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
126215441 12621544 1 I 20160705 20160803 20160804 20160804 EXP FR-ROCHE-1808100 ROCHE 85.00 YR F Y 0.00000 20160804 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
126215441 12621544 1 PS MABTHERA RITUXIMAB 1 Intravenous drip Y 103705 590 MG SOLUTION FOR INFUSION
126215441 12621544 2 C HYDROCORTISONE. HYDROCORTISONE 1 0
126215441 12621544 3 C PERFALGAN ACETAMINOPHEN 1 0
126215441 12621544 4 C POLARAMINE DEXCHLORPHENIRAMINE MALEATE 1 0
126215441 12621544 5 C EMEND APREPITANT 1 0
126215441 12621544 6 C PRIMPERAN METOCLOPRAMIDE HYDROCHLORIDE 1 0
126215441 12621544 7 C XYZALL LEVOCETIRIZINE DIHYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126215441 12621544 1 Chronic lymphocytic leukaemia
126215441 12621544 2 Premedication
126215441 12621544 3 Premedication
126215441 12621544 4 Premedication

Outcome of event

Event ID CASEID OUTC COD
126215441 12621544 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126215441 12621544 Anaphylactic shock
126215441 12621544 Diarrhoea
126215441 12621544 Loss of consciousness
126215441 12621544 Malaise
126215441 12621544 Vomiting

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
126215441 12621544 1 20160705 0