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
115242653 11524265 3 F 20160719 20150918 20160726 PER PHEH2014US019283 NOVARTIS 0.00 F Y 0.00000 20160727 CN COUNTRY NOT SPECIFIED 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
115242653 11524265 1 PS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, QD U 21588 400 MG QD
115242653 11524265 2 C LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown 0.25 MG, UNK U 0 .25 MG
115242653 11524265 3 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown UNK U 0
115242653 11524265 4 C FOCUS 2 Unknown UNK U 0
115242653 11524265 5 C LUTEIN LUTEIN 1 Unknown UNK U 0
115242653 11524265 6 C PRESERVISION MINERALSVITAMINS 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115242653 11524265 1 Leukaemia
115242653 11524265 2 Product used for unknown indication
115242653 11524265 3 Product used for unknown indication
115242653 11524265 4 Product used for unknown indication
115242653 11524265 5 Product used for unknown indication
115242653 11524265 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
115242653 11524265 Fatigue
115242653 11524265 Headache
115242653 11524265 Hypothyroidism
115242653 11524265 Macular degeneration
115242653 11524265 Stress
115242653 11524265 Vitreous floaters

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
115242653 11524265 1 2001 0