Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6148139 | 7206757 | I | 6148139-7 | 20080207 | 20080225 | 20090401 | EXP | 1063481-2008-00006 | CRYOLIFE, INC. | N | MD | GERMANY |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
6148139 | 1011397589 | PS | CARDIAC TISSUE HUMAN | 1 | D | D |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6148139 | OT |
Reactions reported
Event ID | PT |
---|---|
6148139 | PRODUCT QUALITY ISSUE |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6148139 | UF |
Therapies reported
no results found |