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
75919142 7591914 2 F 201603 20160725 20100917 20160930 PER US-ASTRAZENECA-2010SE23832 ASTRAZENECA 789.00 MON F Y 0.00000 20160930 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
75919142 7591914 1 PS SEROQUEL QUETIAPINE FUMARATE 1 Oral D 20639 PROLONGED-RELEASE TABLET
75919142 7591914 2 SS SEROQUEL QUETIAPINE FUMARATE 1 Oral 400.0MG UNKNOWN D 20639 400 MG FILM-COATED TABLET
75919142 7591914 3 SS SEROQUEL QUETIAPINE FUMARATE 1 Oral 300.0MG UNKNOWN D 20639 300 MG PROLONGED-RELEASE TABLET
75919142 7591914 4 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 0 20 MG TABLET QD
75919142 7591914 5 C AMITIZA LUBIPROSTONE 1 0
75919142 7591914 6 C LYNZESS 2 0
75919142 7591914 7 C LIPITOR ATORVASTATIN CALCIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
75919142 7591914 4 Blood cholesterol increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
75919142 7591914 Basedow's disease
75919142 7591914 Diabetes mellitus
75919142 7591914 Drug dose omission
75919142 7591914 Drug hypersensitivity
75919142 7591914 Drug ineffective
75919142 7591914 Emotional disorder
75919142 7591914 Insomnia
75919142 7591914 Thyroid disorder
75919142 7591914 Weight decreased

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
75919142 7591914 4 2002 0