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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5700584 | 6872520 | I | 5700584-7 | 20080317 | 20080409 | DIR | F | N | 148 | LBS | 20080320 | OT | N | Y | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5700584 | 1009768390 | PS | COUMADIN | 1 | ORAL | 1 MG QD PO | N | D | |||
| 5700584 | 1009796994 | SS | ARGINMAX | 2 | ORAL | 3 TABS BID PO NOT RESTARTED | D | D | CASE # 97106-145 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5700584 | 1009768390 | INTRAVENOUS CATHETER MANAGEMENT |
| 5700584 | 1009768390 | PROPHYLAXIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5700584 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5700584 | VULVAL ABSCESS |
| 5700584 | WOUND DRAINAGE |
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 |
|---|---|---|---|---|---|
| 5700584 | 1009768390 | 20080224 | |||
| 5700584 | 1009768390 | 20080304 | |||
| 5700584 | 1009796994 | 20080215 |