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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125199051 | 12519905 | 1 | I | 20160321 | 20160701 | 20160701 | PER | DE-LUPIN PHARMACEUTICALS INC.-E2B_00005196 | LUPIN | 0.00 | A | M | Y | 88.00000 | KG | 20160621 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125199051 | 12519905 | 1 | SS | Sortis | ATORVASTATIN | 1 | Oral | Y | UNKNOWN | 0 | 10 | MG | QD | ||||||
| 125199051 | 12519905 | 2 | SS | Sortis | ATORVASTATIN | 1 | Oral | Y | UNKNOWN | 0 | 10 | MG | QD | ||||||
| 125199051 | 12519905 | 3 | PS | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | Y | UNKNOWN | 78103 | 20 | MG | QD | ||||||
| 125199051 | 12519905 | 4 | SS | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | Y | UNKNOWN | 78103 | 40 | MG | QD | ||||||
| 125199051 | 12519905 | 5 | SS | FLUVASTATIN | FLUVASTATIN SODIUM | 1 | Oral | Y | UNKNOWN | 0 | 40 | MG | QD | ||||||
| 125199051 | 12519905 | 6 | SS | PRAVASTATIN. | PRAVASTATIN | 1 | Oral | Y | UNKNOWN | 77917 | 40 | MG | QD | ||||||
| 125199051 | 12519905 | 7 | SS | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | Y | UNKNOWN | 0 | 5 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125199051 | 12519905 | 1 | Hypercholesterolaemia |
| 125199051 | 12519905 | 2 | Hypercholesterolaemia |
| 125199051 | 12519905 | 3 | Hypercholesterolaemia |
| 125199051 | 12519905 | 4 | Hypercholesterolaemia |
| 125199051 | 12519905 | 5 | Hypercholesterolaemia |
| 125199051 | 12519905 | 6 | Hypercholesterolaemia |
| 125199051 | 12519905 | 7 | Hypercholesterolaemia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125199051 | 12519905 | Depression | |
| 125199051 | 12519905 | Dizziness | |
| 125199051 | 12519905 | Erectile dysfunction | |
| 125199051 | 12519905 | Myalgia | |
| 125199051 | 12519905 | Nausea |
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 |
|---|---|---|---|---|---|---|
| 125199051 | 12519905 | 1 | 1997 | 0 | ||
| 125199051 | 12519905 | 2 | 20120213 | 0 | ||
| 125199051 | 12519905 | 3 | 20080801 | 0 | ||
| 125199051 | 12519905 | 4 | 20110407 | 0 | ||
| 125199051 | 12519905 | 5 | 2011 | 0 | ||
| 125199051 | 12519905 | 6 | 20120202 | 0 | ||
| 125199051 | 12519905 | 7 | 20160210 | 0 |