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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127086041 | 12708604 | 1 | I | 20121217 | 20160825 | 20160901 | 20160901 | EXP | IT-PFIZER INC-2016406150 | PFIZER | 63.00 | YR | F | Y | 62.00000 | KG | 20160901 | MD | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127086041 | 12708604 | 1 | PS | ATORVASTATIN CALCIUM. | ATORVASTATIN CALCIUM | 1 | Oral | UNK | Y | U | 20702 | ||||||||
| 127086041 | 12708604 | 2 | SS | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | UNK | Y | U | 0 | ||||||||
| 127086041 | 12708604 | 3 | SS | PRAVASTATIN. | PRAVASTATIN | 1 | Oral | UNK | Y | U | 0 | ||||||||
| 127086041 | 12708604 | 4 | SS | ROSUVASTATIN CALCIUM. | ROSUVASTATIN CALCIUM | 1 | Oral | Y | U | 0 | |||||||||
| 127086041 | 12708604 | 5 | C | ASPIRINA | ASPIRIN | 1 | UNK | 0 | |||||||||||
| 127086041 | 12708604 | 6 | C | VALSARTAN AND HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDEVALSARTAN | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127086041 | 12708604 | 1 | Type IIa hyperlipidaemia |
| 127086041 | 12708604 | 2 | Type IIa hyperlipidaemia |
| 127086041 | 12708604 | 3 | Type IIa hyperlipidaemia |
| 127086041 | 12708604 | 4 | Type IIa hyperlipidaemia |
| 127086041 | 12708604 | 5 | Hypertension |
| 127086041 | 12708604 | 6 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127086041 | 12708604 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127086041 | 12708604 | Myopathy | |
| 127086041 | 12708604 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |