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
126761482 12676148 2 F 20160706 20160818 20160823 20160829 EXP PHHY2016IT108074 NOVARTIS 80.50 YR M Y 73.00000 KG 20160829 OT IT IT

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
126761482 12676148 1 PS GLIVEC IMATINIB MESYLATE 1 Oral 400 MG, QD (DAILY) 5200 MG Y 21588 400 MG QD
126761482 12676148 2 SS GLIVEC IMATINIB MESYLATE 1 Oral UNK 5200 MG Y 21588
126761482 12676148 3 SS ALLOPURINOL. ALLOPURINOL 1 Oral 300 MG, QD 6000 MG Y 0 300 MG QD
126761482 12676148 4 SS ALLOPURINOL. ALLOPURINOL 1 Oral UNK 6000 MG Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126761482 12676148 1 Chronic myeloid leukaemia
126761482 12676148 3 Hyperuricaemia

Outcome of event

Event ID CASEID OUTC COD
126761482 12676148 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126761482 12676148 Dermatitis exfoliative
126761482 12676148 Drug hypersensitivity
126761482 12676148 Rash

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
126761482 12676148 1 20160624 20160714 0
126761482 12676148 2 20160718 0
126761482 12676148 3 20160617 20160714 0
126761482 12676148 4 20160718 0