Interferon Side Effects
REGISTER
The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Content within the patient forum is user-generated and has not been reviewed by medical professionals. Other sections of the Melanoma Research Foundation website include information that has been reviewed by medical professionals as appropriate. All medical decisions should be made in consultation with your doctor or other qualified medical professional.

Interferon Side Effects

› Forums › General Melanoma Community › Interferon Side Effects

  • Post
    • September 26, 2015 at 8:32 pm
    Tracyd715
    Participant

    Hi everyone. My husband who is stage 3 finished the 20 day round of interferon this past Monday. He had been battling dehydration and nausea the whole time. Halfway through they added steroids and Ativan to his treatment. Wasn't doing any better since finishing Monday so they put him on fluids for 5 days. Ended up at the ER this morning because he still couldn't eat or drink with the nausea and hasn't slept much the past week. They did a CT scan on his abdomen and found lesions on his liver, spleen and lungs. They are hoping the cancer didn't spread but I thought that I read somewhere that this could also be an interferon side effect? Has anyone heard of or experienced this?

Viewing 8 reply threads
  • Replies
      • September 27, 2015 at 9:30 pm
      jpg
      Participant

      Sounds like he has disease growing and he needs to get on newer meds.  Ask the doctor about PD1 or Braf drugs and pronto!

      • September 27, 2015 at 9:30 pm
      jpg
      Participant

      Sounds like he has disease growing and he needs to get on newer meds.  Ask the doctor about PD1 or Braf drugs and pronto!

      • September 27, 2015 at 9:30 pm
      jpg
      Participant

      Sounds like he has disease growing and he needs to get on newer meds.  Ask the doctor about PD1 or Braf drugs and pronto!

      • September 28, 2015 at 1:26 pm
      Gene_S
      Participant

      Make sure you are seeing a melanoma specialist.

      • September 28, 2015 at 1:26 pm
      Gene_S
      Participant

      Make sure you are seeing a melanoma specialist.

      • September 28, 2015 at 1:26 pm
      Gene_S
      Participant

      Make sure you are seeing a melanoma specialist.

      • September 29, 2015 at 7:05 pm
      Tracyd715
      Participant

      We have a melanoma specialist who is working with the oncologist in town. My husband is having another brain Mir now and will be set up for another pet scan. It's so discouraging because he just had both done in June and everything was clear. They are going to put him on Keytruda (?) after the tests and the interferon is more out of his system. Dr said he was giving him 6-12 months. Praying nothing spread to his brain.

      • September 29, 2015 at 7:05 pm
      Tracyd715
      Participant

      We have a melanoma specialist who is working with the oncologist in town. My husband is having another brain Mir now and will be set up for another pet scan. It's so discouraging because he just had both done in June and everything was clear. They are going to put him on Keytruda (?) after the tests and the interferon is more out of his system. Dr said he was giving him 6-12 months. Praying nothing spread to his brain.

      • September 29, 2015 at 7:05 pm
      Tracyd715
      Participant

      We have a melanoma specialist who is working with the oncologist in town. My husband is having another brain Mir now and will be set up for another pet scan. It's so discouraging because he just had both done in June and everything was clear. They are going to put him on Keytruda (?) after the tests and the interferon is more out of his system. Dr said he was giving him 6-12 months. Praying nothing spread to his brain.

Viewing 8 reply threads
  • You must be logged in to reply to this topic.
About the MRF Patient Forum

The MRF Patient Forum is the oldest and largest online community of people affected by melanoma. It is designed to provide peer support and information to caregivers, patients, family and friends. There is no better place to discuss different parts of your journey with this cancer and find the friends and support resources to make that journey more bearable.

The information on the forum is open and accessible to everyone. To add a new topic or to post a reply, you must be a registered user. Please note that you will be able to post both topics and replies anonymously even though you are logged in. All posts must abide by MRF posting policies.

Popular Topics