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
125858991 12585899 1 I 20160628 20160725 20160725 PER US-ASTRAZENECA-2016SE71944 ASTRAZENECA 0.00 F Y 61.20000 KG 20160725 CN 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
125858991 12585899 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral U 21366 5 MG TABLET QD
125858991 12585899 2 C AGGRENOX ASPIRINDIPYRIDAMOLE 1 Oral 25 200 TWICE A DAY 0
125858991 12585899 3 C WELCHOL COLESEVELAM HYDROCHLORIDE 1 Oral 0 1875 MG BID
125858991 12585899 4 C ZETIA EZETIMIBE 1 Oral 0 10 MG QD
125858991 12585899 5 C NIASPAN NIACIN 1 Oral 0 1000 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125858991 12585899 1 Blood cholesterol abnormal
125858991 12585899 2 Anticoagulant therapy
125858991 12585899 3 Blood cholesterol abnormal
125858991 12585899 4 Blood cholesterol abnormal
125858991 12585899 5 Blood cholesterol abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125858991 12585899 Body height decreased
125858991 12585899 Myalgia

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
125858991 12585899 2 2001 0
125858991 12585899 3 2001 0
125858991 12585899 4 2001 0
125858991 12585899 5 2001 0