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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4466779 | 5665028 | I | 4466779-8 | 20040101 | 20040921 | 20040930 | EXP | 2004-02-0972 | SCHERING-PLOUGH CORPORATION | 29 | YR | F | N | 121 | LBS | 20040921 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4466779 | 1005268298 | PS | EULEXIN | 1 | ORAL | 250 MG BID ORAL | Y | D | 18554 | ||
| 4466779 | 1005288525 | C | MIRCETTE (DESOGESTROL/ETHINYL ESTRADIOL) | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4466779 | 1005268298 | HIRSUTISM |
| 4466779 | 1005268298 | POLYCYSTIC OVARIES |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4466779 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4466779 | COLITIS |
| 4466779 | RECTAL HAEMORRHAGE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4466779 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4466779 | 1005268298 | 20040122 | 20040129 |