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
90612981 9061298 1 I 20110305 0 20130208 20130208 DIR 75.00 YR M N 188.00000 LBS 20120918 RN 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
90612981 9061298 1 PS DECITABINE 1 0 0.2 MG/KG
90612981 9061298 3 C NEXIUM 1 0
90612981 9061298 5 C GLYBURIDE 1 0
90612981 9061298 7 C CIPROFLOXACIN 1 0
90612981 9061298 9 C NAMENDA 1 0
90612981 9061298 11 C EXELON 1 0
90612981 9061298 13 C LOPRESSOR 1 0
90612981 9061298 15 C NITRO 1 0
90612981 9061298 17 C PLENDIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90612981 9061298 1 Myelodysplastic syndrome

Outcome of event

Event ID CASEID OUTC COD
90612981 9061298 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
90612981 9061298 Confusional state
90612981 9061298 Dyspnoea
90612981 9061298 Fungal infection
90612981 9061298 Hyponatraemia
90612981 9061298 Liver function test abnormal
90612981 9061298 Neutropenia
90612981 9061298 Pneumonia aspiration
90612981 9061298 Productive cough
90612981 9061298 Pyrexia

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

Event ID CASEID RPSR COD
90612981 9061298 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
90612981 9061298 1 20110110 20110615 0