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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
114418394 | 11441839 | 4 | F | 20160827 | 20150901 | 20160902 | EXP | US-ABBVIE-15P-163-1451397-00 | ABBVIE | 0.00 | M | Y | 0.00000 | 20160902 | CN | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
114418394 | 11441839 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | U | UNKNOWN | 125057 | SOLUTION FOR INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
114418394 | 11441839 | 1 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
114418394 | 11441839 | OT |
114418394 | 11441839 | CA |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
114418394 | 11441839 | Abdominal pain | |
114418394 | 11441839 | Activities of daily living impaired | |
114418394 | 11441839 | Chronic obstructive pulmonary disease | |
114418394 | 11441839 | Congenital diaphragmatic hernia | |
114418394 | 11441839 | Feeling abnormal | |
114418394 | 11441839 | Injury | |
114418394 | 11441839 | Joint range of motion decreased | |
114418394 | 11441839 | Lung disorder | |
114418394 | 11441839 | Mobility decreased | |
114418394 | 11441839 | Rheumatoid arthritis |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |