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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125701912 | 12570191 | 2 | F | 20160507 | 20160712 | 20160719 | 20160722 | EXP | IT-MINISAL02-366307 | IT-TEVA-677062ACC | TEVA | 64.49 | YR | M | Y | 0.00000 | 20160722 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125701912 | 12570191 | 1 | PS | PLAVIX | CLOPIDOGREL BISULFATE | 1 | Unknown | U | 0 | ||||||||||
125701912 | 12570191 | 2 | SS | CARDIOASPIRIN - 100 MG COMPRESSE GASTRORESISTENTI | ASPIRIN | 1 | Oral | 100 MILLIGRAM DAILY; | U | U | 0 | 100 | MG | ||||||
125701912 | 12570191 | 3 | C | ZOPRANOL - 30 MG COMPRESSE RIVESTITE CON FILM | 2 | Oral | 30 MG | U | 0 | 30 | MG | FILM-COATED TABLET | |||||||
125701912 | 12570191 | 4 | C | TORVAST - 80 MG COMPRESSE RIVESTITE CON FILM | 2 | Oral | 80 MG | U | 0 | 80 | MG | FILM-COATED TABLET | |||||||
125701912 | 12570191 | 5 | C | LOPRESOR - 100 MG COMPRESSE RIVESTITE CON FILM | METOPROLOL TARTRATE | 1 | Oral | 100 MG | U | 0 | 100 | MG | FILM-COATED TABLET | ||||||
125701912 | 12570191 | 6 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125701912 | 12570191 | 2 | Myocardial ischaemia |
125701912 | 12570191 | 3 | Product used for unknown indication |
125701912 | 12570191 | 4 | Product used for unknown indication |
125701912 | 12570191 | 5 | Product used for unknown indication |
125701912 | 12570191 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125701912 | 12570191 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125701912 | 12570191 | Abdominal pain | |
125701912 | 12570191 | Haematuria |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |