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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125667621 | 12566762 | 1 | I | 20160529 | 20160707 | 20160718 | 20160718 | EXP | FR-SA-2016SA126867 | AVENTIS | 72.00 | YR | E | M | Y | 0.00000 | 20160718 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125667621 | 12566762 | 1 | SS | IBUPROFEN. | IBUPROFEN | 1 | Oral | U | UNKNOWN | 0 | |||||||||
| 125667621 | 12566762 | 2 | SS | SECTRAL | ACEBUTOLOL HYDROCHLORIDE | 1 | Oral | FROM: LONG TERM | U | UNKNOWN | 0 | ||||||||
| 125667621 | 12566762 | 3 | PS | APROVEL | IRBESARTAN | 1 | Oral | Y | UNKNOWN | 20757 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125667621 | 12566762 | 2 | Myocardial ischaemia |
| 125667621 | 12566762 | 3 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125667621 | 12566762 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125667621 | 12566762 | Acute kidney injury | |
| 125667621 | 12566762 | Bradycardia | |
| 125667621 | 12566762 | Hyperkalaemia | |
| 125667621 | 12566762 | Syncope |
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 |
|---|---|---|---|---|---|---|
| 125667621 | 12566762 | 3 | 20160529 | 0 |