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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125212561 | 12521256 | 1 | I | 20150926 | 20160623 | 20160701 | 20160701 | EXP | CN-BAXTER-2016BAX033932 | BAXTER | 61.00 | YR | F | Y | 53.00000 | KG | 20160701 | MD | CN | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125212561 | 12521256 | 1 | SS | 20% MANNITOL INJECTION | MANNITOL | 1 | Intravenous drip | Y | S1505078 | 0 | 250 | ML | INJECTION | QD | |||||
| 125212561 | 12521256 | 2 | PS | 0.9% SODIUM CHLORIDE INJECTION | SODIUM CHLORIDE | 1 | Unknown | Y | 16677 | 100 | ML | INJECTION | |||||||
| 125212561 | 12521256 | 3 | SS | 0.9% SODIUM CHLORIDE INJECTION | SODIUM CHLORIDE | 1 | Unknown | Y | 16677 | 250 | ML | ||||||||
| 125212561 | 12521256 | 4 | SS | 0.9% SODIUM CHLORIDE INJECTION | SODIUM CHLORIDE | 1 | Intravenous drip | Y | 16677 | 250 | ML | QD | |||||||
| 125212561 | 12521256 | 5 | SS | ALPROSTADIL. | ALPROSTADIL | 1 | Intravenous drip | 2 VIAL | Y | 20150326B | 0 | INJECTION | QD | ||||||
| 125212561 | 12521256 | 6 | SS | CERVUS AND CUCUMIS POLYPEPTIDE | POLYPEPTIDES | 1 | Unknown | 2 VIALS | Y | 0 | |||||||||
| 125212561 | 12521256 | 7 | SS | CERVUS AND CUCUMIS POLYPEPTIDE | POLYPEPTIDES | 1 | Unknown | Y | 0 | ||||||||||
| 125212561 | 12521256 | 8 | SS | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Unknown | Y | 0 | 40 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125212561 | 12521256 | 1 | Swelling |
| 125212561 | 12521256 | 2 | Medication dilution |
| 125212561 | 12521256 | 5 | Cardiovascular disorder |
| 125212561 | 12521256 | 6 | Product used for unknown indication |
| 125212561 | 12521256 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125212561 | 12521256 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125212561 | 12521256 | Condition aggravated | |
| 125212561 | 12521256 | Pruritus | |
| 125212561 | 12521256 | Urticaria |
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 |
|---|---|---|---|---|---|---|
| 125212561 | 12521256 | 1 | 20150919 | 20150927 | 0 | |
| 125212561 | 12521256 | 2 | 20150919 | 0 | ||
| 125212561 | 12521256 | 3 | 20150919 | 20150927 | 0 | |
| 125212561 | 12521256 | 4 | 20150922 | 20150927 | 0 | |
| 125212561 | 12521256 | 5 | 20150922 | 20150927 | 0 | |
| 125212561 | 12521256 | 6 | 20150919 | 20150927 | 0 | |
| 125212561 | 12521256 | 7 | 20150929 | 0 | ||
| 125212561 | 12521256 | 8 | 20150919 | 0 |