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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120485798 | 12048579 | 8 | F | 20160121 | 20160711 | 20160208 | 20160721 | EXP | GB-ALEXION PHARMACEUTICALS INC-A201600441 | ALEXION | 42.67 | YR | F | Y | 0.00000 | 20160721 | CN | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120485798 | 12048579 | 1 | PS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | UNK | 125166 | CONCENTRATE FOR SOLUTION FOR INFUSION | |||||||||
| 120485798 | 12048579 | 2 | SS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 900 MG, Q2W | P0004002 | 125166 | 900 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | QOW | |||||
| 120485798 | 12048579 | 3 | SS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 900 MG, Q2W | P0003801 | 125166 | 900 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | QOW | |||||
| 120485798 | 12048579 | 4 | SS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 900 MG, Q2W | P0004102 | 125166 | 900 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | QOW | |||||
| 120485798 | 12048579 | 5 | SS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 900 MG, Q2W | P0004302 | 125166 | 900 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | QOW | |||||
| 120485798 | 12048579 | 6 | C | PENCILLIN | PENICILLIN | 1 | Oral | 500 MG, BID | 0 | 500 | MG | BID | |||||||
| 120485798 | 12048579 | 7 | C | WARFARIN | WARFARIN | 1 | Unknown | VARYING DOSES, USUALLY 8 MG | 0 | ||||||||||
| 120485798 | 12048579 | 8 | C | COCODAMOL | ACETAMINOPHENCODEINE PHOSPHATE | 1 | Unknown | 20/500 NG | 0 | ||||||||||
| 120485798 | 12048579 | 9 | C | FOLIC ACID. | FOLIC ACID | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120485798 | 12048579 | 1 | Paroxysmal nocturnal haemoglobinuria |
| 120485798 | 12048579 | 6 | Product used for unknown indication |
| 120485798 | 12048579 | 7 | Product used for unknown indication |
| 120485798 | 12048579 | 8 | Product used for unknown indication |
| 120485798 | 12048579 | 9 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120485798 | 12048579 | HO |
| 120485798 | 12048579 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120485798 | 12048579 | Chills | |
| 120485798 | 12048579 | Cough | |
| 120485798 | 12048579 | Decreased appetite | |
| 120485798 | 12048579 | Dysarthria | |
| 120485798 | 12048579 | Fatigue | |
| 120485798 | 12048579 | Headache | |
| 120485798 | 12048579 | Menorrhagia | |
| 120485798 | 12048579 | Nausea | |
| 120485798 | 12048579 | Oropharyngeal pain | |
| 120485798 | 12048579 | Pyrexia | |
| 120485798 | 12048579 | Viral infection |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |