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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6768080 | 7214415 | F | 6768080-6 | 20090601 | 20100609 | 20100614 | EXP | GB-TEVA-199868ISR | TEVA | 63 | YR | M | Y | 20100614 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6768080 | 1013859491 | PS | PREDNISOLONE | 1 | ORAL | 089081 | |||||
| 6768080 | 1013859492 | SS | IBUPROFEN | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6768080 | 1013859491 | DRUG USE FOR UNKNOWN INDICATION |
| 6768080 | 1013859492 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6768080 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6768080 | RENAL IMPAIRMENT |
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 |
|---|---|---|---|---|---|
| 6768080 | 1013859491 | 20080407 | |||
| 6768080 | 1013859492 | 20090420 | 20090602 |