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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7487224 | 7916821 | I | 7487224-4 | 20091101 | 20110411 | 20110518 | PER | US-BAYER-2011-031830 | BAYER HEALTHCARE PHARMACEUTICALS INC. | 43 | YR | F | Y | 60 | KG | 20110518 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7487224 | 1016524437 | SS | DROSPIRENONE AND ETHINYL ESTRADIOL | 1 | UNK | 021098 | |||||
7487224 | 1016524436 | PS | YASMIN | 1 | UNK | 021098 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7487224 | 1016524437 | PRODUCT USED FOR UNKNOWN INDICATION |
7487224 | 1016524436 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
7487224 | HO |
Reactions reported
Event ID | PT |
---|---|
7487224 | CEREBROVASCULAR ACCIDENT |
7487224 | CEREBRAL INFARCTION |
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 |
---|---|---|---|---|---|
7487224 | 1016524437 | 20080901 | 20091101 | ||
7487224 | 1016524436 | 20080101 | 20080901 |