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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4974803 | 6044256 | F | 1 | 4974803-9 | 20051104 | 20060216 | PER | 2005069274 | PFIZER INC | F | N | 20060127 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4974803 | 1007177136 | PS | MYCOBUTIN | 1 | 150 MG | U | U | 50689 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4974803 | 1007177136 | ILL-DEFINED DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4974803 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4974803 | PAIN |
| 4974803 | PYREXIA |
| 4974803 | WHITE BLOOD CELL COUNT DECREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4974803 | CSM |
Therapies reported
| no results found |