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
126709651 12670965 1 I 201510 20160819 20160822 20160822 EXP AR-ROCHE-1817148 ROCHE 67.00 YR M Y 0.00000 20160822 MD AR AR

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
126709651 12670965 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) U 103705 SOLUTION FOR INFUSION
126709651 12670965 2 SS MABTHERA RITUXIMAB 1 Subcutaneous 103705 SOLUTION FOR INJECTION
126709651 12670965 3 C LOSARTAN. LOSARTAN 1 0
126709651 12670965 4 C RIVOTRIL CLONAZEPAM 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126709651 12670965 1 Non-Hodgkin's lymphoma
126709651 12670965 2 Non-Hodgkin's lymphoma
126709651 12670965 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126709651 12670965 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126709651 12670965 Blood pressure increased
126709651 12670965 Dizziness
126709651 12670965 Pallor
126709651 12670965 Pyrexia
126709651 12670965 Tachycardia
126709651 12670965 Tremor

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
126709651 12670965 1 201510 0
126709651 12670965 2 20160818 0