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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
96496094 | 9649609 | 4 | F | 20160809 | 20131028 | 20160816 | EXP | BR-ROCHE-736126 | ROCHE | 0.00 | F | Y | 99.00000 | KG | 20160816 | CN | BR | BR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
96496094 | 9649609 | 1 | PS | MABTHERA | RITUXIMAB | 1 | Intravenous (not otherwise specified) | DOSE: 500 MG/50 ML | U | 103705 | SOLUTION FOR INFUSION | ||||||||
96496094 | 9649609 | 2 | SS | MABTHERA | RITUXIMAB | 1 | Intravenous (not otherwise specified) | U | 103705 | SOLUTION FOR INFUSION | |||||||||
96496094 | 9649609 | 3 | SS | MABTHERA | RITUXIMAB | 1 | Intravenous (not otherwise specified) | MOST RECENT DOSE ON 01/JAN/2016 | U | 103705 | SOLUTION FOR INFUSION | ||||||||
96496094 | 9649609 | 4 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Unknown | 0 | 25 | MG | |||||||||
96496094 | 9649609 | 5 | C | DICLOFENAC | DICLOFENAC | 1 | Unknown | 0 | |||||||||||
96496094 | 9649609 | 6 | C | ENALAPRIL | ENALAPRIL | 1 | Unknown | 0 | |||||||||||
96496094 | 9649609 | 7 | C | CARVEDILOL. | CARVEDILOL | 1 | Unknown | 0 | 25 | MG | TABLET | BID | |||||||
96496094 | 9649609 | 8 | C | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | 0 | |||||||||||
96496094 | 9649609 | 9 | C | PREDNISONE. | PREDNISONE | 1 | Unknown | 0 | |||||||||||
96496094 | 9649609 | 10 | C | LOSARTAN. | LOSARTAN | 1 | Unknown | 0 | 50 | MG | TABLET | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
96496094 | 9649609 | 1 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
96496094 | 9649609 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
96496094 | 9649609 | Arthralgia | |
96496094 | 9649609 | Atrophy | |
96496094 | 9649609 | Cardiac disorder | |
96496094 | 9649609 | Cough | |
96496094 | 9649609 | Ill-defined disorder | |
96496094 | 9649609 | Malaise | |
96496094 | 9649609 | Pain in extremity |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |