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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5902962 | 6775016 | I | 5902962-X | 20080709 | 20080709 | 20080930 | PER | US-BAYER-200828524NA | BAYER HEALTHCARE PHARMACEUTICALS INC. | 41 | YR | F | Y | 20080930 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5902962 | 1010518949 | PS | MIRENA | 1 | INTRA-UTERINE | UNKNOWN | 021225 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5902962 | 1010518949 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5902962 | 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 |
---|---|---|---|---|---|
5902962 | 1010518949 | 20060801 | 20080709 |