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
126093461 12609346 1 I 20091211 20160725 20160801 20160801 EXP DE-ROCHE-1802125 ROCHE 49.05 YR M Y 0.00000 20160801 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
126093461 12609346 1 PS Rituximab RITUXIMAB 1 Unknown 6TH CYCLE DAY 1 U 103705
126093461 12609346 2 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown 6TH CYCLE DAY 1 U 0
126093461 12609346 3 SS CYTARABINE. CYTARABINE 1 Unknown 6TH CYCLE DAY 1 U 0
126093461 12609346 4 SS CISPLATIN. CISPLATIN 1 Unknown 6TH CYCLE DAY 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126093461 12609346 1 Mantle cell lymphoma
126093461 12609346 2 Mantle cell lymphoma
126093461 12609346 3 Mantle cell lymphoma
126093461 12609346 4 Mantle cell lymphoma

Outcome of event

Event ID CASEID OUTC COD
126093461 12609346 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126093461 12609346 Acute kidney injury

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
126093461 12609346 1 20091203 0
126093461 12609346 2 20091203 0
126093461 12609346 3 20091203 0
126093461 12609346 4 20091203 0