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
125423141 12542314 1 I 2016 20160630 20160708 20160708 EXP FR-ASTRAZENECA-2016SE72830 ASTRAZENECA 78.00 YR F Y 0.00000 20160709 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
125423141 12542314 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 19390 MG Y U 21366 10 MG TABLET QD
125423141 12542314 2 C AMLODIPINE AMLODIPINE BESYLATE 1 Oral 0 10 MG QD
125423141 12542314 3 C BISOPROLOL BISOPROLOL 1 Oral 0 10 MG QD
125423141 12542314 4 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Oral 0 25 MG QD
125423141 12542314 5 C LEVOTHYROXINE. LEVOTHYROXINE 1 Oral 100 MCG AND 25 MCG (UNCHANGED) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125423141 12542314 1 Dyslipidaemia

Outcome of event

Event ID CASEID OUTC COD
125423141 12542314 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125423141 12542314 Asthenia
125423141 12542314 Blood creatine phosphokinase increased
125423141 12542314 General physical health deterioration
125423141 12542314 Muscle fatigue
125423141 12542314 Myalgia
125423141 12542314 Nausea
125423141 12542314 Rash

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
125423141 12542314 1 20101110 20160301 0