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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119909093 | 11990909 | 3 | F | 20160914 | 20160202 | 20160921 | EXP | CA-ABBVIE-16K-028-1548389-00 | ABBVIE | 0.00 | M | Y | 91.00000 | KG | 20160921 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119909093 | 11990909 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | Y | UNKNOWN | 125057 | 80 | MG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | /wk | |||||
| 119909093 | 11990909 | 2 | C | PANTOLOC | PANTOPRAZOLE SODIUM | 1 | 0 | ||||||||||||
| 119909093 | 11990909 | 3 | C | CANDESARTAN | CANDESARTAN | 1 | 0 | ||||||||||||
| 119909093 | 11990909 | 4 | C | LYRICA | PREGABALIN | 1 | 0 | ||||||||||||
| 119909093 | 11990909 | 5 | C | SINGULAIR | MONTELUKAST SODIUM | 1 | 0 | ||||||||||||
| 119909093 | 11990909 | 6 | C | SOTALOL. | SOTALOL | 1 | 0 | ||||||||||||
| 119909093 | 11990909 | 7 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | 0 | ||||||||||||
| 119909093 | 11990909 | 8 | C | ADVAIR HFA | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 119909093 | 11990909 | 1 | Crohn's disease |
| 119909093 | 11990909 | 2 | Product used for unknown indication |
| 119909093 | 11990909 | 3 | Product used for unknown indication |
| 119909093 | 11990909 | 4 | Product used for unknown indication |
| 119909093 | 11990909 | 5 | Product used for unknown indication |
| 119909093 | 11990909 | 6 | Product used for unknown indication |
| 119909093 | 11990909 | 7 | Product used for unknown indication |
| 119909093 | 11990909 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 119909093 | 11990909 | HO |
| 119909093 | 11990909 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 119909093 | 11990909 | Intestinal obstruction | |
| 119909093 | 11990909 | Weight 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 |
|---|---|---|---|---|---|---|
| 119909093 | 11990909 | 1 | 20131122 | 20160115 | 0 |