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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
92994754 | 9299475 | 4 | F | 20160921 | 20130521 | 20160927 | EXP | CA-ROCHE-1226509 | ROCHE | 0.00 | M | Y | 0.00000 | 20160927 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
92994754 | 9299475 | 1 | PS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | U | 103976 | 150 | MG | SOLUTION FOR INJECTION | |||||||
92994754 | 9299475 | 2 | C | ADVAIR HFA | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | Unknown | 0 | |||||||||||
92994754 | 9299475 | 3 | C | FLOVENT | FLUTICASONE PROPIONATE | 1 | Unknown | 0 | |||||||||||
92994754 | 9299475 | 4 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | Unknown | 0 | |||||||||||
92994754 | 9299475 | 5 | C | PREDNISONE. | PREDNISONE | 1 | Unknown | 0 | |||||||||||
92994754 | 9299475 | 6 | C | NAPROSYN | NAPROXEN | 1 | Unknown | 0 | |||||||||||
92994754 | 9299475 | 7 | C | PROSCAR | FINASTERIDE | 1 | Unknown | 0 | |||||||||||
92994754 | 9299475 | 8 | C | PARIET | RABEPRAZOLE SODIUM | 1 | Unknown | 0 | |||||||||||
92994754 | 9299475 | 9 | C | METHOTREXATE. | METHOTREXATE | 1 | Unknown | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
92994754 | 9299475 | 1 | Asthma |
92994754 | 9299475 | 2 | Product used for unknown indication |
92994754 | 9299475 | 3 | Product used for unknown indication |
92994754 | 9299475 | 4 | Product used for unknown indication |
92994754 | 9299475 | 5 | Product used for unknown indication |
92994754 | 9299475 | 6 | Product used for unknown indication |
92994754 | 9299475 | 7 | Product used for unknown indication |
92994754 | 9299475 | 8 | Product used for unknown indication |
92994754 | 9299475 | 9 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
92994754 | 9299475 | HO |
92994754 | 9299475 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
92994754 | 9299475 | Aortic stenosis | |
92994754 | 9299475 | Asthma | |
92994754 | 9299475 | Chest discomfort | |
92994754 | 9299475 | Cough | |
92994754 | 9299475 | Dyspnoea exertional | |
92994754 | 9299475 | Forced expiratory volume decreased |
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 |
---|---|---|---|---|---|---|
92994754 | 9299475 | 1 | 20120827 | 0 |