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
115686606 11568660 6 F 2015 20160912 20150929 20160914 EXP CA-ROCHE-1458445 ROCHE 0.00 F Y 98.20000 KG 20160914 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
115686606 11568660 1 PS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) 103705 SOLUTION FOR INFUSION
115686606 11568660 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 690 MG SOLUTION FOR INFUSION QOW
115686606 11568660 3 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) ON 06/AUG/2015, MOST RECENT DOSE RECEIVED. Y 125276 690 MG SOLUTION FOR INFUSION Q3W
115686606 11568660 4 C PREDNISONE. PREDNISONE 1 0
115686606 11568660 5 C RABEPRAZOLE RABEPRAZOLE 1 0
115686606 11568660 6 C VITAMIN D3 CHOLECALCIFEROL 1 0
115686606 11568660 7 C OXYCODONE OXYCODONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115686606 11568660 1 Castleman's disease
115686606 11568660 2 Castleman's disease

Outcome of event

Event ID CASEID OUTC COD
115686606 11568660 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115686606 11568660 Chest pain
115686606 11568660 Colitis
115686606 11568660 Drug ineffective
115686606 11568660 Malaise
115686606 11568660 Off label use
115686606 11568660 Weight increased

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
115686606 11568660 1 20140327 20140417 0
115686606 11568660 2 20141009 0