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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1180959217 | 11809592 | 17 | F | 20150904 | 20160830 | 20151208 | 20160902 | EXP | CA-ROCHE-1631725 | ROCHE | 63.27 | YR | F | Y | 0.00000 | 20160902 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1180959217 | 11809592 | 1 | PS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | U | B2047,B2043,B2045,B2052,B2050,B2059 | 125276 | 576 | MG | SOLUTION FOR INFUSION | ||||||
| 1180959217 | 11809592 | 2 | SS | ACTEMRA | TOCILIZUMAB | 1 | Subcutaneous | 125472 | 162 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk | |||||||
| 1180959217 | 11809592 | 3 | SS | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Unknown | U | 0 | 50 | MG | ||||||||
| 1180959217 | 11809592 | 4 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | U | 0 | ||||||||||
| 1180959217 | 11809592 | 5 | C | FOLIC ACID. | FOLIC ACID | 1 | 0 | ||||||||||||
| 1180959217 | 11809592 | 6 | C | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 1180959217 | 11809592 | 7 | C | LYRICA | PREGABALIN | 1 | 0 | ||||||||||||
| 1180959217 | 11809592 | 8 | C | VOLTAREN | DICLOFENAC SODIUM | 1 | 0 | ||||||||||||
| 1180959217 | 11809592 | 9 | C | DIPHENHYDRAMINE. | DIPHENHYDRAMINE | 1 | Oral | 0 | 50 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 1180959217 | 11809592 | 1 | Rheumatoid arthritis |
| 1180959217 | 11809592 | 2 | Rheumatoid arthritis |
| 1180959217 | 11809592 | 3 | Product used for unknown indication |
| 1180959217 | 11809592 | 4 | Product used for unknown indication |
| 1180959217 | 11809592 | 9 | Premedication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 1180959217 | 11809592 | HO |
| 1180959217 | 11809592 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 1180959217 | 11809592 | Abdominal pain | |
| 1180959217 | 11809592 | Blood pressure increased | |
| 1180959217 | 11809592 | Confusional state | |
| 1180959217 | 11809592 | Diverticulitis | |
| 1180959217 | 11809592 | Drug effect incomplete | |
| 1180959217 | 11809592 | Dysgeusia | |
| 1180959217 | 11809592 | Dyspnoea | |
| 1180959217 | 11809592 | Enuresis | |
| 1180959217 | 11809592 | Fall | |
| 1180959217 | 11809592 | Fatigue | |
| 1180959217 | 11809592 | Flushing | |
| 1180959217 | 11809592 | Gastroenteritis | |
| 1180959217 | 11809592 | Haematoma | |
| 1180959217 | 11809592 | Headache | |
| 1180959217 | 11809592 | Hypertension | |
| 1180959217 | 11809592 | Laceration | |
| 1180959217 | 11809592 | Liver function test increased | |
| 1180959217 | 11809592 | Musculoskeletal chest pain | |
| 1180959217 | 11809592 | Oral herpes | |
| 1180959217 | 11809592 | Pain | |
| 1180959217 | 11809592 | Pain in extremity | |
| 1180959217 | 11809592 | Pneumonitis | |
| 1180959217 | 11809592 | Renal pain | |
| 1180959217 | 11809592 | Stress |
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 |
|---|---|---|---|---|---|---|
| 1180959217 | 11809592 | 1 | 20150904 | 20160425 | 0 | |
| 1180959217 | 11809592 | 2 | 20160628 | 0 | ||
| 1180959217 | 11809592 | 4 | 201605 | 0 | ||
| 1180959217 | 11809592 | 9 | 20160201 | 0 |