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
127772881 12777288 1 I 20160607 20160915 20160924 20160924 EXP GB-MHRA-ADR 23639695 GB-ACCORD-044214 ACCORD 77.00 YR M Y 0.00000 20160924 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
127772881 12777288 1 PS RAMIPRIL. RAMIPRIL 1 Oral EVERY MORNING. Y 202392 10 MG QD
127772881 12777288 2 SS FUROSEMIDE. FUROSEMIDE 1 Oral EVERY MORNING. 2147483647 20 MG QD
127772881 12777288 3 SS ATORVASTATIN ATORVASTATIN 1 Oral AT NIGHT. Y 0 10 MG QD
127772881 12777288 4 C ADCAL-D3 CALCIUM CARBONATECHOLECALCIFEROL 1 0
127772881 12777288 5 C AMLODIPINE AMLODIPINE BESYLATE 1 0
127772881 12777288 6 C ATENOLOL/ATENOLOL HYDROCHLORIDE 2 0
127772881 12777288 7 C BISACODYL. BISACODYL 1 0
127772881 12777288 8 C CARMELLOSE/CARMELLOSE CALCIUM/CARMELLOSE SODIUM 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127772881 12777288 1 Hypertension
127772881 12777288 2 Oedema peripheral
127772881 12777288 3 Hypercholesterolaemia

Outcome of event

Event ID CASEID OUTC COD
127772881 12777288 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127772881 12777288 Acute kidney injury
127772881 12777288 Asthenia
127772881 12777288 Dizziness
127772881 12777288 Dyspnoea
127772881 12777288 Fall
127772881 12777288 Hyponatraemia
127772881 12777288 Rhabdomyolysis

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
127772881 12777288 3 20160609 0