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
125639221 12563922 1 I 201601 20160615 20160716 20160716 PER US-ASTRAZENECA-2016SE66510 ASTRAZENECA 728.00 MON F Y 74.40000 KG 20160716 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
125639221 12563922 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 10 MG TABLET QD
125639221 12563922 2 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 10 MG TABLET QD
125639221 12563922 3 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 10 MG TABLET QD
125639221 12563922 4 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 5 MG TABLET QD
125639221 12563922 5 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 5 MG TABLET QD
125639221 12563922 6 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 5 MG TABLET QD
125639221 12563922 7 C SOTALOL. SOTALOL 1 Oral 0 80 MG QD
125639221 12563922 8 C TRIBENZOR AMLODIPINE BESYLATEHYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 0
125639221 12563922 9 C SLO-MAG 2 Oral DAILY 0
125639221 12563922 10 C VITAMIN D CHOLECALCIFEROL 1 Oral 0 2000 IU QD
125639221 12563922 11 C VITAMIN B VITAMIN B 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125639221 12563922 1 Blood cholesterol increased
125639221 12563922 2 Blood triglycerides abnormal
125639221 12563922 3 Total cholesterol/HDL ratio abnormal
125639221 12563922 4 Blood cholesterol increased
125639221 12563922 5 Blood triglycerides abnormal
125639221 12563922 6 Total cholesterol/HDL ratio abnormal
125639221 12563922 7 Arrhythmia
125639221 12563922 8 Hypertension
125639221 12563922 9 Haemoglobin abnormal
125639221 12563922 10 Haemoglobin abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125639221 12563922 Headache
125639221 12563922 Intentional product misuse
125639221 12563922 Off label use

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
125639221 12563922 1 201601 201605 0
125639221 12563922 2 201601 201605 0
125639221 12563922 3 201601 201605 0
125639221 12563922 4 201605 0
125639221 12563922 5 201605 0
125639221 12563922 6 201605 0
125639221 12563922 7 2008 0
125639221 12563922 8 2012 0
125639221 12563922 9 201605 0
125639221 12563922 10 201601 0