ribavirin information

Any thing i can find out before hand is helpful God bless you all. Thanks so much for all the value information I have found here. Dont really know how to read lot of it dont understand the short cuts and abbreviations .

Solvaldi & Ribavirin could work together. Has anyone heard anything about this ? Also you can go to Web MD & qualify for a $ 5.00 Co-pay for a six month supply. This regiment, S& R is a 12 week program ! Gilead is giving to those that can't afford $ 1000.00 a pill . 12 week treatment for solvadi alone would be Eighty four thousand dollars !

Although not as specific, it contain much of the same information and is readily available to the patient and the doctor. This information label was given to me by my GI to read and discuss regarding issues related to anger and depression and the potential for needing an AD sometime during trt. I would hope all doctors discuss this prior to trt, but this may not be the case. I'm also curious what "psychological evaluations" are being done.

As you mentioned, genotype 2 responds readily to the current interferon/ribavirin combo. You have 80-90% odds of success, versus the 40-45 % success rate with genotype 1, which is the most prevalent strain in North America; however, they both have the potential for deadly results. A biopsy is the most accurate method of determining disease progression; unlike Hep B and HIV, viral load doesn’t *necessarily* correlate with disease severity.

The prescribing information for Epclusa calls for 12 weeks of treatment either alone or with ribavirin.

If you took ribavirin, the wait period is 6 months post treatment. If that is the case, please contact your doctor for advice.

anyways, I was informed that I was approved for 24 weeks worth of the treatment, (the pill ), not Harvoni but another that was as equal (I hope ) I would very much appreciate hearing from anyone who is or has gone thru the treatment so that I can familiarize myself with what to expect and any other information I need or should know about this journey and it's bumpy road.

I am on the last 30 days of treatment with Harvoni combined with ribavirin. Although I have experienced many side effects over the course of treatment they were not dibilitating and did not last more than a few hours before resolving. The main side effect is fatigue that worsens as your day progresses. I have been tuckered out by 6 pm most days and in bed before 8 pm. I am thinking that is due to the Ribavirin. Now that I am in the last month of treatment, the fatigue is not as pronounced.

Health personnel and visitors who are pregnant or trying to become pregnant should also avoid contact with aerosolized ribavirin until more information is available. In one adverse drug report, 3 nurses who worked in the same intensive care unit gave birth to babies with ventricular septal defects. However, only one mother was possibly exposed to ribavirin 5 months prior to estimated conception. A specific causal relationship has not been established.

Just some public info on eltrombopag. I remember somebody was on a clinical trial using eltrombopag or a facsimilie and I think the trial was halted within the first couple of weeks. At least it was halted for the person in it, as I remember. I'm just passing this information onward in case it is of interest to anyone. I thought eltrombopag was still in clinical trial, obviously I'm just here living and learning same as many. ------------------------ Message 3 From: U.S.

You or your healthcare provider should contact the Ribavirin Pregnancy Registry by calling 1-800-593-2214. The Ribavirin Pregnancy Registry collects information about what happens to mothers and their babies if the mother takes Ribavirin tablets while she is pregnant." http://www.drugs.com/pro/ribavirin.html I think once you talk with your Obstetrician and your fiancee's Hep C treating doc, you will have a clearer understanding of what you need to do and what you need to avoid.

Effect of ribavirin in genotype 1 patients with hepatitis C responding to pegylated interferon alfa 2a plus ribavirin. Gastroenterology. 2006;131:1040 1048. 15. Reddy KR, Shiffman ML, Morgan TR, et al. Impact of ribavirin dose reductions in hepatitis C virus genotype 1 patients completing peginterferon alfa 2a/ribavirin treatment. Clin Gastroenterol Hepatol. 2007;5:124 129. So in general... Mitchell L.

1% for subjects receiving SOVALDI + ribavirin for 24 weeks, 11% for subjects receiving peginterferon alfa + ribavirin for 24 weeks and 2% for subjects receiving SOVALDI + peginterferon alfa + ribavirin for 12 weeks." "The most common adverse events (≥ 20%) for SOVALDI + ribavirin combination therapy were fatigue and headache.

hello respected doctors I am hcv infected from 2006 that time I went to my doctor but my sgpt nd other tests were normal so my doctor just write me ribavirin tabs after some time he told me to use interferon I used interferon approximately 3 months I was not mature that time so I don,t pay attension now a days I am in in Ukraine and from last year I m feeling my health is not good so I want to know 1,,, if a person have HCV how many chances are that he also have HIV coz 6 month before my hiv

.The package insert simply says take with food , no designation as to how much or what, follow the link to see more on the subject. http://www.medhelp.org/posts/Hepatitis-C/Starting-Week-12-on-INC---THEN-WHAT-/show/1637168 .

RISK OF SERIOUS DISORDERS AND RIBAVIRIN ASSOCIATED EFFECTS "Significant teratogenic and embryocidal effects have been demonstrated in all animal species exposed to ribavirin. Therefore, COPEGUS is contraindicated in women who are pregnant and in the male partners of women who are pregnant.

Abbott announced at the AASLD meeting in Boston that its triple DAA regimen which produced high rates of SVR both in treatment naive and null responders both with and without Ribavirin, although results with Ribavirin are higher. According to Abbott’s press release, the SVR rates after 12 weeks of treatment were: GT1, treatment naive 97.5% SVR, null responders 93.

For the management of anemia, ribavirin dose reductions should be used (refer to the prescribing information for ribavirin for its dose reduction guidelines). If ribavirin dose reductions are inadequate, discontinuation of INCIVEK should be considered. If ribavirin is permanently discontinued for the management of anemia, INCIVEK must also be permanently discontinued. Ribavirin may be restarted per the dosing modification guidelines for ribavirin.

Ribavirin information

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