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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4504455 | 5682912 | I | 4504455-3 | 20041016 | 20041117 | DIR | 41 | YR | F | N | 62.6 | KG | 20041025 | PH | N | N |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4504455 | 1005398796 | PS | PRIMAXIN | 1 | INTRAVENOUS | 250 MG IVPB BID | Y | D | |||
| 4504455 | 1005427132 | C | D5WS | 2 | |||||||
| 4504455 | 1005427133 | C | STERILE WATER | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4504455 | 1005398796 | OSTEOMYELITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4504455 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4504455 | BACK PAIN |
| 4504455 | NAUSEA |
| 4504455 | VOMITING |
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 |
|---|---|---|---|---|---|
| 4504455 | 1005398796 | 20041007 | 20041016 |