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
70432562 7043256 2 F 2006 20121228 20090707 20121231 EXP PHHY2009MX26997 NOVARTIS 85.51 F Y 0.00000 20121231 CN COUNTRY NOT SPECIFIED MX

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
70432562 7043256 1 PS CO-DIOVAN 1 ORAL 1 DF (80 MG VALS AND 12.5 MG HCTZ), DAILY D 20818 1 DF Tablet
70432562 7043256 2 C PLAVIX 1 1 UKN, DAILY U UNK 0
70432562 7043256 3 C ISOSORBIDE 1 1 UKN, DAILY U UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
70432562 7043256 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
70432562 7043256 LT
70432562 7043256 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
70432562 7043256 Blood glucose increased
70432562 7043256 Cardiac failure
70432562 7043256 Diabetes mellitus
70432562 7043256 Oxygen consumption 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
70432562 7043256 1 200611 0
70432562 7043256 2 200712 0
70432562 7043256 3 201212 0