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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126346201 | 12634620 | 1 | I | 20160731 | 20160801 | 20160809 | 20160809 | PER | BR-BAYER-2016-148825 | BAYER | 30.00 | YR | A | F | Y | 0.00000 | 20160809 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126346201 | 12634620 | 1 | PS | YAZ | DROSPIRENONEETHINYL ESTRADIOL | 1 | Oral | UNK | 21676 | FILM-COATED TABLET | |||||||||
| 126346201 | 12634620 | 2 | C | Miosan | CYCLOBENZAPRINE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126346201 | 12634620 | 1 | Contraception |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126346201 | 12634620 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126346201 | 12634620 | Drug dose omission | |
| 126346201 | 12634620 | Haemorrhage urinary tract | |
| 126346201 | 12634620 | Musculoskeletal pain | |
| 126346201 | 12634620 | Musculoskeletal stiffness | |
| 126346201 | 12634620 | Withdrawal bleed |
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 |
|---|---|---|---|---|---|---|
| 126346201 | 12634620 | 1 | 201508 | 0 |