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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118249602 | 11824960 | 2 | F | 20151118 | 20151229 | 20151210 | 20160101 | EXP | SE-ROCHE-1675667 | ROCHE | 49.00 | YR | F | Y | 0.00000 | 20160101 | MD | SE | SE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118249602 | 11824960 | 1 | PS | XOLAIR | OMALIZUMAB | 1 | Unknown | BATCHNR EFTERSOKS | 103976 | ||||||||||
118249602 | 11824960 | 2 | SS | XOLAIR | OMALIZUMAB | 1 | BATCHNR EFTERSOKS | 103976 | |||||||||||
118249602 | 11824960 | 3 | C | BETAPRED | BETAMETHASONE SODIUM PHOSPHATE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
118249602 | 11824960 | 1 | Asthma |
118249602 | 11824960 | 2 | Hypersensitivity |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
118249602 | 11824960 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
118249602 | 11824960 | Feeling hot | |
118249602 | 11824960 | Swelling face | |
118249602 | 11824960 | Throat irritation |
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 |
---|---|---|---|---|---|---|
118249602 | 11824960 | 1 | 20151117 | 0 |