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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7022032 | 7612662 | I | 7022032-X | 20100830 | 20100830 | 20100930 | PER | US-BAYER-201034995NA | BAYER HEALTHCARE PHARMACEUTICALS INC. | YR | F | Y | 20100930 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7022032 | 1014807828 | PS | MIRENA | 1 | INTRA-UTERINE | CONTINUOUS | UNK | 021225 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7022032 | 1014807828 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 7022032 | DEVICE DISLOCATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |