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
125582461 12558246 1 I 20160521 20160705 20160714 20160714 EXP GB-MHRA-EYC 00141769 PHHY2016GB093007 SANDOZ 89.00 YR F Y 0.00000 20160714 OT 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
125582461 12558246 1 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral 20 MG, QD Y U 75757 20 MG QD
125582461 12558246 2 SS RAMIPRIL. RAMIPRIL 1 Oral 5 MG, BID Y U 0 5 MG BID
125582461 12558246 3 SS SPIRONOLACTONE. SPIRONOLACTONE 1 Oral 25 MG, QD Y U 0 25 MG QD
125582461 12558246 4 C AMITRIPTYLINE AMITRIPTYLINE 1 Oral 25 MG, QD U 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125582461 12558246 1 Product used for unknown indication
125582461 12558246 2 Product used for unknown indication
125582461 12558246 3 Product used for unknown indication
125582461 12558246 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125582461 12558246 OT
125582461 12558246 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125582461 12558246 Abdominal tenderness
125582461 12558246 Acute kidney injury
125582461 12558246 Circulatory collapse
125582461 12558246 Mucosal dryness
125582461 12558246 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
125582461 12558246 1 20160521 0
125582461 12558246 2 20160521 0
125582461 12558246 3 20160521 0