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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118400787 | 11840078 | 7 | F | 20150512 | 20160727 | 20151216 | 20160728 | EXP | CA-ROCHE-1578083 | ROCHE | 65.67 | YR | M | Y | 0.00000 | 20160728 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118400787 | 11840078 | 1 | PS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | Y | 125276 | 674 | MG | SOLUTION FOR INFUSION | |||||||
118400787 | 11840078 | 2 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | Y | 125276 | 680 | MG | SOLUTION FOR INFUSION | |||||||
118400787 | 11840078 | 3 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | Y | 125276 | 656 | MG | SOLUTION FOR INFUSION | |||||||
118400787 | 11840078 | 4 | C | SULPHASALAZINE | SULFASALAZINE | 1 | 0 | ||||||||||||
118400787 | 11840078 | 5 | C | NAPROXEN. | NAPROXEN | 1 | 0 | ||||||||||||
118400787 | 11840078 | 6 | C | METHOTREXATE. | METHOTREXATE | 1 | 0 | ||||||||||||
118400787 | 11840078 | 7 | C | TELMISARTAN. | TELMISARTAN | 1 | 0 | ||||||||||||
118400787 | 11840078 | 8 | C | ZANTAC | RANITIDINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
118400787 | 11840078 | 9 | C | RAPAFLO | SILODOSIN | 1 | 0 | ||||||||||||
118400787 | 11840078 | 10 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
118400787 | 11840078 | 1 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
118400787 | 11840078 | LT |
118400787 | 11840078 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
118400787 | 11840078 | Arthralgia | |
118400787 | 11840078 | Bladder neoplasm | |
118400787 | 11840078 | Blood pressure diastolic decreased | |
118400787 | 11840078 | Blood pressure fluctuation | |
118400787 | 11840078 | Blood urine present | |
118400787 | 11840078 | Cerebrovascular accident | |
118400787 | 11840078 | Drug ineffective | |
118400787 | 11840078 | Haematoma | |
118400787 | 11840078 | Hypotension | |
118400787 | 11840078 | Joint swelling | |
118400787 | 11840078 | No adverse event | |
118400787 | 11840078 | Oxygen saturation decreased | |
118400787 | 11840078 | Pain | |
118400787 | 11840078 | Pain in extremity |
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 |
---|---|---|---|---|---|---|
118400787 | 11840078 | 1 | 20150512 | 0 | ||
118400787 | 11840078 | 2 | 20150609 | 0 | ||
118400787 | 11840078 | 3 | 20160506 | 20160711 | 0 |