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
127891961 12789196 1 I 20160607 20160915 20160928 20160928 EXP GB-MHRA-EYC 00145051 GB-TEVA-694375ACC TEVA 77.00 YR M Y 0.00000 20160928 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
127891961 12789196 1 PS ATORVASTATIN ATORVASTATIN 1 Oral 10 MILLIGRAM DAILY; AT NIGHT. Y U 78773 10 MG QD
127891961 12789196 2 SS FUROSEMIDE. FUROSEMIDE 1 Oral 20 MILLIGRAM DAILY; EVERY MORNING. U 0 20 MG QD
127891961 12789196 3 SS RAMIPRIL. RAMIPRIL 1 Oral 10 MILLIGRAM DAILY; EVERY MORNING. Y U 0 10 MG QD
127891961 12789196 4 C ADCAL-D3 CALCIUM CARBONATECHOLECALCIFEROL 1 0
127891961 12789196 5 C AMLODIPINE AMLODIPINE BESYLATE 1 0
127891961 12789196 6 C ATENOLOL. ATENOLOL 1 0
127891961 12789196 7 C BISACODYL. BISACODYL 1 0
127891961 12789196 8 C CARMELLOSE 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127891961 12789196 1 Hypercholesterolaemia
127891961 12789196 2 Oedema peripheral
127891961 12789196 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127891961 12789196 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127891961 12789196 Acute kidney injury
127891961 12789196 Asthenia
127891961 12789196 Dizziness
127891961 12789196 Dyspnoea
127891961 12789196 Fall
127891961 12789196 Hyponatraemia
127891961 12789196 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
127891961 12789196 1 20160609 0