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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5902959 | 6775014 | I | 5902959-X | 20080711 | 20080711 | 20080930 | PER | US-BAYER-200828744NA | BAYER HEALTHCARE PHARMACEUTICALS INC. | 28 | YR | F | Y | 20080930 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5902959 | 1010518946 | PS | MIRENA | 1 | INTRA-UTERINE | 81053A | 021225 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5902959 | 1010518946 | CONTRACEPTION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5902959 | INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED |
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 |
|---|---|---|---|---|---|
| 5902959 | 1010518946 | 20080707 | 20080711 | 5 | DAY |