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
125873601 12587360 1 I 1998 20160713 20160725 20160725 EXP GB-MHRA-EYC 00140586 GB-TEVA-677540ACC TEVA 55.00 YR M Y 75.00000 KG 20160725 CN 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
125873601 12587360 1 PS LANSOPRAZOLE. LANSOPRAZOLE 1 Oral THE DOSE WAS REDUCED FROM 30 TO 15MG AND THEN GRADUALLY WEANED HIMSELF OFF THAT U VARIOUS 77255 30 MG
125873601 12587360 2 C COLLAGEN COLLAGEN 1 0 200 MG
125873601 12587360 3 C GLUCOSAMINE SULPHATE GLUCOSAMINE 1 0 1 G
125873601 12587360 4 C RAMIPRIL. RAMIPRIL 1 0 10 MG
125873601 12587360 5 C SIMVASTATIN. SIMVASTATIN 1 0 40 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125873601 12587360 1 Barrett's oesophagus

Outcome of event

Event ID CASEID OUTC COD
125873601 12587360 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125873601 12587360 Arthralgia
125873601 12587360 Gout
125873601 12587360 Joint swelling
125873601 12587360 Pain in extremity

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
125873601 12587360 1 19980301 201507 0