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
82980982 8298098 2 F 201506 20160620 20111219 20160815 PER US-ASTRAZENECA-2011SE45430 ASTRAZENECA 1037.00 MON F Y 70.30000 KG 20160816 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
82980982 8298098 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral Y U 0 5 MG TABLET TIW
82980982 8298098 2 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 10 MG SAMPLES IN HALF Y U 0 TABLET
82980982 8298098 3 C ASA ASPIRIN 1 0
82980982 8298098 4 C CALCIUM CALCIUM 1 0
82980982 8298098 5 C VITAMIN D CHOLECALCIFEROL 1 0
82980982 8298098 6 C ZOCOR SIMVASTATIN 1 0
82980982 8298098 7 C LIPITOR ATORVASTATIN CALCIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
82980982 8298098 1 Blood cholesterol abnormal
82980982 8298098 2 Blood cholesterol abnormal
82980982 8298098 4 Prophylaxis
82980982 8298098 5 Vitamin D deficiency

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
82980982 8298098 Arthralgia
82980982 8298098 Blood cholesterol abnormal
82980982 8298098 Fatigue
82980982 8298098 Low density lipoprotein increased
82980982 8298098 Myalgia
82980982 8298098 Off label use
82980982 8298098 Vitamin D decreased
82980982 8298098 Vulvovaginal pruritus
82980982 8298098 Wrong technique in product usage process

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
82980982 8298098 1 2013 2016 0