Vomiting with PD-1

› Forums › General Melanoma Community › Vomiting with PD-1

  • Post
    • January 19, 2015 at 10:01 pm
    mom123
    Participant
      Hello all,
       
       
       
      my son – who is on Merck Anti PD-1 for 7 weeks started vomitng in he last few days. Is this a known side effect?
       
      The drug exhausting him 🙁
       
       
       
      Thanks,
       

       

      Mom
    Viewing 2 reply threads
    • Replies
        • January 19, 2015 at 11:21 pm
        JustMeInCA
        Participant

          It's listed on the FDA sheet. It could be just a bug or something, but I think you should contact his doctor.

          http://www.fda.gov/downloads/Drugs/DrugSafety/UCM417493.pdf

           

          • January 19, 2015 at 11:21 pm
          JustMeInCA
          Participant

            It's listed on the FDA sheet. It could be just a bug or something, but I think you should contact his doctor.

            http://www.fda.gov/downloads/Drugs/DrugSafety/UCM417493.pdf

             

              • January 20, 2015 at 3:05 am
              mom123
              Participant

                Thank you

                • January 20, 2015 at 3:05 am
                mom123
                Participant

                  Thank you

                  • January 20, 2015 at 6:10 pm
                  Maureen038
                  Participant

                    Can you tell us where your son is being treated and who his doctor is? Where is his disease located? Has he been tested for mutations? it would help to know more information so we could give you better advice. People on the board are here to help you.

                    hugs,

                    Maureen 

                    • January 20, 2015 at 6:10 pm
                    Maureen038
                    Participant

                      Can you tell us where your son is being treated and who his doctor is? Where is his disease located? Has he been tested for mutations? it would help to know more information so we could give you better advice. People on the board are here to help you.

                      hugs,

                      Maureen 

                      • January 20, 2015 at 6:10 pm
                      Maureen038
                      Participant

                        Can you tell us where your son is being treated and who his doctor is? Where is his disease located? Has he been tested for mutations? it would help to know more information so we could give you better advice. People on the board are here to help you.

                        hugs,

                        Maureen 

                        • January 23, 2015 at 3:35 am
                        mom123
                        Participant

                          Hi Maureen,

                           

                          Thank you for your reply (just saw it). I have wrote all the information in previous posts ( I will add it to my profile). Generally, he is treated in DFCI, Boston. He is the first pediatric to get the drug and everything is very new to us and the clinical team. the tunor is in his neck (Lymph node) and he is suffering from pain in his neck on a daily basis.

                           

                          Hugs back,

                          Eila

                          • January 23, 2015 at 3:35 am
                          mom123
                          Participant

                            Hi Maureen,

                             

                            Thank you for your reply (just saw it). I have wrote all the information in previous posts ( I will add it to my profile). Generally, he is treated in DFCI, Boston. He is the first pediatric to get the drug and everything is very new to us and the clinical team. the tunor is in his neck (Lymph node) and he is suffering from pain in his neck on a daily basis.

                             

                            Hugs back,

                            Eila

                            • January 23, 2015 at 3:35 am
                            mom123
                            Participant

                              Hi Maureen,

                               

                              Thank you for your reply (just saw it). I have wrote all the information in previous posts ( I will add it to my profile). Generally, he is treated in DFCI, Boston. He is the first pediatric to get the drug and everything is very new to us and the clinical team. the tunor is in his neck (Lymph node) and he is suffering from pain in his neck on a daily basis.

                               

                              Hugs back,

                              Eila

                              • January 20, 2015 at 3:05 am
                              mom123
                              Participant

                                Thank you

                              • January 19, 2015 at 11:21 pm
                              JustMeInCA
                              Participant

                                It's listed on the FDA sheet. It could be just a bug or something, but I think you should contact his doctor.

                                http://www.fda.gov/downloads/Drugs/DrugSafety/UCM417493.pdf

                                 

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