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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125617071 | 12561707 | 1 | I | 20070530 | 20160706 | 20160715 | 20160715 | PER | US-BAYER-2016-134181 | BAYER | 33.00 | YR | A | F | Y | 0.00000 | 20160715 | OT | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125617071 | 12561707 | 1 | PS | YASMIN | DROSPIRENONEETHINYL ESTRADIOL | 1 | Oral | UNK | 21098 | FILM-COATED TABLET | |||||||||
125617071 | 12561707 | 2 | C | IBUPROFEN. | IBUPROFEN | 1 | 0 |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125617071 | 12561707 | OT |
125617071 | 12561707 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125617071 | 12561707 | Deep vein thrombosis | |
125617071 | 12561707 | Pulmonary embolism |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |