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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7022035 | 7612665 | I | 7022035-5 | 20100720 | 20100802 | 20100930 | PER | US-BAYER-201032302NA | BAYER HEALTHCARE PHARMACEUTICALS INC. | 25 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7022035 | 1014807831 | PS | MIRENA | 1 | INTRA-UTERINE | FREQUENCY: CONTINUOUS | TUOO4NF | 021225 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7022035 | 1014807831 | CONTRACEPTION |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
7022035 | DEVICE EXPULSION |
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 |
---|---|---|---|---|---|
7022035 | 1014807831 | 20100405 | 20100720 | 107 | DAY |