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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1026087135 | 10260871 | 35 | F | 20120818 | 20160912 | 20140626 | 20160914 | EXP | CA-ROCHE-1131745 | ROCHE | 57.17 | YR | F | Y | 64.40000 | KG | 20160915 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1026087135 | 10260871 | 1 | PS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | B20071,B20141,B20102,B20131,B20152, | 125276 | 400 | MG | SOLUTION FOR INFUSION | |||||||
| 1026087135 | 10260871 | 2 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | B20071,B20141,B20102,B20131,B20152, | 125276 | 500 | MG | SOLUTION FOR INFUSION | |||||||
| 1026087135 | 10260871 | 3 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | B20071,B20141,B20102,B20131,B20152, | 125276 | 512 | MG | SOLUTION FOR INFUSION | |||||||
| 1026087135 | 10260871 | 4 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | B20071,B20141,B20102,B20131,B20152, | 125276 | 260 | MG | SOLUTION FOR INFUSION | |||||||
| 1026087135 | 10260871 | 5 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | B20071,B20141,B20102,B20131,B20152, | 125276 | 400 | MG | SOLUTION FOR INFUSION | |||||||
| 1026087135 | 10260871 | 6 | SS | NAPROSYN | NAPROXEN | 1 | Unknown | 17581 | |||||||||||
| 1026087135 | 10260871 | 7 | C | FOLIC ACID. | FOLIC ACID | 1 | 0 | ||||||||||||
| 1026087135 | 10260871 | 8 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 1026087135 | 10260871 | 1 | Rheumatoid arthritis |
| 1026087135 | 10260871 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 1026087135 | 10260871 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 1026087135 | 10260871 | Arthralgia | |
| 1026087135 | 10260871 | Arthritis | |
| 1026087135 | 10260871 | Blood cholesterol increased | |
| 1026087135 | 10260871 | Blood pressure diastolic abnormal | |
| 1026087135 | 10260871 | Blood pressure increased | |
| 1026087135 | 10260871 | Blood pressure systolic increased | |
| 1026087135 | 10260871 | Cellulitis | |
| 1026087135 | 10260871 | Chest pain | |
| 1026087135 | 10260871 | Clostridium difficile infection | |
| 1026087135 | 10260871 | Contusion | |
| 1026087135 | 10260871 | Diarrhoea | |
| 1026087135 | 10260871 | Ear infection | |
| 1026087135 | 10260871 | Gastrooesophageal reflux disease | |
| 1026087135 | 10260871 | Heart rate decreased | |
| 1026087135 | 10260871 | Hypertension | |
| 1026087135 | 10260871 | Infusion related reaction | |
| 1026087135 | 10260871 | Limb injury | |
| 1026087135 | 10260871 | Localised infection | |
| 1026087135 | 10260871 | Lower respiratory tract infection | |
| 1026087135 | 10260871 | Musculoskeletal pain | |
| 1026087135 | 10260871 | Nausea | |
| 1026087135 | 10260871 | Nephrolithiasis | |
| 1026087135 | 10260871 | Oropharyngeal pain | |
| 1026087135 | 10260871 | Oxygen saturation decreased | |
| 1026087135 | 10260871 | Pain in extremity | |
| 1026087135 | 10260871 | Pharyngitis | |
| 1026087135 | 10260871 | Sinusitis | |
| 1026087135 | 10260871 | Urinary tract infection | |
| 1026087135 | 10260871 | Vaccination complication | |
| 1026087135 | 10260871 | Vascular rupture | |
| 1026087135 | 10260871 | Vomiting | |
| 1026087135 | 10260871 | Weight decreased | |
| 1026087135 | 10260871 | Weight increased | |
| 1026087135 | 10260871 | White blood cell count 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 |
|---|---|---|---|---|---|---|
| 1026087135 | 10260871 | 1 | 20120816 | 0 | ||
| 1026087135 | 10260871 | 2 | 20121206 | 0 | ||
| 1026087135 | 10260871 | 3 | 20131205 | 0 | ||
| 1026087135 | 10260871 | 4 | 20140619 | 0 | ||
| 1026087135 | 10260871 | 5 | 20140814 | 0 |