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
125143863 12514386 3 F 20140724 20160825 20160630 20160921 PER US-JNJFOC-20160527930 JANSSEN 69.65 YR E M Y 0.00000 20160921 CN US US

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
125143863 12514386 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 10 MG TABLET
125143863 12514386 2 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 22406 10 MG TABLET QD
125143863 12514386 3 SS IBUPROFEN. IBUPROFEN 1 Oral Y N 19012 UNSPECIFIED
125143863 12514386 4 SS IBUPROFEN. IBUPROFEN 1 Oral Y N 19012 200 MG UNSPECIFIED QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125143863 12514386 1 Deep vein thrombosis
125143863 12514386 2 Deep vein thrombosis
125143863 12514386 4 Pain

Outcome of event

Event ID CASEID OUTC COD
125143863 12514386 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125143863 12514386 Upper gastrointestinal haemorrhage

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
125143863 12514386 1 20141114 0
125143863 12514386 2 20140504 20140724 0
125143863 12514386 4 201407 0