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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126439942 | 12643994 | 2 | F | 1999 | 20160810 | 20160811 | 20160816 | EXP | CA-PFIZER INC-2016377290 | PFIZER | 47.00 | YR | F | Y | 0.00000 | 20160816 | CN | CA | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126439942 | 12643994 | 1 | SS | ENBREL | ETANERCEPT | 1 | UNK | 0 | |||||||||||
126439942 | 12643994 | 2 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 25 MG, WEEKLY | 11719 | 25 | MG | /wk | |||||||
126439942 | 12643994 | 3 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 15 MG, WEEKLY | 11719 | 15 | MG | /wk | |||||||
126439942 | 12643994 | 4 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | 20 MG, DAILY | 0 | 20 | MG | |||||||||
126439942 | 12643994 | 5 | SS | HUMIRA | ADALIMUMAB | 1 | UNK | 0 | |||||||||||
126439942 | 12643994 | 6 | SS | REMICADE | INFLIXIMAB | 1 | UNK | 0 | |||||||||||
126439942 | 12643994 | 7 | SS | KINERET | ANAKINRA | 1 | UNK | 0 | |||||||||||
126439942 | 12643994 | 8 | SS | ORENCIA | ABATACEPT | 1 | UNK | 0 | |||||||||||
126439942 | 12643994 | 9 | SS | ACTEMRA | TOCILIZUMAB | 1 | UNK | 0 | |||||||||||
126439942 | 12643994 | 10 | C | FENTANYL. | FENTANYL | 1 | 125 UG, UNK | 0 | 125 | UG | TRANSDERMAL PATCH |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126439942 | 12643994 | 1 | Rheumatoid arthritis |
126439942 | 12643994 | 2 | Rheumatoid arthritis |
126439942 | 12643994 | 10 | Pain |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126439942 | 12643994 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126439942 | 12643994 | Drug ineffective | |
126439942 | 12643994 | Dyspnoea | |
126439942 | 12643994 | Infection | |
126439942 | 12643994 | Liver function test increased | |
126439942 | 12643994 | Osteomyelitis | |
126439942 | 12643994 | Sensitivity to weather change |
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 |
---|---|---|---|---|---|---|
126439942 | 12643994 | 2 | 1999 | 0 | ||
126439942 | 12643994 | 4 | 1999 | 1999 | 0 | |
126439942 | 12643994 | 5 | 2009 | 2009 | 0 | |
126439942 | 12643994 | 7 | 1999 | 1999 | 0 | |
126439942 | 12643994 | 8 | 2010 | 2010 | 0 | |
126439942 | 12643994 | 9 | 201604 | 0 |