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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126530411 | 12653041 | 1 | I | 20160804 | 20160815 | 20160815 | EXP | PHHY2016AU110123 | SANDOZ | 0.00 | F | Y | 0.00000 | 20160815 | CN | AU | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126530411 | 12653041 | 1 | PS | ROSUVASTATIN. | ROSUVASTATIN | 1 | Unknown | 20 MG, UNK | Y | 79171 | 20 | MG | FILM-COATED TABLET | ||||||
| 126530411 | 12653041 | 2 | SS | EZETIMIBE. | EZETIMIBE | 1 | Unknown | Y | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126530411 | 12653041 | 1 | Blood cholesterol |
| 126530411 | 12653041 | 2 | Blood cholesterol |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126530411 | 12653041 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126530411 | 12653041 | Bedridden | |
| 126530411 | 12653041 | Blood cholesterol abnormal | |
| 126530411 | 12653041 | Fatigue |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |