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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122274223 | 12227422 | 3 | F | 20160826 | 20160331 | 20160902 | EXP | PHHY2016GB039719 | SANDOZ | 47.00 | YR | M | Y | 132.00000 | KG | 20160902 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122274223 | 12227422 | 1 | PS | RAMIPRIL. | RAMIPRIL | 1 | Unknown | 10 MG | 019151 | 77514 | 10 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122274223 | 12227422 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122274223 | 12227422 | OT |
| 122274223 | 12227422 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122274223 | 12227422 | Asthenia | |
| 122274223 | 12227422 | Feeling abnormal | |
| 122274223 | 12227422 | Feeling of body temperature change | |
| 122274223 | 12227422 | Hypoaesthesia | |
| 122274223 | 12227422 | Insomnia | |
| 122274223 | 12227422 | Sensory loss | |
| 122274223 | 12227422 | Speech disorder |
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 |
|---|---|---|---|---|---|---|
| 122274223 | 12227422 | 1 | 20130204 | 0 |