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
115565035 11556503 5 F 20080703 20160827 20150925 20160904 EXP US-DSJP-DSU-2015-129601 DAIICHI 0.00 Y 0.00000 20160903 MD 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
115565035 11556503 1 PS BENICAR OLMESARTAN MEDOXOMIL 1 Oral 40 MG, QD 21286 40 MG TABLET QD
115565035 11556503 2 C ASPIRIN /00002701/ ASPIRIN 1 325 MG, QD 0 325 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115565035 11556503 1 Hypertension
115565035 11556503 2 Coagulopathy

Outcome of event

Event ID CASEID OUTC COD
115565035 11556503 HO
115565035 11556503 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115565035 11556503 Acute kidney injury
115565035 11556503 Decreased appetite
115565035 11556503 Depression
115565035 11556503 Diarrhoea haemorrhagic
115565035 11556503 Diverticulum intestinal
115565035 11556503 Gastrointestinal wall thickening
115565035 11556503 Hypotension
115565035 11556503 Malabsorption
115565035 11556503 Pyrexia
115565035 11556503 Retching
115565035 11556503 Surgery
115565035 11556503 Umbilical hernia

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
115565035 11556503 1 200409 20150619 0