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
116624254 11662425 4 F 2007 20160627 20151027 20160711 EXP NO-SUN PHARMACEUTICAL INDUSTRIES LTD-2015RR-105136 RANBAXY 0.00 Y 0.00000 20160711 OT NO NO

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
116624254 11662425 1 PS Pantoprazole PANTOPRAZOLE SODIUM 1 Unknown UNK N U 200794
116624254 11662425 2 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Unknown 40 MG, UNK N U 0 40 MG
116624254 11662425 3 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Unknown 20 MG, DAILY N U 0 20 MG
116624254 11662425 4 SS PANTOZOL PANTOPRAZOLE SODIUM 1 Unknown UNK N U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116624254 11662425 1 Gastrooesophageal reflux disease
116624254 11662425 2 Gastrooesophageal reflux disease
116624254 11662425 3 Gastrooesophageal reflux disease
116624254 11662425 4 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
116624254 11662425 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116624254 11662425 Osteoporosis
116624254 11662425 Pain
116624254 11662425 Paraesthesia
116624254 11662425 Peripheral swelling
116624254 11662425 Tendonitis

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
116624254 11662425 1 2003 2007 0
116624254 11662425 2 2007 2012 0
116624254 11662425 3 2012 2013 0
116624254 11662425 4 2003 2007 0