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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
119421334 | 11942133 | 4 | F | 20150402 | 20160818 | 20160125 | 20160822 | EXP | CA-ROCHE-1535340 | ROCHE | 36.68 | YR | M | Y | 102.15000 | KG | 20160822 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
119421334 | 11942133 | 1 | PS | CELLCEPT | MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE | 1 | Unknown | U | 50722 | ||||||||||
119421334 | 11942133 | 2 | SS | RITUXAN | RITUXIMAB | 1 | Intravenous (not otherwise specified) | 103705 | 1000 | MG | SOLUTION FOR INFUSION | ||||||||
119421334 | 11942133 | 3 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | U | 0 | ||||||||||
119421334 | 11942133 | 4 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
119421334 | 11942133 | 5 | SS | IMURAN | AZATHIOPRINE | 1 | Unknown | 0 | |||||||||||
119421334 | 11942133 | 6 | C | ACTONEL | RISEDRONATE SODIUM | 1 | 0 | ||||||||||||
119421334 | 11942133 | 7 | C | LOSEC | OMEPRAZOLE | 1 | 0 | ||||||||||||
119421334 | 11942133 | 8 | C | REACTINE (CANADA) | CETIRIZINE HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
119421334 | 11942133 | 1 | Product used for unknown indication |
119421334 | 11942133 | 2 | Pemphigus |
119421334 | 11942133 | 3 | Product used for unknown indication |
119421334 | 11942133 | 4 | Product used for unknown indication |
119421334 | 11942133 | 5 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
119421334 | 11942133 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
119421334 | 11942133 | Anxiety | |
119421334 | 11942133 | Apparent death | |
119421334 | 11942133 | Blood urine present | |
119421334 | 11942133 | Drug ineffective | |
119421334 | 11942133 | Eye disorder | |
119421334 | 11942133 | Headache | |
119421334 | 11942133 | Hypersensitivity | |
119421334 | 11942133 | Hypoaesthesia | |
119421334 | 11942133 | Infusion related reaction | |
119421334 | 11942133 | Muscle spasms | |
119421334 | 11942133 | Off label use | |
119421334 | 11942133 | Throat irritation | |
119421334 | 11942133 | Tremor | |
119421334 | 11942133 | 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 |
---|---|---|---|---|---|---|
119421334 | 11942133 | 1 | 201501 | 0 | ||
119421334 | 11942133 | 2 | 20150402 | 0 |