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
89011417 8901141 7 F 201210 20160719 20121109 20160721 EXP CA-ROCHE-1153580 ROCHE 44.47 YR M Y 97.61000 KG 20160721 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
89011417 8901141 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) N B2040 125276 800 MG SOLUTION FOR INFUSION
89011417 8901141 2 C ARAVA LEFLUNOMIDE 1 Oral 0 20 MG
89011417 8901141 3 C TYLENOL WITH CODEINE ACETAMINOPHENCODEINE PHOSPHATE 1 Unknown 0
89011417 8901141 4 C VIMOVO ESOMEPRAZOLE MAGNESIUMNAPROXEN 1 0
89011417 8901141 5 C PREDNISONE. PREDNISONE 1 0
89011417 8901141 6 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0
89011417 8901141 7 C D-FORTE ERGOCALCIFEROL 1 0
89011417 8901141 8 C NORVASC AMLODIPINE BESYLATE 1 0
89011417 8901141 9 C AMLODIPINE AMLODIPINE BESYLATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89011417 8901141 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
89011417 8901141 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
89011417 8901141 Alanine aminotransferase increased
89011417 8901141 Blood pressure diastolic increased
89011417 8901141 Cerebrovascular accident
89011417 8901141 Haematuria
89011417 8901141 Nephrolithiasis
89011417 8901141 Pain
89011417 8901141 Wound

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
89011417 8901141 1 20120614 0