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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
115514194 | 11551419 | 4 | F | 20150910 | 20160801 | 20150925 | 20160811 | EXP | US-ALEXION PHARMACEUTICALS INC-A201503606 | ALEXION | 27.72 | YR | M | Y | 0.00000 | 20160811 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
115514194 | 11551419 | 1 | PS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 900 MG, Q2W | 45731.9297 | MG | N | T2-AD9022B02 | 125166 | 900 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | QOW | ||
115514194 | 11551419 | 2 | C | TACROLIMUS. | TACROLIMUS | 1 | Unknown | UNK | 0 | ||||||||||
115514194 | 11551419 | 3 | C | FOLIC ACID. | FOLIC ACID | 1 | Unknown | UNK | 0 | ||||||||||
115514194 | 11551419 | 4 | C | LOVENOX | ENOXAPARIN SODIUM | 1 | Unknown | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
115514194 | 11551419 | 1 | Paroxysmal nocturnal haemoglobinuria |
115514194 | 11551419 | 2 | Product used for unknown indication |
115514194 | 11551419 | 3 | Product used for unknown indication |
115514194 | 11551419 | 4 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
115514194 | 11551419 | HO |
115514194 | 11551419 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
115514194 | 11551419 | Aplastic anaemia | |
115514194 | 11551419 | Bone marrow failure | |
115514194 | 11551419 | Condition aggravated | |
115514194 | 11551419 | Haemoglobin decreased |
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 |
---|---|---|---|---|---|---|
115514194 | 11551419 | 1 | 20130918 | 20160609 | 0 |