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
125218611 12521861 1 I 20160612 20160623 20160701 20160701 EXP GB-MHRA-EYC 00141222 GB-SA-2016SA118569 AVENTIS 84.00 YR E F Y 0.00000 20160701 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
125218611 12521861 1 PS INDAPAMIDE. INDAPAMIDE 1 Oral Y UNK 18538 2.5 MG
125218611 12521861 2 C ADCAL-D3 CALCIUM CARBONATECHOLECALCIFEROL 1 0
125218611 12521861 3 C ALENDRONIC ACID ALENDRONIC ACID 1 0
125218611 12521861 4 C AMLODIPINE AMLODIPINE BESYLATE 1 0
125218611 12521861 5 C CEFALEXIN CEPHALEXIN 1 0
125218611 12521861 6 C DOSULEPIN HYDROCHLORIDE DOTHIEPIN HYDROCHLORIDE 1 0
125218611 12521861 7 C LATANOPROST. LATANOPROST 1 0
125218611 12521861 8 C LOSARTAN. LOSARTAN 1 0
125218611 12521861 9 C OMEPRAZOLE SODIUM OMEPRAZOLE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125218611 12521861 1 Essential hypertension

Outcome of event

Event ID CASEID OUTC COD
125218611 12521861 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125218611 12521861 Haematemesis
125218611 12521861 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
125218611 12521861 1 20160608 20160613 0