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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121989934 | 12198993 | 4 | F | 20160826 | 20160322 | 20160909 | EXP | GB-TEVA-644257ACC | TEVA | 0.00 | M | Y | 132.00000 | KG | 20160909 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121989934 | 12198993 | 1 | PS | RAMIPRIL. | RAMIPRIL | 1 | Unknown | 019151 | 77470 | 10 | MG | CAPSULE |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
121989934 | 12198993 | OT |
121989934 | 12198993 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
121989934 | 12198993 | Asthenia | |
121989934 | 12198993 | Feeling abnormal | |
121989934 | 12198993 | Feeling of body temperature change | |
121989934 | 12198993 | Hypoaesthesia | |
121989934 | 12198993 | Insomnia | |
121989934 | 12198993 | Sensory loss | |
121989934 | 12198993 | 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 |
---|---|---|---|---|---|---|
121989934 | 12198993 | 1 | 20130204 | 0 |