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
122332802 12233280 2 F 201602 20160715 20160404 20160718 EXP ID-ROCHE-1680079 ROCHE 48.00 YR M Y 0.00000 20160718 CN ID ID

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
122332802 12233280 1 PS MABTHERA RITUXIMAB 1 Unknown U 103705 550 MG
122332802 12233280 2 SS VINCRISTINE VINCRISTINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122332802 12233280 1 Diffuse large B-cell lymphoma
122332802 12233280 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122332802 12233280 HO
122332802 12233280 OT
122332802 12233280 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
122332802 12233280 Anaemia
122332802 12233280 Chills
122332802 12233280 Decreased appetite
122332802 12233280 Drug ineffective
122332802 12233280 General physical health deterioration
122332802 12233280 Hepatitis B
122332802 12233280 Oedema
122332802 12233280 Seizure
122332802 12233280 Thrombocytopenia
122332802 12233280 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
122332802 12233280 1 2015 0