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
107284277 10728427 7 F 201412 20160729 20150122 20160802 EXP BR-ROCHE-1523438 ROCHE 64.18 YR F Y 50.00000 KG 20160802 MD 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
107284277 10728427 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) MOST RECENT IN SEP/2014 U 125276 SOLUTION FOR INFUSION
107284277 10728427 2 C CARVEDILOL. CARVEDILOL 1 0
107284277 10728427 3 C SPIRONOLACTONE. SPIRONOLACTONE 1 0
107284277 10728427 4 C FOLACIN FOLIC ACID 1 0
107284277 10728427 5 C PREDNISOLONE SODIUM PHOSPHATE. PREDNISOLONE SODIUM PHOSPHATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107284277 10728427 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
107284277 10728427 HO
107284277 10728427 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
107284277 10728427 Anaemia
107284277 10728427 Arthropathy
107284277 10728427 Bone pain
107284277 10728427 Fall
107284277 10728427 Femur fracture
107284277 10728427 Gait disturbance
107284277 10728427 Hypersensitivity
107284277 10728427 Malaise
107284277 10728427 Memory impairment
107284277 10728427 Pain
107284277 10728427 Skin ulcer
107284277 10728427 Suture rupture

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
107284277 10728427 1 20140401 20160202 0