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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118939153 | 11893915 | 3 | F | 20150720 | 20160714 | 20160107 | 20160725 | EXP | CA-ROCHE-1689916 | ROCHE | 79.82 | YR | F | Y | 0.00000 | 20160725 | CN | CA | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118939153 | 11893915 | 1 | PS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | U | 103976 | 300 | MG | SOLUTION FOR INJECTION | |||||||
| 118939153 | 11893915 | 2 | SS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | U | 103976 | SOLUTION FOR INJECTION | |||||||||
| 118939153 | 11893915 | 3 | SS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | U | 103976 | SOLUTION FOR INJECTION | |||||||||
| 118939153 | 11893915 | 4 | C | PREDNISONE. | PREDNISONE | 1 | Unknown | UNK | U | 0 | |||||||||
| 118939153 | 11893915 | 5 | C | VENTOLIN | ALBUTEROL SULFATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 118939153 | 11893915 | 6 | C | ADVAIR HFA | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 118939153 | 11893915 | 7 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 118939153 | 11893915 | 8 | C | QVAR | BECLOMETHASONE DIPROPIONATE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118939153 | 11893915 | 1 | Asthma |
| 118939153 | 11893915 | 4 | Product used for unknown indication |
| 118939153 | 11893915 | 5 | Product used for unknown indication |
| 118939153 | 11893915 | 6 | Product used for unknown indication |
| 118939153 | 11893915 | 7 | Product used for unknown indication |
| 118939153 | 11893915 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118939153 | 11893915 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118939153 | 11893915 | Blood pressure systolic increased | |
| 118939153 | 11893915 | Cough | |
| 118939153 | 11893915 | Dizziness | |
| 118939153 | 11893915 | Dyspnoea | |
| 118939153 | 11893915 | Environmental exposure | |
| 118939153 | 11893915 | Epistaxis | |
| 118939153 | 11893915 | Fall | |
| 118939153 | 11893915 | Fatigue | |
| 118939153 | 11893915 | Joint injury | |
| 118939153 | 11893915 | Limb injury | |
| 118939153 | 11893915 | Nausea | |
| 118939153 | 11893915 | Productive cough | |
| 118939153 | 11893915 | Pruritus |
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 |
|---|---|---|---|---|---|---|
| 118939153 | 11893915 | 1 | 20150716 | 0 | ||
| 118939153 | 11893915 | 2 | 20151230 | 0 | ||
| 118939153 | 11893915 | 3 | 20160421 | 0 |