One of the other pressures on me is to do with the Hep C. The doctors are more than keen to have me on Harvoni but I hesitate. I am always cautious when something is called Wonder Drug or a Miracle.  Even moreso nowadays where the profits to Big Pharma are so huge. In the background of each day is the awareness that I may be risking my life by refusing treatment. On the other hand is a great deal of caution. I KNOW they are bending data to suit them because just in my small world of NA I have seen adverse results and dropouts from the treament which the Hospital doesn’t acknowledge at all.

Its heatwave still and once again I am home alone. Too hot to try to go out methinks and I am developing depression and agorophobia. I have run out of fight so I have. Bed. Book. Thats it.

Nonetheless – its not easy to go through each day with a background argument going on. I thought it was too early to know what the results truly were and now I am finding articles confirming that. Here are some samples.


There are a number of sides we have not heard about, ranging from Cardiac Arrest, Respiratory Failure, Mouth Ulcers, Tinnitus, Chest Pain, Lung Damage, etc. I know this because I secured a report from the FDA under a Freedom of Information Act request. I have attached it and hope it goes through for everyone to see. I personally have Tinnitus, Vertigo, Lung and Heart Issues. I am not the only one. The FDA has no requirement to report issues until at least 18 months after the drug goes on the market… bssically for another year, Gilead and the FDA have no responsibility to the public to let them know of additional dangers. I was perfectly healthy except for Hep C until I took Harvoni. If you can wait to take it until the additional information comes out, please do. I wish I had. And in response to the comment that I saw on the this site, no one quit trials, that is not true.

Risk of Hepatitis B Reactivation

The FDA has indicated that there is risk of the Hepatitis B virus becoming an active infection again in any patient who has a current or previous infection with Hepatitis B virus and is being treated with Harvoni, a direct-acting antiviral medicine for Hepatitis C virus. In a few cases, Hepatitis B virus reactivation in patients treated with these types of medicines resulted in serious liver problems or death. In addition to a prominent warning being required on the medication’s labeling, healthcare professionals are being directed to also screen and monitor for the Hepatitis B virus in all patients receiving this treatment.


Last Updated: October 2016


The U.S. Food and Drug Administration (FDA) is warning that serious slowing of the heart rate can occur when the antiarrhythmic drug amiodarone is taken together with either the hepatitis C drug Harvoni (ledipasvir/sofosbuvir) or with Sovaldi (sofosbuvir) taken in combination with another direct acting antiviral for the treatment of hepatitis C infection. We are adding information about serious slowing of the heart rate, known as symptomatic bradycardia, to the Harvoni and Sovaldi labels. We are recommending that health care professionals should not prescribe either Harvoni or Sovaldi combined with another direct acting antiviral, such as the investigational drug daclatasvir or Olysio (simeprevir), with amiodarone. Patients should not stop taking any of their medicines without first talking to their health care professionals.

Harvoni and Sovaldi are used to treat chronic hepatitis C, a viral infection that can last a lifetime and lead to serious liver problems, including cirrhosis or liver cancer. These drugs reduce the amount of hepatitis C virus in the body by preventing the virus from multiplying within the body.

Our review of submitted postmarketing adverse event reports found that patients can develop a serious and life-threatening symptomatic bradycardia when either Harvoni or Sovaldi combined with another direct-acting antiviral is taken together with amiodarone. The reports included the death of one patient due to cardiac arrest and three patients requiring placement of a pacemaker to regulate their heart rhythms. The other patients recovered after discontinuing either the hepatitis C drugs or amiodarone, or both (see Data Summary). The cause of these events could not be determined. Information about this serious risk of bradycardia has been added to the Warnings and Precautions, Drug Interactions, and Postmarketing Experience sections of the drug labels for Harvoni and Sovaldi. We will continue to monitor Harvoni and Sovaldi for risks of serious symptomatic bradycardia and further investigate the reason why the use of amiodarone with these hepatitis C drugs led to the heart-related events.

Health care professionals should not prescribe either Harvoni or Sovaldi combined with another direct-acting antiviral drug with amiodarone. However, in cases where alternative treatment options are unavailable, we recommend heart monitoring in an inpatient hospital setting for the first 48 hours. Subsequently, monitoring in a doctor’s office or self-monitoring of the heart rate should be done every day through at least the first 2 weeks of treatment.

Patients taking either Harvoni or Sovaldi combined with another direct-acting antiviral drug with amiodarone should seek medical attention right away if they experience signs or symptoms of symptomatic bradycardia such as:

  • Near-fainting or fainting
  • Dizziness or light-headedness
  • Malaise
  • Weakness
  • Excessive tiredness
  • Shortness of breath
  • Chest pains
  • Confusion or memory problems

We urge health care professionals and patients to report side effects involving Harvoni, Sovaldi, or amiodarone to the FDA MedWatch program, using the information in the “Contact FDA” box at the bottom of the page.


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