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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7387026 | 7806837 | F | 7387026-3 | 20110101 | 20110315 | 20110331 | PER | US-BAYER-2011-012025 | BAYER HEALTHCARE PHARMACEUTICALS INC. | 29 | YR | F | Y | 20110331 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7387026 | 1016140040 | PS | MIRENA | 1 | INTRA-UTERINE | 20 ?G/D, CONT | 83361A | 021225 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7387026 | 1016140040 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
7387026 | URINARY TRACT INFECTION |
7387026 | PREGNANCY WITH CONTRACEPTIVE DEVICE |
7387026 | DEVICE DISLOCATION |
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 |
---|---|---|---|---|---|
7387026 | 1016140040 | 20090504 |