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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122974782 | 12297478 | 2 | F | 20160920 | 20160422 | 20160926 | EXP | US-ALEXION PHARMACEUTICALS INC-A201602843 | ALEXION | 0.00 | M | Y | 0.00000 | 20160926 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122974782 | 12297478 | 1 | PS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | UNK | U | T3-AE4582B02 | 125166 | CONCENTRATE FOR SOLUTION FOR INFUSION | |||||||
| 122974782 | 12297478 | 2 | SS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 1200 MG, Q10 DAYS | U | 125166 | 1200 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | ||||||
| 122974782 | 12297478 | 3 | SS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 900 MG, Q10 DAYS | U | 125166 | 900 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | ||||||
| 122974782 | 12297478 | 4 | SS | LOVENOX | ENOXAPARIN SODIUM | 1 | Intravenous (not otherwise specified) | UNK | U | 0 | |||||||||
| 122974782 | 12297478 | 5 | C | HEPARIN | HEPARIN SODIUM | 1 | Subcutaneous | UNK, Q8H | 0 | Q8H |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122974782 | 12297478 | 1 | Paroxysmal nocturnal haemoglobinuria |
| 122974782 | 12297478 | 4 | Product used for unknown indication |
| 122974782 | 12297478 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122974782 | 12297478 | OT |
| 122974782 | 12297478 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122974782 | 12297478 | Blood count abnormal | |
| 122974782 | 12297478 | Contusion | |
| 122974782 | 12297478 | Haemorrhage | |
| 122974782 | 12297478 | Inappropriate schedule of drug administration | |
| 122974782 | 12297478 | Incorrect dose administered | |
| 122974782 | 12297478 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |