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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6672589 | 7798109 | I | 6672589-3 | 20090210 | 20100402 | 20100408 | PER | US-BAYER-201018409NA | BAYER HEALTHCARE PHARMACEUTICALS INC. | YR | F | Y | 20100408 | LW | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6672589 | 1013465216 | PS | DROSPIRENONE AND ETHINYL ESTRADIOL | 1 | UNKNOWN | 21098 | |||||
| 6672589 | 1013465217 | SS | YASMIN | 1 | ORAL | UNK | 021098 | ||||
| 6672589 | 1013465218 | SS | YAZ | 1 | ORAL | 021676 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6672589 | 1013465216 | PRODUCT USED FOR UNKNOWN INDICATION |
| 6672589 | 1013465217 | PRODUCT USED FOR UNKNOWN INDICATION |
| 6672589 | 1013465218 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6672589 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6672589 | DEEP VEIN THROMBOSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |