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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
117337352 | 11733735 | 2 | F | 201509 | 20160707 | 20151113 | 20160714 | EXP | IT-ABBVIE-15K-083-1496488-00 | ABBVIE | 75.45 | YR | F | Y | 0.00000 | 20160714 | MD | IT | IT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
117337352 | 11733735 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | Y | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
117337352 | 11733735 | 1 | Psoriasis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
117337352 | 11733735 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
117337352 | 11733735 | Erythrodermic psoriasis | |
117337352 | 11733735 | Neutrophil count increased | |
117337352 | 11733735 | Pleural effusion | |
117337352 | 11733735 | Psoriasis | |
117337352 | 11733735 | Pustular psoriasis | |
117337352 | 11733735 | Skin infection | |
117337352 | 11733735 | Skin lesion | |
117337352 | 11733735 | White blood cell count increased |
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 |
---|---|---|---|---|---|---|
117337352 | 11733735 | 1 | 20130408 | 20151017 | 0 |