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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7583507 | 8016847 | I | 7583507-8 | 20110602 | 20110630 | PER | US-BAYER-2011-048068 | BAYER HEALTHCARE PHARMACEUTICALS INC. | YR | F | Y | 20110630 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7583507 | 1016904591 | PS | YAZ | 1 | 021676 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7583507 | 1016904591 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
7583507 | MENSTRUATION DELAYED |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |