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
127275131 12727513 1 I 20160727 0 20160907 20160907 DIR FDA-CTU 83.00 YR M N 81.80000 KG 20160907 N PH 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
127275131 12727513 1 PS NAPROXEN. NAPROXEN 1 Oral Y D 0 1 DF COATED TABLET PRN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127275131 12727513 1 Pain

Outcome of event

Event ID CASEID OUTC COD
127275131 12727513 LT
127275131 12727513 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127275131 12727513 Abdominal pain
127275131 12727513 Asthenia
127275131 12727513 Epistaxis
127275131 12727513 Faeces discoloured
127275131 12727513 Gastric haemorrhage
127275131 12727513 Gastric ulcer haemorrhage
127275131 12727513 Haematemesis
127275131 12727513 Haemoglobin decreased
127275131 12727513 Hiatus hernia
127275131 12727513 Nausea
127275131 12727513 Radiation associated pain

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
127275131 12727513 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127275131 12727513 1 20160727 0