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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
114923947 | 11492394 | 7 | F | 20140925 | 20160923 | 20150910 | 20160928 | EXP | PHHY2014CA128928 | NOVARTIS | 53.85 | YR | F | Y | 0.00000 | 20160928 | CN | COUNTRY NOT SPECIFIED | CA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
114923947 | 11492394 | 1 | SS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | 375 MG, BIW | U | 0 | 375 | MG | QOW | ||||||
114923947 | 11492394 | 2 | SS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | UNK | U | 0 | |||||||||
114923947 | 11492394 | 3 | SS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | UNK | U | 0 | |||||||||
114923947 | 11492394 | 4 | SS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | UNK | U | 0 | |||||||||
114923947 | 11492394 | 5 | SS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | UNK | U | 0 | |||||||||
114923947 | 11492394 | 6 | PS | DIOVAN | VALSARTAN | 1 | Oral | U | 20665 | ||||||||||
114923947 | 11492394 | 7 | C | ALVESCO | CICLESONIDE | 1 | Unknown | U | 0 | ||||||||||
114923947 | 11492394 | 8 | C | VENTOLIN | ALBUTEROL SULFATE | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
114923947 | 11492394 | 1 | Asthma |
114923947 | 11492394 | 6 | Product used for unknown indication |
114923947 | 11492394 | 7 | Product used for unknown indication |
114923947 | 11492394 | 8 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
114923947 | 11492394 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
114923947 | 11492394 | Blood pressure systolic increased | |
114923947 | 11492394 | Bronchitis | |
114923947 | 11492394 | Cough | |
114923947 | 11492394 | Diarrhoea | |
114923947 | 11492394 | Dizziness | |
114923947 | 11492394 | Drug hypersensitivity | |
114923947 | 11492394 | Fatigue | |
114923947 | 11492394 | Gastrointestinal disorder | |
114923947 | 11492394 | Headache | |
114923947 | 11492394 | Influenza | |
114923947 | 11492394 | Injection site hyperaesthesia | |
114923947 | 11492394 | Injection site hypersensitivity | |
114923947 | 11492394 | Injection site hypoaesthesia | |
114923947 | 11492394 | Injection site pain | |
114923947 | 11492394 | Malaise | |
114923947 | 11492394 | Nausea | |
114923947 | 11492394 | Oropharyngeal pain | |
114923947 | 11492394 | Pain | |
114923947 | 11492394 | Pyrexia |
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 |
---|---|---|---|---|---|---|
114923947 | 11492394 | 1 | 20140911 | 0 | ||
114923947 | 11492394 | 2 | 20140925 | 0 | ||
114923947 | 11492394 | 3 | 20151105 | 0 | ||
114923947 | 11492394 | 4 | 20151217 | 0 | ||
114923947 | 11492394 | 5 | 20160825 | 0 |