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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126941891 | 12694189 | 1 | I | 20160816 | 20160829 | 20160829 | EXP | US-NOVOPROD-506650 | NOVO NORDISK | 0.00 | M | Y | 0.00000 | 20160829 | CN | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126941891 | 12694189 | 1 | PS | NOVOSEVEN | COAGULATION FACTOR VIIA RECOMBINANT HUMAN | 1 | UNKNOWN | DS6L033 | 103665 | POWDER AND SOLVENT FOR SOLUTION FOR INJECTION | |||||||||
126941891 | 12694189 | 2 | SS | KCENTRA | COAGULATION FACTOR IX HUMANCOAGULATION FACTOR VII HUMANCOAGULATION FACTOR X HUMANPROTEIN CPROTEIN S HUMANPROTHROMBIN | 1 | UNKNOWN | UNKNOWN | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126941891 | 12694189 | 1 | Haemorrhage |
126941891 | 12694189 | 2 | Haemorrhage |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126941891 | 12694189 | HO |
126941891 | 12694189 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126941891 | 12694189 | Haemorrhage |
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 |
---|---|---|---|---|---|---|
126941891 | 12694189 | 1 | 201608 | 0 | ||
126941891 | 12694189 | 2 | 201608 | 0 |