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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
111870156 | 11187015 | 6 | F | 20150504 | 20160906 | 20150615 | 20160912 | EXP | US-ALEXION PHARMACEUTICALS INC.-A201502077 | ALEXION | 0.00 | M | Y | 0.00000 | 20160912 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
111870156 | 11187015 | 1 | PS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | UNK | Y | T2-AD4285B01 | 125166 | CONCENTRATE FOR SOLUTION FOR INFUSION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
111870156 | 11187015 | 1 | Paroxysmal nocturnal haemoglobinuria |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
111870156 | 11187015 | OT |
111870156 | 11187015 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
111870156 | 11187015 | Clostridium difficile infection | |
111870156 | 11187015 | Haemoglobin abnormal | |
111870156 | 11187015 | Pain | |
111870156 | 11187015 | Pneumonia | |
111870156 | 11187015 | Systemic inflammatory response syndrome |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |