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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127443411 | 12744341 | 1 | I | 201608 | 20160913 | 20160914 | 20160914 | EXP | US-BEH-2016073414 | CSL BEHRING | 0.00 | M | Y | 0.00000 | 20160915 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127443411 | 12744341 | 1 | PS | KCENTRA | COAGULATION FACTOR IX HUMANCOAGULATION FACTOR VII HUMANCOAGULATION FACTOR X HUMANPROTEIN CPROTEIN S HUMANPROTHROMBIN | 1 | Unknown | UNK | 125421 | INJECTION | |||||||||
| 127443411 | 12744341 | 2 | SS | NOVOSEVEN | COAGULATION FACTOR VIIA RECOMBINANT HUMAN | 1 | Unknown | 5 MG, EVERY FEW HOURS | DS6L033 | 0 | 5 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127443411 | 12744341 | 1 | Haemorrhage |
| 127443411 | 12744341 | 2 | Haemorrhage |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127443411 | 12744341 | HO |
| 127443411 | 12744341 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127443411 | 12744341 | Death |
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 |
|---|---|---|---|---|---|---|
| 127443411 | 12744341 | 1 | 201608 | 0 | ||
| 127443411 | 12744341 | 2 | 201608 | 0 |