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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126154961 | 12615496 | 1 | I | 2015 | 20160726 | 20160802 | 20160802 | EXP | CH-SM-2016-06088 | PHHY2016CH104301 | NOVARTIS | 39.58 | YR | F | Y | 71.00000 | KG | 20160802 | OT | CH | CH |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126154961 | 12615496 | 1 | PS | LESCOL | FLUVASTATIN SODIUM | 1 | Oral | U | 20261 | ||||||||||
| 126154961 | 12615496 | 2 | SS | TRIATEC | RAMIPRIL | 1 | Oral | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126154961 | 12615496 | 1 | Hypercholesterolaemia |
| 126154961 | 12615496 | 2 | Microalbuminuria |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126154961 | 12615496 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126154961 | 12615496 | Abortion spontaneous | |
| 126154961 | 12615496 | Exposure during pregnancy |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |