The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
108013124 10801312 4 F 20160711 20150217 20160713 EXP BR-ROCHE-1528724 ROCHE 0.00 F Y 45.00000 KG 20160713 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
108013124 10801312 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) U 103705 SOLUTION FOR INFUSION
108013124 10801312 2 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) U 103705 SOLUTION FOR INFUSION
108013124 10801312 3 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0
108013124 10801312 4 C ARAVA LEFLUNOMIDE 1 0
108013124 10801312 5 C PREDNISONE. PREDNISONE 1 0
108013124 10801312 6 C FUROSEMIDE. FUROSEMIDE 1 0
108013124 10801312 7 C DICLOFENAC DICLOFENAC 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108013124 10801312 1 Rheumatoid arthritis
108013124 10801312 5 Arthritis
108013124 10801312 7 Pain

Outcome of event

Event ID CASEID OUTC COD
108013124 10801312 OT
108013124 10801312 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
108013124 10801312 Blood pressure fluctuation
108013124 10801312 Haemorrhage
108013124 10801312 Thyroid disorder
108013124 10801312 Uterine cancer
108013124 10801312 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
108013124 10801312 1 20120810 20140913 0
108013124 10801312 2 20160320 0