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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472346 | 6312772 | F | 5472346-X | 20061201 | 20070921 | 20070930 | EXP | US-SHR-US-2007-008924 | BERLEX | 35 | YR | F | Y | 90.7 | KG | 20070928 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472346 | 1008989632 | PS | MIRENA | 1 | INTRA-UTERINE | 20 A?G/DAY, CONT | 021225 | ||||
| 5472346 | 1008989633 | C | CYMBALTA | 1 | ORAL | 60 MG, 1X/DAY | |||||
| 5472346 | 1008989634 | C | PROVIGIL | 1 | ORAL | 200 MG, 2X/DAY |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5472346 | 1008989632 | CONTRACEPTION |
| 5472346 | 1008989633 | DEPRESSION |
| 5472346 | 1008989634 | NARCOLEPSY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5472346 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5472346 | PLATELET COUNT DECREASED |
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 |
|---|---|---|---|---|---|
| 5472346 | 1008989632 | 20041001 | |||
| 5472346 | 1008989633 | 19960901 | |||
| 5472346 | 1008989634 | 19960101 |