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
124833832 12483383 2 F 201604 20160916 20160621 20160921 EXP DE-ROCHE-1778081 ROCHE 73.68 YR F Y 0.00000 20160921 MD DE DE

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
124833832 12483383 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) 500-1000 MG (NOT CONFIRM) Y 103705 SOLUTION FOR INFUSION
124833832 12483383 2 C VIGANTOLETTEN CHOLECALCIFEROL 1 Unknown 0 1000 IU
124833832 12483383 3 C FOLSAURE FOLIC ACID 1 Unknown 0 5 MG
124833832 12483383 4 C CORTISONE CORTISONEHYDROCORTISONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124833832 12483383 1 CREST syndrome
124833832 12483383 3 Folate deficiency

Outcome of event

Event ID CASEID OUTC COD
124833832 12483383 HO
124833832 12483383 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124833832 12483383 Cerebral infarction
124833832 12483383 Cerebrovascular accident
124833832 12483383 Hemiparesis
124833832 12483383 Off label use
124833832 12483383 Weight decreased

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
124833832 12483383 1 20160504 0