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
99486313 9948631 3 F 20140929 20140303 20141001 EXP BR-ROCHE-1334294 ROCHE 0.00 F Y 79.00000 KG 20141001 N CN 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
99486313 9948631 1 PS MABTHERA RITUXIMAB 1 INTRAVENOUS D 103705
99486313 9948631 2 C RIVOTRIL CLONAZEPAM 1 D 0
99486313 9948631 3 C FOLIC ACID. FOLIC ACID 1 D 0
99486313 9948631 4 C VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 D 0
99486313 9948631 5 C PURAN LEVOTHYROXINE SODIUM 1 D 0
99486313 9948631 6 C LEVOFLOXACIN. LEVOFLOXACIN 1 D 0
99486313 9948631 7 C TIBOLONE TIBOLONE 1 D 0
99486313 9948631 8 C SIMVASTATIN. SIMVASTATIN 1 D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
99486313 9948631 1 Rheumatoid arthritis
99486313 9948631 5 Thyroid disorder

Outcome of event

Event ID CASEID OUTC COD
99486313 9948631 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
99486313 9948631 Blood test abnormal
99486313 9948631 Lymphocyte count decreased
99486313 9948631 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
99486313 9948631 1 20130816 20130902 0