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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127115241 | 12711524 | 1 | I | 20160825 | 20160902 | 20160902 | EXP | RU-BAYER-2016-166736 | BAYER | 23.00 | YR | A | F | Y | 0.00000 | 20160902 | CN | RU | RU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127115241 | 12711524 | 1 | PS | Yarina | DROSPIRENONEETHINYL ESTRADIOL | 1 | Oral | UNK | 21098 | FILM-COATED TABLET | |||||||||
| 127115241 | 12711524 | 2 | SS | YAZ | DROSPIRENONEETHINYL ESTRADIOL | 1 | Oral | UNK | 0 | FILM-COATED TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127115241 | 12711524 | 1 | Ovarian rupture |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127115241 | 12711524 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127115241 | 12711524 | Nausea | |
| 127115241 | 12711524 | Off label use | |
| 127115241 | 12711524 | Ovarian rupture | |
| 127115241 | 12711524 | Product use issue | |
| 127115241 | 12711524 | Therapeutic response unexpected | |
| 127115241 | 12711524 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |