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
126623651 12662365 1 I 201403 20160808 20160817 20160817 PER US-ASTRAZENECA-2016SE85947 ASTRAZENECA 681.00 MON F Y 64.90000 KG 20160818 OT 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
126623651 12662365 1 PS ANASTRAZOLE ANASTROZOLE 1 Oral 366 MG 20541 1 MG TABLET QD
126623651 12662365 2 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Oral 0 25 MG BID
126623651 12662365 3 SS TAMOXIFEN TAMOXIFEN 1 Oral UNKNOWN 0 TABLET
126623651 12662365 4 C ASPIRIN. ASPIRIN 1 Oral 0 81 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126623651 12662365 1 Breast cancer
126623651 12662365 2 Hypertension
126623651 12662365 4 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126623651 12662365 Electrocardiogram T wave inversion
126623651 12662365 Hypertension
126623651 12662365 Syncope

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
126623651 12662365 1 2013 0