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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5078717 | 6113342 | I | 5078717-8 | 20060809 | DIR | N | 20060609 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5078717 | 1007572347 | PS | NAFCILLIN SODIUM | 1 | Y | D |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5078717 | RI |
Reactions reported
Event ID | PT |
---|---|
5078717 | LIVER FUNCTION TEST ABNORMAL |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |