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
127839571 12783957 1 I 20160920 20160927 20160927 EXP DE-ASTRAZENECA-2016SF00583 ASTRAZENECA 56.00 YR F Y 120.00000 KG 20160927 CN DE DE

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
127839571 12783957 1 PS BYETTA EXENATIDE 1 Unknown 21773 SOLUTION FOR INJECTION IN PRE-FILLED PEN
127839571 12783957 2 C RAMIPRIL. RAMIPRIL 1 0 5 MG QD
127839571 12783957 3 C RAMIPRIL. RAMIPRIL 1 0 50 MG QD
127839571 12783957 4 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 0 60 MG QD
127839571 12783957 5 C L-THYROXIN LEVOTHYROXINE SODIUM 1 0 100 UG QD
127839571 12783957 6 C JANUMET METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE 1 100 TWICE A DAY 0
127839571 12783957 7 C METOPROLOL. METOPROLOL 1 0 50 MG BID
127839571 12783957 8 C SILVERBETA 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127839571 12783957 2 Hypertension
127839571 12783957 3 Hypertension
127839571 12783957 8 Hypercholesterolaemia

Outcome of event

Event ID CASEID OUTC COD
127839571 12783957 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127839571 12783957 Diarrhoea
127839571 12783957 Hypotension
127839571 12783957 Intestinal haemorrhage
127839571 12783957 Nausea
127839571 12783957 Vomiting
127839571 12783957 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
127839571 12783957 1 201607 20160918 0
127839571 12783957 3 2010 201008 0
127839571 12783957 4 2010 0
127839571 12783957 5 2010 0