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
124919082 12491908 2 F 1998 20160713 20160623 20160727 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-118939 RANBAXY 55.00 YR M Y 75.00000 KG 20160727 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
124919082 12491908 1 PS LANSOPRAZOLE. LANSOPRAZOLE 1 Oral THE DOSE WAS REDUCED FROM 30 TO 15 MG AND THEN GRADUALLY WEANED HIMSELF OFF THAT VARIOUS 202637 30 MG
124919082 12491908 2 C COLLAGEN COLLAGEN 1 Unknown 200 MG, UNK U U 0 200 MG
124919082 12491908 3 C GLUCOSAMINE SULPHATE GLUCOSAMINE 1 Unknown 1 G, UNK U U 0 1 G
124919082 12491908 4 C RAMIPRIL. RAMIPRIL 1 Unknown 10 MG, UNK U U 0 10 MG
124919082 12491908 5 C SIMVASTATIN. SIMVASTATIN 1 Unknown 40 MG, UNK U U 0 40 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124919082 12491908 1 Barrett's oesophagus
124919082 12491908 2 Product used for unknown indication
124919082 12491908 3 Product used for unknown indication
124919082 12491908 4 Product used for unknown indication
124919082 12491908 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124919082 12491908 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124919082 12491908 Arthralgia
124919082 12491908 Gout
124919082 12491908 Joint swelling
124919082 12491908 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
124919082 12491908 1 19980301 201507 0