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
127718051 12771805 1 I 201604 20160913 20160922 20160922 EXP GB-MHRA-EYC 00144940 GB-SA-2016SA169873 AVENTIS 85.00 YR E F Y 0.00000 20160922 PH GB GB

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
127718051 12771805 1 PS INDAPAMIDE. INDAPAMIDE 1 Oral IN THE MORNING. Y UNK 18538 2.5 MG QD
127718051 12771805 2 C CANDESARTAN CANDESARTAN 1 0
127718051 12771805 3 C CLOPIDOGREL CLOPIDOGREL BISULFATE 1 0
127718051 12771805 4 C PARACETAMOL ACETAMINOPHEN 1 0
127718051 12771805 5 C PRAVASTATIN. PRAVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127718051 12771805 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127718051 12771805 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127718051 12771805 Atrial fibrillation
127718051 12771805 Circulatory collapse
127718051 12771805 Hypokalaemia
127718051 12771805 Hyponatraemia

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
127718051 12771805 1 20160501 0