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
127450031 12745003 1 I 20090226 20160912 20160915 20160915 EXP FR-ROCHE-1829174 ROCHE 0.00 F Y 0.00000 20160915 MD FR FR

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
127450031 12745003 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) 20/FEB/2009 (D1), 05/MAR/2009 (D15). ON 28/SEP/2009, SHE RECEIVED HER (D1) RITUXIMAB. ON 13/OCT/2009 U 103705 1 G SOLUTION FOR INFUSION
127450031 12745003 2 C METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 Unknown 0 100 MG
127450031 12745003 3 C PARACETAMOL ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127450031 12745003 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
127450031 12745003 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127450031 12745003 Chest pain
127450031 12745003 Chloasma
127450031 12745003 Dyspnoea
127450031 12745003 Gastrointestinal motility disorder
127450031 12745003 Hyperkalaemia
127450031 12745003 Hypertension
127450031 12745003 Malaise
127450031 12745003 Mitral valve stenosis
127450031 12745003 Muscle spasms
127450031 12745003 Pneumonia
127450031 12745003 Renal failure
127450031 12745003 Syncope
127450031 12745003 Thrombocytopenia

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
127450031 12745003 1 20090220 0