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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125959883 | 12595988 | 3 | F | 2016 | 20160830 | 20160727 | 20160902 | EXP | IE-ALEXION PHARMACEUTICALS INC-A201604735 | ALEXION | 56.54 | YR | F | Y | 0.00000 | 20160902 | PH | IE | IE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125959883 | 12595988 | 1 | PS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 900 MG, Q2W | P0004202 | 125166 | 900 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | QOW | |||||
125959883 | 12595988 | 2 | C | FOLIC ACID. | FOLIC ACID | 1 | Unknown | 0 | TABLET | ||||||||||
125959883 | 12595988 | 3 | C | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Unknown | 0 | TABLET | ||||||||||
125959883 | 12595988 | 4 | C | SALBUTAMOL | ALBUTEROL | 1 | Other | UNK, INHALER | 0 | INHALATION GAS | |||||||||
125959883 | 12595988 | 5 | C | VENTOLIN | ALBUTEROL SULFATE | 1 | Other | 5 MG, QDS | 0 | 5 | MG | ||||||||
125959883 | 12595988 | 6 | C | TAVANIC | LEVOFLOXACIN | 1 | Other | 250 MG, QD | 0 | 250 | MG | QD | |||||||
125959883 | 12595988 | 7 | C | PARACETAMOL | ACETAMINOPHEN | 1 | Other | 500 MG, PRN | 0 | 500 | MG | /yr | |||||||
125959883 | 12595988 | 8 | C | CLOROM | CLARITHROMYCIN | 1 | Unknown | UNK, QD | 0 | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125959883 | 12595988 | 1 | Paroxysmal nocturnal haemoglobinuria |
125959883 | 12595988 | 2 | Product used for unknown indication |
125959883 | 12595988 | 3 | Product used for unknown indication |
125959883 | 12595988 | 4 | Product used for unknown indication |
125959883 | 12595988 | 5 | Product used for unknown indication |
125959883 | 12595988 | 6 | Product used for unknown indication |
125959883 | 12595988 | 7 | Product used for unknown indication |
125959883 | 12595988 | 8 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125959883 | 12595988 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125959883 | 12595988 | Arthralgia | |
125959883 | 12595988 | Bone pain | |
125959883 | 12595988 | Haemoglobin decreased | |
125959883 | 12595988 | Infusion related reaction | |
125959883 | 12595988 | Pain in extremity | |
125959883 | 12595988 | Pelvic pain |
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 |
---|---|---|---|---|---|---|
125959883 | 12595988 | 1 | 20101229 | 0 |