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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123669402 | 12366940 | 2 | F | 20160905 | 20160513 | 20160909 | EXP | SE-PFIZER INC-2016253136 | PFIZER | 59.00 | YR | F | Y | 0.00000 | 20160909 | CN | SE | SE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123669402 | 12366940 | 1 | SS | Trombyl | ASPIRIN | 1 | UNK | Y | 0 | TABLET | |||||||||
| 123669402 | 12366940 | 2 | PS | ATORVASTATIN CALCIUM. | ATORVASTATIN CALCIUM | 1 | 40 MG, UNK | Y | 20702 | 40 | MG | ||||||||
| 123669402 | 12366940 | 3 | SS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | UNK | Y | 74133 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123669402 | 12366940 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123669402 | 12366940 | Faeces discoloured | |
| 123669402 | 12366940 | Haematochezia | |
| 123669402 | 12366940 | Liver function test decreased | |
| 123669402 | 12366940 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 123669402 | 12366940 | 1 | 201602 | 0 | ||
| 123669402 | 12366940 | 2 | 201602 | 201607 | 0 | |
| 123669402 | 12366940 | 3 | 201602 | 0 |