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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118903043 | 11890304 | 3 | F | 20150901 | 20160718 | 20160105 | 20160728 | EXP | IT-MINISAL02-340687 | IT-TEVA-622004ACC | TEVA | 72.03 | YR | M | Y | 0.00000 | 20160728 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118903043 | 11890304 | 1 | PS | RAMIPRIL. | RAMIPRIL | 1 | Oral | 10 MG TOTAL | U | 77470 | 10 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118903043 | 11890304 | 1 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118903043 | 11890304 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118903043 | 11890304 | Bradycardia | |
| 118903043 | 11890304 | Cold sweat | |
| 118903043 | 11890304 | Hyperkalaemia | |
| 118903043 | 11890304 | Medication error | |
| 118903043 | 11890304 | Nausea | |
| 118903043 | 11890304 | Pallor | |
| 118903043 | 11890304 | Presyncope | |
| 118903043 | 11890304 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 118903043 | 11890304 | 1 | 20150901 | 20150901 | 0 |