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
125786701 12578670 1 I 20160714 0 20160720 20160720 DIR 63.70 YR F N 89.90000 KG 20160719 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
125786701 12578670 1 PS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 D D 0 1220 MG
125786701 12578670 2 SS DOXORUBICIN HYDROCHLORIDE. DOXORUBICIN HYDROCHLORIDE 1 0 81 MG
125786701 12578670 3 SS PREDNISONE. PREDNISONE 1 0 1000 MG
125786701 12578670 4 SS RITUXIMAB (MOAB C2B8 ANTI CD20, CHIMERIC) RITUXIMAB 1 0 814 MG
125786701 12578670 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
125786701 12578670 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125786701 12578670 Asthenia
125786701 12578670 Chills
125786701 12578670 Fatigue
125786701 12578670 Heart rate increased
125786701 12578670 Hypotension
125786701 12578670 Mobility decreased
125786701 12578670 Pyrexia
125786701 12578670 Tachycardia

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

Event ID CASEID RPSR COD
125786701 12578670 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125786701 12578670 1 20160707 0
125786701 12578670 2 20160707 0
125786701 12578670 3 20160711 0
125786701 12578670 4 20160707 0
125786701 12578670 5 20160707 0