higher body temp side effects. All of which I knew could happen and am willing to deal with it. I am scheduled to see an oncologist for the low hgb/anemia.
Also I recieved an opthamologist referral because I am experiencing blurry vision in one eye. The doctor fears retinopathy. He has decreased my pegysys now from 180mcg sub q to 135mcg weekly.
Has anyone experienced a decrease in pegasys on tiple therapy and maintained/achieved SRV?
Has anyone had retinopathy during therapy? How was this treated? Did you have to stop treatment? This was an option suggested by my doctor. I do not want to turn back now. Any insight to share?
Thank you!
Thank you for your responce and for sharing your vision history with treatment. I am happy to know it can clear up after treatment is over. I did have a thorough eye exam with in the last 6 months prior to treatment. My blurry vision was present prior to treatment due to an old lasix surgery, but not to the extent it is now and it is only in one eye. It could also be dehydratrion or dry eyes too. I am starting artificial tears, increasing my water intake and I will be relieved to have a physician assessment, which is scheduled in two days. Thank you again.
Welcome to the forum. And, congratulations on your UND status.
I did not reduce Inf. during Tx.
I am wondering if you had a baseline eye exam, including retinal scans, by an opthamologist before treatment started? If you did, then your opthamologist can compare the baseline exam with a current exam. Hopefully this current exam will occur this week, like this Monday, because your treatment and your vision may depend on it.
I do not know how severe your blurred vision is. The severity may be important. I did have blurred vision and worse vision after starting Tx and that has continued throughout 48 weeks of Tx and for the past 9 weeks post Tx. I believe many people have vision changes, especially worse and/ or blurred vision) while on treatment. I also had "showers" of floaters, like large black snowflakes falling. These turned out to be nothing serious. However, what is important is to determine if your blurred vision is just a minor side effect of Tx or if it is a symptom of a major problem, such as retinopathy. Interferon can cause retinal hemorrhages, retinal detachment, cotton wool spots. As an RN, you know these can be serious.
There are a couple of people who did have to stop Tx due to retinal hemorrhages. Hopefully, they will respond to your questions.
Best of luck.
I did not reduce Inf. during Tx.
I am wondering if you had a baseline eye exam, including retinal scans, by an opthamologist before treatment started? If you did, then your opthamologist can compare the baseline exam with a current exam. Hopefully this current exam will occur this week, like this Monday, because your treatment and your vision may depend on it.
I do not know how severe your blurred vision is. The severity may be important. I did have blurred vision and worse vision after starting Tx and that has continued throughout 48 weeks of Tx and for the past 9 weeks post Tx. I believe many people have vision changes, especially worse and/ or blurred vision) while on treatment. I also had "showers" of floaters, like large black snowflakes falling. These turned out to be nothing serious. However, what is important is to determine if your blurred vision is just a minor side effect of Tx or if it is a symptom of a major problem, such as retinopathy. Interferon can cause retinal hemorrhages, retinal detachment, cotton wool spots. As an RN, you know these can be serious.
There are a couple of people who did have to stop Tx due to retinal hemorrhages. Hopefully, they will respond to your questions.
Best of luck.
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