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
126071641 12607164 1 I 20160521 20160726 20160729 20160729 EXP 2016-001212 WARNER CHILCOTT WARNER CHILCOTT 19.00 YR M Y 0.00000 20160729 MD JP JP

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
126071641 12607164 1 PS BENET RISEDRONATE SODIUM 1 Oral U 20835 75 MG TABLET
126071641 12607164 2 SS PREDONINE PREDNISOLONEPREDNISOLONE ACETATEPREDNISOLONE SODIUM SUCCINATE 1 Unknown 0 30 MG
126071641 12607164 3 SS PARIET RABEPRAZOLE SODIUM 1 Oral 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126071641 12607164 1 Osteoporosis prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126071641 12607164 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126071641 12607164 Discomfort
126071641 12607164 Dyspnoea
126071641 12607164 Hepatic function abnormal
126071641 12607164 Internal haemorrhage
126071641 12607164 Nausea
126071641 12607164 Purpura
126071641 12607164 Pyrexia

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
126071641 12607164 2 20160517 0