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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4360252 | 5722862 | I | 4360252-3 | 20040301 | 20040428 | 20040513 | EXP | 200411732FR | AVENTIS PHARMA | 50 | YR | M | N | 20040507 | OT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4360252 | 1004872682 | PS | OFLOXACIN | 1 | AURICULAR (OTIC) | SPRAY, INTRAAURICULAR, A FEW DAYS | 20799 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4360252 | 1004872682 | EAR INFECTION |
Outcome of event
Event ID | OUTC COD |
---|---|
4360252 | DS |
Reactions reported
Event ID | PT |
---|---|
4360252 | TENDONITIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4360252 | FGN |
4360252 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4360252 | 1004872682 | 20040301 | 20040301 |