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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4879673 | 6134423 | F | 1 | 4879673-5 | 20031209 | 20051228 | 20060111 | EXP | 2006P1000005 | PDL BIOPHARMA, INC. | 77 | YR | M | N | 20060110 | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4879673 | 1006816762 | PS | RETEPLASE (RETEPLASE) | 2 | 20 UNK; QD | Y | D | ||||
| 4879673 | 1006844584 | SS | HEPARIN SODIUM | 1 | |||||||
| 4879673 | 1006844585 | SS | SOLPRIN (ACETYLSALICYLATE CALCIUM) | 2 | |||||||
| 4879673 | 1006844587 | C | ATENOLOL | 1 | |||||||
| 4879673 | 1006844594 | C | PRAVACHOL | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4879673 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4879673 | EPISTAXIS |
| 4879673 | HAEMATEMESIS |
| 4879673 | HAEMATURIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4879673 | FGN |
| 4879673 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4879673 | 1006816762 | 20031209 | 20031209 |