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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127111622 | 12711162 | 2 | F | 20160713 | 20160906 | 20160902 | 20160913 | EXP | PHHY2016IT118579 | SANDOZ | 78.79 | YR | M | Y | 0.00000 | 20160913 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127111622 | 12711162 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Oral | 1 DF, QD | 4 | DF | 70733 | 1 | DF | QD | |||||
127111622 | 12711162 | 2 | I | Cardioaspirin | ASPIRIN | 1 | Oral | 100 MG, QD | 19500 | MG | 0 | 100 | MG | GASTRO-RESISTANT TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127111622 | 12711162 | 1 | Pain |
127111622 | 12711162 | 2 | Thrombosis prophylaxis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127111622 | 12711162 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127111622 | 12711162 | Drug interaction | |
127111622 | 12711162 | Haematemesis | |
127111622 | 12711162 | Syncope |
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 |
---|---|---|---|---|---|---|
127111622 | 12711162 | 1 | 20160710 | 20160713 | 0 | |
127111622 | 12711162 | 2 | 20160101 | 20160713 | 0 |