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
76601054 7660105 4 F 20070822 20121227 20101108 20121231 EXP PHHY2010JP72694 NOVARTIS 64.08 YR M Y 43.00000 KG 20121229 OT JP JP

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
76601054 7660105 1 PS ZOMETA 1 INTRAVENOUS DRIP 4 MG, QW4 U 21223 4 MG
76601054 7660105 2 C DECADRON 1 ORAL 1 MG, QD U 0 1 MG QD
76601054 7660105 3 C DECADRON 1 ORAL 1 MG, QD U 0 1 MG QD
76601054 7660105 4 C HONVAN 2 ORAL 50 MG, QD U 0 50 MG QD
76601054 7660105 5 C VESICARE 1 ORAL 5 MG, QD U 0 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
76601054 7660105 1 Metastases to bone
76601054 7660105 2 Prostate cancer
76601054 7660105 4 Prostate cancer
76601054 7660105 5 Hypertonic bladder

Outcome of event

Event ID CASEID OUTC COD
76601054 7660105 HO
76601054 7660105 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
76601054 7660105 General physical health deterioration
76601054 7660105 Malignant neoplasm progression
76601054 7660105 Osteomyelitis

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
76601054 7660105 1 20070110 20071017 0
76601054 7660105 2 20060206 20090113 0
76601054 7660105 3 20090218 20090317 0
76601054 7660105 4 20070822 20071212 0
76601054 7660105 5 20070822 20091015 0