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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 102783755 | 10278375 | 5 | F | 201403 | 20160727 | 20140704 | 20160809 | EXP | JP-ALEXION PHARMACEUTICALS INC.-A201402594 | ALEXION | 26.90 | YR | F | Y | 57.00000 | KG | 20160809 | OT | JP | JP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 102783755 | 10278375 | 1 | PS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 600 MG, QW | 125166 | 600 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | /wk | ||||||
| 102783755 | 10278375 | 2 | SS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 900 MG, Q2W | AA8793B01 | 125166 | 900 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | QOW | |||||
| 102783755 | 10278375 | 3 | C | HEPARIN CALCIUM | HEPARIN CALCIUM | 1 | Intravenous (not otherwise specified) | 5000 IU, QD | 0 | 5000 | IU | QD | |||||||
| 102783755 | 10278375 | 4 | C | WARFARIN | WARFARIN | 1 | Unknown | 3 MG, QD | 0 | 3 | MG | QD | |||||||
| 102783755 | 10278375 | 5 | C | FOLIAMIN | FOLIC ACID | 1 | Unknown | 15 MG, QD | 0 | 15 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 102783755 | 10278375 | 1 | Paroxysmal nocturnal haemoglobinuria |
| 102783755 | 10278375 | 3 | Thrombosis prophylaxis |
| 102783755 | 10278375 | 4 | Product used for unknown indication |
| 102783755 | 10278375 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 102783755 | 10278375 | HO |
| 102783755 | 10278375 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 102783755 | 10278375 | Anaemia | |
| 102783755 | 10278375 | Exposure during pregnancy |
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 |
|---|---|---|---|---|---|---|
| 102783755 | 10278375 | 1 | 20130604 | 0 | ||
| 102783755 | 10278375 | 3 | 20140701 | 20141204 | 0 | |
| 102783755 | 10278375 | 4 | 20141125 | 20150130 | 0 | |
| 102783755 | 10278375 | 5 | 20150203 | 0 |