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
79263113 7926311 3 F 201604 20160531 20110502 20160802 PER US-ASTRAZENECA-2010SE61416 ASTRAZENECA 805.00 MON F Y 71.70000 KG 20160802 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
79263113 7926311 1 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral U 21153
79263113 7926311 2 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 770 MG N U 21366 5 MG TABLET QD
79263113 7926311 3 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 770 MG N U 21366 10 MG TABLET QD
79263113 7926311 4 C TYLENOL ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
79263113 7926311 2 Blood cholesterol increased
79263113 7926311 3 Blood cholesterol increased
79263113 7926311 4 Headache

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
79263113 7926311 Drug dose omission
79263113 7926311 Gastrooesophageal reflux disease
79263113 7926311 Headache
79263113 7926311 Insomnia
79263113 7926311 Malaise
79263113 7926311 Nausea
79263113 7926311 Pain in extremity
79263113 7926311 Sleep disorder due to a general medical condition

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
79263113 7926311 2 201601 201604 0
79263113 7926311 3 201604 20160527 0