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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
103571317 | 10357131 | 7 | F | 201404 | 20160913 | 20140801 | 20160920 | EXP | AU-ALEXION PHARMACEUTICALS INC.-A201402927 | ALEXION | 81.61 | YR | F | Y | 0.00000 | 20160920 | CN | AU | AU |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
103571317 | 10357131 | 1 | PS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 600 MG, QW | 125166 | 600 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | /wk | ||||||
103571317 | 10357131 | 2 | SS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 900 MG, Q2W | 125166 | 900 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | QOW |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
103571317 | 10357131 | 1 | Paroxysmal nocturnal haemoglobinuria |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
103571317 | 10357131 | HO |
103571317 | 10357131 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
103571317 | 10357131 | Arthralgia | |
103571317 | 10357131 | Blood lactate dehydrogenase increased | |
103571317 | 10357131 | Carpal tunnel syndrome | |
103571317 | 10357131 | Cholecystitis | |
103571317 | 10357131 | Cholelithiasis | |
103571317 | 10357131 | Circulatory collapse | |
103571317 | 10357131 | Musculoskeletal pain | |
103571317 | 10357131 | Pain | |
103571317 | 10357131 | Pain in extremity | |
103571317 | 10357131 | Syncope | |
103571317 | 10357131 | Urinary tract infection |
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 |
---|---|---|---|---|---|---|
103571317 | 10357131 | 1 | 201111 | 0 |