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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127166542 | 12716654 | 2 | F | 20160915 | 20160906 | 20160920 | EXP | JP-SA-2016SA161715 | AVENTIS | 0.00 | E | Y | 0.00000 | 20160920 | PH | JP | JP |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127166542 | 12716654 | 1 | PS | PLAVIX | CLOPIDOGREL BISULFATE | 1 | Oral | U | UNK | 20839 |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127166542 | 12716654 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127166542 | 12716654 | Fall | |
127166542 | 12716654 | Haemorrhage subcutaneous | |
127166542 | 12716654 | Skin discolouration |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |