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
127056861 12705686 1 I 20160614 20160824 20160901 20160901 EXP FR-ASTRAZENECA-2016SE91369 ASTRAZENECA 85.00 YR F Y 0.00000 20160901 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
127056861 12705686 1 PS ATACAND CANDESARTAN CILEXETIL 1 Oral 8.0MG UNKNOWN Y 20838 8 MG TABLET
127056861 12705686 2 SS TELMISARTAN. TELMISARTAN 1 Oral 6960 MG Y U 0 80 MG QD
127056861 12705686 3 C CALCIDOSE VITAMIN D CALCIUM CARBONATECHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127056861 12705686 1 Hypertension
127056861 12705686 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127056861 12705686 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127056861 12705686 Acute kidney injury
127056861 12705686 Bacterial colitis
127056861 12705686 Candida infection
127056861 12705686 Chronic gastritis
127056861 12705686 Decreased appetite
127056861 12705686 Dehydration
127056861 12705686 Diarrhoea
127056861 12705686 Diverticulum intestinal
127056861 12705686 Hypokalaemia
127056861 12705686 Hypotension
127056861 12705686 Malnutrition
127056861 12705686 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
127056861 12705686 1 20160716 20160810 0
127056861 12705686 2 20160420 20160715 0