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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126497901 | 12649790 | 1 | I | 20150817 | 20160802 | 20160812 | 20160812 | EXP | FR-009507513-1608FRA003565 | MERCK | 63.34 | YR | M | Y | 75.00000 | KG | 20160812 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126497901 | 12649790 | 1 | PS | EZETROL | EZETIMIBE | 1 | Oral | UNK | Y | 21445 | TABLET | ||||||||
| 126497901 | 12649790 | 2 | SS | AUGMENTIN | AMOXICILLINCLAVULANATE POTASSIUM | 1 | Oral | UNK | Y | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126497901 | 12649790 | 2 | Acute sinusitis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126497901 | 12649790 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126497901 | 12649790 | Cholestatic liver injury | |
| 126497901 | 12649790 | Hepatocellular injury |
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 |
|---|---|---|---|---|---|---|
| 126497901 | 12649790 | 1 | 20150807 | 20150817 | 0 | |
| 126497901 | 12649790 | 2 | 20150812 | 20150817 | 0 |