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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7300032 | 7776947 | F | 7300032-X | 20110207 | 20110217 | EXP | US-BAXTER-2011BH001548 | BAXTER | 63 | YR | F | Y | 20110217 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7300032 | 1015809918 | PS | DIANEAL | 1 | INTRAPERITONEAL | NOWN |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7300032 | 1015809918 | PERITONEAL DIALYSIS |
Outcome of event
Event ID | OUTC COD |
---|---|
7300032 | DE |
Reactions reported
Event ID | PT |
---|---|
7300032 | DEHYDRATION |
7300032 | LACTIC ACIDOSIS |
7300032 | HYPOTENSION |
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 |
---|---|---|---|---|---|
7300032 | 1015809918 | 20110108 |