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
125833351 12583335 1 I 20160606 20160722 20160722 EXP PHHY2016DE079463 NOVARTIS 0.00 A M Y 0.00000 20160722 MD DE DE

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
125833351 12583335 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, UNK Y 22068 600 MG CAPSULE
125833351 12583335 2 C CANDESARTAN CANDESARTAN 1 Oral 16 MG, UNK U 0 16 MG QD
125833351 12583335 3 C AMLODIPINE AMLODIPINE BESYLATE 1 Oral 5 MG, QD U 0 5 MG QD
125833351 12583335 4 C SIMVASTATIN. SIMVASTATIN 1 Oral 20 MG, QD U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125833351 12583335 1 Chronic myeloid leukaemia
125833351 12583335 2 Hypertension
125833351 12583335 3 Hypertension
125833351 12583335 4 Hyperlipidaemia

Outcome of event

Event ID CASEID OUTC COD
125833351 12583335 HO
125833351 12583335 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125833351 12583335 Hypoaesthesia
125833351 12583335 Intermittent claudication
125833351 12583335 Pain
125833351 12583335 Peripheral artery occlusion

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
125833351 12583335 1 201306 201408 0