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
122113894 12211389 4 F 2016 20160705 20160325 20160713 EXP BR-ASTRAZENECA-2016SE32134 ASTRAZENECA 61.00 YR F Y 0.00000 20160713 CN BR BR

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
122113894 12211389 1 PS ATACAND CANDESARTAN CILEXETIL 1 Oral 20838 8 MG TABLET QD
122113894 12211389 2 SS ATACAND CANDESARTAN CILEXETIL 1 Oral 20838 16 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122113894 12211389 1 Blood pressure abnormal
122113894 12211389 2 Blood pressure abnormal

Outcome of event

Event ID CASEID OUTC COD
122113894 12211389 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122113894 12211389 Blood pressure increased
122113894 12211389 Cough
122113894 12211389 Drug dose omission
122113894 12211389 Duodenitis
122113894 12211389 Erosive oesophagitis
122113894 12211389 Gastritis
122113894 12211389 Gastrooesophageal reflux disease
122113894 12211389 Helicobacter infection

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
122113894 12211389 2 2012 0