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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127807431 | 12780743 | 1 | I | 20160923 | 20160926 | 20160926 | EXP | GB-MHRA-ADR 23652984 | GB-009507513-1609GBR011964 | MERCK | 0.00 | M | Y | 0.00000 | 20160926 | CN | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127807431 | 12780743 | 1 | PS | SIMVASTATIN. | SIMVASTATIN | 1 | STARTED A COUPLE OF YEARS AGO. | N | U | 19766 | 40 | MG | TABLET |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127807431 | 12780743 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127807431 | 12780743 | Arthralgia | |
| 127807431 | 12780743 | Back pain | |
| 127807431 | 12780743 | Epistaxis | |
| 127807431 | 12780743 | Liver function test increased | |
| 127807431 | 12780743 | Musculoskeletal pain | |
| 127807431 | 12780743 | Pain in extremity | |
| 127807431 | 12780743 | Visual acuity reduced |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |