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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127814142 | 12781414 | 2 | F | 20141025 | 20160923 | 20160926 | 20160927 | EXP | GB-ABBVIE-16K-167-1736385-00 | ABBVIE | 46.88 | YR | M | Y | 77.00000 | KG | 20160927 | OT | COUNTRY NOT SPECIFIED | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127814142 | 12781414 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | U | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION | ||||||
127814142 | 12781414 | 2 | SS | ALCOHOL. | ALCOHOL | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
127814142 | 12781414 | 3 | C | METHOTREXATE. | METHOTREXATE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127814142 | 12781414 | 1 | Ankylosing spondylitis |
127814142 | 12781414 | 2 | Product used for unknown indication |
127814142 | 12781414 | 3 | Ankylosing spondylitis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127814142 | 12781414 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127814142 | 12781414 | Alcohol abuse | |
127814142 | 12781414 | Intentional overdose |
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 |
---|---|---|---|---|---|---|
127814142 | 12781414 | 1 | 20070312 | 0 |