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
127786081 12778608 1 I 20160909 20160920 20160926 20160926 EXP GB-MHRA-ADR 23647006 GB-ACCORD-044345 ACCORD 51.00 YR M Y 95.00000 KG 20160926 MD 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
127786081 12778608 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 202553 5 MG
127786081 12778608 2 C ATENOLOL/ATENOLOL HYDROCHLORIDE 2 EACH MORNING 50 MG 0 50 MG QD
127786081 12778608 3 C LANSOPRAZOLE. LANSOPRAZOLE 1 EACH EVENING 1 DF 0 1 DF QD
127786081 12778608 4 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 EVERY 6-8 HOURS 0 1 DF
127786081 12778608 5 C RAMIPRIL. RAMIPRIL 1 2.5 MG 0 2.5 MG QD
127786081 12778608 6 C SIMVASTATIN. SIMVASTATIN 1 AT NIGHT 878 DF 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127786081 12778608 1 Hypertension
127786081 12778608 2 Hypertension
127786081 12778608 3 Gastric pH decreased
127786081 12778608 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127786081 12778608 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127786081 12778608 Headache

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
127786081 12778608 1 20140430 0
127786081 12778608 2 20160909 0
127786081 12778608 3 20160909 0
127786081 12778608 4 20160909 0
127786081 12778608 5 20160909 0
127786081 12778608 6 20140415 20160909 0