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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
104767825 | 10476782 | 5 | F | 201204 | 20160831 | 20140925 | 20160901 | EXP | CA-ROCHE-1172178 | ROCHE | 64.38 | YR | F | Y | 73.00000 | KG | 20160901 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
104767825 | 10476782 | 1 | PS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | N | U | UNKNOWN | 125276 | 580 | MG | SOLUTION FOR INFUSION | |||||
104767825 | 10476782 | 2 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | N | U | UNKNOWN | 125276 | 560 | MG | SOLUTION FOR INFUSION | |||||
104767825 | 10476782 | 3 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | N | U | UNKNOWN | 125276 | 400 | MG | SOLUTION FOR INFUSION | |||||
104767825 | 10476782 | 4 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 0 | ||||||||||||
104767825 | 10476782 | 5 | C | IBUPROFEN. | IBUPROFEN | 1 | 0 | ||||||||||||
104767825 | 10476782 | 6 | C | COMBIGAN | BRIMONIDINE TARTRATETIMOLOL MALEATE | 1 | 0 | ||||||||||||
104767825 | 10476782 | 7 | C | LUMIGAN | BIMATOPROST | 1 | 0 | ||||||||||||
104767825 | 10476782 | 8 | C | VITAMIN C | ASCORBIC ACID | 1 | 0 | ||||||||||||
104767825 | 10476782 | 9 | C | ROSUVASTATIN. | ROSUVASTATIN | 1 | Oral | 0 | 10 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
104767825 | 10476782 | 1 | Rheumatoid arthritis |
104767825 | 10476782 | 9 | Hyperlipidaemia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
104767825 | 10476782 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
104767825 | 10476782 | Blood cholesterol increased | |
104767825 | 10476782 | Coeliac disease | |
104767825 | 10476782 | Disease progression | |
104767825 | 10476782 | Haematochezia | |
104767825 | 10476782 | Influenza like illness | |
104767825 | 10476782 | Weight decreased |
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 |
---|---|---|---|---|---|---|
104767825 | 10476782 | 1 | 20120305 | 0 | ||
104767825 | 10476782 | 2 | 20130212 | 0 | ||
104767825 | 10476782 | 3 | 20140312 | 20160804 | 0 | |
104767825 | 10476782 | 9 | 201206 | 0 |