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
125596062 12559606 2 F 20160521 20160713 20160715 20160720 EXP GB-MHRA-ADR 23539418 GB-ACCORD-042276 ACCORD 89.00 YR F Y 0.00000 20160720 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
125596062 12559606 1 PS RAMIPRIL. RAMIPRIL 1 Oral Y 202392 5 MG BID
125596062 12559606 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral Y 112043 20 MG QD
125596062 12559606 3 SS SPIRONOLACTONE. SPIRONOLACTONE 1 Oral Y 24025 25 MG QD
125596062 12559606 4 C AMITRIPTYLINE AMITRIPTYLINE 1 Oral 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125596062 12559606 1 Product used for unknown indication
125596062 12559606 2 Product used for unknown indication
125596062 12559606 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125596062 12559606 OT
125596062 12559606 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125596062 12559606 Abdominal tenderness
125596062 12559606 Acute kidney injury
125596062 12559606 Circulatory collapse
125596062 12559606 Mucosal dryness
125596062 12559606 Viral diarrhoea

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
125596062 12559606 1 20160521 0
125596062 12559606 2 20160521 0
125596062 12559606 3 20160521 0