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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107681234 | 10768123 | 4 | F | 201409 | 20160714 | 20150205 | 20160725 | EXP | DE-ABBVIE-15K-062-1340711-00 | ABBVIE | 48.57 | YR | F | Y | 65.00000 | KG | 20160725 | MD | COUNTRY NOT SPECIFIED | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 107681234 | 10768123 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | QOW | ||||||
| 107681234 | 10768123 | 2 | C | VIGANTOLETTEN | CHOLECALCIFEROL | 1 | 0 | ||||||||||||
| 107681234 | 10768123 | 3 | C | AZATHIOPRINE. | AZATHIOPRINE | 1 | 0 | ||||||||||||
| 107681234 | 10768123 | 4 | C | COLESTYRAMINE | CHOLESTYRAMINE | 1 | 0 | ||||||||||||
| 107681234 | 10768123 | 5 | C | ZINC | ZINCINC CHLORIDE | 1 | 0 | ||||||||||||
| 107681234 | 10768123 | 6 | C | SELEN | SELENIUM | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 107681234 | 10768123 | 1 | Crohn's disease |
| 107681234 | 10768123 | 2 | Product used for unknown indication |
| 107681234 | 10768123 | 3 | Product used for unknown indication |
| 107681234 | 10768123 | 4 | Product used for unknown indication |
| 107681234 | 10768123 | 5 | Product used for unknown indication |
| 107681234 | 10768123 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 107681234 | 10768123 | HO |
| 107681234 | 10768123 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 107681234 | 10768123 | Arthralgia | |
| 107681234 | 10768123 | Ligament rupture |
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 |
|---|---|---|---|---|---|---|
| 107681234 | 10768123 | 1 | 201307 | 0 |