The original 3 week placebo trial did not report any (S)AE's.
The MMRII insert, did say this:
"Only 8 subjects (3 recipients of M-M-R® II with rHA and 5 recipients of M-M-R® II with HSA) experienced a serious adverse experience during the safety follow-up period. None of these 8 serious adverse experiences was determined by the investigato…
The original 3 week placebo trial did not report any (S)AE's.
The MMRII insert, did say this:
"Only 8 subjects (3 recipients of M-M-R® II with rHA and 5 recipients of M-M-R® II with HSA) experienced a serious adverse experience during the safety follow-up period. None of these 8 serious adverse experiences was determined by the investigator to be vaccine-related (see ADVERSE REACTIONS). No subjects died during the study and no subjects were discontinued from the study due to an adverse experience."
The original 3 week placebo trial did not report any (S)AE's.
The MMRII insert, did say this:
"Only 8 subjects (3 recipients of M-M-R® II with rHA and 5 recipients of M-M-R® II with HSA) experienced a serious adverse experience during the safety follow-up period. None of these 8 serious adverse experiences was determined by the investigator to be vaccine-related (see ADVERSE REACTIONS). No subjects died during the study and no subjects were discontinued from the study due to an adverse experience."