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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127125461 | 12712546 | 1 | I | 20160811 | 20160822 | 20160902 | 20160902 | EXP | GB-MHRA-TPP13568190C3364576YC1470938001521 | GB-TEVA-687740ACC | TEVA | 42.00 | YR | M | Y | 85.00000 | KG | 20160902 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127125461 | 12712546 | 1 | PS | RAMIPRIL. | RAMIPRIL | 1 | 5 MILLIGRAM DAILY; DOSE INCREASED FROM 2.5MG | 5 | MG | U | U | 77470 | 5 | MG | QD |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127125461 | 12712546 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127125461 | 12712546 | Cough | |
127125461 | 12712546 | Lethargy | |
127125461 | 12712546 | Rash erythematous |
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 |
---|---|---|---|---|---|---|
127125461 | 12712546 | 1 | 20160811 | 0 |