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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127236101 | 12723610 | 1 | I | 20141031 | 20160902 | 20160908 | 20160908 | EXP | GB-GLENMARK GENERICS (EUROPE) LTD.-2016GMK024173 | GLENMARK | 0.00 | Y | 0.00000 | 20160908 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127236101 | 12723610 | 1 | SS | ROSUVASTATIN CALCIUM. | ROSUVASTATIN CALCIUM | 1 | Oral | UNK | N | 0 | |||||||||
| 127236101 | 12723610 | 2 | PS | PRAVASTATIN SODIUM. | PRAVASTATIN SODIUM | 1 | Oral | UNK | N | 77987 | |||||||||
| 127236101 | 12723610 | 3 | SS | EZETIMIBE. | EZETIMIBE | 1 | Oral | UNK | N | 0 | |||||||||
| 127236101 | 12723610 | 4 | SS | ATORVASTATIN | ATORVASTATIN | 1 | Oral | UNK | N | 0 | |||||||||
| 127236101 | 12723610 | 5 | SS | ATORVASTATIN | ATORVASTATIN | 1 | Oral | UNK | N | 0 | |||||||||
| 127236101 | 12723610 | 6 | SS | CLOFIBRATE | CLOFIBRATE | 1 | Oral | UNK | N | 0 | |||||||||
| 127236101 | 12723610 | 7 | C | IBUPROFEN. | IBUPROFEN | 1 | Unknown | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127236101 | 12723610 | 1 | Blood cholesterol increased |
| 127236101 | 12723610 | 2 | Blood cholesterol increased |
| 127236101 | 12723610 | 3 | Blood cholesterol increased |
| 127236101 | 12723610 | 4 | Blood cholesterol increased |
| 127236101 | 12723610 | 6 | Blood cholesterol increased |
| 127236101 | 12723610 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127236101 | 12723610 | DS |
| 127236101 | 12723610 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127236101 | 12723610 | Arthropathy | |
| 127236101 | 12723610 | Pain |
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 |
|---|---|---|---|---|---|---|
| 127236101 | 12723610 | 1 | 20141019 | 20160819 | 0 | |
| 127236101 | 12723610 | 2 | 20141019 | 20160819 | 0 | |
| 127236101 | 12723610 | 3 | 20141019 | 20160819 | 0 | |
| 127236101 | 12723610 | 4 | 20141019 | 20160819 | 0 | |
| 127236101 | 12723610 | 5 | 20160819 | 0 | ||
| 127236101 | 12723610 | 6 | 20141019 | 20160819 | 0 |