Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125450481 | 12545048 | 1 | I | 20160528 | 20160704 | 20160711 | 20160711 | EXP | IT-MINISAL02-366018 | IT-BAYER-2016-131713 | BAYER | 43.00 | YR | A | F | Y | 79.00000 | KG | 20160711 | CN | IT | IT |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125450481 | 12545048 | 1 | PS | YASMIN | DROSPIRENONEETHINYL ESTRADIOL | 1 | Oral | DAILY DOSE 1 DF | 21098 | 1 | DF | FILM-COATED TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125450481 | 12545048 | 1 | Oral contraception |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125450481 | 12545048 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125450481 | 12545048 | Atrial fibrillation | |
| 125450481 | 12545048 | Pulmonary embolism |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125450481 | 12545048 | 1 | 20160128 | 20160525 | 0 |