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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124995834 | 12499583 | 4 | F | 20160704 | 20160627 | 20160713 | EXP | GB-MHRA-MIDB-85E517C7-8FC0-41C7-B39C-4C5C38DA73FB | GB-PFIZER INC-2016309306 | PFIZER | 85.00 | YR | M | Y | 0.00000 | 20160713 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124995834 | 12499583 | 1 | PS | AMLODIPINE BESILATE | AMLODIPINE BESYLATE | 1 | Unknown | 5 MG, 1X/DAY | 19787 | 5 | MG | QD | |||||||
| 124995834 | 12499583 | 2 | SS | ATENOLOL. | ATENOLOL | 1 | Oral | 25 MG, 1X/DAY | 73676 | 25 | MG | TABLET | QD | ||||||
| 124995834 | 12499583 | 3 | C | SIMVASTATIN. | SIMVASTATIN | 1 | 20 MG, 1X/DAY AT NIGHT | 0 | 20 | MG | QD |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124995834 | 12499583 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124995834 | 12499583 | Loss of consciousness | |
| 124995834 | 12499583 | Lung infection | |
| 124995834 | 12499583 | Nausea | |
| 124995834 | 12499583 | Orthostatic hypotension | |
| 124995834 | 12499583 | Syncope | |
| 124995834 | 12499583 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |