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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 94762224 | 9476222 | 4 | F | 20130226 | 20160722 | 20130826 | 20160728 | EXP | CA-ROCHE-1265249 | ROCHE | 66.72 | YR | F | Y | 0.00000 | 20160728 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 94762224 | 9476222 | 1 | PS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | 300 MG, Q4 WEEKS | Y | 103976 | 300 | MG | SOLUTION FOR INJECTION | ||||||
| 94762224 | 9476222 | 2 | SS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | 300 MG, Q4 WEEKS | Y | 103976 | 300 | MG | SOLUTION FOR INJECTION | ||||||
| 94762224 | 9476222 | 3 | C | ROSUVASTATIN. | ROSUVASTATIN | 1 | Unknown | UNK | U | 0 | |||||||||
| 94762224 | 9476222 | 4 | C | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 94762224 | 9476222 | 5 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 94762224 | 9476222 | 6 | C | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Unknown | U | 0 | ||||||||||
| 94762224 | 9476222 | 7 | C | TELMISARTAN. | TELMISARTAN | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 94762224 | 9476222 | 1 | Asthma |
| 94762224 | 9476222 | 3 | Product used for unknown indication |
| 94762224 | 9476222 | 4 | Product used for unknown indication |
| 94762224 | 9476222 | 5 | Product used for unknown indication |
| 94762224 | 9476222 | 6 | Product used for unknown indication |
| 94762224 | 9476222 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 94762224 | 9476222 | HO |
| 94762224 | 9476222 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 94762224 | 9476222 | Cerebrovascular accident | |
| 94762224 | 9476222 | Myocardial infarction | |
| 94762224 | 9476222 | Pneumonia |
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 |
|---|---|---|---|---|---|---|
| 94762224 | 9476222 | 1 | 20101117 | 0 | ||
| 94762224 | 9476222 | 2 | 201409 | 0 |