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
127275331 12727533 1 I 20160829 20160909 20160909 EXP NO-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-123254 RANBAXY 69.00 YR M Y 0.00000 20160909 OT NO NO

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
127275331 12727533 1 PS TEMOZOLOMIDE. TEMOZOLOMIDE 1 Unknown U U 201742

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127275331 12727533 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127275331 12727533 DE
127275331 12727533 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127275331 12727533 Bone marrow failure
127275331 12727533 Death
127275331 12727533 Decreased appetite
127275331 12727533 Lethargy
127275331 12727533 Weight decreased

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

no results found

Therapies reported

no results found