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
127689921 12768992 1 I 20160902 20160902 20160921 20160921 PER US-ASTRAZENECA-2016SE94487 ASTRAZENECA 18341.00 DY M Y 57.60000 KG 20160922 US 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
127689921 12768992 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral U 21366 20 MG TABLET QD
127689921 12768992 2 SS PRAVASTATIN. PRAVASTATIN 1 Unknown U 0 40 MG QD
127689921 12768992 3 SS ATORVASTATIN ATORVASTATIN 1 Unknown U U 0
127689921 12768992 4 SS ATORVASTATIN ATORVASTATIN 1 Unknown U U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127689921 12768992 1 Blood cholesterol increased
127689921 12768992 2 Blood cholesterol increased
127689921 12768992 3 Blood cholesterol increased
127689921 12768992 4 Blood cholesterol increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127689921 12768992 Blood cholesterol increased
127689921 12768992 Drug dose omission
127689921 12768992 Drug ineffective
127689921 12768992 Eye disorder
127689921 12768992 Fatigue
127689921 12768992 Feeling abnormal
127689921 12768992 Flatulence
127689921 12768992 Malaise
127689921 12768992 Personality change
127689921 12768992 Vision blurred
127689921 12768992 Vomiting

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
127689921 12768992 1 2013 2013 0
127689921 12768992 2 20160623 0
127689921 12768992 4 20160722 0