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
125812542 12581254 2 F 20160702 20160729 20160721 20160805 EXP FR-ASTRAZENECA-2016SE75919 ASTRAZENECA 33523.00 DY M Y 0.00000 20160805 MD FR FR

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
125812542 12581254 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 10 MG TABLET QD
125812542 12581254 2 SS PREVISCAN FLUINDIONE 1 Oral Y U 0 .5 DF QD
125812542 12581254 3 C UROREC SILODOSIN 1 8.0MG UNKNOWN 0 8 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125812542 12581254 1 Dyslipidaemia
125812542 12581254 2 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
125812542 12581254 LT
125812542 12581254 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125812542 12581254 Arthralgia
125812542 12581254 Asthenia
125812542 12581254 Confusional state
125812542 12581254 Fall
125812542 12581254 Haemorrhagic anaemia
125812542 12581254 International normalised ratio increased
125812542 12581254 Muscle haemorrhage
125812542 12581254 Urinary retention

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
125812542 12581254 2 20160702 0
125812542 12581254 3 201606 0