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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127360881 | 12736088 | 1 | I | 20070510 | 20070718 | 20160912 | 20160912 | EXP | DK-DKMA-20071406 | DK-BAYER-DK-2007-027377 | BAYER | 18.00 | YR | A | F | Y | 77.00000 | KG | 20160912 | OT | DK | DK |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127360881 | 12736088 | 1 | PS | YASMIN | DROSPIRENONEETHINYL ESTRADIOL | 1 | Oral | 1 TAB(S), 21D/28D (DAILY DOSE: 1 TAB(S)) | Y | 21676 | 1 | DF | FILM-COATED TABLET | QD | |||||
127360881 | 12736088 | 2 | C | RISPERDAL | RISPERIDONE | 1 | Oral | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127360881 | 12736088 | 1 | Oral contraception |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127360881 | 12736088 | DS |
127360881 | 12736088 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127360881 | 12736088 | Deep vein thrombosis | |
127360881 | 12736088 | Oedema peripheral | |
127360881 | 12736088 | Pain | |
127360881 | 12736088 | Pain in extremity | |
127360881 | 12736088 | Peripheral swelling |
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 |
---|---|---|---|---|---|---|
127360881 | 12736088 | 1 | 200608 | 20070510 | 0 |