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
126095171 12609517 1 I 0 20160729 20160729 DIR 55.00 YR F N 0.00000 0 N PH 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
126095171 12609517 1 PS SPRYCEL DASATINIB 1 Oral N D 0 100 MG QD
126095171 12609517 3 C ZOLPIDEM ZOLPIDEMOLPIDEM TARTRATE 1 0
126095171 12609517 5 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 0
126095171 12609517 7 C AMLODIPINE AMLODIPINE BESYLATE 1 0
126095171 12609517 9 C METOPROLOL. METOPROLOL 1 0
126095171 12609517 11 C ESCITALOPRAM ESCITALOPRAM OXALATE 1 0
126095171 12609517 13 C ACYCLOVIR. ACYCLOVIR 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126095171 12609517 1 Acute lymphocytic leukaemia

Outcome of event

Event ID CASEID OUTC COD
126095171 12609517 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126095171 12609517 Cardiac failure congestive
126095171 12609517 Fatigue
126095171 12609517 Fluid retention

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

Event ID CASEID RPSR COD
126095171 12609517 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126095171 12609517 1 20151112 20160718 0