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
1008318617 10083186 17 F 20110804 20150625 20140417 20150630 EXP CA-ROCHE-1130084 ROCHE 62.47 YR M Y 79.50000 KG 20150630 N OT 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
1008318617 10083186 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) D B20131,B20151,B20172,B20212,B20051, 125276
1008318617 10083186 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) D B20131,B20151,B20172,B20212,B20051, 125276 600 MG
1008318617 10083186 3 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) D B20131,B20151,B20172,B20212,B20051, 125276 600 MG /month
1008318617 10083186 4 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) D B20131,B20151,B20172,B20212,B20051, 125276 560 MG
1008318617 10083186 5 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) D B20131,B20151,B20172,B20212,B20051, 125276 600 MG
1008318617 10083186 6 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) D B20131,B20151,B20172,B20212,B20051, 125276 668.8 MG
1008318617 10083186 7 C METHOTREXATE METHOTREXATE 1 Unknown D 0 20 MG /wk
1008318617 10083186 8 C METHOTREXATE METHOTREXATE 1 Unknown D 0 10 MG /wk
1008318617 10083186 9 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown D 0 200 MG BID
1008318617 10083186 10 C FOLIC ACID. FOLIC ACID 1 Unknown D 0 1 MG
1008318617 10083186 11 C CRESTOR ROSUVASTATIN CALCIUM 1 Unknown D 0 QD
1008318617 10083186 12 C CELEBREX CELECOXIB 1 Unknown D 0 10 MG QD
1008318617 10083186 13 C CELEBREX CELECOXIB 1 Unknown D 0 QD
1008318617 10083186 14 C PANTOLOC PANTOPRAZOLE SODIUM 1 Unknown D 0 40 MG /wk
1008318617 10083186 15 C PANTOLOC PANTOPRAZOLE SODIUM 1 Unknown D 0 200 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1008318617 10083186 1 Rheumatoid arthritis
1008318617 10083186 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
1008318617 10083186 OT
1008318617 10083186 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1008318617 10083186 Abdominal pain
1008318617 10083186 Arthralgia
1008318617 10083186 Arthropathy
1008318617 10083186 Asthenia
1008318617 10083186 Back pain
1008318617 10083186 Blood pressure increased
1008318617 10083186 Cataract
1008318617 10083186 Eye oedema
1008318617 10083186 Fall
1008318617 10083186 Fungal infection
1008318617 10083186 Hypertension
1008318617 10083186 Infusion related reaction
1008318617 10083186 Intracranial aneurysm
1008318617 10083186 Ocular hyperaemia
1008318617 10083186 Onychomycosis
1008318617 10083186 Oxygen saturation decreased
1008318617 10083186 Pain in extremity
1008318617 10083186 Peripheral swelling
1008318617 10083186 Weight decreased
1008318617 10083186 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
1008318617 10083186 1 2005 201009 0
1008318617 10083186 2 20100930 0
1008318617 10083186 3 20130613 0
1008318617 10083186 4 20150304 0
1008318617 10083186 5 20150527 0
1008318617 10083186 6 20150625 0
1008318617 10083186 7 2008 0
1008318617 10083186 8 2008 0
1008318617 10083186 10 2004 0
1008318617 10083186 11 2009 0
1008318617 10083186 12 2006 0
1008318617 10083186 13 2006 0
1008318617 10083186 14 2004 0