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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7023325 | 7613532 | I | 7023325-2 | 20100920 | 20100930 | EXP | US-BAXTER-2010BH023975 | BAXTER | YR | M | Y | 20100930 | CN | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7023325 | 1014813765 | PS | DIANEAL | 1 | INTRAPERITONEAL | UNKNOWN | |||||
7023325 | 1014813766 | SS | DIANEAL | 1 | INTRAPERITONEAL | UNKNOWN |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7023325 | 1014813765 | PERITONEAL DIALYSIS |
7023325 | 1014813766 | PERITONEAL DIALYSIS |
Outcome of event
Event ID | OUTC COD |
---|---|
7023325 | DE |
Reactions reported
Event ID | PT |
---|---|
7023325 | CARDIAC DISORDER |
7023325 | CEREBROVASCULAR ACCIDENT |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
7023325 | 1014813765 | 20100918 | |||
7023325 | 1014813766 | 20100918 |