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
125823291 12582329 1 I 20160708 20160722 20160722 EXP CN-CIPLA LTD.-2016CN09757 CIPLA 0.00 Y 0.00000 20160722 OT CN CN

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
125823291 12582329 1 PS LAMIVUDINE. LAMIVUDINE 1 Oral 100 MG, QD U U 0 100 MG
125823291 12582329 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Unknown 750 MG/M2, ON DAY 1 U U 0 750 MG/M**2
125823291 12582329 3 SS Doxorubicin DOXORUBICIN 1 Unknown 50 MG/M2, ON DAY 1 U U 0 50 MG/M**2
125823291 12582329 4 SS Vincristine VINCRISTINE 1 Unknown 1.2 G/M2, ON DAY 1 U U 0
125823291 12582329 5 SS ENTECAVIR. ENTECAVIR 1 Unknown UNK U U 0
125823291 12582329 6 SS PREDNISONE. PREDNISONE 1 Unknown 60 MG/M2, ON DAYS 1 TO 5 U U 0 60 MG/M**2
125823291 12582329 7 SS Rituximab RITUXIMAB 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125823291 12582329 1 Prophylaxis
125823291 12582329 2 Lymphoma
125823291 12582329 3 Lymphoma
125823291 12582329 4 Lymphoma
125823291 12582329 5 Antiviral treatment
125823291 12582329 6 Lymphoma
125823291 12582329 7 Lymphoma

Outcome of event

Event ID CASEID OUTC COD
125823291 12582329 OT
125823291 12582329 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125823291 12582329 Condition aggravated
125823291 12582329 Hepatic encephalopathy
125823291 12582329 Hepatic failure
125823291 12582329 Hepatitis B DNA increased

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

no results found

Therapies reported

no results found