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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125192931 | 12519293 | 1 | I | 20160307 | 20160701 | 20160701 | PER | DE-LUPIN PHARMACEUTICALS INC.-E2B_00005087 | LUPIN | 0.00 | E | F | Y | 70.00000 | KG | 20160624 | DE | DE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125192931 | 12519293 | 1 | PS | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | Y | UNKNOWN | 78103 | 40 | MG | |||||||
125192931 | 12519293 | 2 | SS | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | DOSE REDUCED | Y | UNKNOWN | 78103 | ||||||||
125192931 | 12519293 | 3 | SS | Atorvastatin | ATORVASTATIN | 1 | Unknown | Y | UNKNOWN | 0 | 80 | MG | |||||||
125192931 | 12519293 | 4 | SS | Atorvastatin | ATORVASTATIN | 1 | Unknown | DOSE REDUCED | Y | UNKNOWN | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125192931 | 12519293 | 1 | Hypercholesterolaemia |
125192931 | 12519293 | 3 | Hypercholesterolaemia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125192931 | 12519293 | Myalgia |
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 |
---|---|---|---|---|---|---|
125192931 | 12519293 | 1 | 2012 | 0 | ||
125192931 | 12519293 | 3 | 201502 | 0 |