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
126063501 12606350 1 I 20160714 0 20160728 20160728 DIR 63.70 YR F N 89.90000 KG 20160727 N MD US

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
126063501 12606350 1 PS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 0 1220 MG
126063501 12606350 2 SS DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 0 81 MG
126063501 12606350 3 SS PREDNISONE. PREDNISONE 1 0 1000 MG
126063501 12606350 4 SS RITUXIMAB (MOAB C2B8 ANTI CD20, CHIMERIC) RITUXIMAB 1 0 814 MG
126063501 12606350 5 SS VINCRISTINE SULFATE. VINCRISTINE SULFATE 1 0 2 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126063501 12606350 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126063501 12606350 Cellulitis
126063501 12606350 Chills
126063501 12606350 Diarrhoea
126063501 12606350 Fatigue
126063501 12606350 Hypotension
126063501 12606350 Pyrexia
126063501 12606350 Tachycardia

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
126063501 12606350 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126063501 12606350 1 20160707 0
126063501 12606350 2 20160707 0
126063501 12606350 3 20160711 0
126063501 12606350 4 20160707 0
126063501 12606350 5 20160707 0