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
126083711 12608371 1 I 20160615 20160615 20160729 20160729 EXP JP-ASTRAZENECA-2016SE72099 ASTRAZENECA 34077.00 DY F Y 52.00000 KG 20160729 PH JP JP

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
126083711 12608371 1 PS FASLODEX FULVESTRANT 1 Intramuscular 2500 MG Y U 21344 500 MG INJECTION
126083711 12608371 2 C FARESTON TOREMIFENE CITRATE 1 Unknown DOSE UNKNOWN 0
126083711 12608371 3 C AZILVA AZILSARTAN KAMEDOXOMIL 1 Oral 0 20 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126083711 12608371 1 Breast cancer female
126083711 12608371 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126083711 12608371 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126083711 12608371 Gait disturbance
126083711 12608371 Muscle spasms
126083711 12608371 Muscular weakness
126083711 12608371 Myalgia
126083711 12608371 Oedema peripheral

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
126083711 12608371 1 20160128 20160615 0