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
126092891 12609289 1 I 20160519 20160727 20160801 20160801 EXP CZ-CZSUKL-16002673 CZ-ROCHE-1805310 ROCHE 72.83 YR F Y 0.00000 20160801 MD CZ CZ

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
126092891 12609289 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) U 103705 2000 MG SOLUTION FOR INFUSION
126092891 12609289 2 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) U 103705 2000 MG SOLUTION FOR INFUSION
126092891 12609289 3 C DETRALEX DIOSMINHESPERIDIN 1 Oral U 0
126092891 12609289 4 C LEFLUNOMID LEFLUNOMIDE 1 Oral U 0 10 MG
126092891 12609289 5 C CELEBREX CELECOXIB 1 Oral U 0
126092891 12609289 6 C VIGANTOL 2 Oral U 0 2 GTT
126092891 12609289 7 C PRESTARIUM NEO PERINDOPRIL ARGININE 1 Unknown U 0 5 MG
126092891 12609289 8 C CALCICHEW CALCIUM CARBONATE 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126092891 12609289 1 Rheumatoid arthritis
126092891 12609289 2 Rheumatoid arthritis
126092891 12609289 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
126092891 12609289 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126092891 12609289 Pneumonia
126092891 12609289 Squamous cell carcinoma of lung

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
126092891 12609289 1 20160229 20160316 0
126092891 12609289 2 20160422 20160513 0