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
888851419 8888514 19 F 20120726 20160711 20121106 20160718 EXP PHHY2012LB067866 NOVARTIS 37.03 YR F Y 0.00000 20160718 CN COUNTRY NOT SPECIFIED LB

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
888851419 8888514 1 PS TASIGNA NILOTINIB 1 Oral 800 MG, QD U 22068 800 MG CAPSULE QD
888851419 8888514 2 C MOSAR PLUS 2 Oral 1 DF, Q8H U 0 1 DF Q8H
888851419 8888514 3 C FLUNAZOL 2 Unknown 1 DF, QW U 0 1 DF /wk
888851419 8888514 4 C METEOSPASM XY 2 Oral 1 DF, Q8H U 0 1 DF Q8H
888851419 8888514 5 C TAVANIC LEVOFLOXACIN 1 Oral 1 DF, QD U 0 1 DF TABLET QD
888851419 8888514 6 C AMOCLAN AMOXICILLINCLAVULANIC ACID 1 Oral 1 DF, Q12H U 0 1 DF TABLET Q12H
888851419 8888514 7 C PARIET RABEPRAZOLE SODIUM 1 Oral 1 DF, QD U 0 1 DF TABLET QD
888851419 8888514 8 C CIPRALEX ESCITALOPRAM OXALATE 1 Oral 1 DF, QD U 0 1 DF TABLET QD
888851419 8888514 9 C ORAVIL 2 Oral UNK UNK, TIW U 0 Q3W
888851419 8888514 10 C EURO-FER 2 Oral 1 UNK, QD U 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
888851419 8888514 1 Chronic myeloid leukaemia
888851419 8888514 2 Product used for unknown indication
888851419 8888514 3 Product used for unknown indication
888851419 8888514 4 Product used for unknown indication
888851419 8888514 5 Product used for unknown indication
888851419 8888514 6 Product used for unknown indication
888851419 8888514 7 Product used for unknown indication
888851419 8888514 8 Product used for unknown indication
888851419 8888514 9 Product used for unknown indication
888851419 8888514 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
888851419 8888514 OT
888851419 8888514 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
888851419 8888514 Abdominal distension
888851419 8888514 Abdominal pain upper
888851419 8888514 Alopecia
888851419 8888514 Anaemia
888851419 8888514 Anxiety
888851419 8888514 Back pain
888851419 8888514 Blood iron decreased
888851419 8888514 Breast fibroma
888851419 8888514 Decreased appetite
888851419 8888514 Dizziness
888851419 8888514 Dysuria
888851419 8888514 Fatigue
888851419 8888514 Headache
888851419 8888514 Hypoglycaemia
888851419 8888514 Hypotension
888851419 8888514 Influenza
888851419 8888514 Intervertebral disc disorder
888851419 8888514 Intervertebral disc protrusion
888851419 8888514 Neck pain
888851419 8888514 Nervousness
888851419 8888514 Pain in extremity
888851419 8888514 Pruritus
888851419 8888514 Pyrexia
888851419 8888514 Rash
888851419 8888514 Renal colic
888851419 8888514 Renal pain
888851419 8888514 Skin burning sensation
888851419 8888514 Vitamin D decreased

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
888851419 8888514 1 20120726 0
888851419 8888514 2 201210 0
888851419 8888514 3 201210 0
888851419 8888514 8 20140301 0
888851419 8888514 9 201602 0
888851419 8888514 10 201602 0