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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125192641 | 12519264 | 1 | I | 20160118 | 20160701 | 20160701 | PER | DE-LUPIN PHARMACEUTICALS INC.-E2B_00004787 | LUPIN | 0.00 | F | Y | 0.00000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125192641 | 12519264 | 1 | PS | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | Y | Y | UNKNOWN | 78103 | ||||||||
| 125192641 | 12519264 | 2 | SS | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | Y | Y | UNKNOWN | 78103 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125192641 | 12519264 | 1 | Cerebrovascular accident |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125192641 | 12519264 | Abdominal discomfort | |
| 125192641 | 12519264 | Cardiac discomfort | |
| 125192641 | 12519264 | Dysphagia | |
| 125192641 | 12519264 | Headache | |
| 125192641 | 12519264 | Memory impairment | |
| 125192641 | 12519264 | Myalgia | |
| 125192641 | 12519264 | Visual impairment |
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 |
|---|---|---|---|---|---|---|
| 125192641 | 12519264 | 1 | 200606 | 20151123 | 0 |