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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126904621 | 12690462 | 1 | I | 20160815 | 20160826 | 20160826 | EXP | GB-B. BRAUN MEDICAL INC.-1056782 | B BRAUN | 24.00 | MON | M | Y | 0.00000 | 20160826 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126904621 | 12690462 | 1 | PS | SODIUM CHLORIDE. | SODIUM CHLORIDE | 1 | 19635 | ||||||||||||
| 126904621 | 12690462 | 2 | SS | BAXTER HEPARIN SODIUM BP INFUSION 1000IU/L | HEPARIN SODIUM | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126904621 | 12690462 | 1 | Catheter management |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126904621 | 12690462 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126904621 | 12690462 | Bleeding time prolonged | |
| 126904621 | 12690462 | Blood pressure systolic decreased | |
| 126904621 | 12690462 | Complication associated with device | |
| 126904621 | 12690462 | Haemorrhage | |
| 126904621 | 12690462 | Overdose |
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 |
|---|---|---|---|---|---|---|
| 126904621 | 12690462 | 1 | 20160728 | 0 | ||
| 126904621 | 12690462 | 2 | 20160728 | 0 |